WO2016112870A1 - Molecular constructs with targeting and effector elements - Google Patents

Molecular constructs with targeting and effector elements Download PDF

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Publication number
WO2016112870A1
WO2016112870A1 PCT/CN2016/071184 CN2016071184W WO2016112870A1 WO 2016112870 A1 WO2016112870 A1 WO 2016112870A1 CN 2016071184 W CN2016071184 W CN 2016071184W WO 2016112870 A1 WO2016112870 A1 WO 2016112870A1
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WO
WIPO (PCT)
Prior art keywords
molecular construct
collagen
linked
group
targeting
Prior art date
Application number
PCT/CN2016/071184
Other languages
French (fr)
Inventor
Tse-Wen Chang
Hsing-Mao CHU
Jou-Han CHEN
Chun-Yu Lin
Chien-Jen Lin
Original Assignee
Tse-Wen Chang
Chu Hsing-Mao
Chen Jou-Han
Chun-Yu Lin
Chien-Jen Lin
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Tse-Wen Chang, Chu Hsing-Mao, Chen Jou-Han, Chun-Yu Lin, Chien-Jen Lin filed Critical Tse-Wen Chang
Priority to RU2017128109A priority Critical patent/RU2696378C2/en
Priority to JP2017537448A priority patent/JP6313530B1/en
Priority to SG11201705323WA priority patent/SG11201705323WA/en
Priority to EP16737095.6A priority patent/EP3244925A4/en
Priority to AU2016207112A priority patent/AU2016207112B2/en
Priority to CN201680004702.4A priority patent/CN107106683B/en
Priority to CA2968141A priority patent/CA2968141C/en
Priority to RU2017144294A priority patent/RU2703952C2/en
Priority to CA2986486A priority patent/CA2986486C/en
Priority to PCT/CN2016/082785 priority patent/WO2016184426A1/en
Priority to EP16795913.9A priority patent/EP3297670A4/en
Priority to JP2018512473A priority patent/JP6602958B2/en
Priority to CN201680029187.5A priority patent/CN107847588B/en
Priority to AU2016264649A priority patent/AU2016264649B2/en
Priority to JP2018511272A priority patent/JP2018527350A/en
Priority to AU2016316202A priority patent/AU2016316202B2/en
Priority to CN201680055855.1A priority patent/CN108431045B/en
Priority to CA2996652A priority patent/CA2996652A1/en
Priority to PCT/CN2016/090296 priority patent/WO2017036255A1/en
Priority to EP16840684.1A priority patent/EP3344659A4/en
Publication of WO2016112870A1 publication Critical patent/WO2016112870A1/en
Priority to IL253295A priority patent/IL253295A0/en
Priority to IL255785A priority patent/IL255785B/en
Priority to IL257751A priority patent/IL257751B/en
Priority to HK18102897.0A priority patent/HK1244425A1/en
Priority to AU2018217311A priority patent/AU2018217311B2/en
Priority to HK18112368.9A priority patent/HK1254280A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
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    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
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Definitions

  • the present disclosure relates to the field of pharmaceuticals; more particularly, to multi-functional molecular constructs, e.g., those having targeting and effector elements for delivering the effector (e.g., therapeutic drug) to targeted sites.
  • multi-functional molecular constructs e.g., those having targeting and effector elements for delivering the effector (e.g., therapeutic drug) to targeted sites.
  • antibodies can neutralize or trap disease-causing mediators, which may be cytokines or immune components present in the blood circulation, interstitial space, or in the lymph nodes.
  • the neutralizing activity inhibits the interaction of the disease-causing mediators with their receptors.
  • fusion proteins of the soluble receptors or the extracellular portions of receptors of cytokines and the Fc portion of IgG which act by neutralizing the cytokines or immune factors in a similar fashion as neutralizing antibodies, have also been developed as therapeutic agents.
  • Fc-mediated mechanisms such as antibody-dependent cellular cytotoxicity (ADCC) and complement-mediated cytolysis (CMC) , are not the intended mechanisms for the antibodies.
  • ADCC antibody-dependent cellular cytotoxicity
  • CMC complement-mediated cytolysis
  • Some therapeutic antibodies bind to certain surface antigens on target cells and render Fc-mediated functions and other mechanisms on the target cells.
  • the most important Fc-mediated mechanisms are antibody-dependent cellular cytotoxicity (ADCC) and complement-mediated cytolysis (CMC) , which both will cause the lysis of the antibody-bound target cells.
  • ADCC antibody-dependent cellular cytotoxicity
  • CMC complement-mediated cytolysis
  • Some antibodies binding to certain cell surface antigens can induce apoptosis of the bound target cells.
  • Antibodies can also serve as carriers of cytotoxic molecules or other therapeutic agents without the antibodies’s erving obvious therapeutic effector functions. In general, those antibodies bind to “tumor-associated” antigens on target cells, but cannot cause cell lysis by themselves. Antibodies specific for CD19 and CD22 on B lymphomas are well known. For many years, those antibodies have been explored as carriers for cytotoxic agents, including radioactive nuclides with very short half-lives, such as 90 Y, 131 I, and 177 Lu. Some antibodies have also been studied as targeting agents for liposomes loaded with cytotoxic drugs, such as doxorubicin, paclitaxel, and amphotericin B.
  • cytotoxic drugs such as doxorubicin, paclitaxel, and amphotericin B.
  • ADC antibody drug conjugates
  • the cytotoxic drug molecules are linked non-selectively to cysteine or lysine residues in the antibody, thereby resulting in a heterogeneous mixture of ADCs with different numbers of drug molecules per ADC.
  • This approach leads to some safety and efficacy issues.
  • the first FDA-approved ADC, gemtuzumab ozogamicin, for treating acute myelogenous leukemia is now withdrawn from the market due to unacceptable toxicity.
  • the bi-valent or multivalent antibodies may contain two or more antigen-binding sites.
  • a number of methods have been reported for preparing multivalent antibodies by covalently linking three or four Fab fragments via a connecting structure.
  • antibodies have been engineered to express tandem three or four Fab repeats.
  • the present disclosure is directed to a linker unit that has at least two different functional elements linked thereto.
  • the linker unit may have linked thereto two different effector elements, one targeting element and one effector element, or one effector element and a polyethylene glycol (PEG) chain for prolonging the circulation time of the linker unit.
  • PEG polyethylene glycol
  • the present linker unit is designed to have at least two different functional groups such that the functional elements can be linked thereto by reacting with the respective functional groups. Accordingly, the present linker unit can serve as a platform for preparing a molecular construct with two or more functional elements.
  • the linker unit comprises a center core and a plurality of linking arms.
  • the center core is a polypeptide core comprising (1) a plurality of lysine (K) resides, in which each K residue and a next K residue are separated by a filler sequence comprising glycine (G) and serine (S) residues, and the number of K residues ranges from 2 to 15; or (2) the sequence of (X aa -K) n , where X aa is a PEGylated amino acid having 2 to 12 repeats of ethylene glycol (EG) unit, and n is an integral from 2 to 15.
  • the filler sequence consists of 2 to 20 amino acid residues.
  • the filler sequence may have the sequence of GS, GGS, GSG, or SEQ ID NOs: 1-16.
  • the center core comprises 2-15 units of the sequence of G 1-5 SK; preferably, the center core comprises the sequence of (GSK) 2-15 .
  • Each of the linking arms is linked to the K residues of the center core via forming an amide linkage between the K residue and the linking arm.
  • the linking arm linked to the center core has a maleimide group at its free-terminus.
  • the linking arm is a PEG chain, preferably having 2 to 20 repeats of EG units.
  • the coupling linking arm is a PEG chain, preferably having 2 to 12 repeats of EG units.
  • amino acid residues having the azide group include L-azidohomoalanine (AHA) , 4-azido-L-phenylalanine, 4-azido-D-phenylalanine, 3-azido-L-alanine, 3-azido-D-alanine, 4-azido-L-homoalanine, 4-azido-D-homoalanine, 5-azido-L-ornithine, 5-azido-d-ornithine, 6-azido-L-lysine, and 6-azido-D-lysine.
  • AHA L-azidohomoalanine
  • 4-azido-L-phenylalanine 4-azido-D-phenylalanine, 3-azido-L-alanine, 3-azido-D-alanine
  • 4-azido-L-homoalanine 4-azido-D-homoalan
  • the strained alkyne group at the free terminus of the coupling arm may be, a cyclooctene group, such as trans-cyclooctene (TCO) group; or a cyclooctyne group, e.g. dibenzocyclooctyne (DBCO) , difluorinated cyclooctyne (DIFO) , bicyclononyne (BCN) , and dibenzocyclooctyne (DICO) group.
  • TCO trans-cyclooctene
  • DBCO dibenzocyclooctyne
  • DIFO difluorinated cyclooctyne
  • BCN bicyclononyne
  • DICO dibenzocyclooctyne
  • the tetrazine group at the free terminus of the coupling arm includes, but is not limited to, 1, 2, 3, 4-tetrazine, 1, 2, 3, 5-tetrazine, and 1, 2, 4, 5-tetrazine, and derivatives thereof, such as, 6-methyl tetrazine.
  • the linker unit further comprises a plurality of first elements.
  • Each of the first elements is linked to one of the linking arms via thiol–maleimide reaction.
  • the first element is an effector element suitable for eliciting an intended effect (e.g., a therapeutic effect) in a subject.
  • the first element may be a targeting element for directing the linker unit to the site of interest.
  • the linker unit further comprises a second element that is different from the first elements.
  • the second element has an azide or alkyne group, so that it is linked to the center core or the coupling arm by coupling with the corresponding alkyne or azide group of the center core or the coupling arm in the presence of Cu (I) as a catalyst in a reaction referred to as “Cu (I) azide-alkyne click chemistry (CuAAC) reaction.
  • the second element when the first element is an effector element, then the second element may be another effector element, which works additively or synergistically with or independently of the first element; alternatively, the second element may be a targeting element or an element for improving the pharmacokinetic property of the linker unit, such as solubility, clearance, half-life, and bioavailability.
  • the first element when the targeting element, then the second element is preferably an effector element or an element for improving the pharmacokinetic property of the linker unit.
  • the linker unit further comprises an optional third element that is different from the first and second elements.
  • the other terminus (i.e., the free terminus that is not linked with the second element) of the center core is optionally a cysteine residue, which can be used to introduce an optional third element.
  • the thiol group of the cysteine residue is reacted with a maleimide group of a PEG chain; and the thus-linked PEG chain is designated as the coupling arm, which has a tetrazine group or a strained alkyne group at its free terminus.
  • the third element is then linked to the coupling arm via iEDDA reaction.
  • the linker unit comprises both the second and third elements
  • at least one of the first and second elements is an effector as described above
  • the third element may be the element for improving the pharmacokinetic property of the linker unit.
  • the element for improving the pharmacokinetic property is a long PEG chain having a molecular weight of about 20,000 to 50,000 daltons.
  • the linker unit according to the first aspect of the present disclosure may find its utility in clinical medicine for the treatment of various diseases.
  • the second aspect of the present disclosure is directed to a method for treating these diseases.
  • the method for treating a particular disease includes the step of administering to the subject in need thereof a therapeutically effective amount of the linker unit according to the above-mentioned aspect and embodiments of the present disclosure.
  • said linker unit may be administered in a pharmaceutical formulation, which comprises a pharmaceutically-acceptable excipient suitable for the intended or desired administration route, in addition to the present linker unit.
  • the present molecular construct is useful in treating an immune disorder, in which the first element is a single-chain variable fragment (scFv) specific for a cytokine or a receptor of the cytokine; or a soluble receptor of the cytokine, while the second element is an scFv specific for a tissue-associated extracellular matrix protein.
  • the first element is an effector element for treating one or more immune disorders
  • the second element is a targeting element that facilitates the delivery of the linker unit to the disease site.
  • Non-limiting examples of the cytokine include tumor necrosis factor- ⁇ (TNF- ⁇ ) , interleukin-17 (IL-17) , IL-1, IL-6, IL-12/IL-23, and B cell activating factor (BAFF)
  • TNF- ⁇ tumor necrosis factor- ⁇
  • IL-17 interleukin-17
  • BAFF B cell activating factor
  • non-limiting examples of the cytokine receptor is the receptor specific for IL-6 (i.e., IL-6R) or IL-17 (i.e., IL-17R)
  • the soluble receptor of a cytokine examples of which include, but are not limited to, the soluble receptor of the cytokine specific for TNF- ⁇ or IL-1.
  • Illustrative examples of the tissue-associated extracellular matrix protein include, but are not limited to, ⁇ -aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, and collagen XI.
  • the first element is an scFv specific for TNF- ⁇ , IL-12/IL-23, IL-17, or IL-17R; and the second element is an scFv specific for collagen I or collagen VII.
  • the linker units suitable for treating immune disorders such as systemic lupus erythematosus (SLE) , cutaneous lupus or Sjogren’s syndrome comprises an scFv specific for BAFF as the first element and an scFv specific for collagen I or collagen VII as the second element.
  • the illustrative linker units comprises the first element, which is an scFv specific for TNF- ⁇ , IL-1, IL-6, IL-12/IL-23, IL-17, IL-6R, or IL-17R; and the second element, which is an scFv specific for collagen II, collagen IX, collagen XI, or ⁇ -aggrecan.
  • the linker units are also suitable for treating inflammatory bowel diseases, e.g., Crohn’s disease and ulcerative colitis, among others.
  • the present linker unit uses an scFv specific for TNF- ⁇ as the first element, and an scFv specific for collagen III or collagen V as the second element.
  • Another set of diseases treatable by the present linker unit is diffused tumor, including, but not limited to, acute lymphocytic leukemia (ALL) , chronic lymphocytic leukemia (CLL) , acute myelogenous leukemia (AML) , chronic myelogenous leukemia (CML) , Hodgkin lymphoma, non-Hodgkin lymphoma, and myeloma.
  • the first element may be a targeting element such as an scFv specific for a first cell surface antigen
  • the second element may be an effector element such as an scFv specific for a second cell surface antigen.
  • the first cell surface antigen suitable for use as the targeting element for treating diffused tumors includes, but is not limited to, CD5, CD19, CD20, CD22, CD23, CD27, CD30, CD33, CD34, CD37, CD38, CD43, CD72a, CD78, CD79a, CD79b, CD86, CD134, CD137, CD138, and CD319.
  • non-limiting examples of the second cell surface antigen suitable for use as the effector element include CD3 and CD16a.
  • the illustrative first element is an scFv specific for CD5, CD19, CD20, CD22, CD23, CD30, CD37, CD79a, or CD79b
  • the illustrative second element is an scFv specific for CD3 or CD16a.
  • the illustrative first element is an scFv specific for CD38, CD78, CD138, or CD319
  • the illustrative second element is an scFv specific for CD3 or CD16a.
  • the illustrative first element for the treatment thereof is an scFv specific for CD5, CD30, or CD43, while the second element is an scFv specific for CD3 or CD16a.
  • the illustrative first element is an scFv specific for CD33 or CD34, while the illustrative second element is an scFv specific for CD3 or CD16a.
  • Still another set of diseases that may be treated by the present linker unit is solid tumor, including, but not limited to, melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, and head and neck squamous cell carcinoma. Additionally, the present linker unit is also suitable for treating advanced, malignant, or metastatic solid tumors.
  • the first element i.e., the targeting element
  • the second element i.e., the effector element
  • the peptide hormone is secretin, cholecystokinin (CCK) , somatostatin, or thyroid-stimulating hormone (TSH) .
  • the growth factor it may be the epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , vascular endothelial growth factor A (VEGF-A) , basic fibroblast growth factor (bFGF) , or hepatocyte growth factor (HGF) .
  • tumor-associated antigen examples include epidermal growth factor receptor (HER1) , HER2, HER3, HER4, carbohydrate antigen 19-9 (CA 19-9) , carbohydrate antigen 125 (CA 125) , carcinoembryonic antigen (CEA) , mucin 1 (MUC 1) , ganglioside GD2, melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) , mesothelin, mucine-related Tn, Sialyl Tn, Globo H, stage-specific embryonic antigen-4 (SSEA-4) , and epithelial cell adhesion molecule (EpCAM) .
  • the cell surface antigen it can be CD3 or CD16a.
  • the tumor-associated antigen may be shed from the solid tumor of a subject and wanders into his/her circulation system.
  • the present method for treating solid tumor comprises the step of, (a) subjecting the subject to a blood dialysis procedure using an antibody specific for one or more tumor-associated antigens to remove the tumor-associated antigens that are shed from the tumor and wanders into the circulation of the subject; and (b) administering the present linker unit for treating the solid tumor.
  • Illustrative linker units suitable for treating osteoporosis include a first element (in this case, an effector element) that is a first scFv specific for receptor activator of nuclear factor ⁇ B (RANKL) ; and a second element (or a targeting element) that is a second scFv specific for collagen I or osteonectin.
  • a first element in this case, an effector element
  • RNKL nuclear factor ⁇ B
  • second element or a targeting element
  • Age-related macular degeneration is another example of the diseases treatable by the present linker unit.
  • Illustrative linker units suitable for treating AMD include a first element of an scFv specific for VEGF-A, and a second element of a long PEG chain having a molecular weight of about 20,000 to 50,000 daltons.
  • the first element is the effector element for treating AMD, while the second element is used to enhance the pharmacokinetic property of the linker unit.
  • the present disclosure is directed to a molecular construct comprising two linker units coupling to each other either directly or indirectly, in which the core of one linker unit is configured to be linked with at least one targeting element while the core of the other linker unit is configured to be linked with at least one effector element.
  • the present molecular construct is advantageous in that the two linker units are coupled to each other via an iEDDA reaction, a SPAAC reaction, or a CuAAC reaction. This design allows for a facile synthesis of a molecular construct with a complex structure.
  • the two linker units respectively carrying different numbers and/or types of functional elements can be independently prepared, and then conjugated together.
  • the molecular construct comprises a first linker unit and a second linker unit.
  • the first linker unit comprises a first center core and one or more linking arms (hereinafter, the first linking arms) and optionally a coupling arm (hereinafter, the first coupling arms) that are respectively linked to the first center core;
  • the second linker unit comprises a second center core and one or more linking arms (hereinafter, the second linking arms) and optionally a coupling arm (hereinafter, the second coupling arm) that are respectively linked to the second center core.
  • the first and second linker units are coupled to each other via iEDDA, SPAAC, or CuAAC reaction occurred between any of the followings: the first and second center cores, the first coupling arm and the second center core, the first and second coupling arms, or the first center core and the second coupling arm.
  • both the first and second center cores have a plurality of amine groups.
  • Each of the linking arms is linked to the center core via forming an amide bond therebetween, for example, between the N-hydroxysuccinimydyl (NHS) group and the amine group.
  • the linking arm After being linked to the center core, the linking arm thus has a maleimide group at the free terminus thereof.
  • a first targeting element and a first effector element are respectively linked to the first and second linking arms via thiol–maleimide reaction.
  • each of the linking arms is a PEG chain having 2-20 repeats of EG units.
  • each of the coupling arms is a PEG chain having 2-12 repeats of EG units.
  • each of the first and second center cores may be a compound core or a polypeptide core.
  • both the first and second center cores are compounds cores of the same or different compound (s) .
  • both the first and second center cores are polypeptide cores having the same or different sequence (s) .
  • one of the two cores is a compound core, while the other is a polypeptide core.
  • Non-limiting examples of the compound suitable for use as the present compound core include, benzene-1, 3, 5-triamine, 2- (aminomethyl) -2-methylpropane-1, 3-diamine, tris (2-aminoethyl) -amine, benzene-1, 2, 4, 5-tetraamine, 3, 3' , 5, 5'-tetraamine-1, 1'-biphenyl, tetrakis- (2-aminoethyl) methane, tetrakis (ethylamine) -hydrazine, N, N, N' , N' , -tetrakis-(aminoethyl) -ethylenediamine, benzene-1, 2, 3, 4, 5, 6-hexaamine, 1-N, 1-N, 3-N, 3-N, 5-N, 5-N-hexakis- (methylamine) -benzene-1, 3, 5-triamine, 1-N, 1-N, 2-N, 2-N, 4-N, 4-N, 5-
  • the coupling arm is linked to one of the plurality of amine groups of the center core by forming an amide bond between the coupling arm and the center core.
  • the free terminus of the coupling arm has an azide, an alkyne, a strained alkyne, or a tetrazine group.
  • the polypeptide suitable for use as the present polypeptide core comprises a plurality of lysine (K) residues; optionally, 2 to 15 K residues. Also, each K residue and the next K residue are separated by a filler sequence comprising glycine (G) and serine (S) residues; optionally, the filler sequence consists of 2 to 20 amino acid residues.
  • the filler sequence may have the sequence of GS, GGS, GSG, or SEQ ID NOs: 1-16.
  • the polypeptide comprises 2-15 units of the sequence of G 1-5 SK, for example, (GSK) 2-15 .
  • the polypeptide core has the sequence of SEQ ID NOs: 17, 18, 19, 21, 22, 23, or 24.
  • the polypeptide core may comprise the sequence of (X aa -K) n , where X aa is a PEGylated amino acid having 2 to 12 repeats of ethylene glycol (EG) unit, and n is an integral from 2 to 15.
  • the polypeptide core has the sequence of SEQ ID NO: 25 or 26.
  • the center core is a polypeptide core, it may comprise a cysteine residue at its N-or C-terminus.
  • the coupling arm is linked to the cysteine residue of the center core via the thiol-maleimide reaction.
  • the coupling arm linked to the cysteine residue has an azide, an alkyne, a strained alkyne, or a tetrazine group at the free-terminus thereof.
  • the first and second linker units may be coupled via various configurations, which are described in detail below, depending on the presence or absence of the first and second coupling arms.
  • a linker unit having a compound core it is preferable that it is linked with another linker unit via a coupling arm (i.e., the first or second coupling arm) , while for a linker unit having a polypeptide core, the need for a coupling arm becomes optional.
  • first and second linker units respectively comprise the coupling arms
  • one of the coupling arms (say, for example, the first coupling arm) has a tetrazine group at the free-terminus thereof
  • the other coupling arm (in this case, the second coupling arm) has a strained alkyne group at the free-terminus thereof, such that the two linker units are coupled via the iEDDA reaction occurred between the two coupling arms (i.e., the first and second coupling arms) .
  • the tetrazine group is 1, 2, 3, 4-tetrazine, 1, 2, 3, 5-tetrazine, and 1, 2, 4, 5-tetrazine, or derivatives thereof, such as, 6-methyl tetrazine; and the strained alkyne group is TCO.
  • the free termini of both coupling arms respectively have an azide group and an alkyne group; in this instance, the two linker units are coupled via the CuAAC reaction occurred between the two coupling arms (i.e., the first and second coupling arms) .
  • one of the coupling arm has an azide group
  • the other of the coupling arm has a strained alkyne group (preferably, DBCO, DIFO, BCN, or DICO) ; accordingly, the two coupling arm can be coupled via the SPAAC reaction.
  • a strained alkyne group preferably, DBCO, DIFO, BCN, or DICO
  • the center core of the other linker unit is a polypeptide core.
  • the first amino acid residue at the N-or C-terminus of one of the second center core is an amino acid residue having an azide group or an alkyne group.
  • the amino acid residue having the azide or alkyne group would undergo CuAAC reaction with the corresponding alkyne or azide group of the first coupling arm of the first linker unit, thereby coupling the first and second linker units.
  • the first amino acid residue at the N-or C-terminus of one of the second center core is an amino acid residue having an azide group, which can be linked to the coupling arm of the first linker unit having a strained alkyne group (preferably, DBCO, DIFO, BCN, or DICO) at the free-terminus via the SPAAC reaction.
  • a strained alkyne group preferably, DBCO, DIFO, BCN, or DICO
  • first and second linker units are coupled without the presence of any coupling arms (that is, the first and second coupling arms) .
  • the first and second coupling arms are directly linked with each other.
  • This configuration mostly occurs between two polypeptide cores.
  • one of the two center cores (say, for example, the first center core) has an amino acid residue having an azide group at the N-or C-terminus thereof, while the other center core (such as the second center core) has an amino acid residue having an alkyne group at the N-or C-terminus thereof.
  • the azide group of the first center core reacts with the alkyne group of the second center core, thereby coupling the first and second linker units.
  • Non-limiting examples of amino acid residues having the azide group include, L-azidohomoalanine (AHA) , 4-azido-L-phenylalanine, 4-azido-D-phenylalanine, 3-azido-L-alanine, 3-azido-D-alanine, 4-azido-L-homoalanine, 4-azido-D-homoalanine, 5-azido-L-ornithine, 5-azido-d-ornithine, 6-azido-L-lysine, and 6-azido-D-lysine.
  • AHA L-azidohomoalanine
  • 4-azido-L-phenylalanine 4-azido-D-phenylalanine, 3-azido-L-alanine, 3-azido-D-alanine
  • 4-azido-L-homoalanine 4-azido-
  • amino acid residues having the alkyne group include, but are not limited to, L-homopropargylglycine (L-HPG) , D-homopropargylglycine (D-HPG) , and beta-homopropargylglycine ( ⁇ -HPG) .
  • L-HPG L-homopropargylglycine
  • D-HPG D-homopropargylglycine
  • ⁇ -HPG beta-homopropargylglycine
  • one of the first and second linker units of the molecular construct further comprises an additional linking arm (hereinafter, the third linking arm) linked to the first or the second linker unit.
  • the third linking arm is configured to be linked with a long PEG chain having a molecular weight of about 20, 000 to 50, 000 daltons via thiol–maleimide reaction.
  • the third linking arm is configured to be linked with a single scFv, as either a targeting element or an effector element.
  • the first and second linking arms are connected with two different effector elements, and the targeting element linked to the third linking arm is an scFv specific for collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, collagen XI, aggrecan, or osteonectin.
  • the first and second linking arms are connected with two different targeting elements, and the effector element is an scFv specific for CD3 or CD16a.
  • the present molecular construct further comprises a third linker unit.
  • the third linker unit comprises a third center core, a linking arm (hereinafter, the third linking arm) , and optionally a coupling arm (hereinafter, the third coupling arm) .
  • the third linker unit is linked to the first or the second linker unit via CuAAC reaction, iEDDA reaction, or SPAAC reaction occurred between any of the followings: the first or the second coupling arm and the third coupling arm, the first or the second center core and the third coupling arm, the first or the second center coupling arm and the third center core, or the first or the second center core and the third center core.
  • the third linking arm of the third linker unit may have a maleimide group at the free terminus thereof, which is used to link a second effector element or targeting element via thiol–maleimide reaction.
  • the targeting/effector element (such as a drug) having an NHS group can be directly linked to the K residue of the first, second, and/or third center core via forming an amide linkage between the NHS group and the K residue without the presence of the linking arm (i.e., the first, second, or third linking arm) .
  • the first, second, and optionally, the third center core may be the same or different.
  • the molecular construct according to the third aspect of the present disclosure may find its utility in clinical medicine for the treatment of various diseases.
  • the fourth aspect of the present disclosure is directed to a method for treating these diseases.
  • the method for treating a particular disease includes the step of administering to the subject in need thereof a molecular construct according to the third aspect of the present disclosure and embodiments thereof in a therapeutically effective amount.
  • said molecular construct may be administered in a pharmaceutical formulation, which comprises a pharmaceutically-acceptable excipient suitable for the intended or desired administration route, in addition to the present molecular construct.
  • the first element is a single-chain variable fragment (scFv) specific for a cytokine or a receptor of the cytokine; or a soluble receptor of the cytokine, while the second element is an scFv specific for a tissue-associated extracellular matrix protein.
  • the first element is an effector element for treating one or more immune disorders, while the second element is a targeting element that facilitates the delivery of the molecular construct to the disease site.
  • Non-limiting examples of the cytokine include tumor necrosis factor- ⁇ (TNF- ⁇ ) , interleukin-17 (IL-17) , IL-1, IL-6, IL-12/IL-23, and B cell activating factor (BAFF)
  • TNF- ⁇ tumor necrosis factor- ⁇
  • IL-17 interleukin-17
  • BAFF B cell activating factor
  • non-limiting examples of the cytokine receptor is the receptor specific for IL-6 (i.e., IL-6R) or IL-17 (i.e., IL-17R)
  • the soluble receptor of a cytokine examples of which include, but are not limited to, the soluble receptor of the cytokine specific for TNF- ⁇ or IL-1.
  • Illustrative examples of the tissue-associated extracellular matrix protein include, but are not limited to, ⁇ -aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, and collagen XI.
  • the first element is an scFv specific for TNF- ⁇ , IL-12/IL-23, IL-17, or IL-17R; and the second element is an scFv specific for collagen I or collagen VII.
  • the molecular constructs suitable for treating immune disorders comprise an scFv specific for BAFF as the first element and an scFv specific for collagen I or collagen VII as the second element.
  • the illustrative molecular constructs comprise a first element that is an scFv specific for TNF- ⁇ , IL-1, IL-6, IL-12/IL-23, IL-17, IL-6R, or IL-17R; and a second element that is an scFv specific for collagen II, collagen IX, collagen XI, or ⁇ -aggrecan.
  • the molecular constructs are also suitable for treating inflammatory bowel diseases, e.g., Crohn’s disease and ulcerative colitis, among others.
  • the present molecular construct uses an scFv specific for TNF- ⁇ as the first element, and an scFv specific for collagen III or collagen V as the second element.
  • Another set of diseases treatable by the present molecular construct is diffused tumor, including, but not limited to, acute lymphocytic leukemia (ALL) , chronic lymphocytic leukemia (CLL) , acute myelogenous leukemia (AML) , chronic myelogenous leukemia (CML) , Hodgkin lymphoma, non-Hodgkin lymphoma, and myeloma.
  • the first element may be a targeting element such as an scFv specific for a first cell surface antigen
  • the second element may be a cytotoxic drug, or an effector element such as an scFv specific for a second cell surface antigen.
  • the first cell surface antigen suitable for use as the targeting element for treating diffused tumor includes, but is not limited to, CD5, CD19, CD20, CD22, CD23, CD27, CD30, CD33, CD34, CD37, CD38, CD43, CD72a, CD78, CD79a, CD79b, CD86, CD134, CD137, CD138, and CD319.
  • non-limiting examples of the second cell surface antigen suitable for use as the effector element include CD3 and CD16a.
  • the first and second cell surface antigens are respectively CD79aand CD79b.
  • the cytotoxic drug suitable for the treatment of diffused tumor includes, but is not limited to, auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin.
  • the illustrative first element is an scFv specific for CD5, CD19, CD20, CD22, CD23, CD30, CD37, CD79a, or CD79b; while the illustrative second element is a cytotoxic drug, or an scFv specific for CD3 or CD16a.
  • the illustrative first element is an scFv specific for CD38, CD78, CD138, or CD319; while the illustrative second element is a cytotoxic drug, or an scFv specific for CD3 or CD16a.
  • the illustrative first element for the treatment thereof is an scFv specific for CD5, CD30, or CD43; while the second element is a cytotoxic drug, or an scFv specific for CD3 or CD16a.
  • the illustrative first element is an scFv specific for CD33 or CD34; while the illustrative second element is a cytotoxic drug, or an scFv specific for CD3 or CD16a.
  • Still another set of diseases that may be treated by the present molecular construct is solid tumor, including, but not limited to, melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, and head and neck squamous cell carcinoma. Additionally, the present molecular construct is also suitable for treating advanced, malignant, or metastatic solid tumors.
  • the first element i.e., the targeting element
  • the second element i.e., the effector element
  • the first element is chosen from a peptide hormone, a growth factor, and a first scFv specific for a tumor-associated antigen
  • the second element i.e., the effector element
  • the second element is a cytotoxic drug, a toll-like receptor (TLR) agonist, a chelator complexed with a radioactive nuclide, a cytokine, or a second scFv specific for a second growth factor, a cell surface antigen, a hapten, or the cytokine.
  • the peptide hormone is secretin, cholecystokinin (CCK) , somatostatin, or thyroid-stimulating hormone (TSH) .
  • the first growth factor it may be the epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , vascular endothelial growth factor A (VEGF-A) , basic fibroblast growth factor (bFGF) , or hepatocyte growth factor (HGF) .
  • tumor-associated antigen examples include epidermal growth factor receptor (HER1) , HER2, HER3, HER4, carbohydrate antigen 19-9 (CA 19-9) , carbohydrate antigen 125 (CA 125) , carcinoembryonic antigen (CEA) , mucin 1 (MUC 1) , ganglioside GD2, melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) , mesothelin, mucine-related Tn, Sialyl Tn, Globo H, stage-specific embryonic antigen-4 (SSEA-4) , and epithelial cell adhesion molecule (EpCAM) .
  • HER1 epidermal growth factor receptor
  • CA 125 carbohydrate antigen 125
  • CEA carcinoembryonic antigen
  • MUC 1 mucin 1
  • MAGE melanoma-associated antigen
  • PSMA prostate-specific membrane antigen
  • the cytotoxic drug used in the molecular construct for the treatment of solid tumors includes, but is not limited to, auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin.
  • Non-limiting TLR agonist includes lipopolysaccharide (LPS) , monophosphoryl lipid A, motolimod, imiquimod, resiquimod, gardiquimod, CpG oligodeoxynucleotide (CpG DON) , lipoteichoic acid, ⁇ -glucan, and zymosan.
  • the chelator is selected from the group consisting of 1, 4, 7, 10-tetraazacyclododecane-1, 4, 7, 10-tetraacetic acid (DOTA) , 1, 4, 7-triaza-cyclo-nonane-1, 4, 7-triacetic acid (NOTA) , 1, 4, 7-triazacyclononane-1, 4-diacetic acid (NODA) , and diethylenetriaminepentaacetic acid (DTPA) ; and the radioactive nuclide is 111 In, 131 I, or 177 Lu.
  • the cytokine it can be selected from the group consisting of IL-2, IFN- ⁇ , IFN- ⁇ , and TNF- ⁇ .
  • the second growth factor capable of being specifically recognized and bound by the second scFv is EGF, mutant EGF, VEGF-A, bFGF, or HGF.
  • the cell surface antigen specifically recognized and bound by the second scFv is selected from the group consisting of CD3, CD16a, CD28, CD134, cytotoxic T-lymphocyte-associated protein 4 (CTLA-4, or CD152) , programmed cell death 1 (PD-1, or CD279) , and programmed cell death 1 ligand 1 (PD-L1, or CD274) .
  • the cytokine specifically recognized and bound by the second scFv is selected from the group consisting of IL-2, IFN- ⁇ , IFN- ⁇ , and TNF- ⁇ ; in these cases, the second scFv is a non-neutralizing scFv.
  • the present method for treating solid tumor comprises the step of, (a) subjecting the subject to a blood dialysis procedure using an antibody specific for one or more tumor-associated antigens to remove the tumor-associated antigens that are shed from the tumor and wander into the circulation of the subject; and (b) administering the present molecular construct for treating the solid tumor.
  • the method further comprises the step of administering to the subject an immunoregulatory effector that is tagged with the same hapten.
  • the hapten is selected from the group consisting of dinitrophenol (DNP) , trinitrophenol (TNP) , and a short peptide having an amino acid sequence of WADWPGPP (SEQ ID NO: 20) ; and the immunoregulatory effector is IFN- ⁇ , IL-2, TNF- ⁇ , and IFN- ⁇ , and an IgG antibody specific for PD-1, PD-L1, CTLA-4, or CD3.
  • Yet another representative disease treatable by the present molecular construct is osteoporosis.
  • Illustrative molecular constructs suitable for treating osteoporosis include a first element (in this case, an effector element) that is a first scFv specific for receptor activator of nuclear factor ⁇ B (RANKL) ; and a second element (e.g., a targeting element) that is a second scFv specific for collagen I or osteonectin.
  • the present disclosure is directed to a fragment crystallizable (Fc) -based molecular construct that has at least one targeting element and at least one effector element linked, directly or indirectly, to a CH2-CH3 domain of an immunoglobulin.
  • Fc fragment crystallizable
  • the design of the present Fc-based molecular construct allows for numerous combinations of a wide range of targeting and effector elements.
  • the present Fc-based molecular construct may serve as a platform for constructing multi-valent molecules.
  • the Fc-based molecular construct comprises a pair of CH2-CH3 segments of an IgG. Fc, a first pair of effector elements, and a first pair of targeting elements.
  • the present Fc-based molecular constructs are intended to be used in the treatment of immune diseases (in particular, autoimmune diseases) or osteoporosis.
  • the first pair of effector elements consists of two effector elements, in which each of the two effector elements is an antibody fragment specific for tumor necrosis factor- ⁇ (TNF- ⁇ ) , interleukin-17 (IL-17) , IL-17 receptor (IL-17R) , IL-1, IL-6, IL-6R, IL-12/IL-23, B cell activating factor (BAFF) , or a receptor activator of nuclear factor kappa-B ligand (RANKL) ; or a soluble receptor of TNF- ⁇ or IL-1.
  • TNF- ⁇ tumor necrosis factor- ⁇
  • IL-17 interleukin-17
  • IL-17R IL-17 receptor
  • IL-1 IL-6
  • IL-6R IL-12/IL-23
  • BAFF B cell activating factor
  • RNKL nuclear factor kappa-
  • the first pair of targeting elements consists of two targeting elements, in which each of the two targeting elements is an antibody fragment specific for ⁇ -aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, collagen XI, or osteonectin.
  • each of the two targeting elements is an antibody fragment specific for ⁇ -aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, collagen XI, or osteonectin.
  • the first pair of effector elements is linked to the N-termini of the pair of CH2-CH3 segments
  • the first pair of targeting elements is linked to the C-termini of the pair of CH2-CH3 segments, and vice versa.
  • the first pair of effectors elements and the first pair of targeting elements is both in the form of single-chain variable fragments (scFvs)
  • the first pair of targeting elements is linked to the N-termini of the first pair of effector elements in a tandem or diabody configuration, thereby forming a pair of bispecific scFvs that are linked to the N-termini of the pair of CH2-CH3 segments.
  • the pair of CH2-CH3 segments is derived from human IgG heavy chain ⁇ 4 or human IgG heavy chain ⁇ 1.
  • the first pair of effector elements or the first pair of the targeting elements takes a Fab configuration (i.e., consisting of the V H -CH1 domain and the V L -C ⁇ domain) ; this Fab fragment is linked to the N-termini of the first and second heavy chains, so that the Fc-based molecular construct adopts an IgG configuration.
  • the pair of elements that is not in the Fab configuration is linked to the C-termini of the pair of CH2-CH3 segments.
  • the Fc-based molecular construct further comprises a second pair of effector elements, which consists of two additional effector elements that are both selected from the group described above for the effector elements.
  • the elements of the second pair of effector elements are different from those of the first pair of effector elements.
  • the second pair of effector elements is linked to the free C-termini of the CH2-CH3 segments.
  • the present Fc-based molecular construct further comprises a second pair of targeting elements, in which the two targeting elements are both selected from the group described above regarding the targeting elements.
  • the elements of the second pair of targeting elements are different from those of the first pair of targeting elements.
  • the second pair of targeting elements is linked to the free C-termini of the CH2-CH3 segments.
  • the targeting elements and effector elements described above can be combined as desired, so as to attain the intended therapeutic effect.
  • Some exemplary combination of the effector element (s) and targeting element (s) for treating immune diseases are provided in the appended claims and discussed in the description section bellow.
  • the present disclosure is directed to methods for treating various diseases.
  • the methods involve the step of administrating an effective amount of the Fc-based molecular constructs according to the fifth aspect and any of the associated embodiments, to a subject in need of such treatment.
  • the present method is directed to the treatment of an immune disease; in particular, an autoimmune disease.
  • the autoimmune disease is rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis.
  • the effector element is an antibody fragment specific for TNF- ⁇ , IL-12/IL-23, IL-1, IL-17, or IL-6, while the targeting element may be an antibody fragment specific for collagen II, collagen IX, collagen XI, or ⁇ -aggrecan.
  • the autoimmune disease is psoriasis.
  • the effector element is an antibody fragment specific for TNF- ⁇ , IL-12/IL-23, or IL-17
  • the targeting element is an antibody fragment specific for collagen I or collagen VII.
  • the autoimmune disease is systemic lupus erythematosus, cutaneous lupus, or Syndrome.
  • the effector element is an antibody fragment specific for BAFF
  • the targeting element is an antibody fragment specific for collagen I, or collagen VII.
  • the autoimmune disease is an inflammatory bowel disease, such as Crohn’s disease or ulcerative colitis.
  • the effector element is an antibody fragment specific for TNF- ⁇
  • the targeting element is an antibody fragment specific for collagen III or collagen V.
  • the present disclosure is directed to an Fc-based molecular construct that, like the molecular construct described above in the fifth aspect of the present disclosure, has at least one targeting element and at least one effector element linked, directly or indirectly, to a CH2-CH3 domain of an immunoglobulin.
  • the molecular construct can be used to treat various cellular proliferative diseases, including diffused tumors and solid tumors.
  • the present disclosure is also advantageous in that, in some embodiments, it utilizes the linker unit according to the first aspect of the present disclosure, which provides a facile means for controlling the amount of the drug (e.
  • the linker unit carrying multiple drug molecules is herein referred to as a drug bundle.
  • drug bundles can be manufactured separately before being conjugated to the antibody molecules, thus avoiding subjecting drug molecules under harsh chemical conditions for the direct conjugation with the antibody molecules.
  • the Fc-based molecular construct comprises a pair of CH2-CH3 segments of an IgG. Fc, a first pair of effector elements, and a first pair of targeting elements.
  • each effector element of the first pair of effector elements is a drug bundle, while each targeting element of the first pair of targeting elements is an antibody fragment specific for a cell surface antigen.
  • the first pair of effector elements is linked to the C-termini of the pair of CH2-CH3 segments, whereas the first pair of targeting elements is linked to the N-termini of the pair of CH2-CH3 segments.
  • the drug bundle comprises a plurality of cytotoxic drug molecules, such as, auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin; while the cell surface antigen targeted by these Fc-based molecular construct is CD5, CD19, CD20, CD22, CD23, CD30, CD33, CD34, CD37, CD38, CD43, CD78, CD79a, CD79b, CD138, or CD319.
  • these Fc-based molecular constructs are useful in the treatment of various diffused tumors.
  • each effector element of the first pair of effector elements is a drug bundle, while each targeting element of the first pair of targeting elements is an antibody fragment specific for a tumor-associated antigen.
  • the first pair of effector elements is linked to the C-termini of the pair of CH2-CH3 segments, whereas the first pair of targeting elements is linked to the N-termini of the pair of CH2-CH3 segments.
  • the drug bundle comprises a plurality of molecules of, a cytotoxic drug, a toll-like receptor (TLR) agonist, or a chelator complexed with a radioactive nuclide
  • the tumor-associated antigen targeted by these Fc-based molecular construct is human epidermal growth factor receptor-1 (HER1) , HER2, HER3, HER4, CA19-9, CA125, carcinoembryonic antigen (CEA) , cell surface-associated mucin 1 (MUC1) , melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) ; mucin-related Tn, Sialyl Tn, Globo H, stage-specific embryonic antigen-4 (SSEA-4) , ganglioside GD2, or epithelial cell adhesion molecule (EpCAM) .
  • HER1 human epidermal growth factor receptor-1
  • each effector element of the first pair of effector elements is a drug bundle or an antibody fragment specific for a cell surface antigen, a growth factor, or a hapten; while each targeting element of the first pair of targeting elements is the growth factor or a peptide hormone.
  • the effector elements are the drug bundles
  • the first pair of effector elements is respectively linked to the C-termini of the pair of CH2-CH3 segments
  • the targeting elements are respectively linked to the N-termini of the pair of CH2-CH3 segments.
  • effector elements are the antibody fragments
  • the effector elements are respectively linked to the N-termini of the pair of CH2-CH3 segments
  • the targeting elements are respectively linked to the C-termini of the pair of CH2-CH3 segments, and vice versa.
  • the Fc-based molecular constructs of this third series provided herein are also useful for use in the treatment of various solid tumors, including malignant and/or metastatic solid tumors; however, the present disclosure is not limited thereto.
  • the cytotoxic drug suitable for use as the effector elements is auristatin, maytansine, doxorubicin, calicheamicin, or camptothecin.
  • TLR agonist include, lipopolysaccharide (LPS) , monophosphoryl lipid A, motolimod, imiquimod, resiquimod, gardiquimod, CpG oligodeoxynucleotide (CpG DON) , lipoteichoic acid, ⁇ -glucan, and zymosan.
  • Some antibody fragments suitable for use as the effector elements are those specific to cell surface antigens such as programmed cell death 1 (PD-1) , programmed cell death 1 ligand 1 (PD-L1) , cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) , CD3, CD16a, CD28, and CD134.
  • PD-1 programmed cell death 1
  • PD-L1 programmed cell death 1 ligand 1
  • CTL-4 cytotoxic T-lymphocyte-associated protein 4
  • CD3, CD16a, CD28, and CD134 CD3, CD16a, CD28, and CD134.
  • Another example is the antibody fragment specific for the growth factor like epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , VEGF-A, basic fibroblast growth factor (bFGF) , and hepatocyte growth factor (HGF) .
  • EGF epidermal growth factor
  • HB-EGF
  • Antibody fragments specific for haptens are also suitable for use herein, and illustrative examples of haptens include dinitrophenol (DNP) , trinitrophenol (TNP) , dansyl, penicillin, p-aminobenzoic acid, or a polypeptide having the amino acid sequence of SEQ ID NO: 20.
  • DNP dinitrophenol
  • TNP trinitrophenol
  • dansyl penicillin
  • p-aminobenzoic acid or a polypeptide having the amino acid sequence of SEQ ID NO: 20.
  • the targeting element (s) may be a growth factor such as EGF, mutant EGF, epiregulin, HB-EGF, VEGF-A, bFGF, and HGF.
  • the targeting element (s) may be a peptide hormone like CCK, somastatin, and TSH.
  • the pair of CH2-CH3 segments is derived from human IgG heavy chain ⁇ 4 or human IgG heavy chain ⁇ 1.
  • the first pair of effector elements e.g., for the third series of Fc-based molecular constructs
  • the first pair of targeting elements e.g., for the first and second series of Fc-based molecular constructs
  • takes a Fab configuration i.e., comprising the V H -CH1 domain and the V L -C ⁇ domain
  • this Fab fragment is linked to the N-termini of the first and second heavy chains so that the Fc-based molecular construct adopts an IgG configuration.
  • the pair of elements that is not in the Fab configuration may be linked to the C-termini of the pair of CH2-CH3 segments.
  • the present Fc-based molecular construct further comprises a peptide extension and a coupling arm.
  • the peptide extension has the sequence of (G 2-4 S) 2-8 C and is linked to the C-terminus of one of the pair of CH2-CH3 segments.
  • the coupling arm is linked to the C-terminus of the coupling arm via thiol-maleimide reaction occurred therebetween.
  • the free terminus of the conjugating arm (that is, the terminus that is not linked to the cysteine residue) is modified with an alkyne, azide, strained alkyne, or tetrazine group, so that the drug bundle is linked thereto via inverse electron demand Diels-Alder (iEDDA) reaction or the strain-promoted azide-alkyne click chemistry (SPAAC) reaction or Copper (I) -catalyzed alkyne-azide cycloaddition (CuAAC) reaction occurred therebetween.
  • iEDDA inverse electron demand Diels-Alder
  • SPAAC strain-promoted azide-alkyne click chemistry
  • CuAAC Copper
  • the drug bundle may be provided as the linker unit according to the first aspect of the present disclosure.
  • the drug bundle comprises a center core, a plurality of first linking arms, and optionally, a second linking arm.
  • the center core may be a compound having a plurality of amine groups or a polypeptide comprising a plurality of lysine (K) residues, according to various embodiments of the present disclosure.
  • Each of the first linking arms has one terminus that is linked to the center core by reacting with the amine groups of the compound core or the K residues of the polypeptide core.
  • the first linking arm also carries a maleimide group at the free terminus thereof, wherein each of the molecules (e.g., molecules of cytotoxic drugs, TLR agonists, or chelator/radioactive nuclide complexes) is linked to the center core via connecting through the first linking arm by reacting with the maleimide group.
  • the molecules e.g., molecules of cytotoxic drugs, TLR agonists, or chelator/radioactive nuclide complexes
  • the amino acid residue at the N-or C-terminus of the center core is a cysteine residue or has an azide group or an alkyne group.
  • the drug bundle may be linked to the peptide extension via the CuAAC reaction occurred between said terminal residue and the C-terminus of the peptide extension.
  • the drug bundle further comprises the second linking arm.
  • the second linking arm has one terminus linked to the center core by reacting with the cysteine residue of the polypeptide core or one amine group of the compound core.
  • the second linking arm also carries an alkyne group, azide group, tetrazine group, or strained alkyne group at the free terminus thereof, so that the drug bundle can be linked to the C-terminus of the peptide extension via the CuAAC reaction or the iEDDA reaction occurred therebetween.
  • the Fc-based molecular construct may further comprise a second pair of effector elements or a second pair of targeting elements.
  • a second pair of targeting elements may be respectively linked to the first pair of targeting elements.
  • each effector element of the first pair of effector elements is a drug bundle comprising the plurality of molecules of the cytotoxic drug
  • each targeting element of the first pair of targeting elements is an scFv specific for HER2
  • each targeting elements of the second pair of targeting elements is an scFv specific for HER1.
  • a second pair of effector elements may be linked, in a tandem or diabody configuration, to the N-termini of the pair of elements that is linked to the N-termini of the pair of CH2-CH3 segments, thereby forming a pair of bispecific scFvs that is linked to the N-termini of the pair of CH2-CH3 segments.
  • the third series of Fc-based molecular construct may further comprise a second pair of targeting elements that is linked, in a tandem or diabody configuration, to the N-termini of the pair of elements that is linked to the N-termini of the pair of CH2-CH3 segments, thereby forming a pair of bispecific scFvs that is linked to the N-termini of the pair of CH2-CH3 segments.
  • the present disclosure is directed to methods for treating various cellular proliferative diseases.
  • the methods involve the step of administrating an effective amount of the Fc-based molecular constructs according to the seventh aspect or any of the associated embodiments, to a subject in need of such treatment.
  • the present method is directed to the treatment of diffused tumors, such as B lymphocyte-derived lymphoma or leukemia, plasmacytoma, multiple myeloma, T-cell derived lymphoma or leukemia, and myelogenous leukemia.
  • diffused tumors such as B lymphocyte-derived lymphoma or leukemia, plasmacytoma, multiple myeloma, T-cell derived lymphoma or leukemia, and myelogenous leukemia.
  • diffused tumors such as B lymphocyte-derived lymphoma or leukemia, plasmacytoma, multiple myeloma, T-cell derived lymphoma or leukemia, and myelogenous leukemia.
  • the present method is also suitable for treating solid tumors in a subject.
  • solid tumors include, but are not limited to, melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, and head and neck squamous cell carcinoma.
  • the second and third series of Fc-based molecular construct of the seventh aspect of the present disclosure are useful in the treatment of the solid tumor.
  • the method comprises the steps of (a) subjecting the subject to a blood dialysis procedure using an antibody fragment specific for one or more tumor-associated antigens to remove the tumor-associated antigens that are shed from the tumor into the circulation of the subject, and then, (b) administering the Fc-based molecular construct of the present disclosure for treating the solid tumor.
  • the present method further comprises the step of administering to the subject an immunoregulatory effector that is tagged with the same hapten, after the administration of the present Fc-based molecular construct.
  • immunoregulatory effector include IFN- ⁇ , IL-2, TNF- ⁇ , and IFN- ⁇ , and an IgG antibody specific for PD-1, PD-L1, CTLA-4, and CD3.
  • the malignant tumor that sheds one or more tumor-associated antigens into the circulation of the subject further comprises the step of, subjecting the subject to a blood dialysis procedure using an antibody fragment specific for the one or more tumor-associated antigens to remove the tumor-associated antigens that are shed from the malignant tumor, prior to the administration of the Fc-based molecular construct.
  • Figure 1A to Figure 1 K are schematic diagrams illustrating linker units according to certain embodiments of the present disclosure.
  • Figure 2 is a schematic diagram illustrating a linker unit having a compound core.
  • Figure 3A to Figure 3D are schematic diagrams illustrating T-E molecular constructs according to some embodiments of the present disclosure.
  • Figure 4 is a schematic diagram that illustrates libraries for constructing molecular constructs according to some embodiments of the present disclosure.
  • Figure 5A and Figure 5B are schematic diagrams that illustrate molecular constructs according to some embodiments of the present disclosure.
  • Figure 6 is a schematic diagram that illustrates a molecular construct according to some embodiments of the present disclosure.
  • Figure 7A and Figure 7B are schematic diagrams illustrating molecular constructs according to various embodiments of the present disclosure.
  • Figures 8A to 8F are schematic diagrams illustrating Fc-based molecular constructs according to various embodiments of the present disclosure.
  • Figures 9A and 9B are schematic diagrams illustrating Fc-based molecular constructs according to various embodiments of the present disclosure.
  • Figures 10A to 10C are schematic diagrams illustrating Fc-based molecular constructs according to various embodiments of the present disclosure.
  • Figure 11 is a schematic diagram illustrating Fc-based molecular constructs according to one embodiment of the present disclosure.
  • Figures 12A to 12C are schematic diagrams illustrating Fc-based molecular constructs according to various embodiments of the present disclosure.
  • Figure 13 shows the reverse phase HPLC elution profile for the purification of TCO-peptide 2.
  • Peptide 2 is SEQ ID NO: 18.
  • Figure 14 shows the reverse phase HPLC profile for the purification of PEG 12 -maleimide-conjugated TCO-peptide 2.
  • Figure 15 shows the mass spectrometry MALDI-TOF result of PEG 12 -maleimide-conjugated TCO-peptide 2.
  • Figures 16A and 16B respectively show the mass spectrometry MALDI-TOF result of PEG 12 -maleimide-conjugated tetrazine-peptide 2 and DBCO-peptide 2.
  • Figure 17 shows the mass spectrometry ESI-TOF result of PEG 12 -maleimide-conjugated tetrazine-peptide 8.
  • Figure 18 shows the mass spectrometry ESI-TOF result of PEG 6 -maleimide-conjugated TCO-peptide 9.
  • Figure 19 shows the mass spectrometry ESI-TOF result of 1, 3, 5-triaminobenzene conjugated with one NHS-PEG 12 -alkyne coupling arm and two NHS-PEG 12 -maleimide linking arms.
  • Figure 20 shows the reverse phase HPLC profile for the purification of TCO-peptide 9 with 5 DM1-SMCC molecules.
  • Figure 21 shows the mass spectrometry result of TCO-peptide 9 with 5 DM1-SMCC molecules.
  • Figure 22 shows that LPS, upon the reaction with dansyl hydrazine, exhibited an emission maximum at 495 nm in fluorescence spectrophotometric analysis.
  • Figure 23 shows mass spectrometric analysis of PEG 5 -NHS conjugated with imiquimod.
  • Figure 24A shows mass spectrometry ESI-TOF result of DOTA-conjugated TCO-peptide 9.
  • Figure 24B shows the mass spectrometric result of Y 3+ -chelated, DOTA-conjugated TCO-peptide 9.
  • Figures 25Aand 25B respectively show SDS-PAGE and ELISA analysis of purified scFv proteins of anti-CD79b antibody 1F10.
  • Figures 25C and Figure 25D respectively show SDS-PAGE and ELISA analysis of purified scFv proteins of anti-collagen VII antibody LH7.2.
  • Figure 26A shows SDS-PAGE analysis of purified scFv of trastuzumab and adalimumab.
  • Figures 26B and 26C respectively show ELISA analyses of purified scFv of trastuzumab and adalimumab.
  • Figures 26D and 26E respectively show SDS-PAGE and ELISA analyses of purified scFv of centuximab.
  • Figure 27A shows SDS-PAGE analysis of the purified scFv of adalimumab.
  • Figure 27B shows ELISA analysis of the purified scFvs of adalimumab.
  • Figure 28A and Figure 28B show, respectively, the ELISA analysis of TCO-conjugated scFv and DBCO-conjugated scFv specific for CD3.
  • Figure 29A is the FPLC elution profile on a synthesized linker unit composed of a free tetrazine functional group and a set of three scFvs specific for human CD79b.
  • Figure 29B shows the SDS-PAGE analysis result.
  • Figure 29C shows the mass spectrometry MALDI-TOF result.
  • Figure 30A and Figure 30B respectively show the SDS-PAGE and mass spectrometry analysis result of tetrazine-peptide 2 conjugated with three scFvs specific for HER2/neu.
  • Figure 30C shows the mass spectrometry result of TCO-peptide 2 conjugated with three scFvs specific for TNF- .
  • Figure 30D and 30E respectively show the SDS-PAGE and mass spectrometry analysis of TCO-peptide 2 conjugated with three scFvs specific for PD-1.
  • Figure 31 shows mass spectrometry analysis result of tetrazine-peptide 2 conjugated with 3 CCK peptides.
  • Figure 32 shows mass spectrometry analysis result of TCO-peptide 7 conjugated with two scFvs specific for CD20.
  • Figure 32 shows mass spectrometry analysis result of TCO-peptide 7 conjugated with two scFvs specific for CD20.
  • Figure 33 shows mass spectrometry analysis result of TCO-peptide 1 conjugated with two scFvs specific for VEGF-A.
  • Figure 34A shows the mass spectrometry analysis result of a molecular construct with three scFvs specific for CD79b and one scFv specific for CD3.
  • Figure 34B shows the mass spectrometry analysis result of a molecular construct with three scFvs specific for HER2/neu and one scFv specific for CD3.
  • Figure 35 shows the SDS-PAGE analysis of the reaction mixtures of TCO-peptide 1 after the conjugation with scFv of anti-VEGF-A and further with tetrazine-20 kDa PEG.
  • Figure 36A and 36B respectively show the SDS-PAGE and mass spectrometric analyses of a molecular construct with a targeting linker unit with three scFvs specific for CD79b and a drug bundle with five DM1 molecules.
  • Figure 37 shows the ELISA analyses of a molecular construct with a targeting linker unit with three scFvs specific for CD79b and a drug bundle with five DM1 molecules.
  • Figure 38 shows the SDS-PAGE analyses of a molecular construct with a targeting linker unit with three scFvs specific for HER2/neu and a drug bundle with five DM1 molecules.
  • Figure 39 shows the mass spectrometric analysis of a molecular construct with a targeting linker unit with three CCK8 peptides and a drug bundle with five DM1 molecules.
  • Figure 40 shows the mass spectrometric analysis of a molecular construct with a targeting linker unit with three CCK8 peptides and a drug bundle with five DOTA groups.
  • Figure 41 shows the SDS-PAGE analysis of the reaction mixtures containing a linker unit of tetrazine-peptide 2 with three scFvs specific for CD79b, a TCO-peptide 7 with two scFvs specific for CD20, and a drug bundle with five DM1.
  • Figure 42 shows the assay results of the biological activity of LPS, before and after modification with dansyl hydrazine.
  • Figure 44 shows the pharmacokinetic pattern of the molecular construct with 3scFv specific for VEGF-A and a 20kDa PEG in mice.
  • Figure 45 shows the cytotoxicity assay results of the molecular construct with three scFvs specific for CD79b and a drug bundle of five DM1.
  • Figure 46 shows the SDS-PAGE analysis of (scFv ⁇ CII) - (scFv ⁇ TNF- ⁇ ) -hIgG4Fc.
  • Figures 47A and 47B show the ELISA results analyzing the binding of (scFv ⁇ CII) - (scFv ⁇ TNF- ⁇ ) -hIgG4Fc to collagen II and TNF- ⁇ .
  • Figures 48A and 48B respectively show the SDS-PAGE and ELISA analysis of the 2-chain (scFv ⁇ CII) - (scFv ⁇ TNF- ⁇ ) -hIgG4. Fc- (scFv ⁇ IL-17) .
  • Figures 49A and 49B respectively show the SDS-PAGE and ELISA analysis of 2-chain (soluble TNF- ⁇ receptor) -IgG1. CH2-CH3-scFv ⁇ collagen II.
  • Figure 50 shows the SDS-PAGE analysis of the 2-chain fusion protein containing intact antibody for human TNF- ⁇ and scFv specific for collagen II.
  • Figures 51A and 51 B respectively show the SDS-PAGE and ELISA analyses of the 2-chain fusion protein containing intact antibody for human IL-17 and scFv specific for collagen VII.
  • Figures 52A and 52B respectively show the SDS-PAGE and ELISA analysis of scFv ⁇ collagen VII-IgG4. CH2-CH3-scFv ⁇ BAFF.
  • Figures 53A and 53B respectively show the SDS-PAGE and ELISA analyses of the 2-chain fusion protein containing intact antibody for human BAFF and scFv specific for collagen VII.
  • Figures 55A and 55B respectively show the SDS-PAGE and ELISA analyses of the 2-chain fusion protein containing intact antibody for human RANKL and scFv specific for human osteonectin.
  • Figures 56A to 56E show the immunostaining of mouse epiphyseal bone with (scFv ⁇ CII) - (scFv ⁇ TNF- ⁇ ) -hIgG4Fc and 2-chain (scFv ⁇ CII) - (scFv ⁇ TNF- ⁇ ) -hIgG4. Fc- (scFv ⁇ IL-17) .
  • Figures 57A-C show the immunostaining of mouse epiphyseal bone with 2-chain (soluble TNF- ⁇ receptor) -IgG1. CH2-CH3-scFv ⁇ collagen II.
  • Figures 58A to 58C show bio-distribution of fluorescence-labeled (scFv ⁇ SPARC) - (scFv ⁇ RANKL) -hIgG4Fc in vivo in BALB/c mice.
  • Figure 59A shows the SDS-PAGE analysis of the 2-chain EGF-CH2-CH3 with a C-terminal extension and a cysteine residue and a 2-chain EGF-CH2-CH3-scFv of anti-PD1.
  • Figure 59B shows SDS-PAGE analysis of 2-chain IgG1. Fc fusion protein conjugated with a linker unit with 2 LPS molecules.
  • Figures 60A and 60B show the ELISA results examining EGF-IgG1.
  • Figure 61A shows the SDS-PAGE analysis of the 2-chain EGF-hIgG1.
  • Figure 61B shows the ELISA analysis examining 2-chain EGF-hIgG1.
  • FIG. 62A shows SDS-PAGE analysis of EGF (S2W/D3V) -IgG1. Fc with C-terminal extension, EGF (S2W/D3V) -IgG1. Fc- (scFv ⁇ PD1) , and EGF (S2W/D3V) -IgG1. Fc- (scFv ⁇ CD3) .
  • Figures 62B to 62E show ELISA analyses of EGF (S2W/D3V) -IgG1.
  • Fc- (scFv ⁇ CD3) in binding to PD-1 or CD3, and ERBB1, ERBB2, and ERBB3.
  • Figure 63 shows SDS-PAGE analysis of somatostatin-hIgG1.
  • Fc somatostatin-hIgG1.
  • Fc- somatostatin-hIgG1.
  • Fc- scFv ⁇ CD3
  • Fc- scFv ⁇ PD-1 .
  • Figure 64 shows the cell staining analysis of EGF-IgG1.
  • Fc EGF-IgG1.
  • Fc- scFv ⁇ PD1
  • Fc- scFv ⁇ CD3
  • EGF S2W/D3V
  • Fc and EGF (S2W/D3V) -IgG1.
  • Fc- (scFv ⁇ CD3) on EGFR-expressing A431 cells.
  • Figure 65 shows the staining analysis of EGF-IgG1.
  • Fc- (scFv ⁇ PD1) on T cells in comparison with anti-PD-1 mAb (panels A to C) as well as the staining analysis of EGF-IgG1.
  • Fc- (scFv ⁇ CD3) on T cells in comparison with anti-CD3 mAb (panels D to F) .
  • Figures 66A and 66B show the T cell –mediated cytolysis of EGFR-expressing of A431 cells upon the incubation with EGF-hIgG.
  • Fc- (scFv ⁇ CD3) Figures 66C and 66D show the degree of cytolysis on MDA-MB-231 cells upon the incubation with EGF (S2W/D3V) -IgG1.
  • Fc- (scFv ⁇ CD3) show the T cell –mediated cytolysis of EGFR-expressing of A431 cells upon the incubation with EGF-hIgG.
  • Fc- (scFv ⁇ CD3) Figures 66C and 66D show the degree of cytolysis on MDA-MB-231 cells upon the
  • Figures 67A to 67C show the time course of T cell-mediated cytolysis of A431 cells upon the incubation with EGF (S2W/D3V) -IgG1.
  • Fc- scFv ⁇ CD3 .
  • Figure 68 shows the degree of cytolysis on A431 by human PBMCs upon the incubation with 2-chain EGFw2v3-IgG1.
  • Fc- (scFv ⁇ PD-1) shows the degree of cytolysis on A431 by human PBMCs upon the incubation with 2-chain EGFw2v3-IgG1.
  • each molecular construct comprises a targeting element (T) and an effector element (E)
  • T targeting element
  • E effector element
  • a targeting element may be an antibody or a ligand for a cell surface receptor, or it may be a molecule that binds such antibody or ligand, thereby indirectly targeting the present molecular construct to the target site (e.g., the surface of the cell of choice) .
  • the localization of the effector (therapeutic agent) in the diseased site will be enhanced or favored with the present molecular constructs as compared to the therapeutic without a targeting function.
  • the localization is a matter of degree or relative proportion; it is not meant for absolute or total localization of the effector to the diseased site.
  • the term “effector element” refers to the portion of a molecular construct that elicits a biological activity (e.g., inducing immune responses, exerting cytotoxic effects and the like) or other functional activity (e.g., recruiting other hapten tagged therapeutic molecules) , once the molecular construct is directed to its target site.
  • the “effect” can be therapeutic or diagnostic.
  • the effector elements encompass those that bind to cells and/or extracellular immunoregulatory factors.
  • the effector element comprises agents such as proteins, nucleic acids, lipids, carbohydrates, glycopeptides, drug moieties (both small molecule drug and biologics) , compounds, elements, and isotopes, and fragments thereof.
  • first, second, third, etc. may be used herein to describe various elements, components, regions, and/or sections, these elements (as well as components, regions, and/or sections) are not to be limited by these terms. Also, the use of such ordinal numbers does not imply a sequence or order unless clearly indicated by the context. Rather, these terms are simply used to distinguish one element from another. Thus, a first element, discussed below, could be termed a second element without departing from the teachings of the exemplary embodiments.
  • link refers to any means of connecting two components either via direct linkage or via indirect linkage between two components.
  • polypeptide refers to a polymer having at least two amino acid residues. Typically, the polypeptide comprises amino acid residues ranging in length from 2 to about 200 residues; preferably, 2 to 50 residues. Where an amino acid sequence is provided herein, L-, D-, or beta amino acid versions of the sequence are also contemplated. Polypeptides also include amino acid polymers in which one or more amino acid residues are an artificial chemical analogue of a corresponding naturally occurring amino acid, as well as to naturally occurring amino acid polymers.
  • amino acids joined by a peptide linkage or by other, “modified linkages” e.g., where the peptide bond is replaced by an ⁇ -ester, a ⁇ -ester, a thioamide, phosphonamide, carbomate, hydroxylate, and the like.
  • conservative substitutions of the amino acids comprising any of the sequences described herein are contemplated.
  • one, two, three, four, or five different residues are substituted.
  • the term “conservative substitution” is used to reflect amino acid substitutions that do not substantially alter the activity (e.g., biological or functional activity and/or specificity) of the molecule.
  • conservative amino acid substitutions involve substitution one amino acid for another amino acid with similar chemical properties (e.g., charge or hydrophobicity) .
  • Certain conservative substitutions include “analog substitutions” where a standard amino acid is replaced by a non-standard (e.g., rare, synthetic, etc. ) amino acid differing minimally from the parental residue. Amino acid analogs are considered to be derived synthetically from the standard amino acids without sufficient change to the structure of the parent, are isomers, or are metabolite precursors.
  • polypeptides comprising at least 80%, preferably at least 85% or 90%, and more preferably at least 95% or 98% sequence identity with any of the sequences described herein are also contemplated.
  • Percentage (%) amino acid sequence identity with respect to the polypeptide sequences identified herein is defined as the percentage of polypeptide residues in a candidate sequence that are identical with the amino acid residues in the specific polypeptide sequence, after aligning the sequences and introducing gaps, if necessary, to achieve the maximum percent sequence identity, and not considering any conservative substitutions as part of the sequence identity. Alignment for purposes of determining percentage sequence identity can be achieved in various ways that are within the skill in the art, for instance, using publicly available computer software such as BLAST, BLAST-2, ALIGN or Megalign (DNASTAR) software. Those skilled in the art can determine appropriate parameters for measuring alignment, including any algorithms needed to achieve maximal alignment over the full length of the sequences being compared.
  • sequence comparison between two polypeptide sequences was carried out by computer program Blastp (protein-protein BLAST) provided online by National Center for Biotechnology Information (NCBI) .
  • NCBI National Center for Biotechnology Information
  • the percentage amino acid sequence identity of a given polypeptide sequence A to a given polypeptide sequence B is calculated by the formula as follows:
  • X is the number of amino acid residues scored as identical matches by the sequence alignment program BLAST in that program's alignment of A and B, and where Y is the total number of amino acid residues in A or B, whichever is shorter.
  • PEGylated amino acid refers to a polyethylene glycol (PEG) chain with one amino group and one carboxyl group.
  • PEG polyethylene glycol
  • the PEGylated amino acid has the formula of NH 2 - (CH 2 CH 2 O) n -COOH.
  • n ranges from 1 to 20; preferably, ranging from 2 to 12.
  • terminal refers to an amino acid residue at the N-or C-end of the polypeptide.
  • terminal refers to a constitutional unit of the polymer (e.g., the polyethylene glycol of the present disclosure) that is positioned at the end of the polymeric backbone.
  • free terminus is used to mean the terminal amino acid residue or constitutional unit is not chemically bound to any other molecular.
  • antigen or “Ag” as used herein is defined as a molecule that elicits an immune response. This immune response may involve a secretory, humoral and/or cellular antigen-specific response.
  • the term “antigen” can be any of a protein, a polypeptide (including mutants or biologically active fragments thereof) , a polysaccharide, a glycoprotein, a glycolipid, a nucleic acid, or a combination thereof.
  • antibody is used in the broadest sense and covers fully assembled antibodies, antibody fragments that bind with antigens, such as antigen-binding fragment (Fab/Fab’ ) , F (ab’ ) 2 fragment (having two antigen-binding Fab portions linked together by disulfide bonds) , variable fragment (Fv) , single chain variable fragment (scFv) , bi-specific single-chain variable fragment (bi-scFv) , nanobodies, unibodies and diabodies.
  • Fab/Fab’ antigen-binding fragment
  • F (ab’ ) 2 fragment having two antigen-binding Fab portions linked together by disulfide bonds
  • variable fragment Fv
  • scFv single chain variable fragment
  • bi-specific single-chain variable fragment bi-scFv
  • nanobodies unibodies and diabodies.
  • an “antibody” refers to a protein consisting of one or more polypeptides substantially encoded by immunoglobulin genes or fragments of immunoglobulin genes.
  • the well-known immunoglobulin genes include the kappa, lambda, alpha, gamma, delta, epsilon, and mu constant region genes, as well as myriad immunoglobulin variable region genes.
  • Light chains are classified as either kappa or lambda.
  • Heavy chains are classified as gamma, mu, alpha, delta, or epsilon, which in turn define the immunoglobulin classes, IgG, IgM, IgA, IgD, and IgE, respectively.
  • a typical immunoglobulin (antibody) structural unit is known to comprise a tetramer.
  • Each tetramer is composed of two identical pairs of polypeptide chains, with each pair having one “light” chain (about 25 kDa) and one “heavy” chain (about 50-70 kDa) .
  • the N-terminus of each chain defines a variable region of about 100 to 110 or more amino acids primarily responsible for antigen recognition.
  • the terms variable light chain (V L ) and variable heavy chain (V H ) refer to these light and heavy chains, respectively.
  • the antibody fragment can be produced by modifying the nature antibody or by de novo synthesis using recombinant DNA methodologies.
  • the antibody and/or antibody fragment can be bispecific, and can be in various configurations.
  • bispecific antibodies may comprise two different antigen binding sites (variable regions) .
  • bispecific antibodies can be produced by hybridoma technique or recombinant DNA technique.
  • bispecific antibodies have binding specificities for at least two different epitopes.
  • the term “specifically binds” as used herein, refers to the ability of an antibody or an antigen-binding fragment thereof, to bind to an antigen with a dissociation constant (Kd) of no more than about 1 ⁇ 10 -6 M, 1 ⁇ 10 -7 M, 1 ⁇ 10 -8 M, 1 ⁇ 10 -9 M, 1 ⁇ 10 -10 M, 1 ⁇ 10 -11 M, 1 ⁇ 10 -12 M, and/or to bind to an antigen with an affinity that is at least two-folds greater than its affinity to a nonspecific antigen.
  • Kd dissociation constant
  • immune disorder refers to a disorder involving deficiency of humoral immunity, deficiency of cell-mediated immunity, combined immunity deficiency, unspecified immunity deficiency, and autoimmune disease.
  • tumor refers to all neoplastic cell growth and proliferation, whether malignant or benign, and all pre-cancerous and cancerous cells and tissues.
  • tumor comprises solid tumors and diffused tumors.
  • solid tumor denotes an abnormal mass of tissue that usually does not contain cysts or liquid areas. Different types of solid tumors are named for the type of cells that form them. Examples of solid tumors include, but are not limited to, sarcomas and carcinomas. Generally, “sarcomas” are cancers arising from connective or supporting tissues such as bone or muscle. “Carcinomas” are cancers arising from glandular cells and epithelial cells, which line body tissues.
  • diffused tumor refers to leukemia and/or hematological malignancy that is formed from hematopoietic (blood-forming) cells and affect blood, bone marrow, or lymph nodes.
  • the example of the diffused tumor includes, but is not limited to, acute lymphocytic leukemia (ALL) , chronic lymphocytic leukemia (CLL) , acute myelogenous leukemia (AML) , chronic myelogenous leukemia (CML) , Hodgkin lymphoma, non-Hodgkin lymphoma, and myeloma.
  • ALL acute lymphocytic leukemia
  • CLL chronic lymphocytic leukemia
  • AML acute myelogenous leukemia
  • CML chronic myelogenous leukemia
  • Hodgkin lymphoma Hodgkin lymphoma
  • non-Hodgkin lymphoma non-Hodgkin lymphoma
  • myeloma my
  • tumor-associated antigen refers to any cancer antigen that is known in the art and includes antigens found on the cancer cell surface, as well as those that are shed from cancerous cell and become soluble (i.e., soluble cancer antigens) .
  • soluble cancer antigens Several cell surface antigens disposed on tumors or normal cells have soluble counterparts.
  • Such antigens include, but are not limited to those found on cancer-associated fibroblasts (CAFs) , tumor endothelial cells (TEC) and tumor-associated macrophages (TAM) .
  • treatment includes preventative (e.g., prophylactic) , curative or palliative treatment; and “treating” as used herein also includes preventative (e.g., prophylactic) , curative or palliative treatment.
  • treating refers to the application or administration of the present molecular construct or a pharmaceutical composition comprising the same to a subject, who has a medical condition a symptom associated with the medical condition, a disease or disorder secondary to the medical condition, or a predisposition toward the medical condition, with the purpose to partially or completely alleviate, ameliorate, relieve, delay onset of, inhibit progression of, reduce severity of, and/or reduce incidence of one or more symptoms or features of said particular disease, disorder, and/or condition.
  • Treatment may be administered to a subject who does not exhibit signs of a disease, disorder, and/or condition, and/or to a subject who exhibits only early signs of a disease, disorder and/or condition, for the purpose of decreasing the risk of developing pathology associated with the disease, disorder and/or condition.
  • an effective amount refers to the quantity of the present recombinant protein that is sufficient to yield a desired therapeutic response.
  • An effective amount of an agent is not required to cure a disease or condition but will provide a treatment for a disease or condition such that the onset of the disease or condition is delayed, hindered or prevented, or the disease or condition symptoms are ameliorated.
  • the effective amount may be divided into one, two, or more doses in a suitable form to be administered at one, two or more times throughout a designated time period.
  • Effective amount will vary with such factors as particular condition being treated, the physical condition of the patient (e.g., the patient's body mass, age, or gender) , the type of subject being treated, the duration of the treatment, the nature of concurrent therapy (if any) , and the specific formulations employed and the structure of the compounds or its derivatives. Effective amount may be expressed, for example, as the total mass of active component (e.g., in grams, milligrams or micrograms) or a ratio of mass of active component to body mass, e.g., as milligrams per kilogram (mg/kg) .
  • application and “administration” are used interchangeably herein to mean the application of a molecular construct or a pharmaceutical composition of the present invention to a subject in need of a treatment thereof.
  • subject and patient are used interchangeably herein and are intended to mean an animal including the human species that is treatable by the molecular construct, pharmaceutical composition, and/or method of the present invention.
  • subject or patient intended to refer to both the male and female gender unless one gender is specifically indicated. Accordingly, the term “subject” or “patient” comprises any mammal, which may benefit from the treatment method of the present disclosure.
  • a “subject” or “patient” include, but are not limited to, a human, rat, mouse, guinea pig, monkey, pig, goat, cow, horse, dog, cat, bird and fowl.
  • the patient is a human.
  • mammal refers to all members of the class Mammalia, including humans, primates, domestic and farm animals, such as rabbit, pig, sheep, and cattle; as well as zoo, sports or pet animals; and rodents, such as mouse and rat.
  • non-human mammal refers to all members of the class Mammalis except human.
  • the present disclosure is based, at least on the construction of the T–E pharmaceuticals that can be delivered to target cells, target tissues or organs at increased proportions relative to the blood circulation, lymphoid system, and other cells, tissues or organs.
  • the therapeutic effect of the pharmaceuticals is increased, while the scope and severity of the side effects and toxicity is decreased.
  • a therapeutic effector is administered at a lower dosage in the form of a T-E molecule, than in a form without a targeting component. Therefore, the therapeutic effector can be administered at lower dosages without losing potency, while lowering side effects and toxicity.
  • Drugs used for many diseases can be improved for better efficacy and safety, if they can be targeted to the disease sites, i.e., if they can be localized or partitioned to the disease sites more favorably than the normal tissues or organs. Following are primary examples of diseases, in which drugs can be improved if they can be preferentially distributed to the disease sites or cells.
  • the diseases, conditions, and/or disorders treatable with the present method is an immune disorder; for example, an autoimmune disorder that includes, but is not limited to, psoriasis, systemic lupus erythematosus (SLE) , cutaneous lupus, Sjogren’s syndrome, rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, and inflammatory bowel disease.
  • SLE systemic lupus erythematosus
  • Sjogren systemic lupus erythematosus
  • rheumatoid arthritis psoriatic arthritis
  • ankylosing spondylitis ankylosing spondylitis
  • autoimmune diseases such as rheumatoid arthritis, systemic lupus erythematosus, syndrome, psoriasis, Crohn’s disease, inflammatory bowel diseases, and others affect connective tissues. Regardless of the etiological nature, whether it is environmental, genetic, epigenetic, or their combinations, the affected tissues are damaged by prolong inflammatory processes. It is rationalized in this invention that in bringing anti-inflammatory therapeutic agents, such as anti-TNF- ⁇ , anti-IL-17, anti-BAFF, anti-IL-6, anti-IL-12/IL-23, to the diseased connective tissues, the components of the extracellular matrix may be employed as target antigens.
  • anti-inflammatory therapeutic agents such as anti-TNF- ⁇ , anti-IL-17, anti-BAFF, anti-IL-6, anti-IL-12/IL-23
  • the target antigens that may be considered include the various types of collagens, laminins, elastins, fibrillins, fibronectins, and tenascins.
  • Connective tissues fill in nearly all parts of the human body. However, due to the structural and functional requirements of the connective tissues in different locations, the types of those extracellular matrix components are different, providing excellent choices for target tissue specificity.
  • TNF- ⁇ e.g., infliximab and adalimumab
  • Fc e.g. etanercept
  • IL-1 interleukin-1
  • Antibodies against the shared p40 protein of IL-12 and IL-23 are approved for psoriatic arthritis or in trials for rheumatoid arthritis.
  • An antibody against IL-6 receptor (tocilizumab) is approved for rheumatoid arthritis and systemic juvenile idiopathic arthritis, and several antibodies against IL-6, e.g., sarilumab and olokizumab, are in clinical trials for treating rheumatoid arthritis.
  • An antibody specific for IL-17 is approved for psoriasis and in clinical trials for rheumatoid arthritis and ankylosing spondylitis.
  • infliximab can cause serious blood disorders, like leukopenia and thrombocytopenia, serious infections, lymphoma and other solid tumors, reactivation of hepatitis B and tuberculosis, and other serious problems.
  • Anakinra causes frequent infections, and severe side effects on the gastrointestinal and the respiratory tracts and the blood forming organs. It is important that the serious side effects of these widely used therapeutic agents be minimized, while retaining or even enhancing their therapeutic effects.
  • rheumatoid arthritis joints of the knees, fingers, toes, and other joints are affected, and in ankylosing spondylitis, joints of the spine and the sacroiliac joint of the pelvis are affected.
  • the articular cartilage in the joints is a smooth cartilage that contains an extracellular matrix.
  • the cartilage is avascular and approximately 60% of the weight is water and the remaining content is composed of collagens and ⁇ -aggrecan, a proteoglycan, and other matrix molecules.
  • Collagen II forms the major fibril in the cartilage.
  • Aggrecan is the second most abundant component in the cartilage.
  • Collagen XI is bound to the surface of the collagen II fibril helping to form fibril networks and collagen IX is associated with collagen II and collagen XI.
  • the cartilage has a large surface and the ⁇ -aggrecan has a structure and shape like a feather.
  • the joints have also ligaments, which connect adjacent bones, such as the cruciate ligaments, and tendons, which connect muscles to the bones.
  • the ligaments and tendons are formed by fibrous network of collagen types I, II, and III, and elastin and fibrillins 1 and 2.
  • the present invention rationalizes that the antagonist for TNF- ⁇ , IL-1, and IL-12/IL-23 can be carried to the diseased joints by using antibody fragments, such as scFv, specific for collagen II, ⁇ -aggrecan, collagen XI or collagen IX, or alternatively, collagen I, elastin or fibrillin 1 as the targeting agent.
  • a preferred anti-collagen II antibody is one that binds to native collagen II in the joints and does not bind to N-terminal and C-terminal propeptides, which are cleaved off during fibril assembly.
  • Psoriasis involves mainly keratinocytes in part of skin in the affected patients.
  • the keratinocytes are in the outmost, epidermis layer of the skin; blood vessels, sweat glands, and collagen fibers are in the middle dermis layer of the skin.
  • the inner layer is hypodermis, where adipose tissues are.
  • the three layers of human skin together are 2-3mm thick. If the anti-inflammatory antibodies are delivered to the dermis layer by scFv specific for collagen I, they can diffuse into the other layers. Or, the antibodies can trap inflammatory cytokines in the three layers of the skin.
  • the dermo-epidermal junction is the area of tissue that joins the epidermal and dermal layers of the skin.
  • the basal cells in the stratum basale of epidermis connect to the basement membrane by the anchoring filament of hemidesmosomes.
  • the cells of the papillary layer of the dermis are attached to the basement membrane by anchoring fibrils, which consist of type VII collagen.
  • Type XVII collagen a transmembrane protein (also referred to as BP180) expressed on keratinocytes, is a structural component of hemidesmosomes, multiprotein complexes at the dermal-epidermal basement membrane zone that mediate adhesion of keratinocytes to the underlying membrane.
  • Laminins are structural non-collagenous glycoproteins present in basement membranes. Among the many types of laminins, types 5, 6, and 10 are specific of the basal lamina present under stratified epithelia.
  • SLE Systemic lupus erythematosus
  • syndrome is an autoimmune disease, in which the immune system attacks the exocrine glands, specifically the salivary and lacrimal glands, which produce saliva and tears, respectively, resulting the symptoms of dry eyes and dry mouth, leading to infections and various other problems. Both of these diseases occur 9 times more frequently in women than in men, especially in women of child-bearing ages 15 to 35.
  • SLE is a systemic autoimmune connective tissue disease and affects many organs and tissues. In general, those tissues and organs, such as the heart, lungs, bladder, and kidneys, which exhibit elasticity and can expand and contract, contain collagen network. In several types of SLE, cutaneous manifestation of inflammatory symptoms is prominent.
  • belimumab For more than 50 years, not a single new therapeutic agent had been developed for SLE, until belimumab, a human monoclonal antibody specific for BAFF was developed and approved. However, the therapeutic effect of belimumab for SLE has been considered to be marginal. Belimumab causes a host of side effects, including more incidences of serious infections and deaths in the treatment group than the placebo group. Interestingly, in a phase II trial on syndrome, belimumab showed more successful results than in SLE.
  • IFN- ⁇ Several monoclonal antibodies specific for IFN- ⁇ , including rontalizumab, sifalimumab, and anifrolumab have been studied in clinical trials for the treatment of SLE. Since IFN- ⁇ is involved in many functions, a systemic administration of an antibody against IFN- ⁇ without localized targeting to disease sites may render serious side effects.
  • Anti-TNF- ⁇ (such as adalimumab) has also been approved for treating Crohn’s disease and ulcerative colitis (aform of inflammatory bowel disease) .
  • the administration of anti-TNF- ⁇ is associated with a range of series side effects, including severe infectious diseases and B cell lymphoma. Therefore, in treating patients with Crohn’s disease or ulcerative colitis with anti-TNF- ⁇ , it will be desirable to distribute the administered anti-TNF- ⁇ in favor of the intestine and colon. It has been found collagen III and type V are relatively abundant in the connective tissues in the intestine and bowel.
  • therapeutic agents include (1) a large number of compounds targeting key cellular regulatory pathways or structural components, or damaging DNA or important cellular machinery, (2) antibodies specific for surface antigens of certain cell types or specific for certain tumor-associated antigens and capable of mediating apoptosis, antibody-dependent cellular cytotoxicity (ADCC) , or complement-mediated cytolysis (CMC) of the targeted cells, (3) antibodies specific for certain tumor-associated antigens, which are conjugated with potent cytotoxic drugs, (4) immunoregulatory cytokines, such as such as interferon- ⁇ (IFN- ⁇ ) , interleukin-2 (IL-2) , or interferon- ⁇ (IFN- ⁇ ) , which can activate the immune system in fighting against malignant cells,
  • IFN- ⁇ interferon- ⁇
  • IL-2 interleukin-2
  • IFN- ⁇ interferon- ⁇
  • therapeutic agents for treating cancer as well as for many other diseases are limited or compromised by their toxicity, because the agents also act on some normal cells to some degrees. Therefore, many therapeutic agents have limited therapeutic windows and therefore, in order to control their toxic effects, they are administered in many of the treated patients at suboptimal doses, as far as therapeutic efficacy is concerned, which are insufficient to achieve satisfactory therapeutic effects.
  • the antibody-drug conjugate approach which is being pursued actively, requires that the tumor-targeting antibodies together with the carried cytotoxic drugs be internalized by the targeted cells expressing the tumor-associated antigens, which the targeting antibodies recognize. This requirement may potentially limit the power of the current antibody-drug conjugate approach, because cells in a tumor express a tumor-associated antigen at varying densities. Those cells expressing relatively low levels may not be killed by the current antibody-drug conjugates during treatment and will grow up as the therapeutic agents are discontinued.
  • the cancer derived from malignantly transformed cells of the lymphoid and myeloid lineages account for a significant proportion among all cancer. Those tumors are generally diffusive and not solid. Thus, the targeting of leukocyte-derived tumors will involve the targeting of the individual tumor cells. Therefore, the identification of the expression of cell-surface antigens of the tumor cells is a key in the targeting of leukocyte-derived tumors.
  • Tumors derived from white blood cells are generally classified into three categories: (1) leukemia found in the blood and bone marrow, (2) lymphoma found in the lymphatic system, and (3) myeloma in many parts of bone marrow and also in the blood.
  • Leukemia has four broad classifications: (1) acute lymphocytic leukemia (ALL) , (2) chronic lymphocytic leukemia (CLL) , (3) acute myelogenous leukemia (AML) , and (4) chronic myelogenous leukemia (CML) .
  • ALL acute lymphocytic leukemia
  • CLL chronic lymphocytic leukemia
  • AML acute myelogenous leukemia
  • CML chronic myelogenous leukemia
  • new types of leukemia such as B cell CLL, T cell CLL, B cell prolymphocytic leukemia, Hairy cell leukemia, and others are been defined.
  • Lymphomas are divided into two categories: (1) Hodgkin lymphomas and (2) non-Hodgkin lymphomas. Of the patients who have lymphomas, about 12% have Hodgkin lymphomas and the rest have non-Hodgkin lymphomas. Of the non-Hodgkin lymphomas, most are B cell-derived and there are many subtypes of B cell non-Hodgkin lymphomas. The rest of the non-Hodgkin lymphomas are T cell lymphomas.
  • Myeloma is derived from antibody-producing plasma cells and is also referred to as plasmacytoma.
  • Myeloma cells are found in bone marrow and can travel in the blood circulation and establish growth in many parts of the bone and hence myeloma is also called multiple myeloma.
  • leukemia, lymphomas, and myeloma are derived from myeloid, lymphoid, and plasma cells
  • diagnosis of the tumor types is often very complex, involving tissue and cellular examinations with histological, immunohistological, morphological, and cellular marker analyses of the biopsied tumor samples.
  • the pluripotent stem cells, the myeloid lineage which differentiate into granulocytes (neutrophils, eosinophils, and basophils) , monocytes and macrophages, and platelets, and the lymphoid lineage, which differentiate into B cells and T cells, undergo many steps of differentiation and maturation, the malignant transformation can occur at any of the differentiation stages.
  • the cancerous transformation may augment and gain certain traits and reduce or lose certain traits.
  • the surface markers or differentiation antigens especially those, which have been assigned a CD (cluster of differentiation) number, have become very useful and often necessary to identify the various leukocytes and immunocytes in the studies of innate and adaptive immunity. Often the identification of a cell type requires a set of markers.
  • ALL is derived from lymphoblasts, precursor B cells, precursor T cells, or B cells.
  • ALL consists of the immunophenotypic subtypes: (1) precursor B cell acute lymphoblastic leukemia, which expresses cell surface markers associated with B cell precursors and precursor T cell acute lymphoblastic leukemia, which express markers of precursor T cells, (2) Burkitt’s lymphoma, which is derived from B cells of the germinal center and express cell surface markers associated with B cells, and (3) acute biphenotypic leukemia, which express markers of both lymphoid and myeloid cells.
  • CLL is also referred to as B-cell CLL (B-CLL) , because CLL is mostly derived from B cells.
  • B-CLL B-cell CLL
  • ALL is derived from lymphoblasts, which are the common precursors of B cells and T cells and CLL is derived from B cells.
  • All CLL cells in a patient are from monoclonal, derived original one B cell of a particular set of V H and V L .
  • the cells of CLL express CD19 and CD20, and characteristically CD5 and CD23.
  • Hodgkin lymphomas are characterized by the presence of Reed-Sternberg cells, which are multi-nucleated giant cells derived from B cells. There are at least four subtypes of Hodgkin lymphomas based on the morphology of Reed-Sternberg cells and the composition of reactive cell infiltrate in the lymph node biopsy specimen: (1) nodular sclerosing Hodgkin lymphoma, (2) mixed-cellularity, (3) lymphocyte-rich or lymphocytic predominance, and (4) lymphocyte depleted. It is well established that Hodgkin lymphoma is derived from mature B cells.
  • Cells of Hodgkin lymphoma depending on its immunophenotype, express a subset of CD15, CD20, CD30, CD79a, and CD138. Most of the cases of non-Hodgkin lymphomas are derived from B cells. There are at least 14 subtypes of B-cell non-Hodgkin lymphomas.
  • B lymphocytes are the source of antigen-specific antibodies and are a critical component of the adaptive immune system for the defense against infectious pathogens.
  • B cells can also be pathogenic and the cause of several types of diseases.
  • B-cell disorders are divided into undesired immunoglobulin production (autoimmune and allergic diseases) and uncontrolled proliferation (lymphomas, leukemia) .
  • B cells have proven to be effective targets for the treatment of multiple autoimmune disorders and B-lineage cancer. Many approaches pertaining to B-cell depletion for the treatment of B cell malignancies and antibody-mediated diseases have been developed with partial success or are in active experimental stages.
  • a number of therapies and drugs have been experimented and a few have been approved for the treatment of multiple myeloma. These include corticosteroids, chemotherapies, proteasome inhibitors, and immunoregulatory compounds.
  • Ig ⁇ (CD79a) /Ig ⁇ (CD79b) is set of antigens that are expressed in association of the B cell receptor (BCR) complex on the surface of cells of the B-cell linage.
  • Ig ⁇ /Ig ⁇ is a heterodimeric transmembrane protein, which is composed of two distinct chains Ig ⁇ and Ig ⁇ stabilized by disulfide bonding.
  • Ig ⁇ /Ig ⁇ forms a complex with the BCR and generates a signal following recognition of antigen by the BCR complex.
  • Ig ⁇ /Ig ⁇ is expressed in the pre-B-cell stage and is early than CD20 for the expression pattern on the B-cell lineage.
  • Ig ⁇ /Ig ⁇ has been considered as attractive target for the B cell depletion therapy in the treatment of non-Hodgkin lymphomas because Ig ⁇ /Ig ⁇ is expressed on B cells and on most non-Hodgkin lymphomas.
  • the mIgD and mIgM are coexpressed on the surface of mature B cells and function as part of BCR.
  • the mIgD contains a unique migis- ⁇ peptide segment of 27 AA, which represents the extracellular portions of the membrane-anchoring segment of mIgD and is located between the CH3 domain and transmembrane segment. It has been proposed that migis- ⁇ peptide provides an antigenic site for targeting mIgD-expressing B cells. The site is present on the mIgD-expressing B cells and not on the secreted IgD.
  • T lymphocyte subsets through their surface molecules and secreted factors mediate a complex network of immunoregulatory activities on humoral and cellular immune effector functions, including the production of different classes of antibodies, the secretion of various cytokines, and the generation of cytotoxic T cells and other cytolytic cells.
  • Many autoimmune diseases are caused by the abnormal activities of T cells against self-components or cells. For example, in type-I diabetes, the insulin-producing ⁇ cells in the islets of Langerhans of pancreas are attacked and killed by autoimmune T cells.
  • the devastating autoimmune diseases such as systemic lupus erythematosus (SLE) , multiple sclerosis, and inflammatory bowel diseases, are caused mainly by T cells.
  • SLE systemic lupus erythematosus
  • multiple sclerosis multiple sclerosis
  • inflammatory bowel diseases are caused mainly by T cells.
  • the rejection reaction toward organ or tissue transplants is mediated mainly by T cells.
  • T cell malignancy There are also a few forms of T cell malignancy.
  • modulating T cell activities or removing T cells has been an active area of drug discovery research.
  • a variety of antibodies and their modified forms against T cell surface antigens, including CD3, CD4, CD8, CD25, and CD28 have been studied in animal models or human clinical trials for treating various human diseases mentioned above.
  • Some antibodies with or without the conjugation with cytotoxic drugs can cause the lysis of the targeted T cell subsets.
  • Some antibodies can cause anergy or an idled, inactive state of T cells without actually lysing the cells.
  • T lymphocytes play major roles in regulating activities of various immunocytes and various other cell types in adaptive and native immunity.
  • therapeutic agents to target lymphocytes, fewer candidates have been successfully developed for targeting T cells than for targeting B cells.
  • therapeutic antibodies that are being developed to target surface antigens of T cell subsets.
  • Antibodies targeting T cell surface antigens can potentially be employed to treat malignant tumors derived from T cells.
  • Antibodies may also be used to modulate T cell activities, either to inhibit them or to enhance them.
  • CML is a clonal bone marrow stem cell disorder and resulted from the malignant transformation of a stem cell or myeloid stem cell, resulting from the chromosome translocation called the Philadelphia chromosome.
  • tumor-associated antigens For example, serum samples from patients with pancreatic tumors and many types of gastrointestinal cancer, including colorectal cancer, esophageal cancer, and hepatocellular carcinoma, contain CA19-9 antigen (carbohydrate antigen 19-9, a sialyl-Lewis A antigen) . The cells of those tumors express CA19-9 on the extracellular matrix on cell surface.
  • CA-125 carbohydrate antigen 125, mucin 16
  • MUC1 cell surface associated glycoprotein mucin 1
  • the ganglioside GD2 is highly expressed on neuroectoderm-derived tumors and sarcomas, including neuroblastoma, retinoblastoma, melanoma, small cell lung cancer, brain tumors, osteosarcoma, rhabdomyosarcoma, Ewing’s sarcoma in children and adolescents, as well as liposarcoma, fibrosarcoma, leiomyosarcoma and other soft tissuesarcoma in adults.
  • neuroectoderm-derived tumors and sarcomas including neuroblastoma, retinoblastoma, melanoma, small cell lung cancer, brain tumors, osteosarcoma, rhabdomyosarcoma, Ewing’s sarcoma in children and adolescents, as well as liposarcoma, fibrosarcoma, leiomyosarcoma and other soft tissuesarcoma in adults.
  • mesothelin is expressed on normal mesothelial cells, it is expressed on many human cancers, mesothelioma, tumors of the pancreas, ovary, lung, and stomach, cholangiocarcinoma, and triple-negative breast cancer.
  • Tn antigen is a structural element on glycoproteins, in which N-acetylgalactosamine (GalNAc) is linked to serine or threonine by a glycosidic bond, i.e. as an O-glycan.
  • GalNAc N-acetylgalactosamine
  • Addition of single monosaccharide residues creates disaccharide antigens: the Thomsen-Friedenreich antigen (TF antigen or T antigen) is formed by substitution with galactose (Gal (b1-3) GalNAc) ; the sialyl-Tn antigen (STn antigen) is formed by substitution with sialic acid (Neu5Ac (a2-6) GalNAc.
  • TN and sialy-Tn are not usually found on healthy cell surfaces, but may be found on cancer cells.
  • Tumor-associated antigens that have been widely studied as markers of tumors or explored as targets for immunological therapies include (1) epidermal growth factor receptors (EGFRs) –human epidermal growth factor 1 (EGFR or HER1) , HER2, HER3, HER4, or their mutants; (2) glycoproteins –CA19-9 (bearing Sialyl Lewis A antigen) , CA125 (bearing mucin 16 or MUC 16) , cell surface-associated mucin 1 (MUC1) , or carcinoembryonic antigen, melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) , or mesothelin, ; (3) mucin-related Tn or Sialyl Tn; (4) the blood group Lewis related Lewis Y , Sialyl Lewis Y , Sialyl Lewis A , or Lewis X ; (5) glycosphingolipids -Globo H or stage-specific embryo
  • CCK cholecystokinin
  • the tumorous cells When malignant transformation occurs to the receptor-bearing cells, the tumorous cells maintain the expression of the receptors. In fact, in many cases, an abnormally high expression of the receptors occurs due to certain mutations in the cells, which are not necessarily in the receptors themselves. The affected cells thus become malignantly transformed.
  • the overexpression of receptors on tumors, e.g., somatostatin receptors are strongly expressed on most neuroendocrine tumors, and the targeting of those receptors for therapeutic and diagnostic (e.g., radio-imaging) purposes have been an active area of research.
  • Neuroendocrine tumors are generally rare, but include a long list of tumors of various cell origins, including those of gastroenteropancreatic neuroendocrine tumors, thyroid gland tumors, Merkel cell carcinoma, adrenomedullary tumors, and many others.
  • EGFRs epidermal growth factor receptors
  • monoclonal antibody trastuzumab specific for HER2/Neu receptor is broadly used for treating HER2-positive breast cancer.
  • Cetuximab specific for EGFR is being used in treating metastatic colon cancer, metastatic non-small cell lung cancer, and head and neck cancer.
  • Pancreatic cancer is one of the most vicious cancers.
  • the pancreatic (ductal or invasive) adenocarcinoma derived from the exocrine cells account for 85% , although those ductal epithelial cells account only for 10% among all cells in the pancreas.
  • the exocrine cells express receptors for the peptide hormones, gastrin, secretin, or cholecystokinin, which are secreted by the cells in the stomach and duodenum, and respond to those hormones and secrete bicarbonate ions and digestive enzymes.
  • the overexpressed receptors for CCK and gastrin in pancreatic cancer and many other types have also been explored as a target for radioimaging.
  • somatostatin and gastrin-releasing peptide are somatostatin and gastrin-releasing peptide.
  • CCK or gastrin of their peptide analogues are coupled with chelating groups for radioactive nuclides.
  • the imaging agents bind to the primary or metastasized tumors containing cells expressing the receptors.
  • Peptide hormones or their analogues carrying radionuclides, lutetium-177, yttrium-90, or indium-111 have also been experimented for treating tumors.
  • CTLA-4 is a protein receptor that down-regulates the immune system.
  • CTLA-4 is found on the surface of T cells, and acts as an "off" switch when bound to CD80 (B7-1) or CD86 (B7-2) on the surface of antigen presenting cells. Such binding prevents the binding of those receptors by CD28, which activates the immune response.
  • a human IgG1 antibody specific for CTLA-4, ipilimumab has been approved for treating melanoma and in clinical studies for treating several other types of cancer. The treatment with ipilimumab has been associated with severe and potential fatal immunological side effects due to T cell activation and proliferation.
  • An anti-PD-L1 antibody, MPDL3280A, is now in Phase II or III clinical trials for triple-negative breast cancer, metastatic non-small cell lung cancer, bladder carcinoma, and renal cell carcinoma.
  • a large number of anti-PD-1 and anti-PD-L1 antibodies are in research or early clinical trials.
  • VEGF-A Vascular endothelial growth factor A
  • angiogenesis blood vessel formation
  • the blood circulation is required for oxygen and nutrient supplies, waste disposal and many other functions.
  • Antibodies specific for VEGF-A such as bevacizumab specific for VEGF-A, are effective as a monotherapy or in combination with chemotherapy in treating a few forms of cancer.
  • bevacizumab is associated with a range of side effects, including hypertension and heightened risk of bleeding, bowel perforation, and necrotizing fasciitis.
  • the immunoregulatory cytokines referred to in this invention are those that are known to be stimulatory and are major drivers in activating immune responses. These cytokines include interleukin-2 (IL-2) , interferon- ⁇ (IFN- ⁇ ) , interferon- ⁇ (IFN- ⁇ ) , and TNF- ⁇ . Among them, IFN- ⁇ , which is a strong activator of T cells, has been approved for use in hairy-cell leukemia, AIDS-related Kaposi's sarcoma, follicular lymphoma, chronic myeloid leukemia and melanoma.
  • IL-2 interleukin-2
  • IFN- ⁇ interferon- ⁇
  • IFN- ⁇ interferon- ⁇
  • TNF- ⁇ TNF- ⁇
  • cytokines act mainly in the microenvironment of the lymphoid system.
  • denosumab An antibody specific for RANKL (CD254) , the ligand of RANK (RANK, receptor activator of nuclear factor ⁇ B) , denosumab, is approved for the treatment of osteoporosis.
  • the development of denosumab represents a major advancement in the care for osteoporosis.
  • the administration of denosumab causes common side effects, such as infections of the urinary and respiratory tracts, cataracts, constipation, rashes, and joint pain. It is hence desirable that the therapeutic agent is carried preferentially to the bone.
  • RANKL is a membrane protein, belonging to the tumor necrosis factor ligand family. RANKL is detected at high levels in the lung, thymus, and lymph nodes. It is also detected at low levels in the bone marrow, stomach, peripheral blood, spleen, placenta, leukocytes, heart, thyroid and skeletal muscle. Since IgG anti-RANKL, such as denosumab, can serve a therapeutic agent for osteoporosis, the molecular constructs of this invention should provide as better therapeutic agents than IgG anti-RANKL.
  • Another target for antibodies for the treatment of osteoporosis is sclerostin, encoded by SOST gene.
  • the glycoprotein is produced and secreted by osteocytes and negatively regulates osteoblastic bone formation.
  • the loss or defective mutation of SOST gene causes progressive bone thickening.
  • a defective mutation in the SOST gene increases bone formation.
  • Antibodies against sclerostin cause increased bone formation, bone mineral density, and stronger bones.
  • the first aspect of the present disclosure pertains to a linker unit that comprises, (1) a center core that comprises 2-15 lysine (K) residues, and (2) 2-15 linking arms respectively linked to the K residues of the center core.
  • the present center core is characterized in having or being linked with an azide group, an alkyne group, a tetrazine group, or a strained alkyne group at its N-or C-terminus.
  • a PEG chain having a N-hydroxysuccinimydyl (NHS) group at one terminus and a maleimide group at the other terminus is linked to the K residue of the center core by forming an amide bond between the NHS group of the PEG chain and the amine group of the K residue.
  • the PEG chain linked to the K residue is referred to as a linking arm, which has a maleimide group at the free-terminus thereof.
  • the center core is a polypeptide that has 8-120 amino acid residues in length and comprises 2 to 15 lysine (K) residues, in which each K residue and the next K residue are separated by a filler sequence.
  • the filler sequence comprises glycine (G) and serine (S) residues; preferably, the filler sequence consists of 2-15 residues selected from G, S, and a combination thereof.
  • the filler sequence can be,
  • the filler sequence placed between two lysine residues may be variations of glycine and serine residues in somewhat random sequences and/or lengths. Longer fillers may be used for a polypeptide with fewer lysine residues, and shorter fillers for a polypeptide with more lysine residues. Hydrophilic amino acid residues, such as aspartic acid and histidine, may be inserted into the filler sequences together with glycine and serine. As alternatives for filler sequences made up with glycine and serine residues, filler sequences may also be adopted from flexible, soluble loops in common human serum proteins, such as albumin and immunoglobulins.
  • the center core comprises 2-15 units of the sequence of G 1-5 SK.
  • the polypeptide comprises the sequence of (GSK) 2-15 ; that is, the polypeptide comprises at least two consecutive units of the sequence of GSK.
  • the present center core may comprises the amino acid sequence of the following,
  • the center core is a polypeptide that comprises the sequence of (X aa -K) n , in which X aa is a PEGylated amino acid having 2 to 12 repeats of ethylene glycol (EG) unit, and n is an integral from 2 to 15.
  • the present center core is characterized in having or being linked with an azide group, an alkyne group, a tetrazine group, or a strained alkyne group at its N-or C-terminus.
  • the present center core comprises, at its N-or C-terminus, an amino acid residue having an azide group or an alkyne group.
  • the amino acid residue having an azide group can be, L-azidohomoalanine (AHA) , 4-azido-L-phenylalanine, 4-azido-D-phenylalanine, 3-azido-L-alanine, 3-azido-D-alanine, 4-azido-L-homoalanine, 4-azido-D-homoalanine, 5-azido-L-ornithine, 5-azido-d-ornithine, 6-azido-L-lysine, or 6-azido-D-lysine.
  • AHA L-azidohomoalanine
  • 4-azido-L-phenylalanine 4-azido-D-phenylalanine
  • 3-azido-L-alanine 3-azido-D-alanine
  • 4-azido-L-homoalanine 4-azido-D-homo
  • Exemplary amino acid having an alkyne group includes, but is not limited to, L-homopropargylglycine (L-HPG) , D-homopropargylglycine (D-HPG) , or beta-homopropargylglycine ( ⁇ -HPG) .
  • L-HPG L-homopropargylglycine
  • D-HPG D-homopropargylglycine
  • ⁇ -HPG beta-homopropargylglycine
  • Xaa is a PEGylated amino acid having specified repeats of EG unit
  • Ac represents the acetyl group
  • G HP represents the HPG residue
  • amino acids containing an azide or alkyne group in their side chains and PEGylated amino acids are available commercially in t-boc (tert-butyloycarbonyl) -or Fmoc (9-fluorenylmethyloxycarbonyl) -protected forms, which are readily applicable in solid-phase peptide synthesis.
  • Xaa is a PEGylated amino acid having specified repeats of EG unit
  • Ac represents the acetyl group
  • a AH represents the AHA residue
  • G HP represents the HPG residue.
  • the present center core is linked with a coupling arm, which has a functional group (e.g., an azide group, an alkyne group, a tetrazine group, or a strained alkyne group) at the free-terminus thereof (that is, the terminus that is not linked to the center core) .
  • a functional group e.g., an azide group, an alkyne group, a tetrazine group, or a strained alkyne group
  • the present center core comprises a cysteine residue at its N-or C-terminus.
  • the coupling arm has a tetrazine group or a strained alkyne group at the free-terminus thereof.
  • These coupling arms have 2-12 EG units.
  • the tetrazine group is 1, 2, 3, 4-tetrazine, 1, 2, 3, 5-tetrazine, 1, 2, 4, 5-tetrazine, or derivatives thereof.
  • Example of strained alkyne group includes, but is not limited to, trans-cyclooctene (TCO) , dibenzocyclooctyne (DBCO) , difluorinated cyclooctyne (DIFO) , bicyclononyne (BCN) , dibenzocyclooctyne (DICO) .
  • TCO trans-cyclooctene
  • DBCO dibenzocyclooctyne
  • DIFO difluorinated cyclooctyne
  • BCN bicyclononyne
  • DICO dibenzocyclooctyne
  • the tetrazine group is 6-methyl-tetrazine.
  • Example of the present center core linked with the coupling arm includes, but is not limited to,
  • the center core has an azide or alkyne group at one terminus and a coupling arm with tetrazine or strained alkyne group at the other terminus. Examples are the following:
  • the polypeptide may also be synthesized using recombinant technology by expressing designed gene segments in bacterial or mammalian host cells. It is preferable to prepare the polypeptide as recombinant proteins if the core has high numbers of lysine residues with considerable lengths. As the length of a polypeptide increases, the number of errors increases, while the purity and/or the yield of the product decrease, if solid-phase synthesis was adopted.
  • a filler sequence ranges from a few amino acid residues to 10-20 residues may be placed between two K residues.
  • the N-terminal or C-terminal residue for those recombinant polypeptides is cysteine.
  • the terminal cysteine residue is then reacted with short bifunctional cross-linkers, which have maleimide group at one end, which reacts with SH group of cysteine residue, and alkyne, azide, tetrazine, or strained alkyne at the other end.
  • PEGylated amino acids with varying lengths (i.e., numbers of repeated ethylene glycol units) may be employed, offering flexibility for solubility and spacing between adjacent amino groups of lysine residues.
  • the center cores may also be constructed to comprise artificial amino acids, such as D-form amino acids, homo-amino acids, N-methyl amino acids etc.
  • the PEGylated amino acids with varying lengths of polyethylene glycol (PEG) are used to construct the center core, because the PEG moieties contained in the amino acid molecules provide conformational flexibility and adequate spacing between conjugating groups, enhance aqueous solubility, and are generally weakly immunogenic.
  • PEG polyethylene glycol
  • the present center has an acetyl group to block the amino group at its N-terminus.
  • the number of the linking arms linked to the center core is mainly determined by the number of lysine resides comprised in the center core. Since there are at least two lysine residues comprised in the present center core, the present linker unit may comprise a plurality of linking arms.
  • the linker unit 10A comprises a center core 11a comprising one HPG (G HP ) residue and four lysine (K) residues respectively separated by filler sequences (denoted by the dots throughout the drawings) .
  • the filler sequences between the HPG residue and K residue or between any two K residues may comprise the same or different amino acid sequences.
  • four linking arms 20a-20d are linked to the lysine residues by forming an amide linkage between the NHS group and the amine group of the lysine reside, respectively.
  • linker unit 10A or any other following linker units are common to other linker units disclosed herein, and hence some or all of these features are also applicable in the following examples, unless it is contradictory to the context of a specific embodiment. However, for the sake of brevity, these common features may not be explicitly repeated below.
  • Figure 1B provides a linker unit 10B according to another embodiment of the present disclosure.
  • the center core 11b comprises one cysteine (C) residue and six lysine (K) residues respectively separated by the filler sequences.
  • the linker unit 10A comprises six linking arms 20a-20f that are respectively linked to the lysine residues.
  • the linking arm is a PEG chain having 2-20 repeats of EG units.
  • the linker unit 1B further comprises a coupling arm 60.
  • a PEG chain having a maleimide group at one end and a functional group at the other end is used to form the coupling arm 60.
  • the coupling arm 60 is linked to the cysteine residue of the center core 11b via thiol–maleimide reaction.
  • the functional group at the free terminus of the coupling arm 60 is a tetrazine group 72.
  • the coupling arm is a PEG chain having 2-12 repeats of EG units.
  • a cleavable bond can be installed in the linking arm.
  • Such a bond is cleaved by acid/alkaline hydrolysis, reduction/oxidation, or enzymes.
  • One embodiment of a class of cleavable PEG chains that can be used to form the coupling arm is NHS-PEG 2-20 -S-S-maleimide, where S-Sis a disulfide bond that can be slowly reduced, while the NHS group is used for conjugating with the amine group of the center core, thereby linking the PEG chain onto the center core.
  • the maleimide group at the free terminus of the linking arm may be substituted by an azide, alkyne, tetrazine, or strained alkyne group.
  • the linking arm that is linked to the K residue of the center core has a maleimide group at its free terminus.
  • a functional element such as, a targeting element or an effector element
  • the functional elements linked to the linking arms are referred to as the first elements.
  • the number of the first elements carried by the present linker unit depends on the number of K residues of the center core (and thus, the number of the linking arms) . Accordingly, one of ordinary skill in the art may adjust the number of the first elements of the linker unit as necessary, for example, to achieve the desired targeting or therapeutic effect.
  • FIG. 1C An example of a linker unit 10C having the first elements is illustrated Figure 1C. Other than the features disused hereafter, Figure 1C is quite similar to Figure 1B.
  • the optional tetrazine group 72 allows for the conjugation with an additional functional element, another molecular construct (see, Part III or Part VII below) .
  • the present linker unit may further comprise a second element in addition to the first element.
  • the second element can be either a targeting element or an effector element.
  • the first element is an effector element, while the second element may be another effector element, which works additively or synergistically with or independently of the first element.
  • the first and second elements exhibit different properties; for example, the first element is a targeting element, and the second element is an effector element, and vice versa.
  • the first element is an effector element
  • the second element is an element capable of improving the pharmacokinetic property of the linker unit, such as solubility, clearance, half-life, and bioavailability.
  • the first element is the targeting element that renders the present linker unit specifically target to a lesion site
  • the second element is the effector element that elicits a therapeutic effect once the present linker unit is delivered to the lesion site.
  • the present linker unit may comprise a plurality of targeting elements as the first elements and one effector element as the second element.
  • the targeting element specifically targets the cell surface antigen expressed on the diffused tumor (e.g., CD5, CD19, CD20, CD22, CD23, CD30, CD37, CD79a, or CD79b) ; while the effector element (e.g., the antibody fragment specific for CD3 or CD16a) recruits T cells or NK cells to kill the tumor cells.
  • the diffused tumor e.g., CD5, CD19, CD20, CD22, CD23, CD30, CD37, CD79a, or CD79b
  • the effector element e.g., the antibody fragment specific for CD3 or CD16a recruits T cells or NK cells to kill the tumor cells.
  • the first element is the effector element and the second element is the targeting element.
  • the present linker unit may comprise one targeting element that specifically targets the tissue-associated extracellular matrix protein (e.g., ⁇ -aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, and collagen XI) and a plurality of effector elements that produce an therapeutic effect on the lesion site.
  • tissue-associated extracellular matrix protein e.g., ⁇ -aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, and collagen XI
  • the center core comprises an amino acid having an azide group (e.g., the AHA residue) at its N-or C-terminus; and accordingly, a second element having an alkyne group is linked to the N-or C-terminus of the center core via the CuAAC reaction.
  • an azide group e.g., the AHA residue
  • the center core comprises an amino acid having an alkyne group (e.g., the HPG residue) at its N-or C-terminus; and a second element having an azide group is thus capable of being linked to the N-or C-terminus of the center core via the “Copper (I) -catalyzed alkyne-azide cycloaddition (CuAAC) ” reaction (or the “click” reaction for short) as exemplified in Scheme 1.
  • CuAAC Copper
  • the CuAAC reaction yields 1, 5 di-substituted 1, 2, 3-triazole.
  • the reaction between alkyne and azide is very selective and there are no alkyne and azide groups in natural biomolecules. Furthermore, the reaction is quick and pH-insensitive. It has been suggested that instead of using copper (I) , such as cuprous bromide or cuprous iodide, for catalyzing the click reaction, it is better to use a mixture of copper (II) and a reducing agent, such as sodium ascorbate to produce copper (I) in situ in the reaction mixture.
  • copper (I) such as cuprous bromide or cuprous iodide
  • the second element can be linked to the N-or C-terminus of the present center core via a copper-free reaction, in which pentamethylcyclopentadienyl ruthenium chloride complex is used as the catalyst to catalyze the azide-alkyne cycloaddition.
  • Figure 1D provides an example of the present linker unit carrying a plurality of first elements and one second element.
  • the center core 11c comprises one HPG (G HP ) residue and five lysine (K) residues.
  • Five linking arms 20a-20e are respectively linked to the five K residues of the center core 11c; and five first elements 30a-30e are respectively linked to said five linking arms 20a-20e via the thiol-maleimide reaction.
  • the linker unit 10D further comprises one second element 50 that is linked to one end of a short PEG chain 62. Before being conjugated with the center core 11c, the other end of the short PEG chain 62 has an azide group.
  • the azide group may reacted with the HPG residue that having an alkyne group via CuAAC reaction, so that the second element 50 is linked to the center core 11c.
  • the solid dot 40 depicted in Figure 1D represents the chemical bond resulted from the CuAAC reaction occurred between the HPG residue and the azide group.
  • the second element is linked to the center core via a coupling arm.
  • the coupling arm has a tetrazine group, which can be efficiently linked to a second element having a TCO group via the inverse electron demand Diels–Alder (iEDDA) reaction (see, scheme 2) .
  • the coupling arm has a TCO group, which is capable of being linked to a second element having a tetrazine group via the iEDDA reaction.
  • the strained cyclooctenes that possess a remarkably decreased activation energy in contrast to terminal alkynes is employed, and thus eliminate the need of an exogenous catalyst.
  • the center core 11d comprises a terminal cysteine (C) residue and five lysine (K) residues.
  • C cysteine
  • K lysine
  • five linking arms 20a-20e are respectively linked to the five K residue of the center core 11d, and then five first elements 30a-30e are respectively linked to the five linking arms 20a-20e via thiol-maleimide reactions.
  • the cysteine residue is linked to the coupling arm 60, which, before being conjugated with the second element, comprises a tetrazine group or a TCO group at its free-terminus.
  • a second element 50 linked with a short PEG chain 62 having a corresponding TCO or tetrazine group can be linked to the coupling arm 60 via the iEDDA reaction.
  • the ellipse 70 as depicted in Figure 1E represents the chemical bond resulted from the iEDDA reaction occurred between the coupling arm 60 and the short PEG chain 62.
  • the coupling arm before the conjugation with a second element, has an azide group.
  • the coupling arm can be linked to the second element having a strained alkyne group (e.g., the DBCO, DIFO, BCN, or DICO group) at the free-terminus of a short PEG chain via SPAAC reaction (see, scheme 3) , and vice versa.
  • a strained alkyne group e.g., the DBCO, DIFO, BCN, or DICO group
  • the linker unit 10F has a structure similar to the linker unit 10E of Figure 1E, except that the coupling arm 60 comprises an azide or a strained alkyne group (e.g., the DBCO, DIFO, BCN, or DICO group) , instead of the tetrazine or TCO group.
  • the second element 50 linked with a short PEG chain 62 may have a corresponding strained alkyne (e.g., DBCO, DIFO, BCN, or DICO) or azide group, so that it can be linked to the coupling arm 60 via the SPAAC reaction.
  • the diamond 90 as depicted in Figure 1F represents the chemical bond resulted from the SPAAC reaction occurred between the coupling arm 60 and the short PEG chain 62.
  • Scheme 4 is an exemplary illustration of the process of preparing the present linker unit.
  • the center core comprising the amino acid sequence of (GSK) 3 and a L-azidohomoalanine (AHA) residue at the C-terminus thereof is prepared.
  • three linking arms are respectively linked to the lysine (K) residues of the center core via forming an amide bond between the NHS group and the amine group; the linking arm linked to the center core has a maleimide (Mal) group at the free-terminus thereof.
  • three anti-A antigen scFvs (scFv ⁇ A) as the first element are respectively linked to the linking arms via the thiol-maleimide reaction.
  • step 4 one anti-B antigen scFv (scFv ⁇ B) as the second element is linked with a short PEG chain that has 4 repeats of EG units and a DBCO group at the free terminus.
  • step 5 the second element is linked to the AHA residue of the center core via the SPAAC reaction.
  • Scheme 5 illustrates another example of the process for preparing the present linker unit.
  • the center core comprising the amino acid sequence of (K-Xaa) 3 and a cysteine residue at the C-terminus thereof is prepared.
  • a PEG chain (as the coupling arm) that has the maleimide (Mal) group at one terminus and a tetrazine group at the other terminus is linked to the cysteine residue via the thiol-maleimide reaction.
  • three linking arm are respectively linked to the lysine (K) residues of the center core.
  • step 5 three anti-A antigen scFvs (scFv ⁇ A) as the first elements are respectively linked to the linking arms via the thiol-maleimide reaction as described in step 4. Meanwhile, in step 5, one anti-B antigen scFv (scFv ⁇ B) as the second element is linked with a short PEG chain that has 3 repeats of EG units and a TCO group at the free terminus. Finally, in step 6, the second element is linked to the coupling arm via the iEDDA reaction.
  • Figure 1G provides an alternative example of the present linker unit (linker unit 10G) , in which five first elements 30 are respectively linked to the lysine residues via the linking arms 20 and the AHA (A AH ) residue of the center core 11e is linked with a PEG chain 80 via the CuAAC reaction.
  • the solid dot 40 depicted in Figure 1G represents the chemical bond resulted from the CuAAC reaction occurred between the AHA residue and the PEG chain 80.
  • Figure 1H provides another example of the present disclosure, in which the N-terminus of the center core 13 is a cysteine residue that is linked to a coupling arm 60.
  • a PEG chain 80 can be efficiently linked to the coupling arm 60 via the iEDDA reaction.
  • the ellipse 70 of the linker unit 10H represents the chemical bond resulted from the iEDDA reaction occurred between the coupling arm 60 and the PEG chain 80.
  • Figure 1I provides an alternative example of the present linker unit, in which the linker unit 10I has a structure similar to the linker unit 10G of Figure 1G, except that the PEG chain 80 is linked to the coupling arm 60 via the SPAAC reaction.
  • the diamond 90 depicted in Figure 1I represents the chemical bond resulted from the SPAAC reaction occurred between the coupling arm 60 and the PEG chain 80.
  • the present linker unit further comprises a third element.
  • one of the N-and C-terminus of the center core is an amino acid having an azide group or an alkyne group
  • the other of the N-and C-terminus of the center core is a cysteine residue.
  • the lysine residues of the center core are respectively linked with the linking arms, each of which has a maleimide group at its free terminus; whereas the cysteine residue of the center core is linked with the coupling arm, which has a tetrazine group or a strained alkyne group at its free terminus.
  • the first element is therefore linked to the linking arm via the thiol-maleimide reaction
  • the second element is linked to the coupling arm via the iEDDA reaction
  • a third element is linked to the terminal amino acid having an azide group or an alkyne group via the CuAAC reaction or SPAAC reaction.
  • the linker unit may have two different kinds of targeting elements and one kind of effector element, two different kinds of effector elements and one kind of targeting element, or one kind of targeting element, one kind of effector element, and one element capable of improving the pharmacokinetic property of the linker unit, such as solubility, clearance, half-life, and bioavailability.
  • the center core 11f has an HPG (G HP ) residue at the N-terminus thereof and a cysteine residue at the C-terminus thereof.
  • the linking arms 20 and the coupling arm 60 are respectively linked to the lysine (K) residues and the cysteine (C) residue of the center core 11f.
  • five first elements 30 are respectively linked to the five linking arms 20, the second element (i.e., the PEG chain) 80 is linked to the coupling arm 60 via the short PEG chain 62, and the third element 50 is linked to the HPG residue.
  • the solid dot 40 indicated the chemical bond resulted from the CuAAC reaction occurred between the HPG residue and the short PEG chain 62; while the ellipse 70 represents the chemical bond resulted from the iEDDA reaction occurred between the coupling arm 60 and the PEG chain 80.
  • Figure 1K provides another embodiment of the present disclosure, in which the linker unit 10K has the similar structure with the linker unit 10J of Figure 1J, except that the short PEG chain 62 is linked with the HPG residue via the SPAAC reaction, instead of the iEDDA reaction.
  • the diamond 90 in Figure 1K represents the chemical bond resulted from the SPAAC reaction occurred between the short PEG chain 62 and the HPG residue.
  • the linking arms have a maleimide group in the free terminus for conjugating with first elements having the sulfhydryl group via the thiol-maleimide reaction. Also, there is one cysteine residue or an amino acid residue with an azide or alkyne group at a terminus of the peptide core for attaching a coupling arm for linking a second element.
  • a conjugating group, other than maleimide, such as azide, alkyne, tetrazine, or strained alkyne may be used for the free terminus of the linking arms, for linking with first elements with a CuAAC, iEDDA, or SPAAC reaction.
  • the cysteine residue (or an amino acid residue with an azide or alkyne group) of the peptide core needs not to be at the N-or C-terminus.
  • two or more of such residues may be incorporated in the peptide core to attach multiple coupling arms for linking a pleural of second elements.
  • the number of the functional elements may be adjusted in accordance with the needs and/or applications.
  • the present linker unit may comprise two elements (i.e., the first and second elements) or three elements (i.e., the first, second, and third elements) in accordance with the requirements of the application (e.g., the disease being treated, the route of administration of the present linker unit, and the binding avidity and/or affinity of the antibody carried by the present linker unit) .
  • the present linker unit is directly delivered into the tissue/organ (e.g., the treatment of eye)
  • one element acting as the effector element may be enough, thus would eliminate the need of a second element acting as the targeting element.
  • the present linker unit when the present linker unit is delivered peripherally (e.g., oral, enteral, nasal, topical, transmucosal, intramuscular, intravenous, or intraperitoneal injection) , it may be necessary for the present linker unit to simultaneously comprise a targeting element that specifically targets the present linker unit to the lesion site; and an effector element that exhibits a therapeutic effect on the lesion site.
  • a targeting element that specifically targets the present linker unit to the lesion site
  • an effector element that exhibits a therapeutic effect on the lesion site.
  • a third element e.g., a second targeting element, a second effector element, or a PEG chain
  • the first element is provided in the form of a bundle.
  • the number of the first element may vary with the number of lysine residue comprised in the center core. If the number of lysine residue in the center core ranges from 2 to 15, then at least two first elements may be comprised in each linker unit.
  • the present linker unit is capable of providing more functional elements (either as targeting elements or as effector elements) at one time, thereby greatly improves the therapeutic effect.
  • a single copy of a targeting or effector element In certain therapeutic applications, it is desirable to have a single copy of a targeting or effector element. For example, in using an scFv for targeting an extracellular matrix protein for delivering a bundle of scFv for neutralizing a pro-inflammatory cytokine, a single copy of the scFv specific for the extracellular protein is desirable, so that unwanted effects due to overly tight binding may be avoided.
  • scFv specific for CD3 or CD16a in using scFv specific for CD3 or CD16a to recruit T cells or NK cells to kill targeted tumor cells bound by a bundle of scFv specific for a tumor-associated antigen on the tumor cells, a single copy of the scFv specific for CD3 or CD16a is desirable, so that unwanted effects due to cross-linking of the CD3 or CD16a may be avoided.
  • the second aspect of the present disclosure pertains to a use of the present linker unit.
  • the present disclosure provides a method for treating different diseases (including immune disorder, diffused tumor, solid tumor, osteoporosis disease, and age-related macular degeneration) , in which the method comprising administering a subject in need thereof a therapeutically effective amount of the present linker unit.
  • a first set of diseases treatable by the present linker unit is the immune disorder.
  • Illustrative linker units suitable for treating immune disorders include a first element that is an antibody fragment specific for a pro-inflammatory cytokine or a receptor of the cytokine; or a soluble receptor specific for the cytokine; and a second element that is an antibody fragment specific to the tissue specific extracellular matrix protein.
  • the present linker unit suitable for treating psoriasis comprises a first element of an scFv specific for TNF- ⁇ , IL-12/IL-23, or IL-17; or the receptor of IL-17; and a second element of an scFv specific for collagen I or collagen VII.
  • the present linker unit suitable for treating systemic lupus erythematosus (SLE) , cutaneous lupus, or Sjogren’s syndrome comprises an scFv specific for BAFF as the first element; and an scFv specific for collagen I or collagen VII as the second element.
  • Some skin diseases such as atopic dermatitis, pemphigus vulgaris, and several types of urticaria, which have obvious inflammatory manifestation in the skin, are not treated with antibodies targeting specific TNF- ⁇ , IL-12/IL-23, IL-17, or BAFF, because those antibodies are not found to be sufficiently efficacious. It is rational to expect that if those anti-inflammatory antibodies are distributed favorable to the skin, they may be able to treat those skin diseases.
  • the present linker unit is used to treat rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis.
  • the first element is an scFv specific for TNF- ⁇ , IL-1, IL-6, IL-12/IL-23, IL-17, IL-6R, or IL-17E; and the second element is an scFv specific for collagen II, collagen IX, collagen XI, or ⁇ -aggrecan.
  • the present linker unit suitable for treating inflammatory bowel disease comprises an scFv specific for TNF- ⁇ as the first element; and an scFv specific for collagen III or collagen V as the second element.
  • the first element of the present linker unit is the antibody fragment specific for the cell surface antigen associated with and/or overexpressed on the diffused tumor; and the second element of the present linker unit is the antibody fragment specific for the cell surface antigen CD3 or CD16a.
  • the cell surface antigen associated with and/or overexpressed on the diffused tumor is CD5, CD19, CD20, CD22, CD23, CD27, CD30, CD33, CD34, CD37, CD38, CD43, CD72a, CD78, CD79a, CD79b, CD86, CD134, CD137, CD138, or CD319.
  • the first element is an scFv specific for CD5, CD19, CD20, CD22, CD23, CD30, CD37, CD79a, or CD79b; and the second element is an scFv specific for CD3 or CD16a.
  • the first element is an scFv specific for CD38, CD78, CD138, or CD319; and the second element is an scFv specific for CD3 or CD16a.
  • the first element is an scFv specific for CD5, CD30, or CD43; and the second element is an scFv specific for CD3 or CD16a.
  • the first element is an scFv specific for CD33 or CD34; and the second element is an scFv specific for CD3 or CD16a.
  • Another set of diseases treatable by the present linker unit is solid tumors, which can be melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, or head and neck squamous cell carcinoma.
  • the first element of the present linker unit is a peptide hormone, a growth factor, or an scFv specific for a tumor-associated antigen; and the second element is an scFv specific for the cell surface antigen CD3 or CD16a.
  • the peptide hormone is secretin, cholecystokinin (CCK) , somatostatin, or thyroid-stimulating hormone (TSH) .
  • the growth factor is selected from the group consisting of epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , vascular endothelial growth factor A (VEGF-A) , basic fibroblast growth factor (bFGF) , and hepatocyte growth factor (HGF) .
  • EGF epidermal growth factor
  • HB-EGF heparin-binding epidermal growth factor
  • VEGF-A vascular endothelial growth factor A
  • bFGF basic fibroblast growth factor
  • HGF hepatocyte growth factor
  • the tumor-associated antigen is selected from the group consisting of human epidermal growth factor receptor (HER1) , HER2, HER3, HER4, carbohydrate antigen 19-9 (CA 19-9) , carbohydrate antigen 125 (CA 125) , carcinoembryonic antigen (CEA) , mucin 1 (MUC 1) , ganglioside GD2, melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) , mesothelin, mucine-related Tn, Sialyl Tn, Globo H, stage-specific embryonic antigen-4 (SSEA-4) , and epithelial cell adhesion molecule (EpCAM) .
  • HER1 human epidermal growth factor receptor
  • the present method for treating solid tumor comprises the step of, (a) subjecting the subject to a blood dialysis procedure using an antibody specific for one or more tumor-associated antigens to remove the tumor-associated antigens that are shed from the tumor and wanders into the circulation of the subject; and (b) administering the present linker unit for treating the solid tumor.
  • the first element of the present disclosure is an scFv specific for receptor activator of nuclear factor ⁇ B (RANKL) ; and the second element of the present disclosure is a second scFv specific for collagen I or osteonectin.
  • RTKL nuclear factor ⁇ B
  • the present linker unit is useful in treating age-related macular degeneration (AMD) , in which the first element of the present linker unit is an scFv specific for VEGF-A; and the second element of the present disclosure is a long PEG chain having a molecular weight of about 20,000 to 50,000 daltons.
  • AMD age-related macular degeneration
  • a molecular construct comprising at least two linker units.
  • the molecular construct may also use linker unit with a compound core (see, below) as one or both of its linker units.
  • at least one of the linker units of the present molecular construct comprises the polypeptide core.
  • at least two linker units of the present molecular construct comprise the polypeptide cores. More preferably, all the linker units of present molecular construct respectively comprise the polypeptide cores.
  • linker unit that employs a compound, instead of the polypeptide, as the center core.
  • the compound is benzene-1, 3, 5-triamine, 2- (aminomethyl) -2-methylpropane-1, 3-diamine, tris (2-aminoethyl) amine, benzene-1, 2, 4, 5-tetraamine, 3, 3', 5, 5'-tetraamine-1, 1'-biphenyl, tetrakis (2-aminoethyl) methane, tetrakis-(ethylamine) hydrazine, N, N, N', N', -tetrakis (aminoethyl) ethylenediamine, benzene-1,2, 3, 4, 5, 6-hexaamine, 1-N, 1-N, 3-N, 3-N, 5-N, 5-N-hexakis (methylamine) -benzene-1,
  • each compound listed above comprises a plurality of amine groups, and thus, a plurality of PEG chains having NHS groups can be linked to the compound via forming an amine linkage between the amine group and the NHS group; the thus-linked PEG chain is designated as linking arm, which has a maleimide group at the free-terminus thereof.
  • At least one of the amine groups of the compound core is linked to another PEG chain, which has an NHS group at one end, and a functional group (e.g., an azide, alkyne, tetrazine, or strained alkyne group) at the other end; the thus-linked PEG chain is designated as coupling arm, which has a functional group at the free-terminus thereof.
  • a functional group e.g., an azide, alkyne, tetrazine, or strained alkyne group
  • two different elements can be respectively linked to the linking arm and/or coupling arm via the thiol-maleimide reaction (the linkage between the element and the linking arm) and the CuAAC reaction, SPAAC reaction or the iEDDA reaction (the linkage between the element and the coupling arm) .
  • the linking arm is a PEG chain having 2-20 repeats of EG units; and the coupling arm is a PEG chain having 2-12 repeats of EG unit.
  • both the linking and coupling arms have 12 repeats of EG unit, in which one terminus of the coupling arm is an NHS group, and the other terminus of the coupling arm is an alkyne group.
  • Schemes 6 and 7 respectively depict the linkages between the center core, and the linking arm and the coupling arm, in which NHS represents NHS ester, Mal represents maleimide group, azide represents azide group, and alkyne represents alkyne group.
  • the requirement of having multiple NH 2 groups exist in a symmetrical and identical orientation in the compound serving as the center core is for the following reason: when one of the NH 2 group is used for connecting a bifunctional linker arm with N-hydroxysuccinimide (NHS) ester group and alkyne, azide, tetrazine, or strained alkyne group, the product, namely, a core with a coupling arm having alkyne, azide, tetrazine or strained alkyne, is homogeneous and may be purified. Such a product can then be used to produce multi-arm linker units with all other NH 2 groups connected to linking arms with maleimide or other coupling groups at the other ends. If a compound with multiple NH 2 groups in non-symmetrical orientations, the product with one bifunctional linking arm/coupling arms is not homogeneous.
  • NHS N-hydroxysuccinimide
  • symmetrical compounds can further be modified to provide center cores with more linking arms/coupling arms.
  • tetrakis (2-aminoethyl) methane which can be synthesized from common compounds or obtained commercially, may be used as a core for constructing linker units with four linking arms/coupling arms.
  • Tetrakis (2-aminoethyl) methane can react with bis (sulfosuccinimidyl) suberate to yield a condensed product of two tetrakis (2-aminoethyl) methane molecules, which can be used as a core for constructing linker units having six linking arms/coupling arms.
  • the linker units respectively having 3 linking arms/coupling arms, 4 linking arms/coupling arms and 6 linking arms/coupling arms, can fulfill most of the need for constructing targeting/effector molecules with joint-linker configuration.
  • the numbers of the linking arm and/or the coupling arm and the element linked thereto may vary with the number of amine groups comprised in the center core. In some preferred embodiments, the numbers of the linking arm/coupling arm and the corresponding linking element linked thereto ranges from about 1-7.
  • FIG. 2 in which benzene-1, 2, 4, 5-tetraamine having 4 amine groups is depicted.
  • Three of the amine groups are respectively linked to the linking arms 20, and one of the amine group is linked to the coupling arm 60, which has an azide group at its free-terminus.
  • Three first elements 30 are then respectively linked to the three linking arms 20 via the thiol-maleimide reactions, and one second element 50 is linked to the coupling arm 60 via the CuAAC reaction.
  • the solid dot 40 as depicted in Figure 2 represents the chemical bond resulted from the CuAAC reaction occurred between the coupling arm 60 and the second element 50.
  • the molecular construct comprises two linker units, and the linker units are coupled to each other via either the CuAAC reaction (using copper or pentamethylcyclopentadienyl ruthenium chloride complex as catalyst) , the SPAAC reaction, or the iEDDA reaction.
  • the linker units is linked with a plurality of first elements, which act as the targeting elements, and the other of the linker units is linked with a plurality of second elements, which act as the effector elements.
  • the molecular construct comprises three linker units, in which the first and second linker units are coupled to each other via the iEDDA reaction, and then, the third linker unit is coupled to the first or second linker unit via the CuAAC reaction.
  • the first and second linker units are coupled to each other via the iEDDA reaction
  • the third linker unit is coupled to the first or second linker unit via the SPAAC reaction.
  • the first, second, and third linker units respectively carry a plurality of first, second, and third elements, in which the first, second, and third elements are different.
  • two of the three elements are targeting elements, and one of the three elements is an effector element.
  • two of the three elements are effector elements, and one of the three elements is a targeting element.
  • one of the three elements is a targeting element, another of the three elements is an effector element, and the other of the three elements is an element capable of improving the pharmacokinetic property of the molecular construct, such as solubility, clearance, half-life, and bioavailability.
  • Figure 3A depicts a molecular construct comprising two linker units (100A, 200A) , which are coupled to each other via the iEDDA reaction.
  • the first linker unit 100A comprises a first center core 110a, a linking arm 120 (as the first linking arm) , and a coupling arm 130a (as the first coupling arm) , in which the linking and coupling arms are respectively linked to the first center core 110a at one ends.
  • the second linker unit 200A comprises a second center core 210a, a linking arm 220 (as the second linking arm) , and a coupling arm 230a (as the second coupling arm) , in which the linking and coupling arms are respectively linked to the second center core 210a at one ends.
  • One of the coupling arms 130a, 230a has a tetrazine group at its free terminus, while the other of the coupling arms 130a, 230a has a TCO group.
  • the coupling arm 130a has a tetrazine group 152 at its free terminus (i.e., the terminus not connected to the first center core 110a)
  • the coupling arm 230a would have a TCO group 154 at its free terminus (i.e., the terminus not connected to the second center core 210a) , and vice versa.
  • the two linker units (100A, 200A) are coupled to each other via the iEDDA reaction occurred between the respective free ends of the coupling arms 130a, 230a.
  • the ellipse 156 as depicted in Figure 3A represents the chemical bond resulted from the iEDDA reaction occurred between the coupling arms 130a, 230a.
  • each of the linking arms 120, 220 has a maleimide group at its free terminus. Accordingly, a first targeting element 140 and a first effector element 240, each has a thiol group are respectively linked to the linking arms 120, 220 via the thiol–maleimide reaction.
  • both the first and second center cores 110a, 210a depicted in Figure 3A are polypeptide cores. According to another embodiment, both the first and second center cores 110a, 210a depicted in Figure 3A are compound cores. According to still another embodiment, one of the first and second center cores 110a, 210a depicted in Figure 3A is a polypeptide core, while the other of the first and second center cores 110a, 210a depicted in Figure 3A is a compound core.
  • Figure 3B provides an alternative embodiment of the present disclosure, in which both the first and second center cores 110b, 210b are polypeptide cores, and are respectively linked to a first targeting element 140 and a first effector element 240 via the linking arms 120, 220.
  • one of the center cores 110b, 210b comprises an amino acid residue having an azide group (e.g., the AHA residue) at it N-or C-terminus
  • the other of the center cores 110b, 210b comprises an amino acid residue having an alkyne group (e.g., the HPG residue) at it N-or C-terminus
  • such configuration allows the center cores 110a, 210a to be directly linked to each other, that is, without connecting through any coupling arms as that depicted in Figure 3A.
  • the center core 110b comprises the amino acid residue having the azide group 162 at its N-or C-terminus
  • the center core 210b would comprises the amino acid residue having the alkyne group 164 at its N-or C-terminus, and vice versa.
  • the linker units 100B, 200B can couple together directly via the CuAAC reaction occurred between the N-or C-terminal amino acid residues of the center cores 110b, 210b.
  • the solid dot 166 as depicted in Figure 3B represents the chemical bond formed between the N-or C-terminal amino acid residues.
  • Figure 3C is another embodiment of the present disclosure.
  • the linker units 100C, 200C have the similar structures as the linker units 100A, 200A, except that the coupling arms 130b, 230b respectively have an azide group 162 and a DBCO group 172, instead of the azide group 152 and the alkyne group 154 as depicted in the linker units 100A, 200A of Figure 3A.
  • the center core 110a is linked with a coupling arm 130b (as the first coupling arm) having an azide group 162 at its free-terminus; and the center core 210a is linked with a coupling arm 230b (as the second coupling arm) having a DBCO group 172 at its free-terminus.
  • the linker units 100C, 200C are then coupled together via the SPAAC reaction occurred between the coupling arms 130b, 230b; and forming the chemical bond 182, depicted as a diamond.
  • both the first and second center cores 110a, 210a depicted in Figure 3C are polypeptide cores. In another embodiment, both the first and second center cores 110a, 210a depicted in Figure 3C are compound cores. In still another embodiment, one of the first and second center cores 110a, 210a depicted in Figure 3C is a polypeptide core, while the other of the first and second center cores 110a, 210a depicted in Figure 3C is a compound core.
  • two linker units can be coupled to each other via the CuAAC reaction occurred between the center core and the coupling arm.
  • the center core 110b comprises a N-or C-terminal amino acid residue that has an azide group 162 (e.g., the AHA residue)
  • the center core 210a is linked with a coupling arm 230b having a TCO group 172 at its free-terminus.
  • the linker units 100B and 200C can be coupled together via the SPAAC reaction occurred between the center core 110b and the coupling arm 230b; and forming the chemical bond 182.
  • the linker units 100B, 200C depicted in Figure 3D respectively comprise polypeptide cores.
  • the center core 100B depicted in Figure 3D is a polypeptide core, while the center core 200C depicted in Figure 3D is a compound core.
  • the linker unit 200B that comprises a N-or C-terminal amino acid residue having an alkyne group 160b (e.g., the HPG residue) , and the linker unit 100C comprising the coupling arm 130b with an azide group 160a at its free-terminus can be coupled together via the azide-alkyne cycloaddition occurred between the center core 210b and the coupling arm 130b.
  • the linker unit comprising a specified number and/or type of targeting/effector element can be prepared independently, then proceed to be coupled together via the CuAAC reaction, the iEDDA reaction, or the SPAAC reaction;
  • the number and kind of the targeting and/or effector elements may vary in accordance with the requirements of application (e.g., the disease being treating, and the binding avidity and/or affinity of the targeting and/or effector element) .
  • the combination of the targeting and effector elements may be adjusted according to specific needs and/or applications.
  • Each of the present targeting and effector elements may vary with such factors like particular condition being treated, the physical condition of the patient, and/or the type of disease being treated.
  • the clinical practitioner may combine the most suitable targeting element and the most suitable effector element so as to achieve the best therapeutic effect.
  • the targeting element may be a growth factor, a peptide hormone, a cytokine, or an antibody fragment; and the effector element may be an immunomodulant, a chelator complexed with a radioactive nuclide, a cytotoxic drug, a cytokine, a soluble receptor, or an antibody; and
  • the CuAAC reaction the iEDDA reaction, or the SPAAC reaction is more efficient in terms of coupling any two linker units.
  • Libraries 1-6 respectively comprise a plurality of linker units 300A, 300B, 300C, 400A, 400B, and 400C that are linked with functional elements.
  • Each linker units 300A, 300B, and 300C are similar in structures; in which each of the linker units 300A, 300B, and 300C comprises one center core 310, one coupling arm 330 linked thereto and has a tetrazine group 350 at its free terminus, and a specified number of the linking arm 320.
  • Linker unit 300A comprises four linking arms 320, and accordingly, four targeting elements 340a can be respectively linked to the four linking arms 320.
  • two targeting elements 340b and five targeting elements 340c can be respectively linked to the linker units 300B and 300C.
  • the targeting elements 340a, 340b, and 340c can be the same or different.
  • each of these linker units comprises one center core 410, one coupling arm 430 linked thereto and has a strained alkyne group 450 at its free terminus, and a specified number of the linking arm 420.
  • three effector elements 440a, five effector elements 440b, and eight effector elements 440c can be respectively linked to the linker units 400A, 400B and 400C.
  • the effector elements 440a, 440b, and 440c can be the same or different.
  • FIG. 5A provides an example of the present molecular construct, in which each of the first and second center cores (310, 410) is linked with three linking arms (320, 420) and one coupling arm (330, 340) .
  • Three of the first targeting elements 340 are respectively linked to the linking arms 320; and three of the first effector elements 440 are respectively linked to the linking arms 420.
  • the two linker units are coupled to each other via the iEDDA reaction occurred between two coupling arms 330, 430, and forming the chemical bond 356.
  • Figure 5B provides another example of the present molecular construct, in which the first and second center cores respectively contain different numbers of amine groups (e.g., lysine residues) , and accordingly, the molecular construct contains non-equal numbers of targeting and effector elements.
  • the first center core 310 is linked to one coupling arm 330, and two linking arms 320.
  • the second center core 410 is linked to one coupling arm 430, and five linking arms 420.
  • two targeting elements 340 are respectively linked to the linking arms 320; and five effector elements 440 are respectively linked to the linking arms 420.
  • the ellipse 356 in Figure 5B represents the linkage between two coupling arms 330, 430.
  • the present molecular construct may further comprise a relatively long PEG chain connected to either the first or second center core, so that the present molecular construct may be segregated further away from the reticuloendothelial system and attains a longer half-life after being administered to a subject.
  • a protein is modified by a PEG chain so as to improve its pharmacokinetic properties and/or to decrease immunogenicity, PEG up to 20,000-50,000 daltons in length, is preferred.
  • linking arms of relatively shorter lengths are used to connect the targeting and effector elements, while a PEG chain of 20,000 to 50,000 daltons is connected to any of the linker units with the purpose of increasing in vivo half-life of the present molecular construct.
  • multiple scFv fragments are used as the targeting and/or effector elements to construct the present molecular construct.
  • the targeting element/effector element pharmaceuticals based on molecular constructs comprising scFv fragments should have longer in vivo half-lives than individual antibody fragments.
  • anti-TNF- ⁇ and anti-IL-12/IL-23 in the treatment of rheumatoid arthritis
  • anti-RANKL in the treatment of osteoporosis
  • anti-VEGF-A in the treatment of the eye disease of age-related macular degeneration
  • a linker unit may comprise a plurality of linking arms, which can be linked to a plurality of functional elements.
  • a linker unit may comprises 5-12 linking arms, which can be linked to 5-12 functional elements. This is especially useful when the functional elements are small molecules, such as cytotoxic drugs or toll-like receptor agonists.
  • the linker unit carrying multiple molecules of a cytotoxic drug is herein referred to as a drug bundle.
  • polypeptide cores can be employed to prepare the molecular construct comprising three linker units.
  • another aspect of the present disclosure is directed to a molecular construct comprising three linker units.
  • the three linker units two of them may be connected to each other via the iEDDA reaction, while the third linker unit is connected to any of the two linker units by the SPAAC reaction or CuAAC reaction.
  • the rationale for constructing a multi-linker unit e.g., three linker units
  • two different sets of targeting elements or two different sets of effector elements can be incorporated therein.
  • the molecular construct comprises three linker units (500, 600, 700A) .
  • the linker units 500, 600, 700A respectively comprise a center core (510, 610, 710) , and an linking arm (520, 620, 720) with a functional element (540, 640, 740) linked thereto.
  • the linker unit 600 is characterized in comprising a cysteine residue at one of its N-or C-terminus that is linked with a coupling arm 630; and an amino acid residue having an azide or alkyne group at the other of its N-or C-terminus.
  • One of the coupling arms 530, 630 has a tetrazine group at its free terminus, and the other of the coupling arms 530, 630 has a strained alkyne group at its free terminus. Accordingly, the linker units 500, 600 can be coupled to each other via the iEDDA reaction occurred between the coupling arms 530, 630 as the linkage manner described in Figure 3A.
  • the center core 710 comprises an amino acid having an alkyne group (e.g., the HPG residue) at its N-or C-terminus; or, when the N-or C-terminal amino acid residue of the center core 610 has an alkyne group (e.g., the HPG residue) , then the center core 710 comprises an amino acid having an azide group (e.g., the AHA residue) at its N-or C-terminus.
  • the center core 710 comprises an amino acid having an azide group (e.g., the AHA residue) at its N-or C-terminus.
  • the linker units 600, 700A can be directly coupled to each other via the CuAAC reaction occurred between the N-or C-terminal amino acid residues of the center cores 610, 710 without the presence of the coupling arms.
  • the ellipse 560 and the solid dot 670 in Figure 7 respectively represent the chemical bonds resulted from the iEDDA reaction and the CuAAC reaction.
  • two of the three linker units may be connected to each other via the iEDDA reaction, while the third linker unit is connected to any of the two linker units by the SPAAC reaction.
  • FIG 7B in which the linker units 500, 600 are coupled together via the iEDDA reaction as described in Figure 7A, whereas the linker unit 700B is linked to the linker unit 600 via the SPAAC reaction occurred between the center core 610 and the coupling arm 730.
  • the diamond 672 in Figure 7B represents the chemical bond resulted from the SPAAC reaction.
  • each number of the functional elements 540, 640, 740 respectively linked to the linker units 100, 200, 300 are different depending on the intended use.
  • the linker units respectively carrying different numbers and/or types of functional elements can be prepared separately as different libraries, and one skilled artisan may select and combine the desired linker units from the libraries in accordance with the various applications.
  • the coupling arm of the present molecular construct described in above aspects and/or embodiments of the present disclosure that has an azide, alkyne, tetrazine, or strained alkyne group at the terminus is designed as a PEG chain having 2-12 repeats of EG units.
  • the linking arm is designed as a PEG chain having 2-20 repeats of EG units.
  • Adopting a polypeptide as the center core provides versatility in the present molecular construct, in which multiple copies or types of targeting/effector elements may be present in one construct, accordingly, enhanced specificity of drug delivery and potency in the intended target sites are achieved.
  • a large number of configurations can be adopted by employing the molecular construct comprising multiple linker units.
  • a few examples are: a first linker unit carrying three scFvs targeting elements, and a second linker unit carrying 5 cytotoxic drugs; a first linker unit carrying three scFvs targeting elements, and a second linker unit carrying three scFvs effector elements; a first linker unit carrying two scFvs of the first set targeting elements, a second linker unit carrying two scFvs of the second set targeting elements, and a third linker unit carrying 5 cytotoxic drugs; a first linker unit carrying 2 bi-scFv targeting elements, and a second linker unit carrying two scFvs effector elements; or a first linker unit carrying three scFvs targeting elements, a second linker unit carrying two scFvs effector elements plus a linking arm attached with a long PEG of 20,000-50,000 daltons for the purpose of increasing pharmacokinetic properties.
  • a bi-functional PEG acting as a linking arm is used to link the antigen-binding fragments of antibodies, which serve as targeting or effector elements, to the amine groups located in the polypeptide core.
  • Each PEG may have NHS group at one end and maleimide group at the other end.
  • the NHS group may couple with amine group in the polypeptide core, while the maleimide group may couple with sulfhydryl group of a cysteine residue of an scFv, bi-scFv, or Fab fragment of an antibody.
  • the scFv and bi-scFv are engineered to have a polypeptide linker with terminal cysteine residue at the C-terminal.
  • Fab may be derived from a whole IgG by pepsin cleavage, and the free sulfhydryl groups are derived from the inter-chain disulfide bond by a mild reduction reaction.
  • Schemes 8-12 provide several working example respectively depicting the coupling and preparation of specified linker units.
  • Scheme 8 is a schematic diagram depicting the preparation of the present molecular construct in accordance with one embodiment of the present disclosure, in which NHS represents NHS ester, Mal represents maleimide group, A AH represents L-azidohomoalanine (AHA) residue, AAH represents homopropargylglycine (HPG) residue, Ac represents acetyl group, and scFv represent single-chain variable fragment.
  • NHS represents NHS ester
  • Mal represents maleimide group
  • a AH represents L-azidohomoalanine (AHA) residue
  • AAH represents homopropargylglycine (HPG) residue
  • Ac represents acetyl group
  • scFv represent single-chain variable fragment.
  • step 1 the first center core comprising the amino acid sequence of (GSK) 3 and a L-azidohomoalanine (AHA) residue at the C-terminus thereof; and the second center core comprising the amino acid sequence of (GSK) 5 and a homopropargylglycine (HPG) residue at the C-terminus thereof, are respectively prepared.
  • the N-terminuses of the first and second center cores are respectively modified with an acetyl group.
  • step 2 the linking arms are respectively linked to the lysine residues in the first and second center cores via forming an amide linkage there between; the linked arm linked to the center core has a maleimide group at the free-terminus.
  • step 3 the first targeting element (i.e., the antibody) having a thiol group (e.g., a cysteine residue) is linked to the linking arm linked with the first center core via the thiol–maleimide reaction; similarly, the effector element (i.e., the drug) having a thiol group is linked to the linking arm linked with the second center core via the thiol–maleimide reaction.
  • step 4 the two linker units are coupled via a CuAAC reaction occurred between the AHA and HPG residues.
  • the targeting/effector element can be linked to the center core in an alternative method.
  • Scheme 9 is a scheme illustrating the coupling of the effector element with the polypeptide core, in which the linking arm is first linked to the center core, and then the effector element (i.e., the drug) is linked to the linking arm via the thiol–maleimide reaction.
  • the effector element i.e., the drug
  • the linking arm is coupled to the linking arm so as to produce a linking arm-effector conjugate (i.e., PEG-drug) ; next, the linking arm-effector conjugate is linked to the center core via forming an amide linkage between the lysine residues and the NHS esters.
  • Scheme 11 provides an example of preparing the present molecular construct, which comprises two linker units; both linker units comprises the amino acid sequence of (K-Xaa 4 ) 3 and a cysteine (C) residue at the C-terminus thereof.
  • two coupling arms are respectively linked to the C residues of the linker units, in which one of the coupling arms has a maleimide (Mal) group at one terminus and a tetrazine group at the other terminus, while the other coupling arm has a Mal group at one terminus and a TCO group at the other terminus.
  • the linking arms are respectively linked to the lysine (K) residues via forming the amide bond between the linking arm and the K residue.
  • step 3 three anti-A antigen scFvs (scFv ⁇ A) and three anti-B antigen scFvs (scFv ⁇ B) are respectively linked to the linking arms of the linker units via the thiol-maleimide reaction.
  • step 4 the two linker unit are coupled to each other via the iEDDA reaction occurred between the tetrazine and TCO group.
  • Scheme 12 provides an example of preparing a molecular construct comprising three linker units, in which two linker units respectively linked with the scFv ⁇ A and scFv ⁇ B are coupled to each other via the iEDDA reaction as described in Scheme 11 and a third linker unit couples with the second linker unit via a CuAAC reaction.
  • the third linker unit is a drug bundle.
  • this reaction scheme can be applied to a third linker unit with other elements, such as scFv.
  • the center linker unit (that is, the second linker unit) comprises an HPG (G HP ) residue at its N-terminus, and accordingly, a drug bundle conjugated with an AHA (A AH ) residue can be linked to the second linker unit via the CuAAC reaction occurred between the HPG and AHA residues.
  • the center linker unit may comprise an AHA residue at its N or C-terminus, and can couple with a third linker unit carrying a coupling arm with a DBCO or another strained alkyne group via a SPAAC reaction.
  • the thus-formed molecular construct in scheme 12 has three functional elements: scFv ⁇ A, scFv ⁇ B, and drug molecule.
  • the molecular constructs with three linker units can carry three sets of scFv, of which two sets as targeting elements and one set as effector elements, or one set as targeting elements and two sets as effector elements.
  • a molecular construct with a total of six scFvs has a molecular weight of about 170,000 daltons.
  • a molecular construct with seven scFvs has a molecular weight of about 200,000 daltons, and a molecular construct with eight scFvs has a molecular weight of about 230,000 daltons.
  • Most of the molecular constructs of this invention have molecular weights smaller than 200,000 daltons, and a few molecular constructs have molecular weights in 200,000-250,000 daltons.
  • bi-scFv bi-specific scFv
  • scFv1-scFv2 e.g., specific for HER2 and HER3
  • scFv3 and scFv4 respectively
  • V L 1-V H 1-V L 2-V H 2 or V H 1-V L 1-V H 2-V L 2 is arranged; in the “diabody” configuration, V L 2-V L 1-V H 1-V H 2 or V H 2-V H 1-V L 1-V L 2 is arranged.
  • Proper linkers with GGGGS (SEQ ID NO: 6) repeats or other sequences are placed between the immunoglobulin domains.
  • each linker unit is prepared freshly and independently, and processed to connecting the targeting or effector elements onto the linker units, and the coupling of the linker units through click reaction without delay.
  • the targeting elements and effector elements are both conjugated to linker units with alkyne groups, and the alkyne group in one of the linker units is then converted to azide with a short homo-bifunctional linker with azide at both ends. The linker units, one with alkyne and the other with azide, are then coupled via a click reaction.
  • the preferred linking arms for this invention are PEG.
  • the length of the linking arms is important for several considerations. It should be long enough to allow flexibility of the linked scFv or other types of functional elements to reach targeted antigenic sites on targeted cell surface without steric constraints; yet not long enough to cause intra-molecular and inter-molecular tangling of the linking arms and their linked scFv fragments or functional elements, or to unnecessarily increase the size of the whole molecular construct for hindering tissue penetration. Linking arms that are too long may also fail to pull antigen molecules to form compacted clusters, if such clusters are required to initiate signal-transducing process for apoptosis or other cellular effects.
  • the optimal length of linking arms for different types of combinations of targeted antigens and their binding agents may be determined by any skilled artisan in the related field without undue experimentation.
  • a PEG arm of about 1, 000-1, 200 daltons (about 25-30 ethylene glycol units) is effective in causing apoptosis. Therefore, PEG linkers of 100 to 1, 000 daltons are suitable for the purpose of the present invention.
  • a linking arm of NHS- (PEG) 12 -Maleimide (approximately 500 daltons) is preferred in a number of molecular construct of this invention.
  • a fully stretched (PEG) 12 has a length of
  • Applicable linking arms and coupling arms are not limited by PEG chains.
  • Peptides comprising glycine, serine and other amino acid hydrophilic residues, and polysaccharides, and other biocompatible linear polymers, which are modified to contain NHS and maleimide groups, can be used.
  • the effector elements in the molecular constructs of this disclosure be released from the linking arms, so that they can get into cells in the targeted site, including cells bound by the targeting elements or surrounding cells, to cause pharmacological effects.
  • a cleavable bond is engineered in the linking arm.
  • Cleavable bonds which are susceptible for cleavage by hydrolysis, acid exposure, reduction, and enzymes, have been developed.
  • peptide segments susceptible to matrix metalloproteinases which are present in inflammatory tissues, have been used in constructing therapeutic constructs.
  • One embodiment of the present invention is to use PEG linkers with S-Sbond adjacent to the maleimide group NHS-PEG 2-12 -S-S-maleimide, wherein S-S is a disulfide bond, which can be slowly reduced.
  • the targeting element described in above-mentioned embodiments is selected from the group consisting of a growth factor, a peptide hormone, a cytokine, and an antibody fragment; and the effector element is an immunomodulant, a chelator complexed with a radioactive nuclide, a cytotoxic drug, a cytokine, a soluble receptor, or an antibody.
  • the antibody is in the form of an antigen-binding fragment (Fab) , a variable fragment (Fv) , a single-chain variable fragment (scFv) , a single domain antibody (sdAb) , or a bi-specific single-chain variable fragment (bi-scFv) .
  • the bi-scFv is a bi-specific tandem scFv or a bi-specific diabody scFv.
  • genes are constructed so that the V L and V H are linked as a single polypeptide in either order (V L -V H or V H -V L ) by a peptide linker of 10-25 amino acid residues with glycine and serine being the major residues.
  • a short stretch with glycine and serine and a terminal residue cysteine is engineered.
  • Recombinant scFv and bi-scFv can be produced in bacteria, such as E. coli and Pseudomonas putida, in yeast, such as Pichia pastoris, or in mammalian cells, such as CHO and HEK293 cell lines.
  • the inventors’ laboratory have produced a large number of IgG antibodies, Fab, scFv and various antibody fragments, Fc-based proteins, and other recombinant antibodies in HEK293 and CHO cell lines for experimentation in in vitro systems and in animal models. Our laboratory has also developed cell lines for producing antibodies for human clinical trials.
  • the HEK293 transient expression system can be conveniently employed to produce up to 1 g of IgG or antibody fragments using a few flasks of 1-2 liters in the research laboratory.
  • the scFv fragments to be used in the molecular constructs of this invention generally do not have a carbohydrate modification, and carbohydrate modification is not required for the binding activity of the scFv to their antigenic targets.
  • scFv small-scale bacterial expression systems have been developed as a manufacturing alternative for producing scFv.
  • E. coli expression systems for recovering scFv in intracellular inclusion bodies, in periplasm, and in secreted form have been employed.
  • the scFv can be purified in most cases with an affinity column with Protein L, which interacts with V H of most ⁇ light chain, or in other cases with ion-exchange columns.
  • the examples of this invention based on the joint-linker platform employ mainly scFv and Fab as the targeting and/or effector elements.
  • specific binding molecules may also be screened from large libraries of binding molecules based on sdAb or other antibody fragments.
  • binding molecules which are not based on immunoglobulin domains but resemble antibodies in having specific binding affinities to selected target molecules, include (1) aptamers, which are oligonucleotides or short peptides selected for binding to target molecules, (2) fynomers, which are small binding proteins derived from the human Fyn SH3 domain, (3) affimers, which are binding proteins derived from the cysteine protein inhibitor family of cystatins, and (4) DARPins (designed ankyrin repeat proteins) , which are genetically engineered proteins with structures derived from the natural ankyrin proteins and consist of 3, 4, or 5 repeat motifs of these proteins. These antibody-mimetics have molecular weights of about 10K to 20K daltons.
  • Cytokines, growth factors, peptide hormone or their natural fragments or synthetic analogues may also be used as targeting or effector elements.
  • Small molecule drugs such as cytotoxic drugs (such as auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin) and immunostimulatory drugs (e.g. motolimod, imiquimod, resiquimod, and gardiquimod) may also be linked as effector elements and carried to diseased target cells or tissues.
  • CpG oligonucleotides CpG oligonucleotides, lipopolysaccharides derived from certain Gram-negative bacteria and glucans (such as zymosan and ⁇ -D-glucan) derived from fungi of especially Aspergillus and Agaricus species have strong immunostimulatory activities and can also be employed as effector elements. Most of those immunostimulatory substances bind to toll-like receptors on various immunocytes and hence activate the immune system.
  • At least one of the targeting element and the effector element of the present molecular construct is the antibody fragment specific for the cell surface antigen.
  • the targeting element is the antibody fragment specific for the cell surface antigen
  • the present construct is capable of specifically targeting to the cell/tissue/organ with the cell surface antigen expressed thereon.
  • the cell surface antigen-specific antibody that employed as the effector element of the present construct it may either activate or inhibit the signaling transduction pathway via binding with the cell surface antigen, and accordingly, regulate the growth/survival/function of the cell/tissue/organ with the cell surface antigen expressed thereon.
  • the cell surface antigen may be selected from the group consisting of, receptor activator of nuclear factor ⁇ B (RANKL) , CD3, CD4, CD5, CD7, CD8, CD10, CD11 c, CD13, CD14, CD15, CD16a, CD19, CD20, CD22, CD23, CD25, CD27, CD28, CD30, CD33, CD34, CD36, CD37, CD38, CD41, CD43, CD52, CD56, CD61, CD64, CD65, CD74, CD78, CD79a, CD79b, CD80, CD86, CD134, CD137, CD138, CD319, cytotoxic T-lymphocyte-associated protein 4 (CTLA-4, or CD152) , programmed cell death 1 (PD-1, or CD279) , and programmed cell death 1 ligand 1 (PD-L1, or CD274) .
  • RNKL receptor activator of nuclear factor ⁇ B
  • the present molecular construct is useful in treating diffused tumors, in which the targeting element is an antibody fragment specific for CD19, CD20, CD38 or CD138; and the effector element is an antibody fragment specific for CD3 or CD16a.
  • the present molecular construct is useful in treating solid tumors, in which the effector element is an antibody fragment specific for PD1.
  • the present molecular construct is useful in treating diffused tumors, in which the targeting element is an antibody fragment specific for CD79a; and the effector element is an antibody fragment specific for CD79b.
  • the present molecular construct is useful in treating diffused tumors, and the targeting element is an antibody fragment specific for CD79b; and the effector element is an antibody fragment specific for CD79a.
  • the targeting element of the present molecular construct is the antibody fragment specific for the tumor-associated antigen, which is selected from the group consisting of human epidermal growth factor receptor (HER1) , human epidermal growth factor receptor 2 (HER2) , human epidermal growth factor receptor 3 (HER3) , human epidermal growth factor receptor (HER4) , carbohydrate antigen 19-9 (CA 19-9) , carbohydrate antigen 125 (CA 125) , mucin 1 (MUC 1) , ganglioside GD2, ganglioside GD3, ganglioside GM2, fucosyl GM1, Neu5GcGM3, melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) , mesothelin, mucine-related Tn, Sialyl Tn, Lewis Y , Sialyl Lewis Y , Lewis A , Lewis x , heparin-binding epi
  • HER1 human epiderma
  • the present molecular construct is useful in treating the breast tumor/cancer, in which the targeting element is an antibody fragment specific for HER1 or HER2.
  • the present molecular construct is useful in treating the prostate tumor/cancer, in which the targeting element is an antibody fragment specific for PSMA.
  • the targeting element of the present molecular construct is the antibody fragment specific for the tissue specific extracellular matrix protein, which is osteonectin, ⁇ -aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, or collagen XI.
  • the present molecular construct is useful in treating rheumatoid arthritis, in which the targeting element is an antibody fragment specific for collagen IX.
  • the present molecular construct is useful in treating psoriasis, in which the targeting element is an antibody fragment specific for VII.
  • the present molecular construct is useful in treating ankylosing spondylitis, in which the targeting element is an antibody fragment specific for ⁇ -aggrecan.
  • the targeting element and the effector element of the present disclosure is the cytokine. In other embodiments of the present disclosure, at least one of the targeting element and the effector element of the present disclosure is the antibody fragment specific for the cytokine.
  • the cytokine is B cell activating factor (BAFF) , interleukin-1 (IL-1) , IL-2, IL-6, IL-12/IL23, IL-17, interferon- ⁇ (IFN- ⁇ ) , IFN- ⁇ , interferon- ⁇ (IFN- ⁇ ) , tumor necrosis factor- ⁇ (TNF- ⁇ ) , or transforming growth factor- ⁇ (TGF- ⁇ ) .
  • BAFF B cell activating factor
  • IL-1 interleukin-1
  • IL-2 interleukin-2
  • IL-6 IL-12/IL23
  • IL-17 interferon- ⁇
  • IFN- ⁇ IFN- ⁇
  • interferon- ⁇ IFN- ⁇
  • TGF- ⁇ tumor necrosis factor- ⁇
  • the targeting element is the cytokine (e.g., TGF- ⁇ )
  • the present molecular construct is capable of specifically targeting to the receptor-expressing cell/tissue/organ (e.g., tumor cell with the TGF- ⁇ receptor expressed thereon) .
  • the cytokine that serves as the effector element of the present molecular construct it may activate the cytokine-associated signaling transduction pathway via binding with the cytokine receptor, and accordingly, generate the therapeutic effect (e.g., IFN- ⁇ as the effector element that binds to IFN- ⁇ receptor and produce the pro-inflammatory or anti-tumor effect) .
  • the effector element being an antibody fragment specific for the cytokine, it may capture and neutralize the cytokine, and thus, inhibit the cytokine-associated signaling transduction pathway (e.g., the antibody neutralizing IL-6 and inhibit IL-6 associated inflammation) .
  • the present molecular construct is useful in treating autoimmune diseases, in which the effector element is an antibody fragment specific for TNF- ⁇ or IL-17.
  • the present molecular construct is useful in treating solid tumors, in which the effector element is IFN- ⁇ or IL-2.
  • the present molecular construct is useful in treating solid tumors, in which the effector element is a non-neutralizing antibody fragment specific for IFN- ⁇ or IL-2.
  • the present molecular construct is useful in treating autoimmune diseases, in which the effector element is an antibody fragment specific for BAFF.
  • the soluble receptor is specific for TNF- ⁇ or IL-1.
  • the soluble receptor is used to capture and neutralize the cytokine without triggering the associated signaling transduction pathway.
  • the targeting element of the present molecular construct is the growth factor.
  • at least one of the targeting element and the effector element of the present disclosure is the antibody fragment specific for the growth factor.
  • the growth factor is selected from the group consisting of epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , vascular endothelial growth factor A (VEGF-A) , basic fibroblast growth factor (bFGF) , and hepatocyte growth factor (HGF) .
  • the targeting element is the growth factor (e.g., EGF)
  • the present molecular construct is capable of specifically targeting to the receptor-expressing cell/tissue/organ (e.g., tumor cell with the EGF receptor expressed thereon) .
  • the effector element being an antibody fragment specific for the growth factor (e.g., VEGF-A)
  • it may capture and neutralize the growth factor-associated signaling transduction pathway (e.g., VEGF-A-induced angiogenesis) .
  • the present molecular construct is useful in treating solid tumors, in which the effector element is an antibody fragment specific for VEGF-A.
  • the targeting element of the present molecular construct is the peptide hormone.
  • at least one of the targeting element and the effector element of the present molecular construct is the antibody fragment specific for the peptide hormone.
  • the peptide hormone is selected from the group consisting of secretin, cholecystokinin (CCK) , gastrin, gastrin-releasing polypeptide, glucagon-like polypeptide 1 (GLP-1) , neuromedin, adrenocorticotropic hormone (ACTH) , thyroid-stimulating hormone (TSH) , gonadotropin-releasing hormone (GnRH) , and somatostatin.
  • the present molecular construct is useful in treating solid tumors, in which the targeting element is CCK or somatostatin.
  • the effector element of the present molecular construct is the antibody fragment specific for the hapten, which is selected from the group consisting of dinitrophenol (DNP) , trinitrophenol (TNP) , dansyl, penicillin, p-aminobenzoic acid, and a short peptide having an amino acid sequence of SEQ ID NO: 20.
  • DNP dinitrophenol
  • TNP trinitrophenol
  • dansyl penicillin
  • p-aminobenzoic acid a short peptide having an amino acid sequence of SEQ ID NO: 20.
  • the effector element is the antibody fragment specific for the hapten, it may be used with an immunoregulatory effector that is tagged with the same hapten.
  • the effector element of the present molecular construct is the immunomodulant.
  • the immunomodulant is a toll-like receptor agonist.
  • the toll-like receptor agonist is selected from the group consisting of lipoteichoic acid, glucan, motolimod, imiquimod, resiquimod, gardiquimod, CpG oligodeoxynucleotide (CpG DON) , lipopolysaccharide (LPS) , monophosphoryl lipid A, and zymosan.
  • the present molecular construct is useful in treating solid tumors, in which the effector element is LPS or imiquimod.
  • the effector element of the present molecular construct is the cytotoxic drug, which is selected from the group consisting of auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin.
  • the radioactive nuclide is 111 In, 131 I, or 177 Lu.
  • the chelator is selected from the group consisting of 1,4, 7, 10-tetraazacyclododecane-1, 4, 7, 10-tetraacetic acid (DOTA) , 1,4, 7-triazacyclononane-1, 4, 7-triacetic acid (NOTA) , 1, 4, 7-triazacyclononane-1, 4-diacetic acid (NODA) , and diethylenetriaminepentaacetic acid (DTPA) .
  • the radioactive nuclide is 90 Y or 111 In
  • the chelator is DOTA.
  • the radioactive nuclide is 111 In, and the chelator is NOTA. In still another working example, the radioactive nuclide is 111 In, and the chelator is NODA. In further another working example, the radioactive nuclide is 90 Y, 111 In, or 177 Lu, and the chelator is DTPA.
  • the preferred targeting or effector elements are Fab, Fv, single-chain Fv (scFv) , single-domain antibody (sdAb) , or other antigen-binding fragments of antibodies.
  • scFv single-chain Fv
  • sdAb single-domain antibody
  • a linker with a sequence of (GGGGS) 2-5 is placed between V L and V H , or between V H and V L .
  • Other sequences of flexible nature and without a rigid secondary structure, such as the linking sequences between CH1 and CH2 domains and CH2 and CH3 domains of some human immunoglobulin isotypes, may also be used.
  • a linker of (GGGGS) 1-3 and a terminal cysteine residue is configured at the C-terminal of the scFv or other antibody fragment, or a growth factor, hormone, or cytokine.
  • the sulfhydryl group is for conjugating with a maleimide group at the end of the linking arms extending from a linker unit.
  • the antibody drug conjugate (ADC) approach which has been pursued very actively in recent years, has an underlined rationale of bringing a payload of a cytotoxic drug to the target cells.
  • ADC antibody drug conjugate
  • DAR drug/antibody ratios
  • the targeting part is limited to two Fab or Fv antigen-binding fragments.
  • the targeting element can accommodate growth factors, cytokines, hormones, in addition to various antibody fragments, and the effector element can accommodate a broad array of effector elements, including small molecular drugs, such as cytotoxic drugs, toll-like receptor agonists, chelators for radioactive nuclides, and proteins, such as scFv for various immune factors, cells, and/or cytokines.
  • small molecular drugs such as cytotoxic drugs, toll-like receptor agonists, chelators for radioactive nuclides, and proteins, such as scFv for various immune factors, cells, and/or cytokines.
  • the specificity of targeting is enhanced by adjusting the number of a particular targeting element and/or including two different sets of targeting elements.
  • the linker unit comprising cytotoxic drug payload can be prepared separately and then conjugating with different IgG antibodies for the preparation of antibody-drug conjugates.
  • a linker unit with any of the followings: 3 or more cytotoxic drugs, 2 or more toll-like receptor agonists (e.g., LPS molecules) , 2 or more chelators for radioactive nuclides (which is also referred to as bundles of cytotoxic drugs, LPS molecules, or chelators) can be conjugated to each of the two C-termini of CH3 domains of IgG molecules specific for certain target antigens.
  • These bundles of cytotoxic drugs, LPS molecules, and chelators may be supplied to academic and industrial laboratories producing antibody drug conjugates for laboratory tests, clinical trials, or commercial distribution.
  • the linker units for a targeting element and for an effector element can be prepared separately before joining.
  • the bundles of cytotoxic drugs, LPS molecules, chelators for radioactive nuclides, or other small molecules can be prepared separately without exposing the antibodies to harsh chemical conditions.
  • the drug to antibody ratios (DAR) can be better controlled than if the drugs are conjugated directly onto antibody molecules.
  • the adoption of the joint-linker platform can accommodate the preparation of various targeting/effector pharmaceutical molecules.
  • Another advantage is that IgG. Fc is not contained in the molecular constructs and can minimize potential Fc-mediated effects, such as complement-mediated activation, when such effects are not desired.
  • an overriding principle of this invention is to carry the therapeutic effectors to the disease sites (e.g., a tumor, an inflammation site and the like) while minimizing an overall systemic immune-enhancing or immunosuppressing effect.
  • the present molecular construct as discussed in Part III, above, possesses both the targeting and effector elements; hence, drug molecules carried by the effector element are directed to the intended target site by the targeting element. Accordingly, target treatment of any disease, condition, and/or disorder may be achieved by proper selection of the targeting and effector elements. Accordingly, another aspect of the present invention is directed to uses of the present molecular constructs (including those with the joint-linker configuration and the Fc-based ones) in the treatment of various diseases, conditions, and/or disorders.
  • Suitable diseases, conditions and/or disorders that may be treated by the present methods include autoimmune diseases (rheumatoid arthritis, psoriasis, SLE, syndrome, and Crohn’s disease) , osteoporosis, diffusive tumors (various types of lymphomas and leukemia) , solid tumors, and dry and wet age-related macular degeneration.
  • autoimmune diseases rheumatoid arthritis, psoriasis, SLE, syndrome, and Crohn’s disease
  • osteoporosis diffusive tumors (various types of lymphomas and leukemia)
  • solid tumors solid tumors
  • dry and wet age-related macular degeneration dry and wet age-related macular degeneration.
  • each of these methods comprises administering to the subject or patient a therapeutically effective amount of the molecular construct according to any of the above-mentioned aspect/embodiments.
  • the targeting elements involved in constructing the targeting/effector pharmaceuticals for treating the above diseases include scFv specific for (1) collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, collagen XI, ⁇ -aggrecan, osteonectin, and some other components of extracellular matrix in joints, skin, or bone, (2) CD19, CD20, CD22, CD30, CD52, CD79a, CD79b; CD38, CD56, CD74, CD78, CD138; or CD319, CD5, CD4, CD7, CD8, CD30; or CD13, CD14, CD15, CD33, CD34, CD36, CD37, CD41, CD61, CD64, CD65, CD11 c and other surface antigens of cells of lymphoid and myeloid lineages and of plasma cells, (3) EGFR, HER2/Neu, HER3, TN, Globo H, GD-2, CA125, CA19-9, and CEA overly expressed on solid tumors.
  • the targeting elements may also be antibodies of hormones, growth factors, or cytokines, in which receptors of hormones, growth factors, or cytokines are expressed on tumor cells or other diseased cells.
  • autoimmune diseases are diseases of the connective tissues, and hence various collagen types can serve as target antigens for shuffling targeting/effector pharmaceuticals to the targeted connective tissues.
  • effector elements for the T-E pharmaceuticals of this invention covers a broad range of molecules, including (1) scFv specific for inflammatory cytokines (such as TNF- ⁇ , IL-12/IL-23, IL-17, IL-1, IL-6, BAFF) , (2) scFv specific for RANKL, (3) scFv for CD3, and CD16a, expressed on T cells and NK cells, (4) scFv specific for PD-1, PD-L1, CTLA-4 and other immune checkpoints, (5) immunoenhancing cytokines (IFN- ⁇ , IFN- ⁇ , IL-2, TNF- ⁇ ) , (6) cytotoxic molecules, (7) TLR agonists (LPS, motolimod, imiquimod, resiquimod, gardiquimod, CpG oligonucleotides, ⁇ -glucan, zymosan) , and (9) chelating agents for radioactive nuclides.
  • inflammatory cytokines such as TNF-
  • This invention rationalizes that the requirement for the strength of binding of targeting element to the targeted molecules is not uniformly same.
  • a tumor-associated antigen on the surface of targeted tumor cells e.g., with scFv specific for CD19, CD38, HER2/Neu, EGFR, CA125
  • the binding avidity of the targeting element to the targeted tumor-associated antigen is high.
  • the specific binding to the targeted cells, in relative to other cells not expressing the antigens will be enhanced.
  • the targeting/effector pharmaceuticals can still bind to those target cells expressing relatively low densities of the targeted antigens.
  • the payloads of effector elements such as a payload of cytotoxic drugs, or immune-enhancing effector elements, have enhanced chances to exhibit their effector functions.
  • the targeting element binds to the targeted antigens in the extracellular matrix in the diseased sites, e.g., scFv specific for collagen II, collagen IX, collagen VII, collagen I, or osteonectin, too tightly. It is possible that if the binding is too strong, it will elicit unwanted immune functions or affect the integrity of the extracellular matrix. It is anticipated that the abundance of the extracellular protein can sequester the therapeutic molecules with the targeting moieties; even the avidity of the targeting moieties in binding their targeted molecules is not high. An equilibrium state of the on-and-off binding of the targeting element of the T-E pharmaceutical will bring about a raised local concentration of the T-E pharmaceuticals.
  • This invention rationalizes that for the targeting with scFv specific for collagen II, collagen I, collagen VII, collagen IX, or osteonectin, the avidity is not too high.
  • the targeting IgG antibody has an affinity constant, Kd ⁇ 1x10 -9 , in binding to the target antigen, only one scFv is incorporated to the pharmaceutical, and for two scFvs to be employed in the pharmaceutical, the affinity of the targeting IgG antibody binding to the target antigen should be lower, 1x10 -8 >Kd>1x10 -9 .
  • anti-IL17 or anti-BAFF to the skin, two targeting elements each with a different binding antigen can be adopted. This will enhance the binding to the aimed target tissue over normal tissues or cells, which express one of the two target antigens.
  • the molecular constructs used for treating autoimmune diseases are designed based on the rationale that if antibodies specific for pro-inflammatory cytokines are carried to the diseased tissues affected by those pro-inflammatory cytokines, the therapeutic efficacy will be enhanced and the side effects decreased.
  • Cytokines unlike hormones, generally do not circulate in the blood stream and act on remote target cells. Cells of the lymph nodes emigrate via the efferent lymph vessel and enter the lymphatic circulation. The products of lymphocytes do not get out the lymph nodes moving upstream against the blood flow coming into the nodes. In fact, administered antibodies can enter lymph nodes via the blood circulation. However, most of the cytokine molecules do not get out of the lymph nodes via blood circulation.
  • the cytokines secreted by the local lymph nodes act on cells in the microenvironment of the lymph nodes. Therefore, if antibodies targeting pro-inflammatory cytokines are channeled to some degrees to the diseased inflammatory tissues, less of the antibodies will go to the lymph nodes, and hence side effects will be decreased, and more of the antibodies will go to the diseased tissue and therapeutic efficacy can be enhanced.
  • an amount of the present molecular construct carrying excess amount of effector element i.e., scFv specific for TNF- ⁇ with an amount that exceeds the total amount of TNF- ⁇ in the blood circulation
  • scFv specific for TNF- ⁇ with an amount that exceeds the total amount of TNF- ⁇ in the blood circulation
  • the remaining amount will be favorably localized to the tissues (including joints) where collagen II is abundant.
  • TNF- ⁇ acts mainly in the microenvironment of the immune system. It has a very short half-life, about 1 hour and there is a minute amount of it in the blood circulation.
  • the administered anti-TNF- ⁇ of this invention will not be mainly present in lymphoid system and neutralize the TNF- ⁇ in the lymphoid system. Therefore, the side effects of anti-TNF- ⁇ in causing serious infections should be decreased.
  • the present method is useful in treating autoimmunity, in which the first targeting element is an scFv specific for ⁇ -aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, and collagen XI; and the first effector element is a an scFv specific for TNF- ⁇ , IL-17, IL-1, IL-6, IL-12/IL-23, BAFF, the receptor of IL-6 (IL-6R) , or the receptor of IL-17 (IL-17R) ; or the soluble receptor of TNF- ⁇ or IL-1.
  • the first targeting element is an scFv specific for ⁇ -aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, and collagen XI
  • the first effector element is a an scFv specific for TNF- ⁇ , IL-17, IL-1, IL-6, IL-12/IL-23, BAFF, the receptor of IL-6 (IL-6R) ,
  • a preferred set of the present inventions is to construct molecular constructs with scFv specific for type I collagen and type VII collagen as the targeting elements and scFv specific for TNF- ⁇ , IL-12/IL-23, or IL-17 as the effector elements.
  • the various T-E molecules based on the “joint-linker” configuration contain scFv specific for collagen I and/or collagen VII as the targeting elements and scFv specific for IL-17 as the effector elements.
  • the present method is employed to treat psoriasis, in which the first targeting element is an scFv specific for collagen I, or collagen VII; and the first effector element is an scFv specific for TNF- ⁇ , IL-12/IL-23, IL-17, or IL-17R.
  • scFv of antibodies specific for BAFF or IFN- ⁇ are to be carried to the skin by targeting elements, scFv specific for collagen I and collagen VII.
  • the various T-E molecules based on the “joint-linker” configuration contain scFv specific for collagen I and/or collagen VII as the targeting elements and scFv specific for BAFF as the effector elements.
  • the present method is suitable for the treatment of SLE, cutaneous lupus, or Sjogren’s syndrome, in which the first targeting element is an scFv specific for collagen I or collagen VII; and the first effector element is an scFv specific for BAFF.
  • the disease treated by the present method is rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis, in which the first targeting element is an scFv specific for collagen II, collagen IX, collagen XI, or ⁇ -aggrecan; and the first effector element is an scFv specific for TNF- ⁇ , IL-1, IL-6, IL-12/IL-23, or IL-17; or IL-6R or IL-17R.
  • the various T-E molecules based on the “joint-linker” configuration contain scFv specific for collagen III and/or collagen V as the targeting elements and scFv specific for TNF- ⁇ as the effector elements.
  • the present method may be used to treat inflammatory bowel disease, in which the first targeting element is an scFv specific for collagen III or collagen V; and the first effector element is an scFv specific for TNF- ⁇ .
  • the inflammatory bowel disease is Crohn’s disease or ulcerative colitis.
  • the present invention rationalizes that a preferred drug targeting approach has two folds of considerations. One is to increase the avidity and specificity of the targeting agents, so that target cells expressing relatively low antigen densities are still bound by the targeting agents. Secondly, the therapeutic agents are brought to diseased tumor tissue, without requiring that the therapeutic agents be internalized into the cells that express a particular tumor-associated antigen. Examples of such therapeutic agents are scFv, which recruit T cells and NK cells for mediating cytolytic effects on the targeted cells.
  • therapeutic agents are toll-like receptor agonists, such as LPS molecules, and scFv specific for immune checkpoints, such as scFv specific for PD-1, PD-L1, and CTLA-4, which elicit immune response in the local sites.
  • toll-like receptor agonists such as LPS molecules
  • scFv specific for immune checkpoints such as scFv specific for PD-1, PD-L1, and CTLA-4
  • bundles of chelating agents for radioactive nuclides is bundles of chelating agents for radioactive nuclides. With many of those therapeutic agents, cytolytic effects on the diseased cells and bystander cells can be elicited in the tissue sites regardless of the levels of tumor-associated antigen expressed by the tumor cells.
  • the present invention thus embodies a number of remedies to increase the relative localization of therapeutic agents in the targeted site.
  • Such a rationalization about specific delivery of therapeutic agents to diseased sites is not limited to therapeutic agents targeting cancer but also therapeutic agents targeting tissues affected by other diseases.
  • the target-specific delivery needs not to be absolute.
  • a preferred set of embodiments of T-E pharmaceuticals of the present invention is the employment of cytotoxic drug bundles in the joint-linker configuration.
  • the potent cytotoxic drugs include auristatin, maytansine, doxorubicin, calicheamicin, camptothecin, and others.
  • a preferred embodiment is that 5-10 cytotoxic molecules are carried in a linker unit.
  • a typical IgG antibody drug conjugates currently approved or under clinical development carry two Fab fragments for targeting and 3 or 4 molecules on the average of a cytotoxic drug for rendering lysis of the target cells.
  • it contains 3-5 scFv specific for a target antigen as the targeting element and 5-10 cytotoxic molecules as the effector element.
  • the targeting specificity and pharmacological effects can be much enhanced in comparison with the typical antibody drug conjugate approach.
  • two sets of scFv for two different antigens on target cells can be employed as the targeting elements, enhancing the specificity of targeting and the uptake or internalization of the bound antibody drug conjugates by the targeted cells.
  • the cytotoxic molecules are conjugated through a PEG or peptide linking arms to increase solubility.
  • the linker unit with the cytotoxic drug payload is prepared separately before the coupling with the linker unit conjugated with the targeting elements. In such an approach, the solubility of the linker unit and the entire molecular constructs should not pose a problem.
  • the molecular constructs described in this section bear a larger binding avidity in binding to the surface antigen of targeted cells but also a larger toxic drug payload than typical antibody drug conjugates that have been approved for clinical uses or are in clinical trials.
  • the inclusion of bundles of cytotoxic drug payload essentially amplifies the potency of the molecular constructs and therefore can increase the specificity of the targeting therapeutic agents. It is anticipated that those therapeutic agents can be administered at a lower dose and can achieve an enhanced therapeutic efficacy and reduced toxicity in treating diffusive and solid tumors.
  • This approach is not only suitable for different types of lymphoma and leukemia derived from B cells, T cells, and other leukocytes but also applicable for tumors that bear cell surface molecules for antibody targeting, such as tumors bearing an antigen belonging to the human epidermal growth factor receptor (EGFR) family, which are often overexpressed on many tumors.
  • EGFR human epidermal growth factor receptor
  • the scFv fragments of anti-CD3 antibodies may also be conjugated to linker units as effector elements for those T-E molecules designed to target tumorous cells.
  • the incorporation of scFv specific for CD3 helps the recruitment of T cells and the attachment of tumor target cells with cytotoxic T cells.
  • the binding by scFv of anti-CD3 induces the activation of T cells, which results in the lysis of the contacted or bridged target cells.
  • the bi-specific antibodies combining anti-CD3 with antibody fragments specific for antigens such as CD20, CD30, and EGFR, can efficiently lyse target cells expressing those antigens.
  • effector mechanisms that can be employed in molecular constructs that enlist targeting functions.
  • Those effector mechanisms include cytotoxic drug payloads and scFv specific for CD3 or CD16a.
  • the assortment of effectors for B cell-derived tumors, T cell-derived tumors, and some other types of leukemia, some of which are in diffusive forms, is different from that for solid tumors.
  • immune-enhancing agents such as LPS
  • the potent immune enhancing IgG and anti-CD28 may be applied and recruited to local tumor sites for stimulating immune activities. Those potent immune enhancers are not applicable as therapeutic effectors for treating various types of leukemia and diffusive tumors.
  • a binding agent For achieving the effect of apoptosis, a binding agent must be able to cross-link and cluster the targeted cell surface molecule, such as B-cell receptors or CD20, effectively.
  • the cross-linking of the surface molecules should achieve a “centrally-focused” cluster of cross-linked molecules, rather than a large number of small aggregates on the targeted cell surface.
  • a number of factors will affect a binding agent in achieving its apoptotic effect.
  • the multiple valence of a binding agent can enhance the cross-linking ability. However, if the binding arms are too many, it will increase the size of the binding agent and affect its ability to penetrate into tissues.
  • the binding agent should effectively bind to the targeted cell surface on a planar surface of a cell.
  • the binding arms such as PEG-scFv
  • the binding arms have a certain degree of flexibility and can reach to the targeted antigenic sites without steric constraints.
  • the binding arms are too long, the cross-linking and clustering effects may not be optimal, or the binding arms reach to cell surface molecules on an adjacent cell.
  • the Fab or scFv fragments can provide more flexibility than whole IgG or F (ab’ ) 2 .
  • CD20 is a transmembrane protein that has provided as a therapeutic target for the treatment of B cell malignancies.
  • CD20 is expressed by over 95%of B lymphocytes throughout their differentiation and maturation pathway, from the pre-B cell stage to the terminally differentiated plasma cells, but is absent on the hematopoietic stem cells.
  • CD20 is believed to exist predominantly as a tetramer on the cell surface.
  • the most widely used B cell-targeting antibody drug is rituximab, which is a chimeric IgG1 monoclonal antibody directed against CD20. Accumulating data indicate that rituximab is effective only for about 50%of the patients with B cell lymphoma.
  • Anti-CD20 antibodies which are approved for clinical uses or in human clinical trials, include chimeric ”C2B8” monoclonal antibody (rituximab) , monoclonal antibody 1F5, and chimeric 2H7 antibody.
  • Antibodies specific for other B cell surface antigens such as CD19 and CD22, generally do not cause lytic effects on B cell-derived tumor cells.
  • scFv specific for a B cell surface antigen such as CD19
  • scFv specific for CD20 can be considered as a targeting element and an effector element.
  • a large number of CD markers on B cells probably can be combined with CD20 under such a rationale, as long as there is some level of CD20 present on the intended target B tumors.
  • the various T-E molecules based on the “joint-linker” configuration contain scFv specific for CD20 and CD19 as the targeting elements and scFv specific for CD3 or CD16a, and bundles of cytotoxic drugs as the effector elements.
  • the preferred embodiments of this invention in the treatment of multiple myeloma are molecular constructs employing 3 or more scFv of one or two antibodies specific for CD38, CD78, CD138, or CD319 as the targeting element and a drug payload with 5-10 cytotoxic drug molecules as the effector element.
  • Other effector elements such as scFv specific for CD3 or CD16a may also be employed.
  • the various T-E molecules based on the “joint-linker” configuration contain scFv specific for CD38 and CD138 as the targeting elements and scFv specific for CD3 or CD16a, and bundles of cytotoxic drugs as the effector elements.
  • the protein In order that a targeted protein on a cell surface can be effectively cross-linked to form a large cluster, the protein must possess two or more antigenic sites for the binding agent to bind (without the help of a secondary cross-linking agent) .
  • a binding agent with even multiple copies of Fab or scFv specific for Ig ⁇ or Ig ⁇ cannot induce productive cross-linking of Ig ⁇ /Ig ⁇ -BCR to form a cluster.
  • T-E molecules which resemble those designed for treating B-cell derived tumors are designed.
  • scFv specific for CD markers of T cells are employed as targeting elements and the effector elements are the same as those for targeting B cell tumors.
  • This invention also pertains to the development of molecular constructs based on fragments of anti-CD3 antibodies for causing T cell anergy or dysfunction partially without inducing T cell activation and cytokine storm. Such constructs can then be used for treating T cell-mediated autoimmune diseases, including type-I diabetes, SLE, multiple sclerosis, inflammatory bowel diseases, etc.
  • scFv specific for CD3 can also be used as the effector element for recruiting T cells for the elimination of the targeted tumor cells.
  • T-E molecules which resemble those designed for treating B-cell derived tumors are designed.
  • scFv specific for CD markers of myeloid lineage cells are employed as targeting elements and the effector elements are the same as those for targeting B cell tumors.
  • the present method is useful in treating the diffused tumor, in which the first targeting element is an scFv specific for CD4, CD5, CD7, CD8, CD10, CD11c, CD13, CD14, CD15, CD19, CD20, CD22, CD23, CD30, CD33, CD34, CD36, CD37, CD38, CD41, CD43, CD56, CD61, CD64, CD65, CD74, CD78, CD79a, CD79b, CD80, CD138, or CD319; and the first effector element is a cytotoxic drug, or an scFv specific for CD3 or CD16a.
  • the first targeting element is an scFv specific for CD4, CD5, CD7, CD8, CD10, CD11c, CD13, CD14, CD15, CD19, CD20, CD22, CD23, CD30, CD33, CD34, CD36, CD37, CD38, CD41, CD43, CD56, CD61, CD64, CD65, CD74, CD78, CD79a, CD
  • the present method is employed to treat B-lymphocyte-derived lymphoma or leukemia, in which the first targeting element is an scFv specific for CD5, CD19, CD20, CD22, CD23, CD30, CD37, CD79a, or CD79b; and the first effector element is the cytotoxic drug, or an scFv specific for CD3 or CD16a.
  • the first targeting element is an scFv specific for CD5, CD19, CD20, CD22, CD23, CD30, CD37, CD79a, or CD79b
  • the first effector element is the cytotoxic drug, or an scFv specific for CD3 or CD16a.
  • the present method is employed in the treatment of B-lymphocyte-derived lymphoma or leukemia, in which one of the first targeting element and the first effector element is an scFv specific for CD79a; and the other of the first targeting element and the first effector element is an scFv specific for CD79b.
  • the present method possesses an effect on T-cell derived lymphoma or leukemia, in which the first targeting element is an scFv specific for CD5, CD30, or CD43; and the first effector element is a cytotoxic drug, or an scFv specific for CD3 or CD16a.
  • the present invention pertains to multi-arm linkers conjugated with antibody fragments specific for the tumor-associated antigens listed above.
  • Many antibodies specific for tumor-associated antigens such as anti-HER2/NEU (trastuzumab) , anti-CA19-9 (derived from clone 1116-NS-19-9) , anti-CA125 (derived from clone OC125) , anti-GD2 (ch14.18 monoclonal antibody) , and anti-Globo H (clone VK9) are readily available for application.
  • the present invention pertains to the employment of scFv or bi-scFv of antibodies specific for those tumor-associated antigens in conjunction with multi-arm linkers for carrying therapeutic agents to tumor sites.
  • Ligands suitable for such an approach include epidermal growth factor (EGF) and its mutants, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , vascular endothelial growth factor A (VEGF-A) , basic fibroblast growth factors (FGF) , hepatocyte growth factors (HGF) , gastrin, CCK, secretin, gastrin-releasing peptide, glucagon-like peptide 1 (GLP-1) , neuromedin, thyroid-stimulating hormone (TSH, or thyrotropin) , adrenocorticotropic hormone (ACTH) , gonadotropin-releasing hormone (GnRH) and somatostatin.
  • EGF epidermal growth factor
  • HB-EGF heparin-binding epidermal growth factor
  • VEGF-A vascular endothelial growth factor A
  • FGF basic fibroblast growth factors
  • HGF hepatocyte growth factors
  • VEGF-A vascular endothelial growth factor
  • VEGF-B vascular endothelial growth factor receptors 1 and 2
  • Trp2-Val3 VEGF receptors 1 and 2
  • Trp2-Arg3 VEGF receptors 1 and 2
  • EGF EGF, 53 a.a., somatostatin, 14 and 28 a.a., secretin, 27 a.a., gastrin, 14-34 a.a., CCK, 8-58 a.a., gastrin-releasing peptide, 27a.a., GLP-1, 37 a.a., the receptor-binding ⁇ chain of thyroid stimulating hormone, 118 a.a., neuromedin, 10 a.a., ACTH, 39 a.a., and GnRH, 10 a.a.
  • VEGF-A is a dimer with two peptides of 120-188 a.a. in length.
  • truncated segments of the hormones or factors or artificially designed peptides have been shown to retain comparable or even stronger binding to their respective receptors.
  • an octapeptide has been designed for the imaging of tumors expressing somatostatin receptors.
  • TLRs toll-like receptors
  • TLR agonists have been approved by FDA for treatment certain cancer and infectious diseases.
  • Bacillus Calmette-Guérin which activates TLR2 and TLR4, has long been used as a vaccine against tuberculosis. It is now approved for use in immunotherapy of in situ bladder carcinoma.
  • Imiquimod a small imidazoquinoline originally developed as a topical antiviral agent, which also binds to TLR7, is approved for actinic keratosis, and superficial basal cell carcinoma.
  • Monophosphoryl lipid A a derivative of lipopolysaccharide (LPS) from Salmonella minnesota, which binds to TLR2 and TLR4, is approved as an adjuvant for a vaccine against papilloma virus, which causes most cases of cervical carcinoma.
  • LPS lipopolysaccharide
  • TLR agonists that have been studied as potential therapeutic immunostimulatory substances include (1) glucans, include ⁇ -D-glucans derived from the cell wall of certain fungi, especially Aspergillus and Agaricus species, and zymosan derived from the cell wall of certain fungi, such as the yeast Saccharomyces cerevisiae, which bind to TLR2 and other receptors of immunocytes, (2) motolimod, a small molecule, which binds to TLR8, (3) imiquimod as explained above, and (4) CpG oligodeoxynucleotides (CpG DON) , short single-stranded synthetic DNA molecules containing a C followed by a G nucleotide, which binds to TLR9.
  • glucans include ⁇ -D-glucans derived from the cell wall of certain fungi, especially Aspergillus and Agaricus species, and zymosan derived from the cell wall of certain fungi, such as the yeast
  • TLR binding agents generally activate dendritic cells, macrophages, natural killer cells, neutrophils, and other immune cells of the native immunity and elicit the production of a large array of inflammatory cytokines, which augment the adaptive immunity.
  • the native and the adaptive immunity act in synergy in the removal of the pathologic elements.
  • LPS derived from Gram-negative bacteria also referred to as endotoxin or exogenous pyrogen
  • endotoxin or exogenous pyrogen is a very strong stimulator of the immune system.
  • LPS binds to CD14/TLR4/MD2 receptor complex on monocytes, dendritic cells, and macrophages, elicits strong responses of the innate immune system, and induces production of inflammatory cytokines.
  • LPS at 1 ⁇ g/kg can induce shock and is a powerful immunostimulatory agent. Systemic administration of unmodified LPS can potentially be very risky.
  • the present invention rationalize if LPS can be tied to a carrier and carried to tumor site, it can elicit in situ powerful local immune response, cause the release of inflammatory cytokines, increase vascular permeability, and recruit various effector cells to the site. This may help lyse the tumor cells in the inflamed tissue. Since cells in a tumor express tumor-associated antigens at varying density, the present approach elicits immune activities to all cells in a tumor site regardless of the cells’ densities of tumor-associated antigens.
  • a preferred embodiment is that three scFvs specific for a tumor-associated antigen are conjugated to one linker unit as the targeting element and 2-3 LPS or monophosphoryl lipid A molecules are conjugated to the other linker unit as the effector element. Additionally, two sets of scFv specific for two tumor-associated antigens may be separately conjugated to two linker units, which are then joined to form the targeting element.
  • LPS can be conjugated to a protein via a linker.
  • the methodology involves the activation of LPS with 1-cyano-4-dimethylaminopyridinium tetrafluoroborate (CDAP) and the coupling with a primary amino group of a protein.
  • CDAP 1-cyano-4-dimethylaminopyridinium tetrafluoroborate
  • the experiment also shows that LPS is conjugated to the protein preserving 70%of its endotoxic activity.
  • the conjugation of LPS to a linker unit of this invention can be achieved by following a similar procedure.
  • Activation of the hydroxyl groups in the carbohydrate element of LPS can be performed by the treatment with CDAP under a mild condition in an aqueous solution.
  • the CDAP-activated LPS is reacted with a NH 2 ----SH cross linker and then with the maleimide groups of the linking arms of a linker unit.
  • T-E molecules are designed for carrying scFv specific for immune checkpoints, such as cytotoxic T-lymphocyte-associated protein 4, or CTLA-4 (CD152) , programmed cell death 1, or PD-1 (CD279) , and programmed cell death 1 ligand 1, or PD-L1 (CD274 or B7-H1) , as effector elements for liberating immunological mechanisms to destroy cancerous cells.
  • scFv specific for immune checkpoints such as cytotoxic T-lymphocyte-associated protein 4, or CTLA-4 (CD152) , programmed cell death 1, or PD-1 (CD279) , and programmed cell death 1 ligand 1, or PD-L1 (CD274 or B7-H1) , as effector elements for liberating immunological mechanisms to destroy cancerous cells.
  • the present invention rationalizes that if those cytokines are recruited to tumor sites, they can elicit strong immune activities or inflammatory activities locally, which then leads to the elimination of the tumors. Therefore, the present invention employs the multi-arm linkers for conjugating scFv or bi-scFv specific for immunoregulatory cytokines rather than the immunoregulatory cytokines themselves.
  • the rationale is to use the scFv to recruit the immunoregulatory cytokines, which are already present in the body and circulating in the blood, and to concentrate them in the tumor site.
  • the cytokine-specific scFv used in these molecular constructs do not neutralize the activities of the cytokines.
  • the scFv also do not have very high binding affinity for the cytokines.
  • Kd in the range of 1-5 x10 -8 is adequate.
  • each of the scFv can potentially recruit multiple molecules of an immunoregulatory cytokine, rendering increased therapeutic effects.
  • Some tumors have two overexpressed tumor-associated markers, e.g., CA19-9 and CCK/gastrin receptors on some gastrointestinal and neuroendocrine tumors, or Globo H and HER2/Neu on some breast tumors.
  • the present invention rationalizes that by employing two guiding mechanisms, each carrying a different effector agent, e.g., one with a cytotoxic drug payload and the other with LPS, the combined therapeutic effects will be stronger and the side effects will be smaller.
  • the molecular conjugate with LPS, anti-PD-1, anti-PD-L1, anti-CTLA4, anti-TNF- ⁇ , anti-IFN- ⁇ , or anti-IFN- ⁇ is applied first, so that an “in-situ” inflammation or immune activation is induced, permitting increased vascular permeability. If the local inflammation or immune activation cannot lead to the complete cytolytic effects on the tumor or diseased cells, a subsequent administration of a molecular construct carrying cytotoxic drug payload can augment the cytolytic effects on the cells bearing the targeted tumor-associated antigen.
  • the therapeutic effectors that can be carried to the targeted solid tumor site by the targeting components include the following: (1) cytotoxic drugs, which kill the bound cells; (2) anti-CD16a or anti-CD3, which induces ADCC or cytotoxic activities; (3) LPS or other TLR agonists, anti-IL-2, anti-TNF- ⁇ , anti-IFN- ⁇ , or anti-IFN- ⁇ , which activate immune activities; (4) anti-PD1, anti-PD-L1, anti-CTLA4, or other immune checkpoint inhibitors, which liberate immune checkpoints and depress inhibitory feedback activities.
  • the therapeutic aim of these agents is to cause the lysis of the tumor cells bearing receptors for the ligand.
  • T-E molecules in joint-linker configuration incorporate scFv specific for HER2/Neu alone or in combination with scFv specific for HER1 as targeting elements and a cytotoxic drug, LPS, or scFv specific for CD3, CD16a, PD1, or VEGF-A as effector elements.
  • Various T-E molecules in joint-linker configuration incorporate scFv specific for GD2 alone or in combination with scFv specific for Globo H as targeting elements and a cytotoxic drug, LPS, or scFv specific for CD3, CD16a, PD1, or VEGF-A as effector elements.
  • T-E molecules in joint-linker configuration incorporate cholecystokinin (CCK) alone or in combination with somatostatin as targeting elements and a cytotoxic drug, LPS, or scFv specific for CD3, CD16a, PD1, or VEGF-A as effector elements.
  • CCK cholecystokinin
  • LPS cytotoxic drug
  • scFv specific for CD3, CD16a, PD1, or VEGF-A a cytotoxic drug
  • scFv specific for CD3, CD16a, PD1, or VEGF-A as effector elements.
  • T-E molecules in joint-linker configuration incorporate scFv specific for prostate-specific membrane antigen (PSMA) as the targeting elements and scFv specific, but non-neutralizing for IL-2, TNF- ⁇ , IFN- ⁇ , or IFN- ⁇ as the effector elements.
  • PSMA prostate-specific membrane antigen
  • growth factors such as EGF or its mutant, epiregulin, HB-EGF, VEGF-A, FGF, HGF, gastrin, CCK, secretin, gastrin-releasing peptide, GLP-1, neuromedin, the ⁇ -chain of TSH, ACTH, GnRH, or somatostatin
  • EGF epiregulin
  • HB-EGF vascular endothelial growth factor
  • VEGF-A FGF
  • HGF gastrin
  • CCK secretin
  • gastrin-releasing peptide GLP-1
  • neuromedin the ⁇ -chain of TSH, ACTH, GnRH, or somatostatin
  • the molecular constructs enlist EGF as a targeting element in IgG. Fc fusion protein configurations.
  • the effector elements include linker units containing cytotoxic molecules or LPS molecules, which are conjugated to the C-terminal peptide linkers.
  • the effectors may also be scFv specific for CD3, CD16a, PD-1, or VEGF-A.
  • Immunoregulatory cytokines such as IFN- ⁇ , TNF- ⁇ , IL-2, and IFN- ⁇ , can be incorporated as effector elements.
  • the scFv or immunoregulatory cytokine can be expressed as part of the recombinant peptide chain.
  • the invention also pertains to a preferred embodiment of T-E molecules that incorporate scFv specific for tumor-associated antigens as targeting elements and scFv specific for haptens as effector elements.
  • haptens include dinitrophenol (DNP) , trinitrophenol (TNP) , dansyl group, penicillin, p-aminobenzoic acid, or short peptides derived from proteins of human cells, viruses, or bacteria, for which antibodies are already available.
  • DNP dinitrophenol
  • TNP trinitrophenol
  • dansyl group penicillin
  • p-aminobenzoic acid or short peptides derived from proteins of human cells, viruses, or bacteria, for which antibodies are already available.
  • a peptide WADWPGPP of 8 amino acid residues which is located in the C ⁇ mX domain of membrane-bound IgE on human B lymphocytes is unique in sequence in the entire protein database, is not physically accessible by antibodies on the B cell surface.
  • T-E molecule of this design When a T-E molecule of this design is administered to a patient with a tumor expressing the tumor-associated antigen the drug aims to target, the T-E molecule binds to the tumor cells and serves as the base in the tumor site to recruit subsequently administered immunoregulatory antibodies, cytokines, or other proteins, which are tagged with the hapten.
  • the hapten tagged on the therapeutic molecule can be engineered via a linker, such as at the C-terminal end of antibodies, such as IgG antibodies specific for PD-1, PD-L1, CTLA4, VEGF-A, CD3, CD28, or immunoregulatory cytokines, such as IL-2, TNF- ⁇ , INF- ⁇ , or INF- ⁇ .
  • the linker and the peptide hapten can be expressed as part of an integral recombinant protein.
  • Bundles of cytotoxic drug payload based on a linker unit may also be tagged with the hapten through a linking arm and be recruited to the tumor site. This treatment strategy will increase the relative distribution of the therapeutic agents in favor of the tumor site and achieve enhanced therapeutic effects and decreased toxicity and side effects.
  • IgG specific for CD3 or CD28 are extremely powerful T cell activators. A systemic application of these antibodies can cause massive cytokine storms. However, if the activation of T cells by anti-CD3 or anti-CD28 antibodies can be administered at much reduced quantities and be concentrated to tumor tissues, their induced effects may be very effective in inducing local immune activities and inflammation and recruiting various immunocytes to counter tumor cells. Thus, a preferred embodiment of the present invention is to tag these antibodies with a hapten. The tagged anti-CD3 or CD28 is then administered at very minute quantities.
  • tumor-associated antigens such as CA19-9, CA125, and carcinoembryonic antigen (CEA)
  • CA19-9, CA125, and carcinoembryonic antigen (CEA) are shed from tumor cells and are present in the blood circulation.
  • the detection and measurements of those antigens in serum samples have become routine assays for the preliminary detection of tumors in people undergoing physical health examination.
  • the assays have also been used to monitor the efficacy of therapy and tumor status post treatments.
  • tumor-associated antigens of other types in serum are not assayed routinely, they are also known to be present in the blood circulation in varying quantities.
  • the keys in achieving therapeutic purposes for drug-conjugated tumor-targeting pharmaceuticals is that the therapeutic agents are specifically brought to the targeted tumor sites and that minimal quantities of the toxic therapeutic agents are trapped by other molecules and tissues.
  • the present invention also pertains to the clearance of circulating tumor-associated antigens, such as CA19-9, CA125, or CEA, when such tumor-associated antigens are the antigenic targets of the targeting elements of the T-E pharmaceuticals of this invention.
  • the clearance of the tumor-associated antigen in the blood can be performed by passing the patient’s plasma through affinity columns packed with resins conjugated with the antibodies specific for the intended tumor-associated antigens in a blood dialysis procedure, prior to the application of the pharmaceuticals of this invention specific for the targeted tumor-associated antigens.
  • the present invention also pertains to the new treatment modality of sequential administrations of a PEG-modified binding agent and a drug-conjugated anti-PEG antibody.
  • the PEG-modified binding agents include protein therapeutics that are conjugated with PEG to improve pharmacokinetic properties and the multi-arm linker-based therapeutics, which employ PEG linking arms, of this invention.
  • the cytolytic effect is enhanced or induced by the use of drug-conjugated anti-PEG IgG or F (ab’ ) 2 .
  • anti-PEG IgG or F (ab’ ) 2 can bind to each strand of PEG and multiple molecules of a cytotoxic drug can be carried by each anti-PEG IgG or F (ab’ ) 2 molecule.
  • the use of the divalent anti-PEG IgG or F (ab’ ) 2 can cause cross-linking of the complexes of targeted surface antigen and the PEG-linked binding agent.
  • the binding by divalent anti-PEG IgG or F (ab’ ) 2 can cause the aggregation of the large complexes (targeted surface antigen plus PEG-linked binding agent plus drug-conjugated divalent anti-PEG IgG or F (ab’ ) 2 and lead to the internalization of such complexes by the target cells.
  • the internalized drug will then cause the cytolysis of the targeted cells.
  • the treatment strategy should be effective in combination with the use of the molecular constructs for targeting tumor-associated antigens.
  • the drug-conjugated anti-PEG IgG can be prepared by engineering the IgG by installing a (GGGGS) 2 linker and a cysteine residue at the C-termini of the ⁇ heavy chains and conjugating to the two sulfhydryl groups with two linker units of cytotoxic dug payloads, each with 3-5 molecules of a cytotoxic drug.
  • the present invention also pertains to the new treatment modality of sequential administrations of PEG-linked antigen-binding fragments of antibodies specific for a tumor associated antigen, such as CEA, Globo H, or SSEA4, and an LPS-conjugated anti-PEG antibody.
  • a tumor associated antigen such as CEA, Globo H, or SSEA4
  • LPS-conjugated anti-PEG antibody elicits strong immune response in the targeted tumor site.
  • a 4-arm PEG linker conjugated with 4 scFv fragments is first administered to a patient with cancer expressing Globo H or SSEA4, followed with a lapse of time, by an LPS-conjugated anti-PEG IgG or F (ab’ ) 2 .
  • the present method is useful for treating the solid tumor.
  • the first targeting element is a peptide hormone, a growth factor, or an antibody fragment specific for a tumor-associated antigen
  • the first effector element is a cytotoxic drug, a toll-like receptor agonist, a chelator complexed with a radioactive nuclide, a cytokine, or an antibody fragment specific for a growth factor, a cell surface antigen, a hapten, or a cytokine.
  • the method further comprises the step of administering to the subject an immunoregulatory effector that is tagged with the same hapten, prior to, concurrent with, or after the administration of the present molecular construct.
  • the solid tumor treatable by the present method may be melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, or head and neck squamous cell carcinoma.
  • the tumor-associated antigen is selected from the group consisting of human epidermal growth factor receptor (HER1) , human epidermal growth factor receptor 2 (HER2) , human epidermal growth factor receptor 3 (HER3) , human epidermal growth factor receptor (HER4) , carbohydrate antigen 19-9 (CA 19-9) , carbohydrate antigen 125 (CA 125) , mucin 1 (MUC 1) , ganglioside GD2, ganglioside GD3, ganglioside GM2, fucosyl GM1, Neu5GcGM3, melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) , mesothelin, mucine-related Tn, Sialyl Tn, Lewis Y , Sialyl Lewis Y , Lewis A , Lewis x , heparin-binding epidermal growth factor (HB-EGF) , Globo H, and stage-specific embryo
  • the peptide hormone is selected from the group consisting of secretin, gastrin, cholecystokinin (CCK) , gastrin-releasing polypeptide, glucagon-like polypeptide 1 (GLP-1) , neuromedin, thyroid-stimulating hormone (TSH) , adrenocorticotropic hormone (ACTH) , gonadotropin-releasing hormone (GnRH) , and somatostatin.
  • the growth factor is selected from the group consisting of epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , vascular endothelial growth factor A (VEGF-A) , basic fibroblast growth factor (bFGF) , and hepatocyte growth factor (HGF) .
  • the first targeting element is EGF, mutant EGF, HB-EGF, VEGF-A, bFGF, or HGF.
  • the first effector element is an scFv specific for EGF, mutant EGF, VEGF-A, bFGF, or HGF.
  • the cell surface antigen is PD-1, PD-L1, CTLA-4, CD3, CD16a, CD28, or CD134.
  • the hapten is dinitrophenol (DNP) , trinitrophenol (TNP) , dansyl, penicillin, p-aminobenzoic acid, or a short peptide having an amino acid sequence of SEQ ID NO: 20.
  • the cytokine is IL-2, IL-10, IL-12, IFN- ⁇ , IFN- ⁇ , TGF- ⁇ , or TNF- ⁇ .
  • the first effector element is a non-neutralizing scFv specific for the cytokine selected from the group consisting of IL-2, IFN- ⁇ , IFN- ⁇ , and TNF- ⁇ .
  • the cytotoxic drug exhibiting a cytotoxic effect on tumor cell can be anti-estrogens (e.g., tamoxifen, raloxifene, and megestrol) , LHRH agonists (e.g., goscrclin and leuprolide) , anti-androgens (e.g., flutamide and bicalutamide) , photodynamic therapies (e.g., vertoporfin, phthalocyanine, photosensitizer Pc4, and demethoxy-hypocrellin A) , nitrogen mustards (e.g., cyclophosphamide, ifosfamide, trofosfamide, chlorambucil, estramustine, and melphalan) , nitrosoureas (e.g., carmustine and lomustine) , alkylsulphonates (e.g., busulfan and treosulfan) , triazene
  • the toll-like receptor agonist is lipoteichoic acid, glucan, motolimod, imiquimod, resiquimod, gardiquimod, CpG oligodeoxynucleotide (CpG DON) , lipopolysaccharide (LPS) , monophosphoryl lipid A, or zymosan.
  • osteonectin also referred to as secreted protein acidic and rich in cysteine (SPARC) .
  • SPARC secreted protein acidic and rich in cysteine
  • Collagen I is a dominant protein in the bone matrix, although it is also present in the connective tissue lining the skin.
  • a set of the present inventions is to construct T-E molecules with scFv specific for osteonectin and/or collagen I as the targeting elements and scFv specific for RANKL or sclerostin as the effector elements.
  • T-E molecules with scFv specific for osteonectin and/or collagen I as the targeting elements and scFv specific for RANKL or sclerostin as the effector elements.
  • the various T-E molecules based on the “joint-linker” configuration contain scFv specific for osteonectin (SPARC) and collagen I as the targeting elements and scFv specific for RANKL as the effector elements.
  • the present method is useful in treating osteoporosis disease, in which the first targeting element is an scFv specific for collagen I or osteonectin; and the first effector element is an scFv specific for receptor activator of nuclear factor ⁇ B (RANKL) .
  • the first targeting element is an scFv specific for collagen I or osteonectin
  • the first effector element is an scFv specific for receptor activator of nuclear factor ⁇ B (RANKL) .
  • immunoglobulin antibody can serve as the base of a targeting or effector element, and its corresponding effector or targeting element can be incorporated at the C-terminal of its two heavy ⁇ chains in the form of scFv domains.
  • Fc-based two-chain IgG. Fc is used as the base of the molecular platform.
  • Each of the polypeptide chain is fused with one or two targeting and one or two effector elements, for a total of two to three elements on each chain.
  • the T-E molecule with an Fc-based configuration will have a total of four to six elements (e.g., scFv, growth factor, or cytokines) .
  • the Fc portion of the molecular constructs also carries Fc-mediated effector functions, ADCC, and/or complement-mediated activation. While in certain other applications, such Fc-mediated effector functions are avoided.
  • targeting elements are positioned at the N-or C-terminus. If the effector elements function by binding to a cell surface component, such as CD3, CD16a, PD-1, PD-L1, or CTLA-4, they should also be positioned at the terminus. If the effector elements function by binding to and neutralizing soluble factors, such as VEGF, TNF- ⁇ , IL-17, or BAFF, they can be positioned between a terminal targeting or effector element and CH2-CH3.
  • a cell surface component such as CD3, CD16a, PD-1, PD-L1, or CTLA-4
  • both the effector element and the targeting element carried by the CH2-CH3 segment (or CH2-CH3 chain) are mostly comprised of amino acid residues, and for the sake of discussion, these molecular constructs are referred to anti-inflammatory molecules with tissue-targeting functions or anti-inflammatory Fc-based molecular construct.
  • the effector element may be an antibody fragment or a soluble receptor, while the targeting element is also an antibody fragment.
  • FIG. 8A is a schematic diagram illustrating an Fc-based molecular construct 800A according to certain embodiments of the present disclosure.
  • the Fc-based molecular construct 800A comprises two identical CH2-CH3 chains 810, a first pair of effector elements E1 linked to the N-termini of the CH2-CH3 chains 810, and a first pair of targeting elements T1 linked to the C-termini of the CH2-CH3 chains 810.
  • both the targeting element T1 and effector element E1 are antibody fragments.
  • the CH2-CH3 chains are adopted from human immunoglobulins ⁇ 1 or ⁇ 4.
  • ⁇ 1 is chosen, when Fc-mediated functions, such as antibody-dependent cellular cytotoxicity (ADCC) and complement-mediated activity (inflammatory activation or target cell lysis) , are desired.
  • ADCC antibody-dependent cellular cytotoxicity
  • complement-mediated activity inflammatory activation or target cell lysis
  • ⁇ 4 is chosen for constructing the present Fc-based molecular constructs.
  • the Fc-based molecular construct 800B illustrated in Figure 8B is quite similar to the Fc-based molecular construct 800A of Figure 8A in structure, except that the two effector elements E1 are respectively linked to the C-termini of the CH2-CH3 chains 810, while the two targeting effectors are respectively linked to the C-termini of the CH2-CH3 chains 810.
  • both the effector elements and targeting elements are linked to the N-termini of the CH2-CH3 chains.
  • the effector element and the targeting element are in the form of single-chain variable fragments (scFvs)
  • the effector element and the targeting element may be linked in a tandem or diabody configuration, thereby forming a bispecific scFv that is linked to the N-terminus of the CH2-CH3 chain.
  • the Fc-based molecular construct 800C ( Figure 8C) comprises an Fc portion, and accordingly, each CH2-CH3 chain 810 has a T1-E1 bispecific scFv linked to the N-terminus thereof.
  • the anti-inflammatory Fc-based molecular constructs can also use a soluble receptor (e.g., the soluble receptor of TNF- ⁇ or IL-1) as the effector element, according to certain embodiments.
  • the Fc-based molecular construct 800D ( Figure 8D) may have two effector elements E1 respectively linked to the N-termini of the CH2-CH3 chains 810, and two targeting elements T1 respectively linked to the C-termini of the CH2-CH3 chains 810. It is also possible that the effector elements and the targeting elements are respectively arranged at the C-and N-termini of the CH2-CH3 chains; see, for example, the Fc-based molecular construct 800E of Figure 8E.
  • the first pair of effector elements or the first pair of the targeting elements takes a Fab configuration (i.e., consisting of the V H -CH1 domain and the V L -C ⁇ domain) ; this Fab fragment is linked to the N-termini of the CH2-CH3 chains, so that the Fc-based molecular construct adopts an IgG configuration.
  • the pair of elements that is not in the Fab configuration may be linked to the C-termini of the pair of CH2-CH3 segments.
  • each of the two targeting elements T1 comprises the V H -CH1 domain 820 and the V L -C ⁇ domain 825, thereby forming a Fab configuration 830 that is linked to the N-termini of the CH2-CH3 chains 810, so that the Fc-based molecular construct 800F adopts the IgG configuration.
  • the pair of effector elements E1 is linked to the C-termini of the pair of CH2-CH3 chains 810.
  • the present Fc-based molecular construct may carry a total of six elements at most.
  • the additional elements may be a second pair of effector elements or a second pair of targeting elements.
  • the Fc-based molecular construct 900A ( Figure 9A) comprises a second pair of targeting elements T2.
  • the targeting elements T1 and T2 are linked in a tandem or diabody configuration to form a bispecific scFv that is linked to the N-terminus of the CH2-CH3 chain 910, and the effector element E1 is linked to the C-terminus of the CH2-CH3 chain 910.
  • the Fc-based molecular construct 900B comprises a second pair of effector elements E2.
  • the effector element E1 and E2 are linked in a tandem or diabody configuration to form a bispecific scFv that is linked to the N-terminus of the CH2-CH3 chain 910, and the targeting element T1 is linked to the C-terminus of the CH2-CH3 chain 910.
  • the effector element is an scFv specific for TNF- ⁇
  • the targeting element is an scFv specific for collagen II or collagen IX, or ⁇ -aggrecan.
  • each of the two effector elements is an scFv specific for IL-17, while the targeting element is an scFv specific for collagen I or collagen VII.
  • each of the two effector elements is an scFv specific for BAFF, and the targeting element is an scFv specific for collagen I or collagen VII.
  • each of the two effector elements is an scFv specific for TNF- ⁇
  • the targeting element is an scFv specific for collagen III or collagen V.
  • the two effector elements are in the form of a Fab specific for RANKL, and the targeting element is an scFv specific for collagen I or osteonectin.
  • the targeting element is an scFv specific for collagen I or osteonectin.
  • such molecular construct may take the configuration of any of those depicted in Figures 8A-8C and 8F.
  • the first pair of effector elements includes an scFv specific for TNF- ⁇ and an scFv specific for IL-17, while the first pair of targeting elements includes an scFv specific for collagen II and an scFv specific for collagen IX.
  • the first pair of effector elements includes an scFv specific for TNF- ⁇ and an scFv specific for IL-17, while the first pair of targeting elements includes an scFv specific for collagen I and an scFv specific for collagen VII.
  • each of the two effector elements is an scFv specific for BAFF, and the targeting element is an scFv specific for collagen I or collagen VII.
  • each of the two effector elements is an scFv specific for RANKL
  • the targeting element is an scFv specific for collagen I or osteonectin.
  • the two effector elements are in the form of a Fab antibody specific for TNF- ⁇ , while the targeting element is an scFv specific for collagen II or collagen IX.
  • the two effector elements are in the form of a Fab antibody specific for IL-17, and the targeting element is an scFv specific for collagen I or collagen VII.
  • the two effector elements are in the form of a Fab antibody specific for BAFF, and the targeting element is an scFv specific for collagen I or collagen VII.
  • the two effector elements are in the form of a Fab antibody specific for TNF- ⁇ , and the targeting element is an scFv specific for collagen III or collagen V.
  • the essence of this invention is the rationalization and conception of the specific combination or pairing of the targeting and effector elements.
  • the adoption of Fc-fusion configuration in the molecular constructs is a preferred embodiment. It is conceivable for those skilled in the arts to link the pairs of targeting and effector elements of this invention employing other molecular platforms, such as peptides, proteins (e.g., albumin) , polysaccharides, polyethylene glycol, and other types of polymers, which serve as a structural base for attaching multiple molecular elements.
  • Another aspect of the present disclosure is directed to the use of the anti-inflammatory Fc-based molecular constructs discussed above in Part V.
  • anti-inflammatory Fc-based molecular constructs used for treating various immune disorders contain an antibody fragment (e.g., scFv, Fab, and the like) specific for collagen II, collagen XI, or ⁇ -aggrecan used as targeting elements and an antibody fragment (e.g., scFv, Fab, and the like) specific for TNF- ⁇ and IL-17 as effector elements.
  • an antibody fragment e.g., scFv, Fab, and the like
  • an antibody fragment e.g., scFv, Fab, and the like
  • the present treatment method involves the administration of a suitable anti-inflammatory Fc-based molecular construct to a subject in need of such treatment.
  • a suitable anti-inflammatory Fc-based molecular construct for treating various immune disorders, in particular, autoimmune diseases, are discussed below.
  • each effector element of the anti-inflammatory Fc-based molecular construct is an antibody fragment specific for TNF- ⁇ , IL-12/IL-23, IL-1, IL-17, or IL-6, while each targeting element is an antibody fragment specific for collagen II, collagen IX, collagen XI, or ⁇ -aggrecan.
  • each effector element of the first pair of effector elements is an scFv specific for TNF- ⁇
  • each targeting element of the first pair of targeting elements is an antibody fragment specific for collagen II.
  • the effector element is an scFv specific for TNF- ⁇ , while the targeting element is an antibody fragment specific for collagen IX.
  • the effector element is an scFv specific for TNF- ⁇ , while the targeting element is an antibody fragment specific for ⁇ -aggrecan.
  • the above-mentioned anti-inflammatory Fc-based molecular constructs may have the configuration of 800A, 800B, or 800C discussed above.
  • Another anti-inflammatory Fc-based molecular construct for treating rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis comprises two effector elements that are in the form of a Fab antibody specific for TNF- ⁇ .
  • both targeting elements of the first pair of targeting elements is scFvs specific for collagen II or scFvs specific for collagen IX. Configurations of these Fc-based molecular constructs are illustrated in Figure 8F, for example.
  • the anti-inflammatory Fc-based molecular construct may comprise effector elements of an antibody fragment specific for TNF- ⁇ , IL-12/IL-23, or IL-17, and targeting elements of an antibody fragment specific for collagen I or collagen VII.
  • the effector elements are scFvs specific for IL-17, while the targeting elements are scFvs specific for collagen I.
  • the effector elements are scFvs specific for IL-17, while the targeting elements are scFvs specific for collagen VII.
  • These anti-inflammatory Fc-based molecular constructs have the configuration of 800A, 800B, or 800C discussed above.
  • Another anti-inflammatory Fc-based molecular construct for treating psoriasis comprises two effector elements that are in the form of a Fab antibody specific for IL-17.
  • both targeting elements of the first pair of targeting elements is scFvs specific for collagen I or scFvs specific for collagen VII. Configurations of these Fc-based molecular constructs are illustrated in Figure 8F, for example.
  • each effector is an antibody fragment specific for BAFF
  • each targeting element is an antibody fragment specific for collagen I or collagen VII.
  • These anti-inflammatory Fc-based molecular constructs may have the configuration illustrated in Figures 8A to 8C.
  • the pair of effector elements may also take the form of a Fab antibody specific for BAFF
  • the pair of targeting elements may be scFvs specific for collagen I or collagen VII, which takes the configuration of the molecular construct 800F illustrated in Figure 8F.
  • each effector is an antibody fragment specific for TNF- ⁇
  • each targeting element is an antibody fragment specific for collagen III or collagen V.
  • Configurations of these Fc-based molecular constructs are illustrated in Figures 8A to 8C, for example.
  • the pair of effector elements may also take the form of a Fab antibody specific for TNF- ⁇
  • the pair of targeting elements may be scFvs specific for collagen III or collagen V, thereby giving the configuration illustrated in Figure 8F.
  • the present anti-inflammatory Fc-based molecular constructs are also applicable in the treatment of osteoporosis.
  • the effector elements are antibody fragments specific for RANKL
  • the targeting elements are antibody fragments specific for collagen I or osteonectin.
  • the antibody fragments specific for RANKL may be scFvs so that the Fc-based molecular construct has the configuration illustrated in Figures 8A to 8C, or they may take the form of a Fab so that the Fc-based molecular construct has the configuration illustrated in Figure 8F.
  • Another aspect of the present disclosure is directed to an Fc-based molecular construct that, like the molecular construct described in Part V above, has at least a pair of targeting elements and at least a pair of effector elements linked, directly or indirectly, to a CH2-CH3 domain of an immunoglobulin.
  • the molecular construct can be used to treat various cellular proliferative diseases, including diffused tumor and solid tumors.
  • the present disclosure is also advantageous in that, in some embodiments, it utilizes the linker unit according to the first aspect of the present disclosure, which provides a facile means for controlling the amount of the cytotoxic drug payload of the present Fc-based molecular construct may take different configurations, which are discussed below, respectively.
  • each effector element of the first pair of effector elements is a drug bundle
  • each targeting element of the first pair of targeting elements is an antibody fragment specific for a cell surface antigen or a tumor associated antigen.
  • the Fc-based molecular constructs for treating tumors may have the configuration of molecular construct 1000A of Figure 10A or molecular construct 1000B of Figure 10B.
  • the effector elements E1 for example, drug bundles
  • the targeting elements T1 in this case, an scFv
  • the molecular construct 1000B has a pair of targeting elements T1 that takes the form of a Fab 1030.
  • the Fab 1030 configuration comprises the V H -CH1 domain 1020 and the V L -C ⁇ domain 1025, and is linked to the N-termini of the pair of CH2-CH3 segments 1010, so that the Fc-based molecular construct 1000A adopts the IgG configuration.
  • the pair of effector elements E1 is linked to the C-termini of the pair of CH2-CH3 chains 1010.
  • the drug bundle may be provided as the linker unit discussed in Part I of the present disclosure (see, for example Figure 1A to Figure 1 C) .
  • the drug bundle comprises a center core, a plurality of linking arms, and optionally, a coupling arm.
  • the center core may be a compound having a plurality of amine groups or a polypeptide comprising a plurality of lysine (K) residues, according to various embodiments of the present disclosure.
  • Each of the linking arms has one terminus that is linked to the center core by reacting with the amine groups of the compound core or the amine side chain of the K residues of the polypeptide core.
  • the amino acid residue at the N-or C-terminus of the center core is a cysteine residue or has an azide group or an alkyne group.
  • the drug bundle is linked to the peptide extension via the SPAAC reaction or CuAAC reaction occurred between said terminal residue and the C-terminus of the peptide extension.
  • the drug bundle is linked to the peptide extension via the CuAAC reaction occurred between said terminal residue and the C-terminus of the peptide extension.
  • the coupling arm also carries an alkyne group, azide group, tetrazine group, or strained alkyne group at the free terminus thereof, so that the drug bundle is linked to the C-terminus of the peptide extension via the iEDDA reaction (for coupling arms with the tetrazine or cyclooctene group) , SPAAC (for coupling arms with the azide or cyclooctyne group) reaction or CuAAC reaction (for coupling arms with the alkyne or azide group) occurred therebetween.
  • iEDDA reaction for coupling arms with the tetrazine or cyclooctene group
  • SPAAC for coupling arms with the azide or cyclooctyne group
  • CuAAC reaction for coupling arms with the alkyne or azide group
  • the present Fc-based molecular construct for treating tumors further comprises a pair of peptide extensions 1050 (see, Figures 10A and 10B) respectively having the sequence of (G 2-4 S) 2-8 C .
  • the pair of peptide extensions 1050 is linked to the C-termini of the pair of CH2-CH3 segments 1010.
  • the cysteine residue at the C-terminus of the peptide extension is linked with a coupling arm 1055 via thiol-maleimide reaction occurred therebetween.
  • the free terminus of the conjugating arm (that is, the terminus that is not linked to the cysteine residue) is modified with an alkyne, azide, strained alkyne, or tetrazine group, so that the drug bundle is linked thereto via iEDDA reaction or the SPAAC or CUAAC reaction occurred therebetween.
  • the coupling arm 1040 of the effector element E1 (in this case, a drug bundle) is linked to the CH2-CH3 segment 1010 via iEDDA reaction.
  • the ellipse 1045 as depicted in Figure 10A represents the chemical bond resulted from the iEDDA reaction occurred between the peptide extension 1050 and the effector element E1.
  • an iEDDA reaction is occurred between a tetrazine group and a cyclooctene group, such as a transcyclooctene (TCO) group.
  • TCO transcyclooctene
  • the effector element E1 is linked to the CH2-CH3 segment 1010 via SPAAC reaction.
  • the diamond 1045 as depicted in Figure 10B represents the chemical bond resulted from the SPAAC reaction occurred between the peptide extension 1050 and the effector element E1.
  • an SPAAC reaction is occurred between an azide group and a strained alkyne group (e.g., a cyclooctyne group, including, dibenzocyclooctyne (DBCO) , difluorinated cyclooctyne (DIFO) , bicyclononyne (BCN) , and dibenzocyclooctyne (DICO) group) .
  • DBCO dibenzocyclooctyne
  • DIFO difluorinated cyclooctyne
  • BCN bicyclononyne
  • DICO dibenzocyclooctyne
  • the pair of effector elements E1 is linked to the CH2-CH3 segment 1010 via iEDDA reaction by forming a chemical bond 1045 between the peptide extension 1050 and the effector element E1.
  • the present disclosure is not limited thereto; rather, the effector elements E1 is linked to the CH2-CH3 segment 1010 via SPAAC reaction or CuAAC reaction in other embodiments.
  • the Fc-based molecular construct that has the configuration illustrated in any of Figure 10A to Figure 10C is applicable in the treatment of diffused tumors.
  • the drug bundle of such Fc-based molecular construct comprises a plurality of cytotoxic drug molecules, such as, auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin.
  • the targeting elements of such Fc-based molecular construct may be an antibody fragment (e.g., scFv, Fab, or the like) specific for cell surface antigen selected from the group consisting of CD5, CD19, CD20, CD22, CD23, CD30, CD33, CD34, CD37, CD38, CD43, CD78, CD79a, CD79b, CD138, and CD319.
  • an antibody fragment e.g., scFv, Fab, or the like
  • CD5 CD19, CD20, CD22, CD23, CD30, CD33, CD34, CD37, CD38, CD43, CD78, CD79a, CD79b, CD138, and CD319.
  • the Fc-based molecular construct that has the configuration illustrated in any of Figure 10A to Figure 10C is applicable in the treatment of solid tumors, including malignant and/or metastatic solid tumors.
  • the drug bundle for use as effector elements comprises multiple cytotoxic drug molecules, e.g., auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin.
  • the drug bundle comprises multiple molecules of TLR agonist, such as, LPS, monophosphoryl lipid A, motolimod, imiquimod, resiquimod, gardiquimod, CpG DON, lipoteichoic acid, ⁇ -glucan, and zymosan.
  • the drug bundle comprises multiple molecules of a chelator (e.g., DOTA, NOTA, NODA, and DTPA) complexed with a radioactive nuclide (e.g., 90 Y, 111 In, and 177 Lu) .
  • a chelator e.g., DOTA, NOTA, NODA, and DTPA
  • a radioactive nuclide e.g. 90 Y, 111 In, and 177 Lu
  • the targeting elements of such Fc-based molecular construct may be an antibody fragment (e.g., scFv, Fab, or the like) specific for HER1, HER2, HER3, HER4, CA19-9, CA125, CEA, MUC1, MAGE, PSMA, PSCA; mucin-related Tn, Sialyl Tn, Globo H, SSEA-4, ganglioside GD2, or EpCAM.
  • the effector element of the first pair of effector elements is a drug bundle comprising multiple cytotoxic drug molecules, while the first and second pairs of targeting elements are scFvs specific for HER2 and scFvs specific for HER1, respectively.
  • each effector element of the first pair of effector elements is a drug bundle
  • each targeting element of the first pair of targeting elements is a growth factor or a peptide hormone
  • the Fc-based molecular constructs are suitable for treating solid tumors (including malignant and/or metastatic ones) may have the configuration of molecular construct 1100 of Figure 11. As illustrated in Figure 11, the effector elements E1 are linked to the C-termini of the pair of CH2-CH3 segments 1110, whereas the targeting elements T are linked to the N-termini of the pair of CH2-CH3 segments 1110.
  • the present molecular construct 1100 further comprises a pair of peptide extensions 1150 respectively having the sequence of (G 2-4 S) 2-8 C, which is linked to the C-termini of the pair of CH2-CH3 segments 1110.
  • the cysteine residue is linked with a coupling arm 1155, and the drug bundle is linked to the coupling arm 1155 via iEDDA reaction, SPAAC reaction, or CuAAC reaction occurred therebetween (see the above discussion regarding Figure 10A) .
  • the coupling arm 1140 of the effector element E1 is linked to the coupling arm 1155 via iEDDA reaction, in which the ellipse 1145 represents the chemical bond resulted from the iEDDA reaction occurred between the coupling arm 1155 and the effector element E1.
  • the present disclosure is not limited thereto; rather, the effector elements E1 is linked to the CH2-CH3 segment 1110 via SPAAC reaction or CuAAC reaction in other embodiments.
  • the drug bundle for use as effector elements comprises multiple cytotoxic drug molecules, e.g., auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin, according to some embodiments.
  • the drug bundle comprises multiple molecules of TLR agonist, such as, LPS, monophosphoryl lipid A, motolimod, imiquimod, resiquimod, gardiquimod, CpG DON, lipoteichoic acid, ⁇ -glucan, and zymosan.
  • the drug bundle comprises multiple molecules of a chelator (e.g., DOTA, NOTA, NODA, and DTPA) complexed with a radioactive nuclide (e.g., 90 Y, 111 In, and 177 Lu) .
  • a chelator e.g., DOTA, NOTA, NODA, and DTPA
  • a radioactive nuclide e.g. 90 Y, 111 In, and 177 Lu
  • targeting elements suitable for use in combination with the above-mentioned drug bundles are growth factors including, but not limited to EGF, mutant EGF, epiregulin, HB-EGF, VEGF-A, bFGF, and HGF.
  • Other targeting elements combinable with the above-mentioned drug bundles are peptide hormones; illustrative examples of which include CCK, somastatin, and TSH.
  • the Fc-based molecular construct comprises an antibody fragment as effector elements and a growth factor or peptide hormone as targeting elements.
  • Such molecular constructs are applicable in the treatment of solid tumors (including malignant and/or metastatic ones) .
  • Figure 12A illustrate a Fc-based molecular construct 1200A, in which the pair of effector elements E1 (in this case, scFvs) is linked to the N-termini of the pair of CH2-CH3 segments 1210, whereas the pair of targeting elements T1 is linked to the C-termini of the pair of CH2-CH3 segments 1210.
  • the effector elements E1 and targeting elements T1 are respectively linked to the C-and N-termini of the pair of CH2-CH3 segments 1210.
  • the antibody fragment may also take the form of a Fab, according to certain embodiments of the present disclosure.
  • the Fc-based molecular construct 1200C of Figure 12C comprises a pair of effector elements E1 in the form of a Fab 1230.
  • the Fab 1230 configuration comprises the V H -CH1 domain 1220 and the V L -C ⁇ domain 1225; the Fab 1230 is linked to the N-termini of the pair of CH2-CH3 segments 1210 so that the Fc-based molecular construct 1200A adopts the IgG configuration.
  • the pair of targeting elements T1 is linked to the C-termini of the pair of CH2-CH3 chains 1210.
  • the antibody fragments suitable for use as the effector elements are those specific to cell surface antigens such as PD-1, PD-L1, CTLA-4, CD3, CD16a, CD28, and CD134.
  • Another example of the effector element is the antibody fragment specific for the growth factor like EGF, mutant EGF, epiregulin, HB-EGF, VEGF-A, bFGF, and HGF.
  • Antibody fragments specific for haptens are also suitable for use as effector elements, and illustrative examples of haptens include DNP, TNP, dansyl, penicillin, p-aminobenzoic acid, and a polypeptide having the amino acid sequence of SEQ ID NO: 20.
  • the targeting element may be a growth factor such as EGF, mutant EGF, epiregulin, HB-EGF, VEGF-A, bFGF, and HGF.
  • the targeting element may be a peptide hormone like CCK, somastatin, and TSH.
  • the essence of this invention is the rationalization and conception of the specific combination or pairing of the targeting and effector elements.
  • the adoption of Fc-fusion configuration in the molecular constructs is a preferred embodiment. It is conceivable for those skilled in the arts to link the pairs of targeting and effector elements of this invention employing other molecular platforms, such as peptides, proteins (e.g., albumin) , polysaccharides, polyethylene glycol, and other types of polymers, which serve as a structural base for attaching multiple molecular elements.
  • the Fc-based molecular constructs of Part VII above are also useful in the treatment of various tumors, including diffused tumors and solid tumors.
  • the present disclosure also covers method for treating tumors by using the Fc-based molecular construct in Part VII.
  • the method comprises the administration of the present Fc-based molecular construct or a pharmaceutical comprising the same in an effective amount to a subject in need of such treatment.
  • the pharmacologic purpose is to lyse the targeted cells expressing those antigens.
  • the molecular construct bear Fc-mediated functions, such as ADCC or complement-mediated cytolysis.
  • Fc-mediated functions such as ADCC or complement-mediated cytolysis.
  • the molecular construct can be joined with effector elements that elicit strong immune-destruction functions, such as scFv specific for CD3 or CD16a, or immunoregulatory functions, such as scFv specific for PD-1, PD-L1, CTLA-4, the Fc-mediated functions may not be crucial.
  • the IgG molecules may also be linked at the termini of the two heavy chains with bundles of cytotoxic molecules, LPS molecules, or chelating groups for radioactive nuclides.
  • Fc region (paired CH2-CH3 domains) of human IgG1 mediates antibody-dependent cellular cytotoxicity (ADCC) and complement-mediated cytolysis (CMC) .
  • ADCC antibody-dependent cellular cytotoxicity
  • CMC complement-mediated cytolysis
  • the present invention rationalizes that those Fc-mediated functions can be maintained, while increasing the binding avidity of an antibody’s binding ability. It is known that some proportions of cells in tumor, which express low densities of targeted antigens, are resistant to the targeting therapeutic antibodies. For example, cells expressing low levels of HER2/Neu in breast tumor or CD20 in B cell lymphoma are not killed by trastuzumab or rituximab, respectively.
  • the molecular conjugates of this invention with much higher binding avidity may bind sufficiently strongly to those cells and mediate cytolytic mechanism on them.
  • Fc ⁇ RI CD64
  • Fc ⁇ RIIa CD32
  • Fc ⁇ RIIIb CD16b
  • Fc ⁇ RIIIa CD16a
  • a preferred embodiment of this invention is to conjugate scFv of antibodies specific for Fc ⁇ RIIIa to multi-arm linkers, which are conjugated with scFv for various antigenic targets (e.g., CD20, EGFR) and tumor-associated antigens expressed on various cell targets.
  • antigenic targets e.g., CD20, EGFR
  • a bi-specific antibody with one Fab specific for HER2/Neu and one Fab specific for Fc ⁇ RIIIa is superior to anti-HER2/Neu antibody trastuzumab in lysing tumor cells expressing low density of HER2 antigen.
  • the molecular construct of this invention has higher avidity for both HER2/Neu and should have higher lytic activities toward tumor cells expressing very low HER2/Neu.
  • the present Fc-based molecular construct uses drug bundles comprising multiple cytotoxic drug molecules as effector elements, and antibody fragments specific for a suitable cell surface antigen as targeting elements.
  • the present method is used to treat B lymphocyte-derived lymphoma or leukemia.
  • the cell surface antigens targeted by the present Fc-based molecular construct are cell surface antigens on human B lymphocytes, such as CD5, CD19, CD20, CD22, CD23, CD30, CD37 CD43, CD79a, and CD79b.
  • the diffused tumor treatable by the present method is plasmacytoma or multiple myeloma, and the cell surface antigens targeted in these cases are those on human plasma cells, including CD38, CD78, CD138, and CD319.
  • the present method involves the treatment of T-cell derived lymphoma or leukemia using molecular constructs that target cell surface antigens on human T cells, such as CD5, CD30, and CD43.
  • the cell surface antigens targeted by the molecular construct used are those on human myeloid lineage leukocytes, like CD33 and CD34.
  • the present Fc-based molecular construct uses drug bundles as effector elements and antibody fragments specific for a suitable tumor-associated antigen as targeting elements to treat solid tumors, such as melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, and head and neck squamous cell carcinoma.
  • solid tumors such as melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, and head and neck squamous cell carcinoma.
  • the method for treating solid tumors further comprises the step of subjecting the subject to a blood dialysis procedure using an antibody fragment specific for one or more tumor-associated antigens to remove the tumor-associated antigens that are shed from the tumor into the circulation of the subject, prior to the administration of the molecular construct.
  • the method for treating solid tumors involves the use of Fc-based molecular construct with drug bundles or antibody fragments specific for cell surface antigens, growth factors or haptens as effector elements, and growth factors or peptide hormones as targeting elements.
  • Fc-based molecular construct with drug bundles or antibody fragments specific for cell surface antigens, growth factors or haptens as effector elements, and growth factors or peptide hormones as targeting elements.
  • Illustrative examples of such molecular construct include those discussed above in Part VII- (iii) .
  • the solid tumor treatable by these molecular constructs are melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, or head and neck squamous cell carcinoma.
  • the molecular construct uses drug bundles of cytotoxic drug molecules as effector elements and EGF or its mutants as targeting elements.
  • the molecular construct uses scFvs specific for CD3, CD16a, PD-1, or VEGF as effector elements and EGF or its mutants as targeting elements.
  • the effector elements are antibody fragments specific for hapten.
  • the method further comprises the step of administering to the subject an immunoregulatory effector that is tagged with the same hapten after the administration of the molecule construct.
  • the immunoregulatory effector can be IFN- ⁇ , IL-2, TNF- ⁇ , and IFN- ⁇ , and an IgG antibody specific for PD-1, PD-L1, CTLA-4, or CD3.
  • the pair of CH2-CH3 segments is derived from human IgG heavy chain ⁇ 1, and the molecular construct uses drug bundles of cytotoxic drug molecules or LPS molecules as effector elements and EGF or its mutants, epiregulin, HB-EGF, VEGF-A, FGF, HGF, CCK, somastatin, or TSH as targeting elements.
  • the pair of CH2-CH3 segments is derived from human IgG heavy chain ⁇ 1, and the molecular construct uses scFvs specific for human CD3, CD16a, PD-1, PD-L1, or VEGF-A as effector elements and EGF or its mutants, epiregulin, HB-EGF, VEGF-A, FGF, HGF, CCK, somastatin, or TSH as targeting elements.
  • Example 1 Synthesis of peptide 1 (SEQ ID NO: 17) , peptide 2 (SEQ ID NO: 18) , and peptide 3 (SEQ ID NO: 19) as peptide cores, and conjugation of SH group of cysteine residue with maleimide-PEG 3 -transcyclooctene (TCO) as conjugating arm
  • Peptides 1 to 3 were synthesized by solid-phase peptide synthesis method and purified with reverse phase high-performance liquid chromatography (HPLC) using Shimadzu Nexera-i LC-2040C 3D HPLC system to 95%purity.
  • HPLC reverse phase high-performance liquid chromatography
  • the reverse phase HPLC used a Kromasil 100-5C18 column (250 mm X 4.6 mm; 5 ⁇ m) , with a mobile phase of acetonitrile and 0.1%trifluoroacetic acid, a linear gradient of 10%to 45%acetonitrile over 15 minutes, at a flow rate of 1.0 mL/min and a column temperature of 25°C.
  • the purified peptide was dissolved in 100 mM sodium phosphate buffer (pH 7.0) containing 50 mM NaCl and 5 mM EDTA at a final concentration of 2 mM.
  • the dissolved peptide was reduced by 1 mM tris (2-carboxyethyl) phosphine (TCEP) at 25°C for 2 hours.
  • TCEP 2-carboxyethyl phosphine
  • TCEP 2-carboxyethyl phosphine
  • the peptide and maleimide-PEG 3 -TCO were mixed at a 1/10 ratio and incubated at pH 7.0 and 25°C for 24 hours.
  • TCO-conjugated peptides were purified by reverse phase HPLC on a Supelco C18 column (250 mm X 10 mm; 5 ⁇ m) , using a mobile phase of acetonitrile and 0.1%trifluoroacetic acid, a linear gradient of 0%to 100%acetonitrile over 30 minutes, at a flow rate of 1.0 mL/min and a column temperature of 25°C.
  • Figure 13 showed the reverse phase HPLC elution profile for the purification of TCO-peptide 2; with the peak of the TCO-peptide 2 being indicated with an arrow.
  • the present TCO-peptide 2 as illustrated below, had a m.w. of 2078.9 daltons.
  • the present TCO-peptide 3 as illustrated below, had a m.w. of 3380.8 daltons.
  • Example 2 Synthesis of peptides 1 and 2 as peptide cores, and conjugation of SH group of cysteine residue with maleimide-PEG 4 -tetrazine as conjugating arm
  • Peptides 1 and 2 were prepared as in Example 1, and then dissolved in 100 mM sodium phosphate buffer (pH 7.0) containing 50 mM NaCl and 5 mM EDTA at 2 mM final concentration. The dissolved peptide was reduced by 1 mM TCEP at 25°C for 2 hours.
  • maleimide-PEG 4 -tetrazine Conju-probe Inc.
  • the peptide and maleimide-PEG 4 -tetrazine were mixed at a 1/5 ratio and incubated at pH 7.0 and 4°C for 24 hours.
  • Tetrazine-conjugated peptides were purified by reverse phase HPLC on a Supelco C18 column (250 mm X 10 mm; 5 ⁇ m) , using a mobile phase of acetonitrile and 0.1%trifluoroacetic acid, a linear gradient of 0%to 100%acetonitrile over 30 minutes, at a flow rate of 1.0 mL/min and a column temperature of 25°C.
  • the identification of said two synthesized tetrazine-peptides was carried out by mass spectrometry MALDI-TOF set forth in the preceding Example.
  • the present tetrazine-peptide 2 as illustrated below, had a m.w. of 2185.2 daltons.
  • Example 3 Synthesis of peptides 1 and 2 as peptide cores, and conjugation of SH group of cysteine residue with maleimide-PEG 5 -DBCO as conjugating arm
  • Peptides 1 and 2 were prepared as in the earlier Example.
  • the peptide was dissolved in 100 mM sodium phosphate buffer (pH 7.0) containing 50 mM NaCl and 5 mM EDTA at 2 mM final concentration.
  • the dissolved peptide was reduced by 1 mM TCEP at 25°C for 2 hours.
  • DBCO dibenzylcyclooctyne
  • DBCO-conjugated peptides were purified by reverse phase HPLC on a Supelco C18 column (250 mm X 10 mm; 5 ⁇ m) , using a mobile phase of acetonitrile and 0.1%trifluoroacetic acid, a linear gradient of 0%to 100%acetonitrile over 30 minutes, at a flow rate of 1.0 mL/min and a column temperature of 25°C.
  • the identification of the two synthesized DBCO-peptides was carried out by mass spectrometry MALDI-TOF.
  • the present DBCO-peptide 2 as illustrated below, had a m.w. of 2213.9 daltons.
  • Example 4 Synthesis of peptide 4 (SEQ ID NO: 21) , peptide 5 (SEQ ID NO: 22) , and peptide 6 (SEQ ID NO: 23) as peptide cores
  • Peptides 4 to 6 were synthesized by solid-phase peptide synthesis method, and then purified by reverse phase HPLC to 95%purity.
  • the unnatural amino acids, homopropagylglycine (G HP ) and azidohomoalanine (A AH ) contained an alkyne and an azide group, respectively.
  • the reverse phase HPLC used a Supelco C18 column (250 mm X 4.6 mm; 5 ⁇ m) , with a mobile phase of acetonitrile and 0.1%trifluoroacetic acid, a linear gradient of 2%to 90%acetonitrile over 30 minutes, at a flow rate of 1.0 mL/min and a column temperature of 25°C.
  • the identification of said three synthesized peptides was carried out by mass spectrometry MALDI-TOF.
  • the present peptide 4 had a molecular weight of 1317.0 daltons; the present peptide 5 had a m.w. of 1589.9 daltons; while the present peptide 6 had a m.w. of 1634.66 daltons.
  • Peptide 7 was synthesized, and the conjugation of the crosslinkers was performed as described in above examples.
  • the synthesized TCO-peptide 7 and tetrazine-peptide 7 were examined using MALDI-TOF.
  • Example 6 Synthesis of peptide 8 (SEQ ID NO: 25) as peptide core, and conjugation of SH group of cysteine residue with maleimide-PEG 3 -TCO, maleimide-PEG 4 -tetrazine or maleimide-PEG 5 -DBCO as conjugating arm
  • Peptide 8 (Ac-C-Xaa-K-Xaa-K-Xaa-K; wherein Xaa was a PEGylated amino acid with 2 EG units; SEQ ID NO: 25) was synthesized by solid-phase peptide synthesis method and then purified using reverse phase HPLC to 95%purity.
  • the reversed phase HPLC was conducted using a Kromasil 100-5C18 column (250 mm X 4.6 mm; 5 ⁇ m) , with a mobile phase of water and 0.1%TFA, a linear gradient of 10 %to 40 %acetonitrile over 12 minutes, at a flow rate of 1.0 mL/min and a column temperature of 25°C.
  • the identification of the synthesized peptide 8 was carried out by mass spectrometry ESI-MS. High resolution and high mass accuracy experiments were done on a LTQ Orbitrap XL ETD mass spectrometer (Thermo Fisher Scientific, San Jose, CA) equipped with standard ESI ion source. Mass ESI-TOF analyses were performed by GRC Mass Core Facility of Genomics Research Center, Academia Sinica, Taipei, Taiwan. The sample of the synthesized peptide showed a strong molecular ion at 981.9, corresponding to [M-H] - , indicating that the actual molecular weight of the PEGylated peptide was 983.0 daltons.
  • the present TCO-peptide 8 as illustrated below, had a m.w. of 1478.87 daltons.
  • the present tetrazine-peptide 8 as illustrated below, had a m.w. of 1584.92 daltons.
  • the present DBCO-peptide 8 as illustrated below, had a m.w. of 1613.8 daltons
  • Example 7 Synthesis of peptide 9 (SEQ ID NO: 26) as peptide core, and conjugation of SH group of cysteine residue with maleimide-PEG 3 -TCO as conjugating arm
  • Peptide 9 (Ac-C-Xaa-K-Xaa-K-Xaa-K-Xaa-K-Xaa-K-Xaa-K-Xaa-K; wherein Xaa was a PEGylated amino acid with 6 EG units; SEQ ID NO: 26) was prepared as set forth in an earlier Example. The identification of the synthesized peptide 9 was carried out by mass spectrometry ESI-MS. The sample of the synthesized peptide showed a strong molecular ion at 828.0, corresponding to [M+3H] 3+ , indicating that the actual molecular weight of the PEGylated peptide was 2480.7 daltons.
  • the conjugation of the crosslinker was performed as set forth in above examples, and then examined with mass spectrometry ESI-MS.
  • Example 8 Synthesis of linker unit by conjugating NHS-PEG 12 -maleimide to NH 2 groups of TCO-peptides 1 and 2
  • the identification of the PEG 12 -maleimide-conjugated TCO-peptide 1 and peptide 2 was carried out by mass spectrometry MALDI-TOF.
  • the present PEG 12 -maleimide-conjugated TCO-peptide 1 was a peptide core-based linker unit carrying one coupling arm with a TCO group and two PEG linking arms with maleimide groups.
  • the present PEG 12 -maleimide-conjugated TCO-peptide 2 was a peptide core-based linker unit carrying one coupling arm with a TCO group and three PEG linking arms with maleimide groups.
  • the present PEG 12 -maleimide-conjugated tetrazine-peptide 2 carried one coupling arm with a tetrazine group and three PEG linking arms with maleimide groups.
  • Figure 16A showed the mass spectrometry MALDI-TOF result, indicating that the construct had a m.w. of 4461 daltons.
  • the present PEG 12 -maleimide-conjugated DBCO-peptide 1 carried one linking arm with a DBCO group and two PEG linking arms with maleimide groups.
  • Figure 16B showed the mass spectrometry MALDI-TOF result, indicating that the construct had had a m.w. of 3445 daltons.
  • the present PEG 12 -maleimide-conjugated peptide 4 had a m.w. of 2817.3 daltons; it was a peptide core-based linker unit carrying one alkyne group and two PEG linking arms with maleimide groups.
  • the present PEG 12 -maleimide-conjugated peptide 5 (illustrated below) had a m.w. of 3839.2 daltons; it was a peptide core-based linker unit carrying one alkyne group and three PEG linking arms with maleimide groups.
  • PEG 12 -maleimide-conjugated peptide 6 (illustrated below) had a m.w. of 3811.5 daltons; it was a peptide core-based linker unit carrying one azide group and three PEG linking arms with maleimide groups.
  • Two linking arms of PEG 12 -maleimide were attached to a peptide core, the peptide 7 from the preceding Examples.
  • the conjugation of NHS-PEG 12 -maleimide to the NH 2 groups of the lysine residues of the peptide core was performed as described above, and the identification was carried out by mass spectrometry MALDI-TOF.
  • the present PEG 12 -maleimide-conjugated TCO-peptide 7 had a m.w. of 3237.63 daltons; it was a peptide core-based linker unit carrying one an alkyne group, one coupling arm with a TCO group, and two PEG linking arms with maleimide groups.
  • Example 12 Synthesis of linker unit by conjugating NHS-PEG 12 -maleimide to NH2 groups of TCO-peptide 8 and tetrazine-peptide 8
  • Three linking arms of PEG 12 -maleimide were attached to the peptide cores, TCO-peptide 8 and tetrazine-peptide 8.
  • the conjugation of NHS-PEG 12 -maleimide to the NH2 groups of the lysine residues of the peptide core was performed as in Example 8, and the identification was carried out by mass spectrometry MALDI-TOF.
  • the present PEG 12 -maleimide-conjugated TCO-peptide 8 (illustrated below) had a m.w. of 3774.9 daltons; it was a linker unit based on PEGylated amino acid and lysine; it carried one coupling arm with a TCO group and three PEG linking arms with maleimide groups.
  • Example 14 Synthesis of linker unit with 1, 3, 5-triaminobenzene conjugated with 1 NHS-PEG 12 -alkyne linking arm and 2 NHS-PEG 12 -maleimide linking arms
  • 1, 3, 5-triaminobenzene was purchased from BOC Sciences, Creative Dynamics Inc., NY, USA, and NHS-PEG 12 -alkyne linking arm and NHS-PEG 12 -maleimide from Thermo Fisher Scientific Inc. Waltham, MA, USA.
  • the conjugation of the linking arms employed a two-step procedure as shown in scheme 13.
  • step (i) 1, 3, 5-triaminobenzene was dissolved in the conjugation buffer (phosphate buffered saline, PBS, PH 7.2) at 1 mM and NHS-PEG 12 -alkyne crosslinker was added to 1, 3, 5-triaminobenzene solution at 1 mM final concentration (1:1 molar ratio) .
  • step (ii) NHS-PEG 12 -maleimide crosslinker was added to the incubated solution in the step (i) at 10 mM final concentration (1:30 molar ratio) .
  • step (ii) 30 ⁇ l of the 250 mM NHS-PEG 12 -maleimide stock solution was added to 125 ⁇ l of incubated solution; then 845 ⁇ l of the conjugation buffer was added to make the final solution 1 ml.
  • the reaction mixtures were incubated for 2 hours at room temperature.
  • DM1-SMCC which was N 2 ’-Deacetyl-N 2 ’- (3-mercapto-1-oxopropyl) -maytansine (DM1) modified by a linker, succinimidyl-4- (N-maleimidom-ethyl) cyclohexan-1-carboxylate (SMCC) , was purchased from ALB Technology Inc., Hong Kong, China. TCO-peptide 9 with free amine groups was dissolved in 100 mM sodium phosphate buffered at pH 7.5.
  • DM1-SMCC was added to the TCO-peptide 9 solution at 1 mM final concentration (25-fold molar excess over the 0.04 mM TCO-peptide 9 solution) by adding 4 ⁇ l of the 250 mM DM1-SMCC solution per milliliter of NH 2 -containing TCO-peptide 9 solution.
  • the reaction mixtures were incubated for 24 hours at room temperature.
  • the reaction product was separated by HPLC and then lyophilized.
  • the TCO-peptide 9 with five DM1-SMCC molecules was purified by reverse phase HPLC on a Supelco C18 column (250 mm X 4.6 mm; 5 ⁇ m) , using a mobile phase of acetonitrile and 0.1%trifluoroacetic acid, a linear gradient of 30%to 100%acetonitrile over 30 minutes, at a flow rate of 1.0 mL/min and a column temperature of 25°C.
  • Figure 20 showed the reverse phase HPLC profile for the purification of TCO-peptide 9 with five DM1-SMCC molecules (also referred to as a drug bundle) ; the peak being indicated with an arrow.
  • the present drug bundle was composed of a linker unit with a free TCO functional group and a set of five DM1 molecules as effector elements.
  • LPS from Salmonella enterica sv. Minnesota (Cat No. L2137, Sigma) was chromatographically purified on the Superdex 200 10/300 Tricon column (HR, GE Healthcare) in an Explorer FPLC system.
  • the elution buffer 50 mM HEPES, pH7.5, was used.
  • the sample was injected and eluted isocratically at 0.5 mL/min and collected in 1-mL fractions.
  • the fractions containing LPS were then dialyzed against MilliQ water using a 3500 MWCO membrane at 4°Covernight. The dialyzed LPS were lyophilized for subsequent conjugation.
  • the purified LPS was activated as follows. An amount of 1 ml of 2 mg/ml of an aqueous LPS solution was vortexed for 3 min and sonicated for 15 min at 25°C. Then, 1 ml of 4.5 mM sodium deoxycholate (NaDC) was added; 100 ⁇ l of 2.5 mM EDTA solution was added. The mixture was stirred for 30 minutes at 37°C, sonicated for 15 minutes, and stirred for another 30 minutes at 37°C. 40 ⁇ l of 100 mg/ml 1-cyano-4-dimethylaminopyridinium tetrafluoroborate (CDAP) in acetonitrile was added. After 30 seconds, 40 ⁇ l of 0.2M aqueous triethylamine (TEA) was added. The mixture was kept at 25°Cfor further 150 seconds with stirring to allow activation of LPS by CDAP
  • CDAP 1-cyano-4-dimethylaminopyridinium tetrafluo
  • LPS derived from Salmonella enterica sv. Minnesota was reacted with dansyl hydrazine to introduce a hydrazine group for subsequent coupling with amine group on a linker unit. Briefly, 1 ml of 2.0 mg/ml dansyl hydrazine in 0.1 M sodium borate buffer, pH 9.3, was added to the CDAP-activated LPS. The mixture was left to react overnight in the dark at 25°Cunder stirring. The reaction was quenched by adding 100 ⁇ l of ethanolamine. The unreacted dansyl hydrazine was removed by dialysis against Milli-Q water using a 3, 500 MWCO dialysis membrane for 24 hours at 4°Cin the dark.
  • the sample was characterized using fluorescence spectroscopy by measuring the emission spectra under the excitation at 325 nm.
  • Figure 22 showed that LPS, upon the reaction with dansyl hydrazine, exhibited an emission maximum at 495 nm in fluorescence spectrophotometric analysis.
  • the identification of the purified LPS and the dansyl-activated LPS was carried out by mass spectrometry MALDI-TOF.
  • the purified LPS had a m.w. of 3143 daltons; the dansyl-activated LPS had a m.w. of 3651 daltons, indicating one LPS conjugated with two dansyl hydrazine molecules; one dansyl hydrazine molecule had a m.w. of 265 daltons.
  • the present drug bundle was composed of a linker unit with a free TCO functional group and a set of two LPS molecules as effector elements.
  • Example 17 Conjugation of a imiquimod molecule with NHS-PEG 6 -maleimide-conjugated TCO-peptide 9
  • the present drug bundle was composed of a linker unit with a free TCO functional group and a set of five imiquimod molecules as effector elements.
  • DOTA-NHS (1, 4, 7, 10-tetraazacyclododecane-1, 4, 7, 10-tetraacetic acid N-hydroxy-succinimide ester) was purchased from Macrocyclics, Inc. Dallas, USA.
  • Conjugation of DOTA-NHS to TCO-peptide 9 employed a two-step procedure as illustrated in Scheme 14. In the first step, TCO-peptide 9 was dissolved in the conjugation buffer (phosphate buffered saline, PBS, with 5 mM EDTA pH 7.0) at 1 mM. The reaction mixtures were incubated for overnight at room temperature.
  • the conjugation buffer phosphate buffered saline, PBS, with 5 mM EDTA pH 7.0
  • the DOTA-NHS ester was added to the incubated solution at 100 mM final concentration (1:100 molar ratio or 1:20 equivalent ratio) . Since the DOTA-NHS ester was acidic because of containing TFA, the pH of the solution was adjusted to 8.0 in order to activate the NHS ester-NH 2 coupling reaction. The reaction mixtures were incubated overnight at room temperature.
  • Scheme 15 showed the chelation of five Y 3+ ions by DOTA-conjugated TCO-peptide 9.
  • Y (NO 3 ) 3 solution was added to the reaction mixtures at a 1:100 molar ratio, incubated for 2 hours at room temperature.
  • Free DOTA-NHS and Y 3+ ions were removed from reaction mixtures by using NAP-10 Sephadex G-25 column.
  • DOTA-conjugated TCO-peptide 9 with bound Y 3+ ions was analyzed by mass spectroscopy MALDI-TOF. Mass spectrometric analysis showed that the sample of DOTA-conjugated TCO-peptide 9 with bound Y 3+ ions had a m.w. of 5355 daltons ( Figure 24B) .
  • the present drug bundle which was composed of a linker unit with a free TCO functional group and a set of five DOTA groups respectively chelating an Y 3+ ion as effector elements.
  • Example 20 Isolation of V H and V L sequences from hybridoma cell lines producing monoclonal antibodies respectively specific for human CD79a, CD79b, and collagen VII for the preparation of scFv
  • Mouse B cell hybridoma 24C10 producing anti-CD79a antibody and hybridoma 1F10 producing anti-CD79b antibody were generated in our laboratory employing standard hybridoma methodology.
  • the mouse hybridoma line LH7.2 specific for human collagen VII was a gift from Prof. Irene M. Leigh, University of Dundee, U. K. Poly (A) + RNA was reverse-transcribed with a SuperScript III RT-PCR system (Invitrogen, Carlsbad, USA) , and the first strand cDNA was synthesized.
  • variable region of 24C10, 1F10, and LH7.2 cDNA of V H and V L were amplified by PCR using a set of DNA primers provided by Ig-primer Sets (Novagen, Madison, USA) according to the manufacturer’s instructions. The sequences of V H and V L for all clones were determined.
  • Expi293F cells were seeded at a density of 2.0 ⁇ 10 6 viable cells/ml in Expi293F expression medium and maintained for 18–24 hours prior to transfection to ensure that cells were actively dividing at the time of transfection.
  • 7.5 ⁇ 10 8 cells in 255 ml medium in a 2-liter Erlenmeyer shaker flask were transfected by ExpiFectamine TM 293 transfection reagent.
  • transfected cells were incubated at 37°Cfor 16 to 18 hours post-transfection in an orbital shaker (125 rpm) and the cells were added ExpiFectamine TM 293 transfection enhancer 1 and enhancer 2 to the shaker flask, and incubated for another 6 days.
  • Culture supernatants were harvested and scFv proteins in the media were purified using Protein L affinity chromatography.
  • Figures 25A and 25B respectively showed SDS-PAGE and ELISA analysis of purified scFv proteins of anti-CD79b antibody 1F10.
  • Figures 25C and Figure 25D respectively showed SDS-PAGE and ELISA analysis of purified scFv proteins of anti-collagen VII antibody LH7.2.
  • Example 22 Production of scFv of trastuzumab, rituximab, centuximab, nivolumab, ipilimumab, ranibizumab, adalimumab, and mutated teplizumab by HEK293 overexpression system
  • the scFv derived from those antibodies were designed to contain a flexible linker of GGGGSGGGGS and a terminal cysteine residue at the C-terminus.
  • the cysteine residue provides a sulfhydryl group for conjugation with maleimide group present at the free ends of liking arms in various linker units.
  • To produce the scFv of trastuzumab, rituximab, centuximab, nivolumab, ranibizumab, adalimumab, and a mutated teplizumab we used the V H and V L DNA sequences of those humanized antibodies without further codon optimization.
  • DNA sequences encoding V L -GSTSGSGKPGSGEGSTKG-V H - (GGGGS) 2 -C were synthesized.
  • the teplizumab antibody molecule contains a cysteine residue in CDR3 of V H , which interferes with SH-maleimide conjugation explained above.
  • amino acid sequences of the scFv of trastuzumab, rituximab, centuximab, nivolumab, ranibizumab, adalimumab, and the mutated teplizumab, prepared for the experiments of this invention are set forth in SEQ ID NOs: 35 to 42, respectively.
  • ExpiFectamine TM 293 transfection kit (Life Technologies, Carlsbad, USA) consisting of the Expi293F TM cell line, the cationic lipid-based ExpiFectamine TM 293 Reagent and ExpiFectamine TM 293 transfection Enhancers 1 and 2, and the medium (Gibco, New York, USA) .
  • Expi293F cells were seeded at a density of 2.0 ⁇ 10 6 viable cells/ml in Expi293F expression medium and maintained for 18 to 24 hours prior to transfection to ensure that the cells were actively dividing at the time of transfection.
  • 7.5 ⁇ 10 8 cells in 255ml medium in a 2-liter Erlenmeyer shaker flask were transfected by ExpiFectamine TM 293 transfection reagent.
  • the transfected cells were incubated at 37°Cfor 16 to 18 hours post-transfection in an orbital shaker (125 rpm) and the cells were added ExpiFectamine TM 293 transfection enhancer 1 and enhancer 2 to the shaker flask, and incubated for another 5 to 6 days.
  • Culture supernatants were harvested and scFv proteins in the media were purified using Protein L affinity chromatography. In our experience with adalimumab and trastuzumab scFv proteins, over 300 mg of purified scFv could be obtained from the 1 liter culture.
  • Figure 26A showed SDS-PAGE (10%) analysis of purified scFv of trastuzumab (lane 1) and adalimumab (lane 2)
  • Figures 26B and 26C respectively showed ELISA analyses of purified scFv of trastuzumab and adalimumab
  • Figures 26D and 26E respectively showed SDS-PAGE and ELISA analyses of purified scFv of centuximab, in which the trastuzumab scFv (anti-HER2 scFv) was used as a negative control.
  • Example 23 Production of scFv of adalimumab by an yeast Pichia expression system
  • the intended scFv constructs were the same as in the preceding Example, while the signal peptides used were different.
  • DNA sequence of scFv of adalimumab was synthesized and subcloned using primers (forward 5’-GTATCTCTCGAGAAAAGAGATATTCAGATGACGCAATCCCC-3’ (SEQ ID NO: 43) and reverse 5’-GTATCTGCGGCCGCTTAACAGGAGCCACCGCCAC-3’ (SEQ ID NO: 44) ) containing XhoI and NotI restriction sites into pPICZ ⁇ expression vector, in which the Kex2 signal peptide allowed for extracellular secretion of scFv of adalimumab.
  • the expression plasmid was then transformed into Pichia pastoris by electroporation.
  • ELISA was performed to measure the expression levels of scFv of adalimumab. Out of 480 transformants, five were selected for further protein induction and examination by SDS-PAGE. The clone scFv_1-A2 was selected for subsequent large-scale fermentation.
  • the high-yield clone scFv_1-A2 was inoculated in 100 mL of buffered glycerol-complex medium (BMGY, containing 1%yeast extract, 2%peptone, 100 mM K 3 PO 4 , 1.34 YNB, 0.4 mg/L biotin and 1%glycerol, pH 6.0) and cultured at 30°C, 200 rpm for 24 hours. On the next day, the culture was changed to a fermentation condition maintaining at 30°C, 30%of dissolved oxygen and pH 6.0. After being fermented for 24 hours, nitrogen source (YE, peptone) and methanol (0.5%, v/v) was added to induce protein expression. The culture supernatant was harvested for protein purification.
  • BMGY buffered glycerol-complex medium
  • YE peptone
  • methanol methanol
  • FIG. 27A showed SDS-PAGE analysis of the purified scFv of adalimumab
  • Figure 27B showed ELISA analysis of the purified scFvs of adalimumab.
  • the size of the scFv was as expected and the yeast-produced scFv of adalizumab bound to human TNF- ⁇ equally well as Expi-293F-produced scFv of adalizumab.
  • the peptide analogue of CCK (CGGGGSDY (SO 4 H) L (N) GWL (N) DF-NH 2 ; SEQ ID NO: 45) was designed to be composed of an 8-amino acid segment of CCK with three unusual amino acid residues and a consecutive N-terminal extension of six amino acid residues (CGGGGS) with a cysteine residue at the terminal.
  • the tyrosine residue (Y) was sulfated at its OH group on the aromatic ring and X was a norleucine residue.
  • the cysteine residue provided an SH group for conjugation with PEG-maleimide linking arms of the linker unit according to the present disclosure.
  • the peptide was custom-synthesized by Kelowna Inc., Taipei, Taiwan.
  • the DNA sequence encoding SEQ ID NO: 42 was synthesized and expressed as in the above Examples.
  • the sequences of V L and V H of scFv specific for CD3 were those of V L and V H of mutated Teplizumab.
  • the cysteine residue at the C-terminal end of the purified scFv of the mutated teplizumab was reduced by incubating 5 mM DTT at room temperature for 4 hours with gentle shaking.
  • the buffer of reduced anti-CDthree scFvs was exchanged to sodium phosphate buffer (100 mM sodium phosphate, pH7.0, 50 mM NaCl, and 5 mM EDTA) by using NAP-10 Sephadex G-25 column. After the reduction reaction and buffer exchange, conjugation was conducted overnight at room temperature in a reaction molar ratio of 1:1 ( [Mal-PEG 3 -TCO or Mal-PEG 5 -DBCO: [scFv] ] . The excess crosslinker was removed by a desalting column and the TCO-conjugated and DBCO-conjugated scFv products were analyzed.
  • Example 26 Conjugation of three scFvs specific for CD79b to three PEG 12 -maleimide linking arms based on tetrazine-peptide 2
  • This example aimed to demonstrate that three scFvs could be conjugated to the three PEG 12 -maleimide linking arms based on tetrazine-peptide 2.
  • 1F10 scFv Prior to conjugation with the tetrazine-peptide 2 that had three PEG 12 -maleimide linking arms, 1F10 scFv was incubated with DTT at a molar ratio of 2:1 ( [DTT] : [scFv] ) at 25°Cfor 4 hours with gentle shaking to keep its C-terminal cysteine in reduced form.
  • the buffer of reduced 1F10 scFv was exchanged to maleimide-SH coupling reaction buffer (100 mM sodium phosphate, pH 7.0, 50 mM NaCl and 5 mM EDTA) by using an NAP-10 Sephadex G-25 column (GE Healthcare) .
  • maleimide-SH coupling reaction buffer 100 mM sodium phosphate, pH 7.0, 50 mM NaCl and 5 mM EDTA
  • NAP-10 Sephadex G-25 column GE Healthcare
  • Example 27 Purification of the targeting linker unit containing three scFvs specific for CD79b linked to the three PEG 12 -maleimide linking arms based on tetrazine-peptide 2
  • the reaction mixture of the preceding example was applied to a size exclusion chromatography column S75.
  • the PEG 12 -maleimide-conjugated tetrazine-peptide 2 conjugated with three scFvs specific for CD79b was separated from the free scFv, free PEG 12 -maleimide-conjugated tetrazine-peptide 2 and the PEG 12 -maleimide-conjugated tetrazine-peptide 2 conjugated with 1 and two scFvs specific for CD79b by size exclusion chromatography column S75.
  • Figure 29A was the FPLC elution profile on a synthesized targeting linker unit composed of a linker unit with a free tetrazine functional group and a set of three scFvs specific for human CD79b as targeting elements.
  • the product i.e., the PEG 12 -maleimide-conjugated tetrazine-peptide 2 having a free tetrazine functional group and being conjugated with a set of three scFvs specific for CD79b
  • the product i.e., the PEG 12 -maleimide-conjugated tetrazine-peptide 2 having a free tetrazine functional group and being conjugated with a set of three scFvs specific for CD79b
  • Example 28 Analysis of targeting linker unit containing three scFvs specific for CD79b linked to the three PEG 12 -maleimide linking arms based on tetrazine-peptide 2 by mass spectrometry MALDI-TOF
  • the sample of the targeting linker unit of three scFvs specific for CD79b linked to the three PEG 12 -maleimide linking arms based on tetrazine-peptide 2 was confirmed by using mass spectrometry MALDI-TOF.
  • the median of experimental molecular weight was consistent with the median of theoretical molecular weight of three 1 F10 scFv conjugated to tetrazine-peptide 2 with three PEG 12 -maleimide linking arms.
  • the present targeting linker unit had the median molecular weight of 85996 daltons. Illustrated below is the present targeting linker unit that was composed of a linker unit with a free tetrazine functional group and a set of three scFvs specific for human CD79b as targeting elements.
  • Example 29 Preparation of targeting linker unit based on tetrazine-peptide 2 with three scFvs specific for HER2/neu
  • FIG. 30A showed the SDS-PAGE analysis of the synthesized product, indicating that the preparation was relatively pure. However, molecules with substantial PEG component generally migrate slowly in SDS-PAGE than proteins with the same molecular weight.
  • Figure 30B showed the mass spectrometric analysis, indicating that the purified linker unit had a m.w. of 86120 daltons. Illustrated below is the present targeting linker unit, which was composed of a linker unit with one free tetrazine functional group and a set of three scFvs specific for human HER2/neu as targeting elements.
  • Example 30 Preparation of effector linker units based on TCO-peptide 2 with three scFvs specific for TNF- ⁇ or PD-1
  • FIG. 30C Shown in Figure 30C was the mass spectrometric analysis of the present effector linker unit that was composed of a linker unit with a free TCO functional group and a set of three scFv specific for human TNF- ⁇ as effector elements (illustrated below) . As indicated in Figure 30C, this effector linker unit had a molecular weight of 86134 daltons.

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Abstract

The present disclosure provides various molecular constructs having a targeting element and an effector element. Methods for treating various diseases using such molecular constructs are also disclosed.

Description

MOLECULAR CONSTRUCTS WITH TARGETING AND EFFECTOR ELEMENTS
CROSS-REFERENCE TO RELATED APPLICATIONS
This application relates to and claims the benefit of U.S. Provisional Application No. 62/104405, filed January 16, 2015, U.S. Provisional Application No. 62/114,427, filed February 10, 2015, and U.S. Provisional Application No. 62/137737, filed March 24, 2015； the contents of the applications are incorporated herein by reference in their entirety.
BACKGROUND OF THE INVENTION
1. Field of the Invention
The present disclosure relates to the field of pharmaceuticals； more particularly, to multi-functional molecular constructs, e.g., those having targeting and effector elements for delivering the effector (e.g., therapeutic drug) to targeted sites.
2. Description of the Related Art
The continual advancement of a broad array of methodologies for screening and selecting monoclonal antibodies (mAbs) for targeted antigens has helped the development of a good number of therapeutic antibodies for many diseases that were regarded as untreatable just a few years ago. According to Therapeutic Antibody Database, approximately 2,800 antibodies have been studied or are being planned for studies in human clinical trials, and approximately 80 antibodies have been approved by governmental drug regulatory agencies for clinical uses. The large amount of data on the therapeutic effects of antibodies has provided information concerning the pharmacological mechanisms how antibodies act as therapeutics.
One major pharmacologic mechanism for antibodies acting as therapeutics is that, antibodies can neutralize or trap disease-causing mediators, which may be cytokines or immune components present in the blood circulation, interstitial space, or in the lymph nodes. The neutralizing activity inhibits the interaction of the disease-causing mediators with their receptors. It should be noted that fusion proteins of the soluble receptors or the extracellular portions of receptors of cytokines and the Fc portion of IgG, which act by  neutralizing the cytokines or immune factors in a similar fashion as neutralizing antibodies, have also been developed as therapeutic agents.
Several therapeutic antibodies that have been approved for clinical applications or subjected to clinical developments mediate their pharmacologic effects by binding to receptors, thereby blocking the interaction of the receptors with their ligands. For those antibody drugs, Fc-mediated mechanisms, such as antibody-dependent cellular cytotoxicity (ADCC) and complement-mediated cytolysis (CMC) , are not the intended mechanisms for the antibodies.
Some therapeutic antibodies bind to certain surface antigens on target cells and render Fc-mediated functions and other mechanisms on the target cells. The most important Fc-mediated mechanisms are antibody-dependent cellular cytotoxicity (ADCC) and complement-mediated cytolysis (CMC) , which both will cause the lysis of the antibody-bound target cells. Some antibodies binding to certain cell surface antigens can induce apoptosis of the bound target cells.
Antibodies can also serve as carriers of cytotoxic molecules or other therapeutic agents without the antibodies’s erving obvious therapeutic effector functions. In general, those antibodies bind to “tumor-associated” antigens on target cells, but cannot cause cell lysis by themselves. Antibodies specific for CD19 and CD22 on B lymphomas are well known. For many years, those antibodies have been explored as carriers for cytotoxic agents, including radioactive nuclides with very short half-lives, such as 90Y, 131I, and 177Lu. Some antibodies have also been studied as targeting agents for liposomes loaded with cytotoxic drugs, such as doxorubicin, paclitaxel, and amphotericin B. The field of antibody drug conjugates (ADC) has experienced an explosive phase of research and development in recent years, mainly attributing to the development of extremely cytotoxic drugs, such as auristatin, maytansine, calicheamicin, and camptothecin, and of methodologies for conjugating the cytotoxic molecules onto antibody molecules. Those ADCs have been designed to target diffusive (or liquid) tumors of the blood, lymphoid system, and bone marrow, including various types of lymphomas and leukemia, expressing one or more unique CD markers. Some ADCs are also being developed for solid tumors. A few of this new generation of antibody drug conjugates have been approved for clinical uses and many  are in clinical trials.
However, in the first generation of ADCs, the cytotoxic drug molecules are linked non-selectively to cysteine or lysine residues in the antibody, thereby resulting in a heterogeneous mixture of ADCs with different numbers of drug molecules per ADC. This approach leads to some safety and efficacy issues. For example, the first FDA-approved ADC, gemtuzumab ozogamicin, for treating acute myelogenous leukemia, is now withdrawn from the market due to unacceptable toxicity.
The concept and methodology for preparing antibodies with dual specificities germinated more than three decades ago. In recent year, the advancement in recombinant antibody engineering methodologies and the drive to develop improved medicine has stimulated the development bi-specific antibodies adopting a large variety of structural configurations.
For example, the bi-valent or multivalent antibodies may contain two or more antigen-binding sites. A number of methods have been reported for preparing multivalent antibodies by covalently linking three or four Fab fragments via a connecting structure. For example, antibodies have been engineered to express tandem three or four Fab repeats.
Several methods for producing multivalent antibodies by employing synthetic crosslinkers to associate, chemically, different antibodies or binding fragments have been disclosed. One approach involves chemically cross-linking three, four, and more separately Fab fragments using different linkers. Another method to produce a construct with multiple Fabs that are assembled to one-dimensional DNA scaffold was provided. Those various multivalent Ab constructs designed for binding to target molecules differ among one another in size, half-lives, flexibility in conformation, and ability to modulate the immune system. In view of the foregoing, several reports have been made for preparing molecular constructs with a fixed number of effector elements or with two or more different kinds of functional elements (e.g., at least one targeting element and at least one effector element) . However, it is often difficult to build a molecular construct with a particular combination of the targeting and effector elements either using chemical synthesis or recombinant technology. Accordingly, there exists a need in the related art to provide novel molecular platforms to build a more versatile molecule suitable for covering  applications in a wide range of diseases.
SUMMARY
The following presents a simplified summary of the disclosure in order to provide a basic understanding to the reader. This summary is not an extensive overview of the disclosure and it does not identify key/critical elements of the present invention or delineate the scope of the present invention. Its sole purpose is to present some concepts disclosed herein in a simplified form as a prelude to the more detailed description that is presented later.
<I> Peptide Core-Based Multi-Arm Linkers
In the first aspect, the present disclosure is directed to a linker unit that has at least two different functional elements linked thereto. For example, the linker unit may have linked thereto two different effector elements, one targeting element and one effector element, or one effector element and a polyethylene glycol (PEG) chain for prolonging the circulation time of the linker unit. The present linker unit is designed to have at least two different functional groups such that the functional elements can be linked thereto by reacting with the respective functional groups. Accordingly, the present linker unit can serve as a platform for preparing a molecular construct with two or more functional elements.
According to various embodiments of the present disclosure, the linker unit comprises a center core and a plurality of linking arms. The center core is a polypeptide core comprising (1) a plurality of lysine (K) resides, in which each K residue and a next K residue are separated by a filler sequence comprising glycine (G) and serine (S) residues, and the number of K residues ranges from 2 to 15； or (2) the sequence of (Xaa-K) n, where Xaa is a PEGylated amino acid having 2 to 12 repeats of ethylene glycol (EG) unit, and n is an integral from 2 to 15. Optionally, the filler sequence consists of 2 to 20 amino acid residues. In various embodiments, the filler sequence may have the sequence of GS, GGS, GSG, or SEQ ID NOs: 1-16. According to some embodiments of the present disclosure, the center core comprises 2-15 units of the sequence of G1-5SK； preferably, the center core comprises the sequence of (GSK) 2-15. Each of the linking arms is linked to the K residues of the center core via forming an amide linkage between the K residue and the  linking arm. The linking arm linked to the center core has a maleimide group at its free-terminus. Also, the amino acid residue at the N-or C-terminus of the center core has an azide group or an alkyne group； alternatively or additionally, the amino acid residue at the N-or C-terminus of the center core is a cysteine (C) residue, in which the thiol group of the amino acid residue is linked with a coupling arm having an azide group, an alkyne group, a tetrazine group or a strained alkyne group at the free terminus of the coupling arm.
In some embodiments, the linking arm is a PEG chain, preferably having 2 to 20 repeats of EG units. Also, the coupling linking arm is a PEG chain, preferably having 2 to 12 repeats of EG units.
Regarding amino acid residues having the azide group, non-limiting examples of said amino acid residues include L-azidohomoalanine (AHA) , 4-azido-L-phenylalanine, 4-azido-D-phenylalanine, 3-azido-L-alanine, 3-azido-D-alanine, 4-azido-L-homoalanine, 4-azido-D-homoalanine, 5-azido-L-ornithine, 5-azido-d-ornithine, 6-azido-L-lysine, and 6-azido-D-lysine. As to the amino acid residues having the alkyne group, illustrative examples thereof include L-homopropargylglycine (L-HPG) , D-homopropargylglycine (D-HPG) , and beta-homopropargylglycine (β-HPG) .
When the amino acid residues at the N-or C-terminus of the center core is the cysteine residue, the strained alkyne group at the free terminus of the coupling arm may be, a cyclooctene group, such as trans-cyclooctene (TCO) group； or a cyclooctyne group, e.g. dibenzocyclooctyne (DBCO) , difluorinated cyclooctyne (DIFO) , bicyclononyne (BCN) , and dibenzocyclooctyne (DICO) group. Alternatively, the tetrazine group at the free terminus of the coupling arm includes, but is not limited to, 1, 2, 3, 4-tetrazine, 1, 2, 3, 5-tetrazine, and 1, 2, 4, 5-tetrazine, and derivatives thereof, such as, 6-methyl tetrazine.
According to various embodiments of the present disclosure, the linker unit further comprises a plurality of first elements. Each of the first elements is linked to one of the linking arms via thiol–maleimide reaction. According to various optional embodiments of the present disclosure, the first element is an effector element suitable for eliciting an intended effect (e.g., a therapeutic effect) in a subject. Alternatively, the first element may be a targeting element for directing the linker unit to the site of interest.
Still optionally, the linker unit further comprises a second element that is different from the first elements. In some embodiments, the second element has an azide or alkyne group, so that it is linked to the center core or the coupling arm by coupling with the corresponding alkyne or azide group of the center core or the coupling arm in the presence of Cu (I) as a catalyst in a reaction referred to as “Cu (I) azide-alkyne click chemistry (CuAAC) reaction. ” Alternatively, in some embodiments, the second element having an azide or cyclooctyne group is linked to the center core or the coupling arm by coupling with the corresponding cyclooctyne or azide group of the center core or the coupling arm via “strain-promoted azide-alkyne click chemistry (SPAAC) reaction” . Still alternatively, in certain embodiments, the second element having a tetrazine or cyclooctene group is linked to the center core or the coupling arm by coupling with the corresponding cyclooctene or tetrazine group of the center core or the coupling arm via “inverse electron demand Diels–Alder (iEDDA) reaction” . In optional embodiments of the present disclosure, when the first element is an effector element, then the second element may be another effector element, which works additively or synergistically with or independently of the first element； alternatively, the second element may be a targeting element or an element for improving the pharmacokinetic property of the linker unit, such as solubility, clearance, half-life, and bioavailability. In some other optional embodiments, when the first element is the targeting element, then the second element is preferably an effector element or an element for improving the pharmacokinetic property of the linker unit.
In certain embodiments, the linker unit further comprises an optional third element that is different from the first and second elements. In the case where the second element is directly linked to the center core, the other terminus (i.e., the free terminus that is not linked with the second element) of the center core is optionally a cysteine residue, which can be used to introduce an optional third element. Specifically, the thiol group of the cysteine residue is reacted with a maleimide group of a PEG chain； and the thus-linked PEG chain is designated as the coupling arm, which has a tetrazine group or a strained alkyne group at its free terminus. Accordingly, the third element is then linked to the coupling arm via iEDDA reaction. In the case where the linker unit comprises both the second and third elements, it is preferable that at least one of the first and second elements is an effector as described above, while the third element may be the element for improving the pharmacokinetic property of the linker unit. One example of the element for improving the  pharmacokinetic property is a long PEG chain having a molecular weight of about 20,000 to 50,000 daltons.
<II> Uses of Peptide Core-Based Multi-Arm Linkers
The linker unit according to the first aspect of the present disclosure may find its utility in clinical medicine for the treatment of various diseases. Hence, the second aspect of the present disclosure is directed to a method for treating these diseases. According to various embodiments of the present disclosure, the method for treating a particular disease includes the step of administering to the subject in need thereof a therapeutically effective amount of the linker unit according to the above-mentioned aspect and embodiments of the present disclosure. As could be appreciated, said linker unit may be administered in a pharmaceutical formulation, which comprises a pharmaceutically-acceptable excipient suitable for the intended or desired administration route, in addition to the present linker unit.
Various illustrative combinations of the first and second elements of the present linker unit for treating some particular diseases are disclosed below for facilitating the understanding of some embodiments of the present disclosure.
According to some embodiments of the present disclosure, the present molecular construct is useful in treating an immune disorder, in which the first element is a single-chain variable fragment (scFv) specific for a cytokine or a receptor of the cytokine； or a soluble receptor of the cytokine, while the second element is an scFv specific for a tissue-associated extracellular matrix protein. In these cases, the first element is an effector element for treating one or more immune disorders, while the second element is a targeting element that facilitates the delivery of the linker unit to the disease site.
Non-limiting examples of the cytokine include tumor necrosis factor-α (TNF-α) , interleukin-17 (IL-17) , IL-1, IL-6, IL-12/IL-23, and B cell activating factor (BAFF) , while non-limiting examples of the cytokine receptor is the receptor specific for IL-6 (i.e., IL-6R) or IL-17 (i.e., IL-17R) . As for the soluble receptor of a cytokine, examples of which include, but are not limited to, the soluble receptor of the cytokine specific for TNF-α or IL-1. Illustrative examples of the tissue-associated extracellular matrix protein include, but are not  limited to, α-aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, and collagen XI.
According to some specific but illustrative examples of linker units suitable for treating psoriasis, the first element is an scFv specific for TNF-α, IL-12/IL-23, IL-17, or IL-17R； and the second element is an scFv specific for collagen I or collagen VII.
In some optional examples, the linker units suitable for treating immune disorders such as systemic lupus erythematosus (SLE) , cutaneous lupus or Sjogren’s syndrome comprises an scFv specific for BAFF as the first element and an scFv specific for collagen I or collagen VII as the second element.
For treating rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis, the illustrative linker units comprises the first element, which is an scFv specific for TNF-α, IL-1, IL-6, IL-12/IL-23, IL-17, IL-6R, or IL-17R； and the second element, which is an scFv specific for collagen II, collagen IX, collagen XI, or α-aggrecan.
The linker units are also suitable for treating inflammatory bowel diseases, e.g., Crohn’s disease and ulcerative colitis, among others. In these cases, the present linker unit uses an scFv specific for TNF-α as the first element, and an scFv specific for collagen III or collagen V as the second element.
Another set of diseases treatable by the present linker unit is diffused tumor, including, but not limited to, acute lymphocytic leukemia (ALL) , chronic lymphocytic leukemia (CLL) , acute myelogenous leukemia (AML) , chronic myelogenous leukemia (CML) , Hodgkin lymphoma, non-Hodgkin lymphoma, and myeloma. In these embodiments, the first element may be a targeting element such as an scFv specific for a first cell surface antigen, whereas the second element may be an effector element such as an scFv specific for a second cell surface antigen.
The first cell surface antigen suitable for use as the targeting element for treating diffused tumors includes, but is not limited to, CD5, CD19, CD20, CD22, CD23, CD27, CD30, CD33, CD34, CD37, CD38, CD43, CD72a, CD78, CD79a, CD79b, CD86, CD134, CD137, CD138, and CD319. On the other hand, non-limiting examples of the second cell surface antigen suitable for use as the effector element include CD3 and CD16a.
For the treatment of B-lymphocyte-derived lymphoma or leukemia, the illustrative first element is an scFv specific for CD5, CD19, CD20, CD22, CD23, CD30, CD37, CD79a, or CD79b, while the illustrative second element is an scFv specific for CD3 or CD16a.
To treat plasmacytoma or multiple myeloma, the illustrative first element is an scFv specific for CD38, CD78, CD138, or CD319, while the illustrative second element is an scFv specific for CD3 or CD16a.
Regarding T-cell derived lymphoma or leukemia, the illustrative first element for the treatment thereof is an scFv specific for CD5, CD30, or CD43, while the second element is an scFv specific for CD3 or CD16a.
For treating myelogenous leukemia, the illustrative first element is an scFv specific for CD33 or CD34, while the illustrative second element is an scFv specific for CD3 or CD16a. 
Still another set of diseases that may be treated by the present linker unit is solid tumor, including, but not limited to, melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, and head and neck squamous cell carcinoma. Additionally, the present linker unit is also suitable for treating advanced, malignant, or metastatic solid tumors.
To construct a linker unit for treating solid tumors, the first element (i.e., the targeting element) is chosen from a peptide hormone, a growth factor, and a first scFv specific for a tumor-associated antigen； whereas the second element (i.e., the effector element) is a second scFv specific for a cell surface antigen.
For example, the peptide hormone is secretin, cholecystokinin (CCK) , somatostatin, or thyroid-stimulating hormone (TSH) . Regarding the growth factor, it may be the epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , vascular endothelial growth factor A (VEGF-A) , basic fibroblast growth factor (bFGF) , or hepatocyte growth factor (HGF) . Illustrative examples of the tumor-associated antigen include epidermal growth factor receptor (HER1) , HER2, HER3, HER4, carbohydrate antigen 19-9 (CA 19-9) , carbohydrate antigen 125 (CA 125) ,  carcinoembryonic antigen (CEA) , mucin 1 (MUC 1) , ganglioside GD2, melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) , mesothelin, mucine-related Tn, Sialyl Tn, Globo H, stage-specific embryonic antigen-4 (SSEA-4) , and epithelial cell adhesion molecule (EpCAM) . As to the cell surface antigen, it can be CD3 or CD16a.
In some instances, the tumor-associated antigen may be shed from the solid tumor of a subject and wanders into his/her circulation system. In these cases, the present method for treating solid tumor comprises the step of, (a) subjecting the subject to a blood dialysis procedure using an antibody specific for one or more tumor-associated antigens to remove the tumor-associated antigens that are shed from the tumor and wanders into the circulation of the subject； and (b) administering the present linker unit for treating the solid tumor.
Yet another representative disease treatable by the present linker unit is osteoporosis. Illustrative linker units suitable for treating osteoporosis include a first element (in this case, an effector element) that is a first scFv specific for receptor activator of nuclear factor κB (RANKL) ； and a second element (or a targeting element) that is a second scFv specific for collagen I or osteonectin.
Age-related macular degeneration (AMD) is another example of the diseases treatable by the present linker unit. Illustrative linker units suitable for treating AMD include a first element of an scFv specific for VEGF-A, and a second element of a long PEG chain having a molecular weight of about 20,000 to 50,000 daltons. In this case, the first element is the effector element for treating AMD, while the second element is used to enhance the pharmacokinetic property of the linker unit.
<III> Molecular Constructs with Targeting and Effector Moieties
In the third aspect, the present disclosure is directed to a molecular construct comprising two linker units coupling to each other either directly or indirectly, in which the core of one linker unit is configured to be linked with at least one targeting element while the core of the other linker unit is configured to be linked with at least one effector element. The present molecular construct is advantageous in that the two linker units are coupled to each other via an iEDDA reaction, a SPAAC reaction, or a CuAAC reaction. This design  allows for a facile synthesis of a molecular construct with a complex structure. According to the principles and spirits of the present disclosure, the two linker units respectively carrying different numbers and/or types of functional elements can be independently prepared, and then conjugated together. In this way, it becomes feasible for a skilled artisan to construct libraries of molecular constructs respectively carrying different functional elements, and then select and combine two molecular constructs (or linker units) from the libraries to generate a desired constructs, depending on the needs and/or intended applications. Moreover, the number of functional elements per linker unit may be controlled by adjusting the number of specific functional group (s) of the core.
According to one embodiment of the present disclosure, the molecular construct comprises a first linker unit and a second linker unit. Specifically, the first linker unit comprises a first center core and one or more linking arms (hereinafter, the first linking arms) and optionally a coupling arm (hereinafter, the first coupling arms) that are respectively linked to the first center core； the second linker unit comprises a second center core and one or more linking arms (hereinafter, the second linking arms) and optionally a coupling arm (hereinafter, the second coupling arm) that are respectively linked to the second center core. The first and second linker units are coupled to each other via iEDDA, SPAAC, or CuAAC reaction occurred between any of the followings: the first and second center cores, the first coupling arm and the second center core, the first and second coupling arms, or the first center core and the second coupling arm.
According to the embodiments of the present disclosure, both the first and second center cores have a plurality of amine groups. Each of the linking arms is linked to the center core via forming an amide bond therebetween, for example, between the N-hydroxysuccinimydyl (NHS) group and the amine group. After being linked to the center core, the linking arm thus has a maleimide group at the free terminus thereof. In the presence of the maleimide group, a first targeting element and a first effector element are respectively linked to the first and second linking arms via thiol–maleimide reaction.
According to some embodiments of the present disclosure, each of the linking arms is a PEG chain having 2-20 repeats of EG units. Also, each of the coupling arms is a PEG chain having 2-12 repeats of EG units.
According to various embodiments of the present disclosure, each of the first and second center cores may be a compound core or a polypeptide core. In some examples, both the first and second center cores are compounds cores of the same or different compound (s) . In certain preferred embodiments, both the first and second center cores are polypeptide cores having the same or different sequence (s) . Alternatively, one of the two cores is a compound core, while the other is a polypeptide core.
Non-limiting examples of the compound suitable for use as the present compound core include, benzene-1, 3, 5-triamine, 2- (aminomethyl) -2-methylpropane-1, 3-diamine, tris (2-aminoethyl) -amine, benzene-1, 2, 4, 5-tetraamine, 3, 3' , 5, 5'-tetraamine-1, 1'-biphenyl, tetrakis- (2-aminoethyl) methane, tetrakis (ethylamine) -hydrazine, N, N, N' , N' , -tetrakis-(aminoethyl) -ethylenediamine, benzene-1, 2, 3, 4, 5, 6-hexaamine, 1-N, 1-N, 3-N, 3-N, 5-N, 5-N-hexakis- (methylamine) -benzene-1, 3, 5-triamine, 1-N, 1-N, 2-N, 2-N, 4-N, 4-N, 5-N, 5-N-octakis-(methylamine) -benzene-1, 2, 4, 5-triamine, and N, N-bis [ (1-amino-3, 3-diaminoethyl) -pentyl] methane-diamine.
In the case where the center core is a compound core, the coupling arm is linked to one of the plurality of amine groups of the center core by forming an amide bond between the coupling arm and the center core. Meanwhile, the free terminus of the coupling arm has an azide, an alkyne, a strained alkyne, or a tetrazine group.
According to some embodiments of the present disclosure, the polypeptide suitable for use as the present polypeptide core comprises a plurality of lysine (K) residues； optionally, 2 to 15 K residues. Also, each K residue and the next K residue are separated by a filler sequence comprising glycine (G) and serine (S) residues； optionally, the filler sequence consists of 2 to 20 amino acid residues. In various embodiments, the filler sequence may have the sequence of GS, GGS, GSG, or SEQ ID NOs: 1-16. In some embodiments, the polypeptide comprises 2-15 units of the sequence of G1-5SK, for example, (GSK) 2-15. In one embodiment, the polypeptide core has the sequence of SEQ ID NOs: 17, 18, 19, 21, 22, 23, or 24.
Alternatively, the polypeptide core may comprise the sequence of (Xaa-K) n, where Xaa is a PEGylated amino acid having 2 to 12 repeats of ethylene glycol (EG) unit, and n is an  integral from 2 to 15. In one embodiment, the polypeptide core has the sequence of SEQ ID NO: 25 or 26.
In the case where the center core is a polypeptide core, it may comprise a cysteine residue at its N-or C-terminus. In these instances, the coupling arm is linked to the cysteine residue of the center core via the thiol-maleimide reaction. The coupling arm linked to the cysteine residue has an azide, an alkyne, a strained alkyne, or a tetrazine group at the free-terminus thereof.
The first and second linker units may be coupled via various configurations, which are described in detail below, depending on the presence or absence of the first and second coupling arms. For a linker unit having a compound core, it is preferable that it is linked with another linker unit via a coupling arm (i.e., the first or second coupling arm) , while for a linker unit having a polypeptide core, the need for a coupling arm becomes optional.
When the first and second linker units respectively comprise the coupling arms, then one of the coupling arms (say, for example, the first coupling arm) has a tetrazine group at the free-terminus thereof, and the other coupling arm (in this case, the second coupling arm) has a strained alkyne group at the free-terminus thereof, such that the two linker units are coupled via the iEDDA reaction occurred between the two coupling arms (i.e., the first and second coupling arms) . Preferably, the tetrazine group is 1, 2, 3, 4-tetrazine, 1, 2, 3, 5-tetrazine, and 1, 2, 4, 5-tetrazine, or derivatives thereof, such as, 6-methyl tetrazine； and the strained alkyne group is TCO. The same rule also applies in the case where the free termini of both coupling arms respectively have an azide group and an alkyne group； in this instance, the two linker units are coupled via the CuAAC reaction occurred between the two coupling arms (i.e., the first and second coupling arms) . Alternatively, one of the coupling arm has an azide group, and the other of the coupling arm has a strained alkyne group (preferably, DBCO, DIFO, BCN, or DICO) ； accordingly, the two coupling arm can be coupled via the SPAAC reaction. These configurations may occur between two linker units, where both units have either compound cores or polypeptide cores, as well as in situations where one linker unit has a compound core, while the other has a polypeptide core.
When only one linker unit has the coupling arm (as an example, the first linker unit with the first coupling arm) , the center core of the other linker unit (for example, the second  center core) is a polypeptide core. In this case, the first amino acid residue at the N-or C-terminus of one of the second center core is an amino acid residue having an azide group or an alkyne group. In some embodiments, the amino acid residue having the azide or alkyne group would undergo CuAAC reaction with the corresponding alkyne or azide group of the first coupling arm of the first linker unit, thereby coupling the first and second linker units. Alternatively, the first amino acid residue at the N-or C-terminus of one of the second center core is an amino acid residue having an azide group, which can be linked to the coupling arm of the first linker unit having a strained alkyne group (preferably, DBCO, DIFO, BCN, or DICO) at the free-terminus via the SPAAC reaction. This configuration may occur between two linker units, where both units have polypeptide cores, or in situations where one linker unit has a compound core, while the other has a polypeptide core.
It is also possible that the first and second linker units are coupled without the presence of any coupling arms (that is, the first and second coupling arms) . In other words, the first and second coupling arms are directly linked with each other. This configuration mostly occurs between two polypeptide cores. Specifically, one of the two center cores (say, for example, the first center core) has an amino acid residue having an azide group at the N-or C-terminus thereof, while the other center core (such as the second center core) has an amino acid residue having an alkyne group at the N-or C-terminus thereof. In this way, the azide group of the first center core reacts with the alkyne group of the second center core, thereby coupling the first and second linker units.
Non-limiting examples of amino acid residues having the azide group include, L-azidohomoalanine (AHA) , 4-azido-L-phenylalanine, 4-azido-D-phenylalanine, 3-azido-L-alanine, 3-azido-D-alanine, 4-azido-L-homoalanine, 4-azido-D-homoalanine, 5-azido-L-ornithine, 5-azido-d-ornithine, 6-azido-L-lysine, and 6-azido-D-lysine. Illustrative examples of amino acid residues having the alkyne group include, but are not limited to, L-homopropargylglycine (L-HPG) , D-homopropargylglycine (D-HPG) , and beta-homopropargylglycine (β-HPG) .
According to some embodiments of the present disclosure, one of the first and second linker units of the molecular construct further comprises an additional linking arm (hereinafter, the third linking arm) linked to the first or the second linker unit.
In some embodiments, the third linking arm is configured to be linked with a long PEG chain having a molecular weight of about 20, 000 to 50, 000 daltons via thiol–maleimide reaction. Optionally, the third linking arm is configured to be linked with a single scFv, as either a targeting element or an effector element. In some examples, the first and second linking arms are connected with two different effector elements, and the targeting element linked to the third linking arm is an scFv specific for collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, collagen XI, aggrecan, or osteonectin. In other examples, the first and second linking arms are connected with two different targeting elements, and the effector element is an scFv specific for CD3 or CD16a.
In other embodiments, the present molecular construct further comprises a third linker unit. The third linker unit comprises a third center core, a linking arm (hereinafter, the third linking arm) , and optionally a coupling arm (hereinafter, the third coupling arm) . In this case, the third linker unit is linked to the first or the second linker unit via CuAAC reaction, iEDDA reaction, or SPAAC reaction occurred between any of the followings: the first or the second coupling arm and the third coupling arm, the first or the second center core and the third coupling arm, the first or the second center coupling arm and the third center core, or the first or the second center core and the third center core.
Regarding the third linking arm of the third linker unit, it may have a maleimide group at the free terminus thereof, which is used to link a second effector element or targeting element via thiol–maleimide reaction.
As would be appreciated, the targeting/effector element (such as a drug) having an NHS group can be directly linked to the K residue of the first, second, and/or third center core via forming an amide linkage between the NHS group and the K residue without the presence of the linking arm (i.e., the first, second, or third linking arm) .
According to various embodiments of the present disclosure, the first, second, and optionally, the third center core may be the same or different.
<IV> Uses of Molecular Constructs with Targeting and Effector Moieties
The molecular construct according to the third aspect of the present disclosure may find its utility in clinical medicine for the treatment of various diseases. Hence, the fourth  aspect of the present disclosure is directed to a method for treating these diseases. According to various embodiments of the present disclosure, the method for treating a particular disease includes the step of administering to the subject in need thereof a molecular construct according to the third aspect of the present disclosure and embodiments thereof in a therapeutically effective amount. As could be appreciated, said molecular construct may be administered in a pharmaceutical formulation, which comprises a pharmaceutically-acceptable excipient suitable for the intended or desired administration route, in addition to the present molecular construct.
Various illustrative combinations of the first and second elements of the present molecular construct for treating some particular diseases are disclosed below for facilitating the understanding of some embodiments of the present disclosure.
In some embodiments, the first element is a single-chain variable fragment (scFv) specific for a cytokine or a receptor of the cytokine； or a soluble receptor of the cytokine, while the second element is an scFv specific for a tissue-associated extracellular matrix protein. In these cases, the first element is an effector element for treating one or more immune disorders, while the second element is a targeting element that facilitates the delivery of the molecular construct to the disease site.
Non-limiting examples of the cytokine include tumor necrosis factor-α (TNF-α) , interleukin-17 (IL-17) , IL-1, IL-6, IL-12/IL-23, and B cell activating factor (BAFF) , while non-limiting examples of the cytokine receptor is the receptor specific for IL-6 (i.e., IL-6R) or IL-17 (i.e., IL-17R) . As for the soluble receptor of a cytokine, examples of which include, but are not limited to, the soluble receptor of the cytokine specific for TNF-α or IL-1. Illustrative examples of the tissue-associated extracellular matrix protein include, but are not limited to, α-aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, and collagen XI.
According to some specific but illustrative examples of molecular constructs suitable for treating psoriasis, the first element is an scFv specific for TNF-α, IL-12/IL-23, IL-17, or IL-17R； and the second element is an scFv specific for collagen I or collagen VII.
In some optional examples, the molecular constructs suitable for treating immune disorders, such as systemic lupus erythematosus (SLE) , cutaneous lupus, or Sjogren’s syndrome, comprise an scFv specific for BAFF as the first element and an scFv specific for collagen I or collagen VII as the second element.
For treating rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis, the illustrative molecular constructs comprise a first element that is an scFv specific for TNF-α, IL-1, IL-6, IL-12/IL-23, IL-17, IL-6R, or IL-17R； and a second element that is an scFv specific for collagen II, collagen IX, collagen XI, or α-aggrecan.
The molecular constructs are also suitable for treating inflammatory bowel diseases, e.g., Crohn’s disease and ulcerative colitis, among others. In these cases, the present molecular construct uses an scFv specific for TNF-α as the first element, and an scFv specific for collagen III or collagen V as the second element.
Another set of diseases treatable by the present molecular construct is diffused tumor, including, but not limited to, acute lymphocytic leukemia (ALL) , chronic lymphocytic leukemia (CLL) , acute myelogenous leukemia (AML) , chronic myelogenous leukemia (CML) , Hodgkin lymphoma, non-Hodgkin lymphoma, and myeloma. In these embodiments, the first element may be a targeting element such as an scFv specific for a first cell surface antigen, whereas the second element may be a cytotoxic drug, or an effector element such as an scFv specific for a second cell surface antigen.
The first cell surface antigen suitable for use as the targeting element for treating diffused tumor includes, but is not limited to, CD5, CD19, CD20, CD22, CD23, CD27, CD30, CD33, CD34, CD37, CD38, CD43, CD72a, CD78, CD79a, CD79b, CD86, CD134, CD137, CD138, and CD319. On the other hand, non-limiting examples of the second cell surface antigen suitable for use as the effector element include CD3 and CD16a. Alternatively, the first and second cell surface antigens are respectively CD79aand CD79b. The cytotoxic drug suitable for the treatment of diffused tumor includes, but is not limited to, auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin.
For the treatment of B-lymphocyte-derived lymphoma or leukemia, the illustrative first element is an scFv specific for CD5, CD19, CD20, CD22, CD23, CD30, CD37, CD79a, or  CD79b； while the illustrative second element is a cytotoxic drug, or an scFv specific for CD3 or CD16a.
To treat plasmacytoma or multiple myeloma, the illustrative first element is an scFv specific for CD38, CD78, CD138, or CD319； while the illustrative second element is a cytotoxic drug, or an scFv specific for CD3 or CD16a.
Regarding T-cell derived lymphoma or leukemia, the illustrative first element for the treatment thereof is an scFv specific for CD5, CD30, or CD43； while the second element is a cytotoxic drug, or an scFv specific for CD3 or CD16a.
For treating myelogenous leukemia, the illustrative first element is an scFv specific for CD33 or CD34； while the illustrative second element is a cytotoxic drug, or an scFv specific for CD3 or CD16a.
Still another set of diseases that may be treated by the present molecular construct is solid tumor, including, but not limited to, melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, and head and neck squamous cell carcinoma. Additionally, the present molecular construct is also suitable for treating advanced, malignant, or metastatic solid tumors.
To construct a molecular construct for treating solid tumors, the first element (i.e., the targeting element) is chosen from a peptide hormone, a growth factor, and a first scFv specific for a tumor-associated antigen； whereas the second element (i.e., the effector element) is a cytotoxic drug, a toll-like receptor (TLR) agonist, a chelator complexed with a radioactive nuclide, a cytokine, or a second scFv specific for a second growth factor, a cell surface antigen, a hapten, or the cytokine.
For example, the peptide hormone is secretin, cholecystokinin (CCK) , somatostatin, or thyroid-stimulating hormone (TSH) . Regarding the first growth factor, it may be the epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , vascular endothelial growth factor A (VEGF-A) , basic fibroblast growth factor (bFGF) , or hepatocyte growth factor (HGF) . Illustrative examples of the  tumor-associated antigen include epidermal growth factor receptor (HER1) , HER2, HER3, HER4, carbohydrate antigen 19-9 (CA 19-9) , carbohydrate antigen 125 (CA 125) , carcinoembryonic antigen (CEA) , mucin 1 (MUC 1) , ganglioside GD2, melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) , mesothelin, mucine-related Tn, Sialyl Tn, Globo H, stage-specific embryonic antigen-4 (SSEA-4) , and epithelial cell adhesion molecule (EpCAM) .
As the cytotoxic drug suitable for treating diffused tumors, the cytotoxic drug used in the molecular construct for the treatment of solid tumors includes, but is not limited to, auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin. Non-limiting TLR agonist includes lipopolysaccharide (LPS) , monophosphoryl lipid A, motolimod, imiquimod, resiquimod, gardiquimod, CpG oligodeoxynucleotide (CpG DON) , lipoteichoic acid, β-glucan, and zymosan. The chelator is selected from the group consisting of 1, 4, 7, 10-tetraazacyclododecane-1, 4, 7, 10-tetraacetic acid (DOTA) , 1, 4, 7-triaza-cyclo-nonane-1, 4, 7-triacetic acid (NOTA) , 1, 4, 7-triazacyclononane-1, 4-diacetic acid (NODA) , and diethylenetriaminepentaacetic acid (DTPA) ； and the radioactive nuclide is 111In, 131I, or 177Lu. As to the cytokine, it can be selected from the group consisting of IL-2, IFN-α, IFN-γ, and TNF-α. The second growth factor capable of being specifically recognized and bound by the second scFv is EGF, mutant EGF, VEGF-A, bFGF, or HGF. The cell surface antigen specifically recognized and bound by the second scFv is selected from the group consisting of CD3, CD16a, CD28, CD134, cytotoxic T-lymphocyte-associated protein 4 (CTLA-4, or CD152) , programmed cell death 1 (PD-1, or CD279) , and programmed cell death 1 ligand 1 (PD-L1, or CD274) . The cytokine specifically recognized and bound by the second scFv is selected from the group consisting of IL-2, IFN-α, IFN-γ, and TNF-α； in these cases, the second scFv is a non-neutralizing scFv.
In some instances, some tumor-associated antigens may be shed from the solid tumor of a subject and wanders into the circulation system of the subject. In these cases, the present method for treating solid tumor comprises the step of, (a) subjecting the subject to a blood dialysis procedure using an antibody specific for one or more tumor-associated antigens to remove the tumor-associated antigens that are shed from the tumor and wander into the circulation of the subject； and (b) administering the present molecular construct for treating the solid tumor.
According to some embodiments of the present disclosure, when the second element is the second scFv specific for the hapten, then the method further comprises the step of administering to the subject an immunoregulatory effector that is tagged with the same hapten. In the embodiments, the hapten is selected from the group consisting of dinitrophenol (DNP) , trinitrophenol (TNP) , and a short peptide having an amino acid sequence of WADWPGPP (SEQ ID NO: 20) ； and the immunoregulatory effector is IFN-α, IL-2, TNF-α, and IFN-γ, and an IgG antibody specific for PD-1, PD-L1, CTLA-4, or CD3.
Yet another representative disease treatable by the present molecular construct is osteoporosis. Illustrative molecular constructs suitable for treating osteoporosis include a first element (in this case, an effector element) that is a first scFv specific for receptor activator of nuclear factor κB (RANKL) ； and a second element (e.g., a targeting element) that is a second scFv specific for collagen I or osteonectin.
<V> Anti-Inflammatory Molecules with Tissue-Targeting Functions
In the fifth aspect, the present disclosure is directed to a fragment crystallizable (Fc) -based molecular construct that has at least one targeting element and at least one effector element linked, directly or indirectly, to a CH2-CH3 domain of an immunoglobulin. The design of the present Fc-based molecular construct allows for numerous combinations of a wide range of targeting and effector elements. Hence, the present Fc-based molecular construct may serve as a platform for constructing multi-valent molecules.
According to certain embodiments of the present disclosure, the Fc-based molecular construct comprises a pair of CH2-CH3 segments of an IgG. Fc, a first pair of effector elements, and a first pair of targeting elements.
In some embodiments, the present Fc-based molecular constructs are intended to be used in the treatment of immune diseases (in particular, autoimmune diseases) or osteoporosis. In this case, the first pair of effector elements consists of two effector elements, in which each of the two effector elements is an antibody fragment specific for tumor necrosis factor-α (TNF-α) , interleukin-17 (IL-17) , IL-17 receptor (IL-17R) , IL-1, IL-6, IL-6R, IL-12/IL-23, B cell activating factor (BAFF) , or a receptor activator of nuclear factor kappa-B ligand (RANKL) ； or a soluble receptor of TNF-α or IL-1. Further, the first pair of  targeting elements consists of two targeting elements, in which each of the two targeting elements is an antibody fragment specific for α-aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, collagen XI, or osteonectin. In the case where the first pair of effector elements is linked to the N-termini of the pair of CH2-CH3 segments, the first pair of targeting elements is linked to the C-termini of the pair of CH2-CH3 segments, and vice versa. Alternatively, when the first pair of effectors elements and the first pair of targeting elements is both in the form of single-chain variable fragments (scFvs) , then the first pair of targeting elements is linked to the N-termini of the first pair of effector elements in a tandem or diabody configuration, thereby forming a pair of bispecific scFvs that are linked to the N-termini of the pair of CH2-CH3 segments.
In certain embodiments, the pair of CH2-CH3 segments is derived from human IgG heavy chain γ4 or human IgG heavy chain γ1.
In some examples, the first pair of effector elements or the first pair of the targeting elements takes a Fab configuration (i.e., consisting of the VH-CH1 domain and the VL-Cκdomain) ； this Fab fragment is linked to the N-termini of the first and second heavy chains, so that the Fc-based molecular construct adopts an IgG configuration. In these cases, the pair of elements that is not in the Fab configuration is linked to the C-termini of the pair of CH2-CH3 segments.
According to other embodiments, the Fc-based molecular construct further comprises a second pair of effector elements, which consists of two additional effector elements that are both selected from the group described above for the effector elements. According to various embodiments, the elements of the second pair of effector elements are different from those of the first pair of effector elements. In these embodiments, the second pair of effector elements is linked to the free C-termini of the CH2-CH3 segments.
Alternatively, the present Fc-based molecular construct further comprises a second pair of targeting elements, in which the two targeting elements are both selected from the group described above regarding the targeting elements. According to various embodiments, the elements of the second pair of targeting elements are different from those of the first pair of targeting elements. In these embodiments, the second pair of targeting elements is linked to the free C-termini of the CH2-CH3 segments.
According to various optional embodiments, the targeting elements and effector elements described above can be combined as desired, so as to attain the intended therapeutic effect. Some exemplary combination of the effector element (s) and targeting element (s) for treating immune diseases are provided in the appended claims and discussed in the description section bellow.
<VI> Uses of Anti-Inflammatory Molecules with Tissue-Targeting Functions
In the sixth aspect, the present disclosure is directed to methods for treating various diseases. Generally, the methods involve the step of administrating an effective amount of the Fc-based molecular constructs according to the fifth aspect and any of the associated embodiments, to a subject in need of such treatment.
In certain embodiments, the present method is directed to the treatment of an immune disease； in particular, an autoimmune disease.
According to some embodiments of the present disclosure, the autoimmune disease is rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis. In this case, the effector element is an antibody fragment specific for TNF-α, IL-12/IL-23, IL-1, IL-17, or IL-6, while the targeting element may be an antibody fragment specific for collagen II, collagen IX, collagen XI, or α-aggrecan.
According to various embodiments, the autoimmune disease is psoriasis. In this case, the effector element is an antibody fragment specific for TNF-α, IL-12/IL-23, or IL-17, while the targeting element is an antibody fragment specific for collagen I or collagen VII.
According to some other embodiments, the autoimmune disease is systemic lupus erythematosus, cutaneous lupus, or
Figure PCTCN2016071184-appb-000001
Syndrome. In this case, the effector element is an antibody fragment specific for BAFF, and the targeting element is an antibody fragment specific for collagen I, or collagen VII.
According to some embodiments, the autoimmune disease is an inflammatory bowel disease, such as Crohn’s disease or ulcerative colitis. In this case, the effector element is an antibody fragment specific for TNF-α, and the targeting element is an antibody fragment specific for collagen III or collagen V.
Another disease treatable by the method proposed herein is osteoporosis. According to embodiments of the present disclosure, the effector element for treating osteoporosis comprises an antibody fragment specific for RANKL, while the targeting element comprises an antibody fragment specific for collagen I or osteonectin.
<VII> Molecular Constructs for Treating Tumors
In the seventh aspect, the present disclosure is directed to an Fc-based molecular construct that, like the molecular construct described above in the fifth aspect of the present disclosure, has at least one targeting element and at least one effector element linked, directly or indirectly, to a CH2-CH3 domain of an immunoglobulin. By selecting the effector element (s) and targeting element (s) of the present Fc-based molecular construct, the molecular construct can be used to treat various cellular proliferative diseases, including diffused tumors and solid tumors. The present disclosure is also advantageous in that, in some embodiments, it utilizes the linker unit according to the first aspect of the present disclosure, which provides a facile means for controlling the amount of the drug (e. g., cytotoxic drugs) payload of the present Fc-based molecular construct. The linker unit carrying multiple drug molecules is herein referred to as a drug bundle. Such drug bundles can be manufactured separately before being conjugated to the antibody molecules, thus avoiding subjecting drug molecules under harsh chemical conditions for the direct conjugation with the antibody molecules.
According to various embodiments of the present disclosure, the Fc-based molecular construct comprises a pair of CH2-CH3 segments of an IgG. Fc, a first pair of effector elements, and a first pair of targeting elements.
For a first series of Fc-based molecular constructs according to this aspect, each effector element of the first pair of effector elements is a drug bundle, while each targeting element of the first pair of targeting elements is an antibody fragment specific for a cell surface antigen. In these cases, the first pair of effector elements is linked to the C-termini of the pair of CH2-CH3 segments, whereas the first pair of targeting elements is linked to the N-termini of the pair of CH2-CH3 segments. According to various embodiments of the present disclosure, the drug bundle comprises a plurality of cytotoxic drug molecules, such as, auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin； while the cell  surface antigen targeted by these Fc-based molecular construct is CD5, CD19, CD20, CD22, CD23, CD30, CD33, CD34, CD37, CD38, CD43, CD78, CD79a, CD79b, CD138, or CD319. As an example, rather than a limitation, these Fc-based molecular constructs are useful in the treatment of various diffused tumors.
In a second series of Fc-based molecular constructs according to this aspect, each effector element of the first pair of effector elements is a drug bundle, while each targeting element of the first pair of targeting elements is an antibody fragment specific for a tumor-associated antigen. In these cases, the first pair of effector elements is linked to the C-termini of the pair of CH2-CH3 segments, whereas the first pair of targeting elements is linked to the N-termini of the pair of CH2-CH3 segments. According to various embodiments of the present disclosure, the drug bundle comprises a plurality of molecules of, a cytotoxic drug, a toll-like receptor (TLR) agonist, or a chelator complexed with a radioactive nuclide, whereas the tumor-associated antigen targeted by these Fc-based molecular construct is human epidermal growth factor receptor-1 (HER1) , HER2, HER3, HER4, CA19-9, CA125, carcinoembryonic antigen (CEA) , cell surface-associated mucin 1 (MUC1) , melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) ； mucin-related Tn, Sialyl Tn, Globo H, stage-specific embryonic antigen-4 (SSEA-4) , ganglioside GD2, or epithelial cell adhesion molecule (EpCAM) . As an example, but not a limitation, these Fc-based molecular constructs are useful in the treatment of various solid tumors, including malignant and/or metastatic solid tumors.
For a third series of Fc-based molecular constructs according to this aspect, each effector element of the first pair of effector elements is a drug bundle or an antibody fragment specific for a cell surface antigen, a growth factor, or a hapten； while each targeting element of the first pair of targeting elements is the growth factor or a peptide hormone. In the case where the effector elements are the drug bundles, the first pair of effector elements is respectively linked to the C-termini of the pair of CH2-CH3 segments, whereas the targeting elements are respectively linked to the N-termini of the pair of CH2-CH3 segments. Alternatively, when the effector elements are the antibody fragments, then the effector elements are respectively linked to the N-termini of the pair of CH2-CH3  segments, whereas the targeting elements are respectively linked to the C-termini of the pair of CH2-CH3 segments, and vice versa.
By selecting the effector element (s) and the targeting element (s) , the Fc-based molecular constructs of this third series provided herein are also useful for use in the treatment of various solid tumors, including malignant and/or metastatic solid tumors； however, the present disclosure is not limited thereto.
According to embodiments of the present disclosure, the cytotoxic drug suitable for use as the effector elements is auristatin, maytansine, doxorubicin, calicheamicin, or camptothecin. Illustrative examples of TLR agonist include, lipopolysaccharide (LPS) , monophosphoryl lipid A, motolimod, imiquimod, resiquimod, gardiquimod, CpG oligodeoxynucleotide (CpG DON) , lipoteichoic acid, β-glucan, and zymosan. Chelators suitable for use herein include, but are not limited to, 1, 4, 7, 10-Tetra-aza-cyclo-dodecane-N,
Figure PCTCN2016071184-appb-000002
-tetraacetic acid (DOTA) , 1, 4, 7-Triaza-cyclononane-1, 4, 7-triacetic acid (NOTA) , 1, 4, 7-triazacyclooctane-1, 4-diacetic acid-7-p-isothiocyanobenzyl (NODA) , or diethylene triamine pentaacetic acid (DTPA) . Non-limiting examples of radioactive nuclides to be complexed with the above-mentioned chelators or the like include 90Y, 111In, and 177Lu.
Some antibody fragments suitable for use as the effector elements are those specific to cell surface antigens such as programmed cell death 1 (PD-1) , programmed cell death 1 ligand 1 (PD-L1) , cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) , CD3, CD16a, CD28, and CD134. Another example is the antibody fragment specific for the growth factor like epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , VEGF-A, basic fibroblast growth factor (bFGF) , and hepatocyte growth factor (HGF) . Antibody fragments specific for haptens are also suitable for use herein, and illustrative examples of haptens include dinitrophenol (DNP) , trinitrophenol (TNP) , dansyl, penicillin, p-aminobenzoic acid, or a polypeptide having the amino acid sequence of SEQ ID NO: 20.
As to the targeting element (s) suitable for use in this series of Fc-based molecular constructs, the targeting element (s) may be a growth factor such as EGF, mutant EGF,  epiregulin, HB-EGF, VEGF-A, bFGF, and HGF. Alternatively, the targeting element (s) may be a peptide hormone like CCK, somastatin, and TSH.
The Fc-based molecular constructs according to this aspect of the present disclosure share some common structural features, which are summarized below.
In certain embodiments, the pair of CH2-CH3 segments is derived from human IgG heavy chain γ4 or human IgG heavy chain γ1.
In some examples, the first pair of effector elements (e.g., for the third series of Fc-based molecular constructs) or the first pair of targeting elements (e.g., for the first and second series of Fc-based molecular constructs) takes a Fab configuration (i.e., comprising the VH-CH1 domain and the VL-Cκ domain) ； this Fab fragment is linked to the N-termini of the first and second heavy chains so that the Fc-based molecular construct adopts an IgG configuration. In these cases, the pair of elements that is not in the Fab configuration may be linked to the C-termini of the pair of CH2-CH3 segments.
According to certain embodiments, the present Fc-based molecular construct further comprises a peptide extension and a coupling arm. Specifically, the peptide extension has the sequence of (G2-4S) 2-8C and is linked to the C-terminus of one of the pair of CH2-CH3 segments. In such cases, the coupling arm is linked to the C-terminus of the coupling arm via thiol-maleimide reaction occurred therebetween. Also, before being conjugated with the drug bundle, the free terminus of the conjugating arm (that is, the terminus that is not linked to the cysteine residue) is modified with an alkyne, azide, strained alkyne, or tetrazine group, so that the drug bundle is linked thereto via inverse electron demand Diels-Alder (iEDDA) reaction or the strain-promoted azide-alkyne click chemistry (SPAAC) reaction or Copper (I) -catalyzed alkyne-azide cycloaddition (CuAAC) reaction occurred therebetween. 
When the effector element is a drug bundle, the drug bundle may be provided as the linker unit according to the first aspect of the present disclosure. Specifically, the drug bundle comprises a center core, a plurality of first linking arms, and optionally, a second linking arm. The center core may be a compound having a plurality of amine groups or a polypeptide comprising a plurality of lysine (K) residues, according to various embodiments of the present disclosure. Each of the first linking arms has one terminus that is linked to  the center core by reacting with the amine groups of the compound core or the K residues of the polypeptide core. The first linking arm also carries a maleimide group at the free terminus thereof, wherein each of the molecules (e.g., molecules of cytotoxic drugs, TLR agonists, or chelator/radioactive nuclide complexes) is linked to the center core via connecting through the first linking arm by reacting with the maleimide group.
In the case where the center core is the polypeptide core, then the amino acid residue at the N-or C-terminus of the center core is a cysteine residue or has an azide group or an alkyne group.
For polypeptide cores with a terminal amino acid residue having the azide group or the alkyne group, the drug bundle may be linked to the peptide extension via the CuAAC reaction occurred between said terminal residue and the C-terminus of the peptide extension.
For polypeptide cores with a terminal residue that is cysteine, or for compound cores, the drug bundle further comprises the second linking arm. The second linking arm has one terminus linked to the center core by reacting with the cysteine residue of the polypeptide core or one amine group of the compound core. The second linking arm also carries an alkyne group, azide group, tetrazine group, or strained alkyne group at the free terminus thereof, so that the drug bundle can be linked to the C-terminus of the peptide extension via the CuAAC reaction or the iEDDA reaction occurred therebetween.
According to some optional embodiments of the present disclosure, the Fc-based molecular construct may further comprise a second pair of effector elements or a second pair of targeting elements.
For the second series of Fc-based molecular constructs, a second pair of targeting elements may be respectively linked to the first pair of targeting elements. For example, in certain embodiments, each effector element of the first pair of effector elements is a drug bundle comprising the plurality of molecules of the cytotoxic drug, each targeting element of the first pair of targeting elements is an scFv specific for HER2, and each targeting elements of the second pair of targeting elements is an scFv specific for HER1.
For the third series of Fc-based molecular constructs, a second pair of effector elements may be linked, in a tandem or diabody configuration, to the N-termini of the pair of elements that is linked to the N-termini of the pair of CH2-CH3 segments, thereby forming a pair of bispecific scFvs that is linked to the N-termini of the pair of CH2-CH3 segments. Alternatively, the third series of Fc-based molecular construct may further comprise a second pair of targeting elements that is linked, in a tandem or diabody configuration, to the N-termini of the pair of elements that is linked to the N-termini of the pair of CH2-CH3 segments, thereby forming a pair of bispecific scFvs that is linked to the N-termini of the pair of CH2-CH3 segments.
<VIII> Uses of Molecular Constructs for Treating Tumors
In the eighth aspect, the present disclosure is directed to methods for treating various cellular proliferative diseases. Generally, the methods involve the step of administrating an effective amount of the Fc-based molecular constructs according to the seventh aspect or any of the associated embodiments, to a subject in need of such treatment.
In certain embodiments, the present method is directed to the treatment of diffused tumors, such as B lymphocyte-derived lymphoma or leukemia, plasmacytoma, multiple myeloma, T-cell derived lymphoma or leukemia, and myelogenous leukemia. As discussed above, the first series of Fc-based molecular constructs of the seventh aspect of the present disclosure are useful in the treatment of the diffused tumor. Illustrative examples of the cell surface antigen (s) targeted by the present Fc-based molecular construct when treating a specific diffused tumor are provided in the appended claims and discussed in the description section bellow.
As discussed above, the present method is also suitable for treating solid tumors in a subject. Examples of solid tumors include, but are not limited to, melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, and head and neck squamous cell carcinoma. As discussed above, the second and third series of Fc-based molecular construct of the seventh aspect of the present disclosure are useful in the treatment of the solid tumor. Some exemplary combination of the effector element (s) and  targeting element (s) for treating solid tumors are provided in the appended claims and discussed in the description section bellow.
According to some optional embodiments of the present disclosure, when treating the solid tumor, the method comprises the steps of (a) subjecting the subject to a blood dialysis procedure using an antibody fragment specific for one or more tumor-associated antigens to remove the tumor-associated antigens that are shed from the tumor into the circulation of the subject, and then, (b) administering the Fc-based molecular construct of the present disclosure for treating the solid tumor.
In the cases where the Fc-based molecular construct uses an antibody fragment specific for a hapten as the effector element, the present method further comprises the step of administering to the subject an immunoregulatory effector that is tagged with the same hapten, after the administration of the present Fc-based molecular construct. Non-limiting examples of the immunoregulatory effector include IFN-α, IL-2, TNF-α, and IFN-γ, and an IgG antibody specific for PD-1, PD-L1, CTLA-4, and CD3.
According to some embodiments of the present disclosure, the malignant tumor that sheds one or more tumor-associated antigens into the circulation of the subject, and the method further comprises the step of, subjecting the subject to a blood dialysis procedure using an antibody fragment specific for the one or more tumor-associated antigens to remove the tumor-associated antigens that are shed from the malignant tumor, prior to the administration of the Fc-based molecular construct.
BRIEF DESCRIPTION OF THE DRAWINGS
The present description will be better understood from the following detailed description read in light of the accompanying drawings briefly discussed below.
Figure 1A to Figure 1 K are schematic diagrams illustrating linker units according to certain embodiments of the present disclosure.
Figure 2 is a schematic diagram illustrating a linker unit having a compound core.
Figure 3A to Figure 3D are schematic diagrams illustrating T-E molecular constructs according to some embodiments of the present disclosure.
Figure 4 is a schematic diagram that illustrates libraries for constructing molecular constructs according to some embodiments of the present disclosure.
Figure 5A and Figure 5B are schematic diagrams that illustrate molecular constructs according to some embodiments of the present disclosure.
Figure 6 is a schematic diagram that illustrates a molecular construct according to some embodiments of the present disclosure.
Figure 7A and Figure 7B are schematic diagrams illustrating molecular constructs according to various embodiments of the present disclosure.
Figures 8A to 8F are schematic diagrams illustrating Fc-based molecular constructs according to various embodiments of the present disclosure.
Figures 9A and 9B are schematic diagrams illustrating Fc-based molecular constructs according to various embodiments of the present disclosure.
Figures 10A to 10C are schematic diagrams illustrating Fc-based molecular constructs according to various embodiments of the present disclosure.
Figure 11 is a schematic diagram illustrating Fc-based molecular constructs according to one embodiment of the present disclosure.
Figures 12A to 12C are schematic diagrams illustrating Fc-based molecular constructs according to various embodiments of the present disclosure.
Figure 13 shows the reverse phase HPLC elution profile for the purification of TCO-peptide 2. Peptide 2 is SEQ ID NO: 18.
Figure 14 shows the reverse phase HPLC profile for the purification of PEG12-maleimide-conjugated TCO-peptide 2.
Figure 15 shows the mass spectrometry MALDI-TOF result of  PEG12-maleimide-conjugated TCO-peptide 2.
Figures 16A and 16B respectively show the mass spectrometry MALDI-TOF result of PEG12-maleimide-conjugated tetrazine-peptide 2 and DBCO-peptide 2.
Figure 17 shows the mass spectrometry ESI-TOF result of PEG12-maleimide-conjugated tetrazine-peptide 8.
Figure 18 shows the mass spectrometry ESI-TOF result of PEG6-maleimide-conjugated TCO-peptide 9.
Figure 19 shows the mass spectrometry ESI-TOF result of 1, 3, 5-triaminobenzene conjugated with one NHS-PEG12-alkyne coupling arm and two NHS-PEG12-maleimide linking arms.
Figure 20 shows the reverse phase HPLC profile for the purification of TCO-peptide 9 with 5 DM1-SMCC molecules.
Figure 21 shows the mass spectrometry result of TCO-peptide 9 with 5 DM1-SMCC molecules.
Figure 22 shows that LPS, upon the reaction with dansyl hydrazine, exhibited an emission maximum at 495 nm in fluorescence spectrophotometric analysis.
Figure 23 shows mass spectrometric analysis of PEG5-NHS conjugated with imiquimod.
Figure 24A shows mass spectrometry ESI-TOF result of DOTA-conjugated TCO-peptide 9. Figure 24B shows the mass spectrometric result of Y3+-chelated, DOTA-conjugated TCO-peptide 9.
Figures 25Aand 25B respectively show SDS-PAGE and ELISA analysis of purified scFv proteins of anti-CD79b antibody 1F10. Figures 25C and Figure 25D respectively show SDS-PAGE and ELISA analysis of purified scFv proteins of anti-collagen VII antibody LH7.2.
Figure 26A shows SDS-PAGE analysis of purified scFv of trastuzumab and  adalimumab. Figures 26B and 26C respectively show ELISA analyses of purified scFv of trastuzumab and adalimumab. Figures 26D and 26E respectively show SDS-PAGE and ELISA analyses of purified scFv of centuximab.
Figure 27A shows SDS-PAGE analysis of the purified scFv of adalimumab. Figure 27B shows ELISA analysis of the purified scFvs of adalimumab.
Figure 28A and Figure 28B show, respectively, the ELISA analysis of TCO-conjugated scFv and DBCO-conjugated scFv specific for CD3.
Figure 29A is the FPLC elution profile on a synthesized linker unit composed of a free tetrazine functional group and a set of three scFvs specific for human CD79b. Figure 29B shows the SDS-PAGE analysis result. Figure 29C shows the mass spectrometry MALDI-TOF result.
Figure 30A and Figure 30B respectively show the SDS-PAGE and mass spectrometry analysis result of tetrazine-peptide 2 conjugated with three scFvs specific for HER2/neu. Figure 30C shows the mass spectrometry result of TCO-peptide 2 conjugated with three scFvs specific for TNF- . Figure 30D and 30E respectively show the SDS-PAGE and mass spectrometry analysis of TCO-peptide 2 conjugated with three scFvs specific for PD-1.
Figure 31 shows mass spectrometry analysis result of tetrazine-peptide 2 conjugated with 3 CCK peptides.
Figure 32 shows mass spectrometry analysis result of TCO-peptide 7 conjugated with two scFvs specific for CD20.
Figure 32 shows mass spectrometry analysis result of TCO-peptide 7 conjugated with two scFvs specific for CD20.
Figure 33 shows mass spectrometry analysis result of TCO-peptide 1 conjugated with two scFvs specific for VEGF-A.
Figure 34A shows the mass spectrometry analysis result of a molecular construct with three scFvs specific for CD79b and one scFv specific for CD3. Figure 34B shows the  mass spectrometry analysis result of a molecular construct with three scFvs specific for HER2/neu and one scFv specific for CD3.
Figure 35 shows the SDS-PAGE analysis of the reaction mixtures of TCO-peptide 1 after the conjugation with scFv of anti-VEGF-A and further with tetrazine-20 kDa PEG.
Figure 36A and 36B respectively show the SDS-PAGE and mass spectrometric analyses of a molecular construct with a targeting linker unit with three scFvs specific for CD79b and a drug bundle with five DM1 molecules.
Figure 37 shows the ELISA analyses of a molecular construct with a targeting linker unit with three scFvs specific for CD79b and a drug bundle with five DM1 molecules.
Figure 38 shows the SDS-PAGE analyses of a molecular construct with a targeting linker unit with three scFvs specific for HER2/neu and a drug bundle with five DM1 molecules.
Figure 39 shows the mass spectrometric analysis of a molecular construct with a targeting linker unit with three CCK8 peptides and a drug bundle with five DM1 molecules.
Figure 40 shows the mass spectrometric analysis of a molecular construct with a targeting linker unit with three CCK8 peptides and a drug bundle with five DOTA groups.
Figure 41 shows the SDS-PAGE analysis of the reaction mixtures containing a linker unit of tetrazine-peptide 2 with three scFvs specific for CD79b, a TCO-peptide 7 with two scFvs specific for CD20, and a drug bundle with five DM1.
Figure 42 shows the assay results of the biological activity of LPS, before and after modification with dansyl hydrazine.
Figure 43 shows the assay results of the biological activity of imiquimod upon the conjugation with PEG linking arm.
Figure 44 shows the pharmacokinetic pattern of the molecular construct with 3scFv specific for VEGF-A and a 20kDa PEG in mice.
Figure 45 shows the cytotoxicity assay results of the molecular construct with three  scFvs specific for CD79b and a drug bundle of five DM1.
Figure 46 shows the SDS-PAGE analysis of (scFv α CII) - (scFv α TNF-α) -hIgG4Fc.
Figures 47A and 47B show the ELISA results analyzing the binding of (scFv α CII) - (scFv α TNF-α) -hIgG4Fc to collagen II and TNF-α.
Figures 48A and 48B respectively show the SDS-PAGE and ELISA analysis of the 2-chain (scFv α CII) - (scFv α TNF-α) -hIgG4. Fc- (scFv α IL-17) .
Figures 49A and 49B respectively show the SDS-PAGE and ELISA analysis of 2-chain (soluble TNF-α receptor) -IgG1. CH2-CH3-scFv α collagen II.
Figure 50 shows the SDS-PAGE analysis of the 2-chain fusion protein containing intact antibody for human TNF-α and scFv specific for collagen II.
Figures 51A and 51 B respectively show the SDS-PAGE and ELISA analyses of the 2-chain fusion protein containing intact antibody for human IL-17 and scFv specific for collagen VII.
Figures 52A and 52B respectively show the SDS-PAGE and ELISA analysis of scFv α collagen VII-IgG4. CH2-CH3-scFv α BAFF.
Figures 53A and 53B respectively show the SDS-PAGE and ELISA analyses of the 2-chain fusion protein containing intact antibody for human BAFF and scFv specific for collagen VII.
Figures 54A and 54B respectively show the SDS-PAGE and ELISA analyses of the 2-chain (scFv α SPARC) - (scFv α RANKL) -hIgG4. Fc molecular construct.
[Rectified under Rule 91, 23.02.2016]
Figures 55A and 55B respectively show the SDS-PAGE and ELISA analyses of the 2-chain fusion protein containing intact antibody for human RANKL and scFv specific for human osteonectin.
Figures 56A to 56E show the immunostaining of mouse epiphyseal bone with (scFv α CII) - (scFv α TNF-α) -hIgG4Fc and 2-chain (scFv α CII) - (scFv α TNF-α) -hIgG4. Fc- (scFv α IL-17) .
Figures 57A-C show the immunostaining of mouse epiphyseal bone with 2-chain (soluble TNF-α receptor) -IgG1. CH2-CH3-scFv α collagen II.
Figures 58A to 58C show bio-distribution of fluorescence-labeled (scFv α SPARC) - (scFv α RANKL) -hIgG4Fc in vivo in BALB/c mice.
Figure 59A shows the SDS-PAGE analysis of the 2-chain EGF-CH2-CH3 with a C-terminal extension and a cysteine residue and a 2-chain EGF-CH2-CH3-scFv of anti-PD1. Figure 59B shows SDS-PAGE analysis of 2-chain IgG1. Fc fusion protein conjugated with a linker unit with 2 LPS molecules.
Figures 60A and 60B show the ELISA results examining EGF-IgG1. Fc- (scFv α PD1) in binding to various PD-1 and ERBB！ .
Figure 61A shows the SDS-PAGE analysis of the 2-chain EGF-hIgG1. Fc- (scFv α CD3) molecular construct. Figure 61B shows the ELISA analysis examining 2-chain EGF-hIgG1. Fc- (scFv α CD3) in binding to ERBB！ , ERBB2, and ERBB3.
Figure 62A shows SDS-PAGE analysis of EGF (S2W/D3V) -IgG1. Fc with C-terminal extension, EGF (S2W/D3V) -IgG1. Fc- (scFv α PD1) , and EGF (S2W/D3V) -IgG1. Fc- (scFv α CD3) . Figures 62B to 62E show ELISA analyses of EGF (S2W/D3V) -IgG1. Fc- (scFv α PD1) . and EGF (S2W/D3V) -IgG1. Fc- (scFv α CD3) in binding to PD-1 or CD3, and ERBB1, ERBB2, and ERBB3.
Figure 63 shows SDS-PAGE analysis of somatostatin-hIgG1. Fc, somatostatin-hIgG1. Fc- (scFv α CD3) , and somatostatin-hIgG1. Fc- (scFv α PD-1) .
Figure 64 shows the cell staining analysis of EGF-IgG1. Fc, EGF-IgG1. Fc- (scFv α PD1) , EGF-IgG1. Fc- (scFv α CD3) , EGF (S2W/D3V) -IgG1. Fc, and EGF (S2W/D3V) -IgG1. Fc- (scFv α CD3) on EGFR-expressing A431 cells.
Figure 65 shows the staining analysis of EGF-IgG1. Fc- (scFv α PD1) and EGF (S2W/D3V) -IgG1. Fc- (scFv α PD1) on T cells in comparison with anti-PD-1 mAb (panels A to C) , as well as the staining analysis of EGF-IgG1. Fc- (scFv α CD3) and  EGF(S2W/D3V) -IgG1. Fc- (scFv α CD3) on T cells in comparison with anti-CD3 mAb (panels D to F) .
Figures 66A and 66B show the T cell –mediated cytolysis of EGFR-expressing of A431 cells upon the incubation with EGF-hIgG. Fc-scFv α CD3 and EGF (S2W/D3V) -IgG1. Fc- (scFv α CD3) . Figures 66C and 66D show the degree of cytolysis on MDA-MB-231 cells upon the incubation with EGF (S2W/D3V) -IgG1. Fc- (scFv α CD3) .
Figures 67A to 67C show the time course of T cell-mediated cytolysis of A431 cells upon the incubation with EGF (S2W/D3V) -IgG1. Fc- (scFv α CD3) .
Figure 68 shows the degree of cytolysis on A431 by human PBMCs upon the incubation with 2-chain EGFw2v3-IgG1. Fc- (scFv α PD-1) .
In accordance with common practice, the various described features/elements are not drawn to scale but instead are drawn to best illustrate specific features/elements relevant to the present invention. Also, like reference numerals and designations in the various drawings are used to indicate like elements/parts, where possible.
DESCRIPTION
The detailed description provided below in connection with the appended drawings is intended as a description of the present examples and is not intended to represent the only forms in which the present example may be constructed or utilized. The description sets forth the functions of the example and the sequence of steps for constructing and operating the example. However, the same or equivalent functions and sequences may be accomplished by different examples.
For convenience, certain terms employed in the specification, examples and appended claims are collected here. Unless otherwise defined herein, scientific and technical terminologies employed in the present disclosure shall have the meanings that are commonly understood and used by one of ordinary skill in the art.
Unless otherwise required by context, it will be understood that singular terms shall include plural forms of the same and plural terms shall include the singular. Specifically, as  used herein and in the claims, the singular forms “a” and “an” include the plural reference unless the context clearly indicated otherwise. Also, as used herein and in the claims, the terms “at least one” and “one or more” have the same meaning and include one, two, three, or more. Furthermore, the phrases “at least one of A, B, and C” , “at least one of A, B, or C” and “at least one of A, B and/or C, ” as use throughout this specification and the appended claims, are intended to cover A alone, B alone, C alone, A and B together, B and C together, A and C together, as well as A, B, and C together.
Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contains certain errors necessarily resulting from the standard deviation found in the respective testing measurements. Also, as used herein, the term “about” generally means within 10％, 5％, 1％, or 0.5％ of a given value or range. Alternatively, the term “about” means within an acceptable standard error of the mean when considered by one of ordinary skill in the art. Other than in the operating/working examples, or unless otherwise expressly specified, all of the numerical ranges, amounts, values and percentages such as those for quantities of materials, durations of times, temperatures, operating conditions, ratios of amounts, and the likes thereof disclosed herein should be understood as modified in all instances by the term “about. ” Accordingly, unless indicated to the contrary, the numerical parameters set forth in the present disclosure and attached claims are approximations that can vary as desired. At the very least, each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques. Ranges can be expressed herein as from one endpoint to another endpoint or between two endpoints. All ranges disclosed herein are inclusive of the endpoints, unless specified otherwise.
This present disclosure pertains generally to molecular constructs, in which each molecular construct comprises a targeting element (T) and an effector element (E) , and these molecular constructs are sometimes referred to as “T-E molecules” , “T-E pharmaceuticals” or “T-E drugs” in this document.
As used herein, the term “targeting element” refers to the portion of a molecular construct that directly or indirectly binds to a target of interest (e.g., a receptor on a cell surface or a protein in a tissue) thereby facilitates the transportation of the present molecular construct into the interested target. In some example, the targeting element may direct the molecular construct to the proximity of the target cell. In other cases, the targeting element specifically binds to a molecule present on the target cell surface or to a second molecule that specifically binds a molecule present on the cell surface. In some cases, the targeting element may be internalized along with the present molecular construct once it is bound to the interested target, hence is relocated into the cytosol of the target cell. A targeting element may be an antibody or a ligand for a cell surface receptor, or it may be a molecule that binds such antibody or ligand, thereby indirectly targeting the present molecular construct to the target site (e.g., the surface of the cell of choice) . The localization of the effector (therapeutic agent) in the diseased site will be enhanced or favored with the present molecular constructs as compared to the therapeutic without a targeting function. The localization is a matter of degree or relative proportion； it is not meant for absolute or total localization of the effector to the diseased site.
According to the present invention, the term “effector element” refers to the portion of a molecular construct that elicits a biological activity (e.g., inducing immune responses, exerting cytotoxic effects and the like) or other functional activity (e.g., recruiting other hapten tagged therapeutic molecules) , once the molecular construct is directed to its target site. The “effect” can be therapeutic or diagnostic. The effector elements encompass those that bind to cells and/or extracellular immunoregulatory factors. The effector element comprises agents such as proteins, nucleic acids, lipids, carbohydrates, glycopeptides, drug moieties (both small molecule drug and biologics) , compounds, elements, and isotopes, and fragments thereof.
Although the terms, first, second, third, etc., may be used herein to describe various elements, components, regions, and/or sections, these elements (as well as components, regions, and/or sections) are not to be limited by these terms. Also, the use of such ordinal numbers does not imply a sequence or order unless clearly indicated by the context. Rather, these terms are simply used to distinguish one element from another. Thus, a first  element, discussed below, could be termed a second element without departing from the teachings of the exemplary embodiments.
Here, the terms “link, ” “couple, ” and “conjugates” are used interchangeably to refer to any means of connecting two components either via direct linkage or via indirect linkage between two components.
The term “polypeptide” as used herein refers to a polymer having at least two amino acid residues. Typically, the polypeptide comprises amino acid residues ranging in length from 2 to about 200 residues； preferably, 2 to 50 residues. Where an amino acid sequence is provided herein, L-, D-, or beta amino acid versions of the sequence are also contemplated. Polypeptides also include amino acid polymers in which one or more amino acid residues are an artificial chemical analogue of a corresponding naturally occurring amino acid, as well as to naturally occurring amino acid polymers. In addition, the term applies to amino acids joined by a peptide linkage or by other, “modified linkages” (e.g., where the peptide bond is replaced by an α-ester, a β-ester, a thioamide, phosphonamide, carbomate, hydroxylate, and the like.
In certain embodiments, conservative substitutions of the amino acids comprising any of the sequences described herein are contemplated. In various embodiments, one, two, three, four, or five different residues are substituted. The term “conservative substitution” is used to reflect amino acid substitutions that do not substantially alter the activity (e.g., biological or functional activity and/or specificity) of the molecule. Typically, conservative amino acid substitutions involve substitution one amino acid for another amino acid with similar chemical properties (e.g., charge or hydrophobicity) . Certain conservative substitutions include “analog substitutions” where a standard amino acid is replaced by a non-standard (e.g., rare, synthetic, etc. ) amino acid differing minimally from the parental residue. Amino acid analogs are considered to be derived synthetically from the standard amino acids without sufficient change to the structure of the parent, are isomers, or are metabolite precursors.
In certain embodiments, polypeptides comprising at least 80％, preferably at least 85％ or 90％, and more preferably at least 95％ or 98％ sequence identity with any of the sequences described herein are also contemplated.
"Percentage (％) amino acid sequence identity" with respect to the polypeptide sequences identified herein is defined as the percentage of polypeptide residues in a candidate sequence that are identical with the amino acid residues in the specific polypeptide sequence, after aligning the sequences and introducing gaps, if necessary, to achieve the maximum percent sequence identity, and not considering any conservative substitutions as part of the sequence identity. Alignment for purposes of determining percentage sequence identity can be achieved in various ways that are within the skill in the art, for instance, using publicly available computer software such as BLAST, BLAST-2, ALIGN or Megalign (DNASTAR) software. Those skilled in the art can determine appropriate parameters for measuring alignment, including any algorithms needed to achieve maximal alignment over the full length of the sequences being compared. For purposes herein, sequence comparison between two polypeptide sequences was carried out by computer program Blastp (protein-protein BLAST) provided online by Nation Center for Biotechnology Information (NCBI) . The percentage amino acid sequence identity of a given polypeptide sequence A to a given polypeptide sequence B (which can alternatively be phrased as a given polypeptide sequence A that has a certain ％ amino acid sequence identity to a given polypeptide sequence B) is calculated by the formula as follows:
Figure PCTCN2016071184-appb-000003
where X is the number of amino acid residues scored as identical matches by the sequence alignment program BLAST in that program's alignment of A and B, and where Y is the total number of amino acid residues in A or B, whichever is shorter.
The term “PEGylated amino acid” as used herein refers to a polyethylene glycol (PEG) chain with one amino group and one carboxyl group. Generally, the PEGylated amino acid has the formula of NH2- (CH2CH2O) n-COOH. In the present disclosure, the value of n ranges from 1 to 20； preferably, ranging from 2 to 12.
As used herein, the term “terminus” with respect to a polypeptide refers to an amino acid residue at the N-or C-end of the polypeptide. With regard to a polymer, the term “terminus” refers to a constitutional unit of the polymer (e.g., the polyethylene glycol of the present disclosure) that is positioned at the end of the polymeric backbone. In the present  specification and claims, the term “free terminus” is used to mean the terminal amino acid residue or constitutional unit is not chemically bound to any other molecular.
The term “antigen” or “Ag” as used herein is defined as a molecule that elicits an immune response. This immune response may involve a secretory, humoral and/or cellular antigen-specific response. In the present disclosure, the term “antigen” can be any of a protein, a polypeptide (including mutants or biologically active fragments thereof) , a polysaccharide, a glycoprotein, a glycolipid, a nucleic acid, or a combination thereof.
In the present specification and claims, the term “antibody” is used in the broadest sense and covers fully assembled antibodies, antibody fragments that bind with antigens, such as antigen-binding fragment (Fab/Fab’ ) , F (ab’ ) 2 fragment (having two antigen-binding Fab portions linked together by disulfide bonds) , variable fragment (Fv) , single chain variable fragment (scFv) , bi-specific single-chain variable fragment (bi-scFv) , nanobodies, unibodies and diabodies. “Antibody fragments” comprise a portion of an intact antibody, preferably the antigen-binding region or variable region of the intact antibody. Typically, an “antibody” refers to a protein consisting of one or more polypeptides substantially encoded by immunoglobulin genes or fragments of immunoglobulin genes. The well-known immunoglobulin genes include the kappa, lambda, alpha, gamma, delta, epsilon, and mu constant region genes, as well as myriad immunoglobulin variable region genes. Light chains are classified as either kappa or lambda. Heavy chains are classified as gamma, mu, alpha, delta, or epsilon, which in turn define the immunoglobulin classes, IgG, IgM, IgA, IgD, and IgE, respectively. A typical immunoglobulin (antibody) structural unit is known to comprise a tetramer. Each tetramer is composed of two identical pairs of polypeptide chains, with each pair having one “light” chain (about 25 kDa) and one “heavy” chain (about 50-70 kDa) . The N-terminus of each chain defines a variable region of about 100 to 110 or more amino acids primarily responsible for antigen recognition. The terms variable light chain (VL) and variable heavy chain (VH) refer to these light and heavy chains, respectively. According to embodiments of the present disclosure, the antibody fragment can be produced by modifying the nature antibody or by de novo synthesis using recombinant DNA methodologies. In certain embodiments of the present disclosure, the antibody and/or antibody fragment can be bispecific, and can be in various configurations. For example, bispecific antibodies may comprise two different antigen binding sites (variable regions) .  In various embodiments, bispecific antibodies can be produced by hybridoma technique or recombinant DNA technique. In certain embodiments, bispecific antibodies have binding specificities for at least two different epitopes.
The term “specifically binds” as used herein, refers to the ability of an antibody or an antigen-binding fragment thereof, to bind to an antigen with a dissociation constant (Kd) of no more than about 1×10-6 M, 1×10-7 M, 1×10-8 M, 1×10-9 M, 1×10-10 M, 1×10-11 M, 1×10-12 M, and/or to bind to an antigen with an affinity that is at least two-folds greater than its affinity to a nonspecific antigen.
The term “immune disorder” as used herein refers to a disorder involving deficiency of humoral immunity, deficiency of cell-mediated immunity, combined immunity deficiency, unspecified immunity deficiency, and autoimmune disease.
The term “tumor” as used herein, refers to all neoplastic cell growth and proliferation, whether malignant or benign, and all pre-cancerous and cancerous cells and tissues. In the present specification and claims, the term “tumor” comprises solid tumors and diffused tumors.
The term “solid tumor” as used herein, denotes an abnormal mass of tissue that usually does not contain cysts or liquid areas. Different types of solid tumors are named for the type of cells that form them. Examples of solid tumors include, but are not limited to, sarcomas and carcinomas. Generally, “sarcomas” are cancers arising from connective or supporting tissues such as bone or muscle. “Carcinomas” are cancers arising from glandular cells and epithelial cells, which line body tissues.
The term “diffused tumor” as used herein refers to leukemia and/or hematological malignancy that is formed from hematopoietic (blood-forming) cells and affect blood, bone marrow, or lymph nodes. The example of the diffused tumor includes, but is not limited to, acute lymphocytic leukemia (ALL) , chronic lymphocytic leukemia (CLL) , acute myelogenous leukemia (AML) , chronic myelogenous leukemia (CML) , Hodgkin lymphoma, non-Hodgkin lymphoma, and myeloma.
The term “tumor-associated antigen” (TAA) as used herein refers to any cancer antigen that is known in the art and includes antigens found on the cancer cell surface, as well as  those that are shed from cancerous cell and become soluble (i.e., soluble cancer antigens) . Several cell surface antigens disposed on tumors or normal cells have soluble counterparts. Such antigens include, but are not limited to those found on cancer-associated fibroblasts (CAFs) , tumor endothelial cells (TEC) and tumor-associated macrophages (TAM) .
The term “treatment” as used herein includes preventative (e.g., prophylactic) , curative or palliative treatment； and “treating” as used herein also includes preventative (e.g., prophylactic) , curative or palliative treatment. In particular, the term “treating” as used herein refers to the application or administration of the present molecular construct or a pharmaceutical composition comprising the same to a subject, who has a medical condition a symptom associated with the medical condition, a disease or disorder secondary to the medical condition, or a predisposition toward the medical condition, with the purpose to partially or completely alleviate, ameliorate, relieve, delay onset of, inhibit progression of, reduce severity of, and/or reduce incidence of one or more symptoms or features of said particular disease, disorder, and/or condition. Treatment may be administered to a subject who does not exhibit signs of a disease, disorder, and/or condition, and/or to a subject who exhibits only early signs of a disease, disorder and/or condition, for the purpose of decreasing the risk of developing pathology associated with the disease, disorder and/or condition.
The term “effective amount” as used herein refers to the quantity of the present recombinant protein that is sufficient to yield a desired therapeutic response. An effective amount of an agent is not required to cure a disease or condition but will provide a treatment for a disease or condition such that the onset of the disease or condition is delayed, hindered or prevented, or the disease or condition symptoms are ameliorated. The effective amount may be divided into one, two, or more doses in a suitable form to be administered at one, two or more times throughout a designated time period. The specific effective or sufficient amount will vary with such factors as particular condition being treated, the physical condition of the patient (e.g., the patient's body mass, age, or gender) , the type of subject being treated, the duration of the treatment, the nature of concurrent therapy (if any) , and the specific formulations employed and the structure of the compounds or its derivatives. Effective amount may be expressed, for example, as the total mass of active  component (e.g., in grams, milligrams or micrograms) or a ratio of mass of active component to body mass, e.g., as milligrams per kilogram (mg/kg) .
The terms “application” and “administration” are used interchangeably herein to mean the application of a molecular construct or a pharmaceutical composition of the present invention to a subject in need of a treatment thereof.
The terms “subject” and “patient” are used interchangeably herein and are intended to mean an animal including the human species that is treatable by the molecular construct, pharmaceutical composition, and/or method of the present invention. The term “subject” or “patient” intended to refer to both the male and female gender unless one gender is specifically indicated. Accordingly, the term “subject” or “patient” comprises any mammal, which may benefit from the treatment method of the present disclosure. Examples of a “subject” or “patient” include, but are not limited to, a human, rat, mouse, guinea pig, monkey, pig, goat, cow, horse, dog, cat, bird and fowl. In an exemplary embodiment, the patient is a human. The term “mammal” refers to all members of the class Mammalia, including humans, primates, domestic and farm animals, such as rabbit, pig, sheep, and cattle； as well as zoo, sports or pet animals； and rodents, such as mouse and rat. The term “non-human mammal” refers to all members of the class Mammalis except human.
The present disclosure is based, at least on the construction of the T–E pharmaceuticals that can be delivered to target cells, target tissues or organs at increased proportions relative to the blood circulation, lymphoid system, and other cells, tissues or organs. When this is achieved, the therapeutic effect of the pharmaceuticals is increased, while the scope and severity of the side effects and toxicity is decreased. It is also possible that a therapeutic effector is administered at a lower dosage in the form of a T-E molecule, than in a form without a targeting component. Therefore, the therapeutic effector can be administered at lower dosages without losing potency, while lowering side effects and toxicity.
Diseases that can benefit from better drug targeting
Drugs used for many diseases can be improved for better efficacy and safety, if they can be targeted to the disease sites, i.e., if they can be localized or partitioned to the  disease sites more favorably than the normal tissues or organs. Following are primary examples of diseases, in which drugs can be improved if they can be preferentially distributed to the disease sites or cells.
I Immune disorder
According to the design of molecular constructs of the present disclosure, the diseases, conditions, and/or disorders treatable with the present method is an immune disorder； for example, an autoimmune disorder that includes, but is not limited to, psoriasis, systemic lupus erythematosus (SLE) , cutaneous lupus, Sjogren’s syndrome, rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, and inflammatory bowel disease.
Most of the autoimmune diseases, such as rheumatoid arthritis, systemic lupus erythematosus, 
Figure PCTCN2016071184-appb-000004
syndrome, psoriasis, Crohn’s disease, inflammatory bowel diseases, and others affect connective tissues. Regardless of the etiological nature, whether it is environmental, genetic, epigenetic, or their combinations, the affected tissues are damaged by prolong inflammatory processes. It is rationalized in this invention that in bringing anti-inflammatory therapeutic agents, such as anti-TNF-α, anti-IL-17, anti-BAFF, anti-IL-6, anti-IL-12/IL-23, to the diseased connective tissues, the components of the extracellular matrix may be employed as target antigens. The target antigens that may be considered include the various types of collagens, laminins, elastins, fibrillins, fibronectins, and tenascins. Connective tissues fill in nearly all parts of the human body. However, due to the structural and functional requirements of the connective tissues in different locations, the types of those extracellular matrix components are different, providing excellent choices for target tissue specificity.
The advantages of choosing extracellular components over cell surface antigens for targeting the anti-inflammatory therapeutic agents are that the choices of selectivity among the various types of matrix proteins and the abundant amounts of the extracellular matrix proteins. Furthermore, because cells are not used as antigenic targets, the potential harmful effects of direct binding to cells by anti-inflammatory agents can be avoided.
I- (i) Rheumatoid arthritis, Psoriatic Arthritis, or Ankylosing Spondylitis
Several antibodies against TNF-α, e.g., infliximab and adalimumab, and fusion proteins  of TNF-α receptor and IgG. Fc (e.g. etanercept) are approved or in human clinical trials for use to treat rheumatoid arthritis, ankylosing spondylitis, and other autoimmune diseases. The extracellular portion the receptor for interleukin-1 (IL-1) , anakinra, is approved for treating rheumatoid arthritis. Antibodies against the shared p40 protein of IL-12 and IL-23, e.g., ustekinumab and briakinumab, are approved for psoriatic arthritis or in trials for rheumatoid arthritis. An antibody against IL-6 receptor (tocilizumab) is approved for rheumatoid arthritis and systemic juvenile idiopathic arthritis, and several antibodies against IL-6, e.g., sarilumab and olokizumab, are in clinical trials for treating rheumatoid arthritis. An antibody specific for IL-17 (secukinumab) is approved for psoriasis and in clinical trials for rheumatoid arthritis and ankylosing spondylitis.
While those therapeutic agents can alleviate severe symptoms better than previously available medications, they cause a range of serious side effects in some treated patients. For example, infliximab can cause serious blood disorders, like leukopenia and thrombocytopenia, serious infections, lymphoma and other solid tumors, reactivation of hepatitis B and tuberculosis, and other serious problems. Anakinra causes frequent infections, and severe side effects on the gastrointestinal and the respiratory tracts and the blood forming organs. It is important that the serious side effects of these widely used therapeutic agents be minimized, while retaining or even enhancing their therapeutic effects.
In rheumatoid arthritis, joints of the knees, fingers, toes, and other joints are affected, and in ankylosing spondylitis, joints of the spine and the sacroiliac joint of the pelvis are affected. In the diseased joints, the surface of the bones and the articular cartilage lining the bone surfaces are attacked by the inflammatory immune components in the joints. The articular cartilage in the joints is a smooth cartilage that contains an extracellular matrix. The cartilage is avascular and approximately 60％ of the weight is water and the remaining content is composed of collagens and α-aggrecan, a proteoglycan, and other matrix molecules. Collagen II forms the major fibril in the cartilage. Aggrecan is the second most abundant component in the cartilage. Collagen XI is bound to the surface of the collagen II fibril helping to form fibril networks and collagen IX is associated with collagen II and collagen XI. The cartilage has a large surface and the α-aggrecan has a structure and shape like a feather. In addition to the cartilage formation, the joints have also ligaments,  which connect adjacent bones, such as the cruciate ligaments, and tendons, which connect muscles to the bones. The ligaments and tendons are formed by fibrous network of collagen types I, II, and III, and elastin and fibrillins 1 and 2.
The present invention rationalizes that the antagonist for TNF-α, IL-1, and IL-12/IL-23 can be carried to the diseased joints by using antibody fragments, such as scFv, specific for collagen II, α-aggrecan, collagen XI or collagen IX, or alternatively, collagen I, elastin or fibrillin 1 as the targeting agent. A preferred anti-collagen II antibody is one that binds to native collagen II in the joints and does not bind to N-terminal and C-terminal propeptides, which are cleaved off during fibril assembly. A preferred anti-aggrecan antibody is one that binds to whole native α-aggrecan molecules and does not bind to fragments that are cleaved off and released into the blood circulation. By adopting the present molecular construct with scFv of anti-collagen II as targeting agent, in comparison with regular IgG against TNF-α, IL-1, and IL12/IL-23, larger proportions of the present therapeutic agents can be carried to the diseased sites and less amounts of the therapeutic agents will be present in other irrelevant, normal tissues, especially, lymphoid organs, and hence fewer side effects will occur.
I- (ii) Psoriasis
Most patients with psoriasis or plaque psoriasis present inflammatory symptoms primarily in the skin and not in other tissues and organs. Psoriasis involves mainly keratinocytes in part of skin in the affected patients. A systematic administration of monoclonal antibodies anti-TNF-α, anti-IL-12/IL-23, and anti-IL-17 or anti-IL-17 receptor (anti-IL-17R) or other anti-inflammatory agents, such as anti-IL6, causes unwanted side effects, as discussed in the preceding section. The serious adverse side effects of all these immune modulating antibodies have been well documented.
A number of membrane or extracellular proteins, such as filaggrin, collagen I, which are expressed at much higher levels in the skin tissues than most of other tissues, probably can be considered as the target proteins to shuffle therapeutic agents to the skin. Filaggrin is present in the tight junction between cells and is probably accessible by antibodies in the diseased tissue sites. While collagen I is also present in the bone matrix and many parts of the body, it is present in the dermis layer of the skin in abundant proportions.
For damping the inflammatory activity caused by the diseased keratinocytes, which manifests psoriatic symptoms, it is not necessary to deliver the anti-inflammatory antibody drugs to be in contact with the keratinocytes. The keratinocytes are in the outmost, epidermis layer of the skin； blood vessels, sweat glands, and collagen fibers are in the middle dermis layer of the skin. The inner layer is hypodermis, where adipose tissues are. The three layers of human skin together are 2-3mm thick. If the anti-inflammatory antibodies are delivered to the dermis layer by scFv specific for collagen I, they can diffuse into the other layers. Or, the antibodies can trap inflammatory cytokines in the three layers of the skin.
Several proteins present at the dermo-epidermal junction may also be employed as targets for carrying therapeutic agents to the skin. These include type VII collagen, type XVII collagen, and  laminins type  5, 6, or 10. The dermo-epidermal junction is the area of tissue that joins the epidermal and dermal layers of the skin. The basal cells in the stratum basale of epidermis connect to the basement membrane by the anchoring filament of hemidesmosomes. The cells of the papillary layer of the dermis are attached to the basement membrane by anchoring fibrils, which consist of type VII collagen. Type XVII collagen, a transmembrane protein (also referred to as BP180) expressed on keratinocytes, is a structural component of hemidesmosomes, multiprotein complexes at the dermal-epidermal basement membrane zone that mediate adhesion of keratinocytes to the underlying membrane. Laminins are structural non-collagenous glycoproteins present in basement membranes. Among the many types of laminins,  types  5, 6, and 10 are specific of the basal lamina present under stratified epithelia.
I- (iii) Systemic Lupus Erythematosus (SLE) , Cutaneous Lupus, or Sjogren’s Syndrome
Systemic lupus erythematosus (SLE) is an autoimmune disease involving multiple autoantigens, such as nucleic acids, histones, and other nuclear proteins. 
Figure PCTCN2016071184-appb-000005
syndrome is an autoimmune disease, in which the immune system attacks the exocrine glands, specifically the salivary and lacrimal glands, which produce saliva and tears, respectively, resulting the symptoms of dry eyes and dry mouth, leading to infections and various other problems. Both of these diseases occur 9 times more frequently in women  than in men, especially in women of child-bearing ages 15 to 35. SLE is a systemic autoimmune connective tissue disease and affects many organs and tissues. In general, those tissues and organs, such as the heart, lungs, bladder, and kidneys, which exhibit elasticity and can expand and contract, contain collagen network. In several types of SLE, cutaneous manifestation of inflammatory symptoms is prominent.
For more than 50 years, not a single new therapeutic agent had been developed for SLE, until belimumab, a human monoclonal antibody specific for BAFF was developed and approved. However, the therapeutic effect of belimumab for SLE has been considered to be marginal. Belimumab causes a host of side effects, including more incidences of serious infections and deaths in the treatment group than the placebo group. Interestingly, in a phase II trial on 
Figure PCTCN2016071184-appb-000006
 syndrome, belimumab showed more successful results than in SLE.
In addition to BAFF, researchers have been searching other therapeutic targets for SLE. While not a single inflammatory cytokine has been identified as mainly responsible for the pathological process in SLE, the expression of a group of genes known as downstream events of type 1 interferon stimulation, which is termed “type 1 interferon signature” , has been documented in many studies. The pathogenesis of SLE has been found to be associated with the activation of toll-like receptors 7 and 9 (TLR 7 and TLR9) , which induce the expression of a group of genes similar to that resulting from the activation by IFN-α.
Several monoclonal antibodies specific for IFN-α, including rontalizumab, sifalimumab, and anifrolumab have been studied in clinical trials for the treatment of SLE. Since IFN-α is involved in many functions, a systemic administration of an antibody against IFN-α without localized targeting to disease sites may render serious side effects.
I- (iv) Inflammatory Bowel Disease
Anti-TNF-α (such as adalimumab) has also been approved for treating Crohn’s disease and ulcerative colitis (aform of inflammatory bowel disease) . However, as described in an earlier section, the administration of anti-TNF-α is associated with a range of series side effects, including severe infectious diseases and B cell lymphoma. Therefore, in treating patients with Crohn’s disease or ulcerative colitis with anti-TNF-α, it will be desirable to  distribute the administered anti-TNF-α in favor of the intestine and colon. It has been found collagen III and type V are relatively abundant in the connective tissues in the intestine and bowel.
II Tumor
Several classes of large numbers of therapeutic agents have been developed and experimented in animal models and in human clinical trials for the treatment of malignant tumors, including diffused and solid tumors and primary and metastatic tumors of varying clinical stages. These therapeutic agents, some of which have been approved by governmental regulatory agencies for use in patients, include (1) a large number of compounds targeting key cellular regulatory pathways or structural components, or damaging DNA or important cellular machinery, (2) antibodies specific for surface antigens of certain cell types or specific for certain tumor-associated antigens and capable of mediating apoptosis, antibody-dependent cellular cytotoxicity (ADCC) , or complement-mediated cytolysis (CMC) of the targeted cells, (3) antibodies specific for certain tumor-associated antigens, which are conjugated with potent cytotoxic drugs, (4) immunoregulatory cytokines, such as such as interferon-α (IFN-α) , interleukin-2 (IL-2) , or interferon-γ (IFN-γ) , which can activate the immune system in fighting against malignant cells, (5) antibodies targeting certain cell surface markers of B and T lymphocytes, e.g., anti-CD20 rituximab, (6) antibodies targeting growth factor receptors, e.g., anti-HER2/Neu trastuzumab and anti-EGFR cetuximab, (7) antibodies targeting vascular endothelial growth factor-A (VEGF-A) for inhibiting angiogenesis, e.g., bevacizumab, and (8) antibodies binding to immune checkpoints, such as PD1 (programmed cell death protein 1, CD279) , e.g., nivolumab, PD-L1 (programmed cell death protein ligand 1, CD274) , e.g., MPDL3280A, CTLA4 (cytotoxic T-lymphocyte protein 4, CD152) , e.g., ipilimumab, which inhibit the negative feedback of immune reactions and allow continual activation of on-going immune responses.
The usefulness of therapeutic agents for treating cancer as well as for many other diseases is limited or compromised by their toxicity, because the agents also act on some normal cells to some degrees. Therefore, many therapeutic agents have limited therapeutic windows and therefore, in order to control their toxic effects, they are  administered in many of the treated patients at suboptimal doses, as far as therapeutic efficacy is concerned, which are insufficient to achieve satisfactory therapeutic effects.
The antibody-drug conjugate approach, which is being pursued actively, requires that the tumor-targeting antibodies together with the carried cytotoxic drugs be internalized by the targeted cells expressing the tumor-associated antigens, which the targeting antibodies recognize. This requirement may potentially limit the power of the current antibody-drug conjugate approach, because cells in a tumor express a tumor-associated antigen at varying densities. Those cells expressing relatively low levels may not be killed by the current antibody-drug conjugates during treatment and will grow up as the therapeutic agents are discontinued.
II- (i) Diffused Tumor
II- (i) -A Targeting cancerous cells originated from leukocytes
The cancer derived from malignantly transformed cells of the lymphoid and myeloid lineages account for a significant proportion among all cancer. Those tumors are generally diffusive and not solid. Thus, the targeting of leukocyte-derived tumors will involve the targeting of the individual tumor cells. Therefore, the identification of the expression of cell-surface antigens of the tumor cells is a key in the targeting of leukocyte-derived tumors. 
Tumors derived from white blood cells (leukocytes) are generally classified into three categories: (1) leukemia found in the blood and bone marrow, (2) lymphoma found in the lymphatic system, and (3) myeloma in many parts of bone marrow and also in the blood.
Leukemia has four broad classifications: (1) acute lymphocytic leukemia (ALL) , (2) chronic lymphocytic leukemia (CLL) , (3) acute myelogenous leukemia (AML) , and (4) chronic myelogenous leukemia (CML) . However, as advanced diagnostic and analytic methods are being developed, new types of leukemia, such as B cell CLL, T cell CLL, B cell prolymphocytic leukemia, Hairy cell leukemia, and others are been defined.
Lymphomas are divided into two categories: (1) Hodgkin lymphomas and (2) non-Hodgkin lymphomas. Of the patients who have lymphomas, about 12％ have Hodgkin lymphomas and the rest have non-Hodgkin lymphomas. Of the non-Hodgkin lymphomas,  most are B cell-derived and there are many subtypes of B cell non-Hodgkin lymphomas. The rest of the non-Hodgkin lymphomas are T cell lymphomas.
Myeloma is derived from antibody-producing plasma cells and is also referred to as plasmacytoma. Myeloma cells are found in bone marrow and can travel in the blood circulation and establish growth in many parts of the bone and hence myeloma is also called multiple myeloma.
While leukemia, lymphomas, and myeloma are derived from myeloid, lymphoid, and plasma cells, the diagnosis of the tumor types is often very complex, involving tissue and cellular examinations with histological, immunohistological, morphological, and cellular marker analyses of the biopsied tumor samples. Since the pluripotent stem cells, the myeloid lineage, which differentiate into granulocytes (neutrophils, eosinophils, and basophils) , monocytes and macrophages, and platelets, and the lymphoid lineage, which differentiate into B cells and T cells, undergo many steps of differentiation and maturation, the malignant transformation can occur at any of the differentiation stages. Furthermore, the cancerous transformation may augment and gain certain traits and reduce or lose certain traits.
The surface markers or differentiation antigens, especially those, which have been assigned a CD (cluster of differentiation) number, have become very useful and often necessary to identify the various leukocytes and immunocytes in the studies of innate and adaptive immunity. Often the identification of a cell type requires a set of markers.
For antibody-based therapeutic approaches for targeting cancer of the leukocyte origin, identification of the surface markers of a targeted tumor is very useful and powerful. However, among the patients who have been diagnosed to have the same type of tumor, the surface markers can vary over a large range in terms of density.
II- (i) -B Surface markers on B cell-derived lymphocytic leukemia and lymphoma
Both ALL and CLL are not solid tumors. ALL is derived from lymphoblasts, precursor B cells, precursor T cells, or B cells. ALL consists of the immunophenotypic subtypes: (1) precursor B cell acute lymphoblastic leukemia, which expresses cell surface markers associated with B cell precursors and precursor T cell acute lymphoblastic leukemia, which  express markers of precursor T cells, (2) Burkitt’s lymphoma, which is derived from B cells of the germinal center and express cell surface markers associated with B cells, and (3) acute biphenotypic leukemia, which express markers of both lymphoid and myeloid cells.
CLL is also referred to as B-cell CLL (B-CLL) , because CLL is mostly derived from B cells. Thus, the major difference of the cellular origin between ALL and CLL is that ALL is derived from lymphoblasts, which are the common precursors of B cells and T cells and CLL is derived from B cells. All CLL cells in a patient are from monoclonal, derived original one B cell of a particular set of VH and VL. The cells of CLL express CD19 and CD20, and characteristically CD5 and CD23.
Hodgkin lymphomas are characterized by the presence of Reed-Sternberg cells, which are multi-nucleated giant cells derived from B cells. There are at least four subtypes of Hodgkin lymphomas based on the morphology of Reed-Sternberg cells and the composition of reactive cell infiltrate in the lymph node biopsy specimen: (1) nodular sclerosing Hodgkin lymphoma, (2) mixed-cellularity, (3) lymphocyte-rich or lymphocytic predominance, and (4) lymphocyte depleted. It is well established that Hodgkin lymphoma is derived from mature B cells. Cells of Hodgkin lymphoma, depending on its immunophenotype, express a subset of CD15, CD20, CD30, CD79a, and CD138. Most of the cases of non-Hodgkin lymphomas are derived from B cells. There are at least 14 subtypes of B-cell non-Hodgkin lymphomas.
B lymphocytes are the source of antigen-specific antibodies and are a critical component of the adaptive immune system for the defense against infectious pathogens. However, B cells can also be pathogenic and the cause of several types of diseases. B-cell disorders are divided into undesired immunoglobulin production (autoimmune and allergic diseases) and uncontrolled proliferation (lymphomas, leukemia) . B cells have proven to be effective targets for the treatment of multiple autoimmune disorders and B-lineage cancer. Many approaches pertaining to B-cell depletion for the treatment of B cell malignancies and antibody-mediated diseases have been developed with partial success or are in active experimental stages. These include therapeutic antibodies that target human B-cell surface antigens, such as CD19, CD20, CD22, CD37, CD79a/CD79b, and isotype-specific Ig receptor. Some of such antibodies can cause lysis of B cells.  Some other antibodies will cause B cell lysis when the antibodies are conjugated with cytotoxic drugs.
Multiple myeloma, also referred to as plasma cell myeloma, is the second most common hematological malignancies (after non-Hodgkin lymphoma) , constituting 1％ of all cancers and 2％ of all cancer deaths. Multiple myeloma produces large quantities of myeloma proteins and occupies bone marrow and manifests a series of symptoms, including bone pain, anemia, renal failure, infection, and neurological problems. Multiple myeloma is derived from the malignant transformation of plasma cells, which differentiate from B lymphocytes. However, cells of multiple myeloma do not express the most common B cell markers, such as CD19, CD20, and CD22.
A number of therapies and drugs have been experimented and a few have been approved for the treatment of multiple myeloma. These include corticosteroids, chemotherapies, proteasome inhibitors, and immunoregulatory compounds.
II- (i) -C Unique B cell antigens Igα, Igβ and migis-δ as targets of antibodies
Igα (CD79a) /Igβ (CD79b) is set of antigens that are expressed in association of the B cell receptor (BCR) complex on the surface of cells of the B-cell linage. Igα/Igβ is a heterodimeric transmembrane protein, which is composed of two distinct chains Igα and Igβ stabilized by disulfide bonding. Igα/Igβ forms a complex with the BCR and generates a signal following recognition of antigen by the BCR complex. During the development of B cell maturation, Igα/Igβ is expressed in the pre-B-cell stage and is early than CD20 for the expression pattern on the B-cell lineage. Igα/Igβ has been considered as attractive target for the B cell depletion therapy in the treatment of non-Hodgkin lymphomas because Igα/Igβ is expressed on B cells and on most non-Hodgkin lymphomas.
The mIgD and mIgM are coexpressed on the surface of mature B cells and function as part of BCR. The mIgD contains a unique migis-δ peptide segment of 27 AA, which represents the extracellular portions of the membrane-anchoring segment of mIgD and is located between the CH3 domain and transmembrane segment. It has been proposed that migis-δ peptide provides an antigenic site for targeting mIgD-expressing B cells. The site is present on the mIgD-expressing B cells and not on the secreted IgD.
II- (i) -D T cell tumors
T lymphocyte subsets through their surface molecules and secreted factors mediate a complex network of immunoregulatory activities on humoral and cellular immune effector functions, including the production of different classes of antibodies, the secretion of various cytokines, and the generation of cytotoxic T cells and other cytolytic cells. Many autoimmune diseases are caused by the abnormal activities of T cells against self-components or cells. For example, in type-I diabetes, the insulin-producing β cells in the islets of Langerhans of pancreas are attacked and killed by autoimmune T cells. The devastating autoimmune diseases, such as systemic lupus erythematosus (SLE) , multiple sclerosis, and inflammatory bowel diseases, are caused mainly by T cells. Furthermore, the rejection reaction toward organ or tissue transplants is mediated mainly by T cells.
There are also a few forms of T cell malignancy. Thus, modulating T cell activities or removing T cells has been an active area of drug discovery research. A variety of antibodies and their modified forms against T cell surface antigens, including CD3, CD4, CD8, CD25, and CD28 have been studied in animal models or human clinical trials for treating various human diseases mentioned above. Some antibodies with or without the conjugation with cytotoxic drugs can cause the lysis of the targeted T cell subsets. Some antibodies can cause anergy or an idled, inactive state of T cells without actually lysing the cells.
T lymphocytes play major roles in regulating activities of various immunocytes and various other cell types in adaptive and native immunity. In the development of therapeutic agents to target lymphocytes, fewer candidates have been successfully developed for targeting T cells than for targeting B cells. However, there have been increasing numbers of therapeutic antibodies that are being developed to target surface antigens of T cell subsets. Antibodies targeting T cell surface antigens can potentially be employed to treat malignant tumors derived from T cells. Antibodies may also be used to modulate T cell activities, either to inhibit them or to enhance them.
II- (i) -E Myelogenous leukemia
AML is derived from myeloid stem cells or myeloid blasts, the precursors for the mature granulocytes and monocytes. Many of the subtypes of AML are caused by mutagens, which cause chromosomal translocations or loss of certain gene segments. Cells of AML derived from various differentiation stages express some subsets of surface markers of CD13, CD14, CD15, CD33, CD34, CD36, CD41, CD61, CD64, CD65, and CD11c. Cells of AML derived from the early precursor myeloid stages express CD34, which is a surface marker of pluripotent stem cells, and CD33, which is a marker of immature myeloid cells. Cells of AML derived from many myeloid differentiation stages express CD15, a marker of mature myeloid cells. CML is a clonal bone marrow stem cell disorder and resulted from the malignant transformation of a stem cell or myeloid stem cell, resulting from the chromosome translocation called the Philadelphia chromosome.
II- (ii) Solid Tumor
II- (ii) -A Solid Tumor and tumor-associated antigens
Cells of many types of tumors express certain antigens on cell surface at elevated levels compared to those on normal cells. Those antigens are referred to as tumor-associated antigens. For example, serum samples from patients with pancreatic tumors and many types of gastrointestinal cancer, including colorectal cancer, esophageal cancer, and hepatocellular carcinoma, contain CA19-9 antigen (carbohydrate antigen 19-9, a sialyl-Lewis A antigen) . The cells of those tumors express CA19-9 on the extracellular matrix on cell surface. Similarly, serum samples from patients with ovarian cancer, endometrial cancer, fallopian tube cancer, and some other types of cancer have elevated CA-125 (carbohydrate antigen 125, mucin 16) and the cells of those tumors express CA125. Overexpression of cell surface associated glycoprotein mucin 1 (MUC1) is often associated with colon, breast, ovarian, lung, and pancreatic cancer.
The ganglioside GD2 is highly expressed on neuroectoderm-derived tumors and sarcomas, including neuroblastoma, retinoblastoma, melanoma, small cell lung cancer, brain tumors, osteosarcoma, rhabdomyosarcoma, Ewing’s sarcoma in children and adolescents, as well as liposarcoma, fibrosarcoma, leiomyosarcoma and other soft tissuesarcoma in adults.
While mesothelin is expressed on normal mesothelial cells, it is expressed on many human cancers, mesothelioma, tumors of the pancreas, ovary, lung, and stomach, cholangiocarcinoma, and triple-negative breast cancer.
Tn antigen is a structural element on glycoproteins, in which N-acetylgalactosamine (GalNAc) is linked to serine or threonine by a glycosidic bond, i.e. as an O-glycan. Addition of single monosaccharide residues creates disaccharide antigens: the Thomsen-Friedenreich antigen (TF antigen or T antigen) is formed by substitution with galactose (Gal (b1-3) GalNAc) ； the sialyl-Tn antigen (STn antigen) is formed by substitution with sialic acid (Neu5Ac (a2-6) GalNAc. TN and sialy-Tn are not usually found on healthy cell surfaces, but may be found on cancer cells.
Tumor-associated antigens that have been widely studied as markers of tumors or explored as targets for immunological therapies include (1) epidermal growth factor receptors (EGFRs) –human epidermal growth factor 1 (EGFR or HER1) , HER2, HER3, HER4, or their mutants； (2) glycoproteins –CA19-9 (bearing Sialyl LewisA antigen) , CA125 (bearing mucin 16 or MUC 16) , cell surface-associated mucin 1 (MUC1) , or carcinoembryonic antigen, melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) , or mesothelin, ； (3) mucin-related Tn or Sialyl Tn； (4) the blood group Lewis related LewisY, Sialyl LewisY, Sialyl LewisA, or LewisX； (5) glycosphingolipids -Globo H or stage-specific embryonic antigen-4 (SSEA-4) ； or (6) gangliosides -GD2, GD3, GM2, fucosyl GM1, or Neu5GcGM3.
II- (ii) -B Growth factors, peptide hormones, and cytokines as targeting agents for cells overexpressing receptors
A number of growth factors, peptide hormones and regulatory cytokines regulate important physiological processes in a human body. These substances mediate their functions through interacting with their receptors on different cell types. The most prominent are endocrine or exocrine cells in organs or compartments or organs bearing function-specific receptors, which respond to growth factors, hormones, or cytokines. For example, the exocrine cells in the pancreas bear receptors that respond to secretin, gastrin, and cholecystokinin (CCK) from duodenum and stomach during food intake and digestive process.
When malignant transformation occurs to the receptor-bearing cells, the tumorous cells maintain the expression of the receptors. In fact, in many cases, an abnormally high expression of the receptors occurs due to certain mutations in the cells, which are not necessarily in the receptors themselves. The affected cells thus become malignantly transformed. The overexpression of receptors on tumors, e.g., somatostatin receptors are strongly expressed on most neuroendocrine tumors, and the targeting of those receptors for therapeutic and diagnostic (e.g., radio-imaging) purposes have been an active area of research. Neuroendocrine tumors are generally rare, but include a long list of tumors of various cell origins, including those of gastroenteropancreatic neuroendocrine tumors, thyroid gland tumors, Merkel cell carcinoma, adrenomedullary tumors, and many others.
Examples of this line of research are numerous. The over-expression of the family of epidermal growth factor receptors (EGFRs) in breast cancer, lung cancer, colon cancer, and many other types of carcinoma is well documented. For example, monoclonal antibody trastuzumab specific for HER2/Neu receptor is broadly used for treating HER2-positive breast cancer. Cetuximab specific for EGFR is being used in treating metastatic colon cancer, metastatic non-small cell lung cancer, and head and neck cancer. Small molecular inhibitors, such as gefitinib and erlotinib, which interrupts the tyrosine kinase domain in EGFR, have also been developed for the treatment of several type of cancer.
Pancreatic cancer is one of the most vicious cancers. Among the various types of pancreatic cancers, the pancreatic (ductal or invasive) adenocarcinoma derived from the exocrine cells account for 85％ , although those ductal epithelial cells account only for 10％ among all cells in the pancreas. The exocrine cells express receptors for the peptide hormones, gastrin, secretin, or cholecystokinin, which are secreted by the cells in the stomach and duodenum, and respond to those hormones and secrete bicarbonate ions and digestive enzymes. The overexpressed receptors for CCK and gastrin in pancreatic cancer and many other types have also been explored as a target for radioimaging. Other hormones and receptors, which are under active investigation, are somatostatin and gastrin-releasing peptide. In such radio-imaging approaches, CCK or gastrin of their peptide analogues are coupled with chelating groups for radioactive nuclides. In the imaging procedure, the imaging agents bind to the primary or metastasized tumors containing cells expressing the receptors. Peptide hormones or their analogues carrying  radionuclides, lutetium-177, yttrium-90, or indium-111, have also been experimented for treating tumors.
II- (ii) -C Immune checkpoints as targets
CTLA-4 is a protein receptor that down-regulates the immune system. CTLA-4 is found on the surface of T cells, and acts as an "off" switch when bound to CD80 (B7-1) or CD86 (B7-2) on the surface of antigen presenting cells. Such binding prevents the binding of those receptors by CD28, which activates the immune response. A human IgG1 antibody specific for CTLA-4, ipilimumab, has been approved for treating melanoma and in clinical studies for treating several other types of cancer. The treatment with ipilimumab has been associated with severe and potential fatal immunological side effects due to T cell activation and proliferation.
PD-1 is expressed on the surface of activated T cells. If PD-1 is blocked by its ligand, PD-L1, the T cell becomes inactive. This is a way that the body regulates the immune system to avoid an overreaction of immune responses. Many cancer cells make PD-L1 and thereby disarm the T cells and inhibit them from attacking the cancer cells. Two human antibodies against PD-1, pembrolizumab and nivolumab, have been approved for treating unresectable or metastatic melanoma, which no longer respond to other drugs, and squamous non-small cell lung cancer. An anti-PD-L1 antibody, MPDL3280A, is now in Phase II or III clinical trials for triple-negative breast cancer, metastatic non-small cell lung cancer, bladder carcinoma, and renal cell carcinoma. A large number of anti-PD-1 and anti-PD-L1 antibodies are in research or early clinical trials.
Many researchers are exploring other targets, such as OX40, CD137, and CD27 on the activated T cells and their corresponding ligands, OX40L, CD137L, and CD137 the antigen-presenting cells or tumor cells for releasing the brakes of T cell activation. Those pathways are considered to be milder in T-cell activation strength than the CTLA-4 and PD-1 pathways.
While antibodies specific for PD-I or PD-L1 look very promising for treating several types of cancer, the current clinical development suggest that those antibodies will require the combination with chemotherapies, other antibodies, or targeted therapies. Also, the  antibodies also cause a range of severe side effects. We rationalize that if the antibodies specific for immune checkpoints were carried to the targeted tumor site, better therapeutic efficacy could be achieved, and fewer side effects would occur.
II- (ii) -D Vascular endothelial growth factor as targets
Vascular endothelial growth factor A (VEGF-A) is essential for angiogenesis (blood vessel formation) as the tumor grows. The blood circulation is required for oxygen and nutrient supplies, waste disposal and many other functions. Antibodies specific for VEGF-A, such as bevacizumab specific for VEGF-A, are effective as a monotherapy or in combination with chemotherapy in treating a few forms of cancer. However, bevacizumab is associated with a range of side effects, including hypertension and heightened risk of bleeding, bowel perforation, and necrotizing fasciitis.
II- (ii) -E Immunoregulatory cytokines as cancer therapeutic agents
The immunoregulatory cytokines referred to in this invention are those that are known to be stimulatory and are major drivers in activating immune responses. These cytokines include interleukin-2 (IL-2) , interferon-α (IFN-α) , interferon-γ (IFN-γ) , and TNF-α. Among them, IFN-α, which is a strong activator of T cells, has been approved for use in hairy-cell leukemia, AIDS-related Kaposi's sarcoma, follicular lymphoma, chronic myeloid leukemia and melanoma. However, clinical studies so far have not established major therapeutic utilities of those immunoregulatory cytokines in treating tumors, mainly because the therapeutic doses of those cytokines in systematic administrations are limited by the side effects of the cytokines. In general, cytokines act mainly in the microenvironment of the lymphoid system.
III Osteoporosis Disease
An antibody specific for RANKL (CD254) , the ligand of RANK (RANK, receptor activator of nuclear factor κ B) , denosumab, is approved for the treatment of osteoporosis. The development of denosumab represents a major advancement in the care for osteoporosis. However, the administration of denosumab causes common side effects, such as infections of the urinary and respiratory tracts, cataracts, constipation, rashes, and joint pain. It is hence desirable that the therapeutic agent is carried preferentially to the bone.
RANKL is a membrane protein, belonging to the tumor necrosis factor ligand family. RANKL is detected at high levels in the lung, thymus, and lymph nodes. It is also detected at low levels in the bone marrow, stomach, peripheral blood, spleen, placenta, leukocytes, heart, thyroid and skeletal muscle. Since IgG anti-RANKL, such as denosumab, can serve a therapeutic agent for osteoporosis, the molecular constructs of this invention should provide as better therapeutic agents than IgG anti-RANKL.
Another target for antibodies for the treatment of osteoporosis is sclerostin, encoded by SOST gene. The glycoprotein is produced and secreted by osteocytes and negatively regulates osteoblastic bone formation. The loss or defective mutation of SOST gene causes progressive bone thickening. A defective mutation in the SOST gene increases bone formation. Antibodies against sclerostin cause increased bone formation, bone mineral density, and stronger bones. The phase I and II clinical trials of two humanized monoclonal antibodies against sclerostin, blosozumab and romosozumab, indicated that the antibody treatment is associated with increased bone mineral density and bone formation and decreased bone resorption.
In light of the foregoing discussion, two types of molecular platforms for constructing the T-E molecules of this invention are provided in the present disclosure. One is based on the “linker unit” configuration (see, Part I to Part IV below) , and the other is based on the “Fc” configuration (see, Part V to Part VIII below) . Detailed discussion relating to the structure of said two configurations are provided below, as well as the practical applications of each molecular construct.
PART I Peptide Core-Based Multi-Arm Linkers
The first aspect of the present disclosure pertains to a linker unit that comprises, (1) a center core that comprises 2-15 lysine (K) residues, and (2) 2-15 linking arms respectively linked to the K residues of the center core. The present center core is characterized in having or being linked with an azide group, an alkyne group, a tetrazine group, or a strained alkyne group at its N-or C-terminus.
In the preparation of the present linker unit, a PEG chain having a N-hydroxysuccinimydyl (NHS) group at one terminus and a maleimide group at the other  terminus is linked to the K residue of the center core by forming an amide bond between the NHS group of the PEG chain and the amine group of the K residue. In the present disclosure, the PEG chain linked to the K residue is referred to as a linking arm, which has a maleimide group at the free-terminus thereof.
According to the embodiments of the present disclosure, the center core is a polypeptide that has 8-120 amino acid residues in length and comprises 2 to 15 lysine (K) residues, in which each K residue and the next K residue are separated by a filler sequence.
According to embodiments of the present disclosure, the filler sequence comprises glycine (G) and serine (S) residues； preferably, the filler sequence consists of 2-15 residues selected from G, S, and a combination thereof. For example, the filler sequence can be,
Figure PCTCN2016071184-appb-000007
The filler sequence placed between two lysine residues may be variations of glycine  and serine residues in somewhat random sequences and/or lengths. Longer fillers may be used for a polypeptide with fewer lysine residues, and shorter fillers for a polypeptide with more lysine residues. Hydrophilic amino acid residues, such as aspartic acid and histidine, may be inserted into the filler sequences together with glycine and serine. As alternatives for filler sequences made up with glycine and serine residues, filler sequences may also be adopted from flexible, soluble loops in common human serum proteins, such as albumin and immunoglobulins.
According to certain preferred embodiments of the present disclosure, the center core comprises 2-15 units of the sequence of G1-5SK. Alternatively, the polypeptide comprises the sequence of (GSK) 2-15； that is, the polypeptide comprises at least two consecutive units of the sequence of GSK. For example, the present center core may comprises the amino acid sequence of the following,
Figure PCTCN2016071184-appb-000008
in which Ac represents the acetyl group.
According to certain embodiments of the present disclosure, the center core is a polypeptide that comprises the sequence of (Xaa-K) n, in which Xaa is a PEGylated amino acid having 2 to 12 repeats of ethylene glycol (EG) unit, and n is an integral from 2 to 15.
As described above, the present center core is characterized in having or being linked with an azide group, an alkyne group, a tetrazine group, or a strained alkyne group at its N-or C-terminus. According to some embodiments of the present disclosure, the present center core comprises, at its N-or C-terminus, an amino acid residue having an azide group or an alkyne group. The amino acid residue having an azide group can be, L-azidohomoalanine (AHA) , 4-azido-L-phenylalanine, 4-azido-D-phenylalanine, 3-azido-L-alanine, 3-azido-D-alanine, 4-azido-L-homoalanine, 4-azido-D-homoalanine, 5-azido-L-ornithine, 5-azido-d-ornithine, 6-azido-L-lysine, or 6-azido-D-lysine. For example, the present center core may have the sequence of,
Ac- (GSK) 2-7- (G2-4S) 1-8-AAH,
Ac-AAH- (SG2-4) 1-8- (GSK) 2-7,
Ac-AAH- (SG2-4) 0-7- (GSK) 2-6- (G2-4S) 1-8-C,
Ac-C- (SG2-4) 0-7- (GSK) 2-6- (G2-4S) 1-8-AAH,
Ac-K- (Xaa2-12-K) 2-4-Xaa2-12-AAH,
Ac-AAH-Xaa2-12-K- (Xaa2-12-K) 2-4,
Ac-AAH-Xaa2-12-K- (Xaa2-12-K) 1-3-Xaa2-12-C, or
Ac-C-Xaa2-12-K- (Xaa2-12-K) 1-3-Xaa2-12-AAH,
in which Xaa is a PEGylated amino acid having specified repeats of EG unit, Ac represents the acetyl group, and AAH represents the AHA residue.
Exemplary amino acid having an alkyne group includes, but is not limited to, L-homopropargylglycine (L-HPG) , D-homopropargylglycine (D-HPG) , or beta-homopropargylglycine (β-HPG) . In this case, the present center core may have the sequence of,
Ac- (GSK) 2-7- (G2-4S) 1-8-GHP,
Ac-GHP- (SG2-4) 1-8- (GSK) 2-7,
Ac-GHP- (SG2-4) 0-7- (GSK) 2-6- (G2-4S) 1-8-C,
Ac-C- (SG2-4) 0-7- (GSK) 2-6- (G2-4S) 1-8-GHP,
Ac-K- (Xaa2-12-K) 2-4-Xaa2-12-GHP,
Ac-GHP-Xaa2-12-K- (Xaa2-12-K) 2-4,
Ac-GHP-Xaa2-12-K- (Xaa2-12-K) 1-3-Xaa2-12-C, or
Ac-C-Xaa2-12-K- (Xaa2-12-K) 1-3-Xaa2-12-GHP,
in which Xaa is a PEGylated amino acid having specified repeats of EG unit, Ac represents the acetyl group, and GHP represents the HPG residue.
It is noted that many of the amino acids containing an azide or alkyne group in their side chains and PEGylated amino acids are available commercially in t-boc (tert-butyloycarbonyl) -or Fmoc (9-fluorenylmethyloxycarbonyl) -protected forms, which are readily applicable in solid-phase peptide synthesis.
According to some working examples of the present disclosure, the center core may comprise the sequence of,
Figure PCTCN2016071184-appb-000009
Figure PCTCN2016071184-appb-000010
in which Xaa is a PEGylated amino acid having specified repeats of EG unit, Ac represents the acetyl group, AAH represents the AHA residue, and GHP represents the HPG residue.
Alternatively, the present center core is linked with a coupling arm, which has a functional group (e.g., an azide group, an alkyne group, a tetrazine group, or a strained alkyne group) at the free-terminus thereof (that is, the terminus that is not linked to the center core) . In these cases, the present center core comprises a cysteine residue at its N-or C-terminus. To prepare a linker unit linked with a coupling arm, a PEG chain having a maleimide group at one terminus and a functional group at the other terminus is linked to the cysteine residue of the center core via thiol-maleimide reaction occurred between the maleimide group of the PEG chain and the thiol group of the cysteine residue. In the present disclosure, the PEG chain linked to the cysteine residue of the center core is referred to as the coupling arm, which has a functional group at the free-terminus thereof.
Preferably, the coupling arm has a tetrazine group or a strained alkyne group at the free-terminus thereof. These coupling arms have 2-12 EG units. According to the embodiments of the present disclosure, the tetrazine group is 1, 2, 3, 4-tetrazine, 1, 2, 3, 5-tetrazine, 1, 2, 4, 5-tetrazine, or derivatives thereof. Example of strained alkyne group includes, but is not limited to, trans-cyclooctene (TCO) , dibenzocyclooctyne (DBCO) , difluorinated cyclooctyne (DIFO) , bicyclononyne (BCN) , dibenzocyclooctyne (DICO) . According to some embodiments of the present disclosure, the tetrazine group is 6-methyl-tetrazine.
Example of the present center core linked with the coupling arm includes, but is not limited to,
Ac- (GSK) 2-7- (G2-4S) 1-8-C-Xaa2-12-tetrazine,
Ac- (GSK) 2-7- (G2-4S) 1-8-C-Xaa2-12-strained alkyne,
Ac-K- (Xaa2-12-K) 2-4-Xaa2-12-C-Xaa2-12-tetrazine,
Ac-K- (Xaa2-12-K) 2-4-Xaa2-12-C-Xaa2-12-strained alkyne,
Tetrazine-Xaa2-12-C (Ac) - (SG2-4) 1-8- (GSK) 2-7,
Stained alkyne-Xaa2-12-C (Ac) - (SG2-4) 1-8- (GSK) 2-7,
Tetrazine-Xaa2-12-C (Ac) -Xaa2-12-K- (Xaa2-12-K) 2-4, and
Strained alkyne-Xaa2-12-C (Ac) -Xaa2-12-K- (Xaa2-12-K) 2-4.
Alternatively, the center core has an azide or alkyne group at one terminus and a coupling arm with tetrazine or strained alkyne group at the other terminus. Examples are the following:
Ac-AAH- (SG2-4) 0-7- (GSK) 2-6- (G2-4S) 1-8-C-Xaa2-12-tetrazine,
Ac-AAH- (SG2-4) 0-7- (GSK) 2-6- (G2-4S) 1-8-C-Xaa2-12-strained alkyne,
Tetrazine-Xaa2-12-C (Ac) - (SG2-4) 0-7- (GSK) 2-6- (G2-4S) 1-8-AAH,
Strained alkyne-Xaa2-12-C (Ac) - (SG2-4) 0-7- (GSK) 2-6- (G2-4S) 1-8-AAH,
Ac-AAH-Xaa2-12-K- (Xaa2-12-K) 1-3-Xaa2-12-C-Xaa2-12-tetrazine,
Ac-AAH-Xaa2-12-K- (Xaa2-12-K) 1-3-Xaa2-12-C-Xaa2-12-strained alkyne,
Tetrazine-Xaa2-12-C (Ac) -Xaa2-12-K- (Xaa2-12-K) 1-3-Xaa2-12-AAH,
Strained alkyne-Xaa2-12-C (Ac) -Xaa2-12-K- (Xaa2-12-K) 1-3-Xaa2-12-AAH,
Ac-GHP- (SG2-4) 0-7- (GSK) 2-6- (G2-4S) 1-8-C-Xaa2-12-tetrazine,
Ac-GHP- (SG2-4) 0-7- (GSK) 2-6- (G2-4S) 1-8-C-Xaa2-12-strained alkyne,
Tetrazine-Xaa2-12-C (Ac) - (SG2-4) 0-7- (GSK) 2-6- (G2-4S) 1-8-GHP,
Strained alkyne-Xaa2-12-C (AC) - (SG2-4) 0-7- (GSK) 2-6- (G2-4S) 1-8-GHP,
Ac-GHP-Xaa2-12-K- (Xaa2-12-K) 1-3-Xaa2-12-C-Xaa2-12-tetrazine,
Ac-GHP-Xaa2-12-K- (Xaa2-12-K) 1-3-Xaa2-12-C-Xaa2-12-strained alkyne,
Tetrazine-Xaa2-12-C (Ac) -Xaa2-12-K- (Xaa2-12-K) 1-3-Xaa2-12-GHP, and
Strained alkyne-Xaa2-12-C (Ac) -Xaa2-12-K- (Xaa2-12-K) 1-3-Xaa2-12-GHP.
The polypeptide may also be synthesized using recombinant technology by expressing designed gene segments in bacterial or mammalian host cells. It is preferable to prepare the polypeptide as recombinant proteins if the core has high numbers of lysine residues with considerable lengths. As the length of a polypeptide increases, the number of errors increases, while the purity and/or the yield of the product decrease, if solid-phase synthesis was adopted. To produce a polypeptide in bacterial or mammalian host cells, a filler sequence ranges from a few amino acid residues to 10-20 residues may be placed between two K residues. Further, since AHA and HPG are not natural amino acids encoded by the genetic codes, the N-terminal or C-terminal residue for those recombinant polypeptides is  cysteine. After the recombinant proteins are expressed and purified, the terminal cysteine residue is then reacted with short bifunctional cross-linkers, which have maleimide group at one end, which reacts with SH group of cysteine residue, and alkyne, azide, tetrazine, or strained alkyne at the other end.
The synthesis of a polypeptide using PEGylated amino acids involves fewer steps than that with regular amino acids such as glycine and serine resides. In addition, PEGylated amino acids with varying lengths (i.e., numbers of repeated ethylene glycol units) may be employed, offering flexibility for solubility and spacing between adjacent amino groups of lysine residues. Other than PEGylated amino acids, the center cores may also be constructed to comprise artificial amino acids, such as D-form amino acids, homo-amino acids, N-methyl amino acids etc. Preferably, the PEGylated amino acids with varying lengths of polyethylene glycol (PEG) are used to construct the center core, because the PEG moieties contained in the amino acid molecules provide conformational flexibility and adequate spacing between conjugating groups, enhance aqueous solubility, and are generally weakly immunogenic. The synthesis of PEGylated amino acid-containing center core is similar to the procedures for the synthesis of regular polypeptides.
Optionally, for stability purpose, the present center has an acetyl group to block the amino group at its N-terminus.
As could be appreciated, the number of the linking arms linked to the center core is mainly determined by the number of lysine resides comprised in the center core. Since there are at least two lysine residues comprised in the present center core, the present linker unit may comprise a plurality of linking arms.
Reference is now made to Figure 1A. As illustrated, the linker unit 10A comprises a center core 11a comprising one HPG (GHP) residue and four lysine (K) residues respectively separated by filler sequences (denoted by the dots throughout the drawings) . The filler sequences between the HPG residue and K residue or between any two K residues may comprise the same or different amino acid sequences. In this example, four linking arms 20a-20d are linked to the lysine residues by forming an amide linkage between the NHS group and the amine group of the lysine reside, respectively. As could be appreciated, certain features discussed above regarding the linker unit 10A or any other following linker  units are common to other linker units disclosed herein, and hence some or all of these features are also applicable in the following examples, unless it is contradictory to the context of a specific embodiment. However, for the sake of brevity, these common features may not be explicitly repeated below.
Figure 1B provides a linker unit 10B according to another embodiment of the present disclosure. The center core 11b comprises one cysteine (C) residue and six lysine (K) residues respectively separated by the filler sequences. In this example, the linker unit 10A comprises six linking arms 20a-20f that are respectively linked to the lysine residues. According to the embodiments of the present disclosure, the linking arm is a PEG chain having 2-20 repeats of EG units.
Unlike the liker unit 10A of Figure 1A, the linker unit 1B further comprises a coupling arm 60. As discussed above, a PEG chain having a maleimide group at one end and a functional group at the other end is used to form the coupling arm 60. In this way, the coupling arm 60 is linked to the cysteine residue of the center core 11b via thiol–maleimide reaction. In this example, the functional group at the free terminus of the coupling arm 60 is a tetrazine group 72. According to the embodiments of the present disclosure, the coupling arm is a PEG chain having 2-12 repeats of EG units.
When the release of effector elements at the targeted site is required, a cleavable bond can be installed in the linking arm. Such a bond is cleaved by acid/alkaline hydrolysis, reduction/oxidation, or enzymes. One embodiment of a class of cleavable PEG chains that can be used to form the coupling arm is NHS-PEG2-20-S-S-maleimide, where S-Sis a disulfide bond that can be slowly reduced, while the NHS group is used for conjugating with the amine group of the center core, thereby linking the PEG chain onto the center core. The maleimide group at the free terminus of the linking arm may be substituted by an azide, alkyne, tetrazine, or strained alkyne group.
According to certain embodiments of the present disclosure, the linking arm that is linked to the K residue of the center core has a maleimide group at its free terminus. In this way, a functional element (such as, a targeting element or an effector element) having a thiol group may react with the maleimide group of the linking arm via the thiol–maleimide reaction so that the functional element is linked to the linking arm. For the sake of  illustration, the functional elements linked to the linking arms are referred to as the first elements. As could be appreciated, the number of the first elements carried by the present linker unit depends on the number of K residues of the center core (and thus, the number of the linking arms) . Accordingly, one of ordinary skill in the art may adjust the number of the first elements of the linker unit as necessary, for example, to achieve the desired targeting or therapeutic effect.
An example of a linker unit 10C having the first elements is illustrated Figure 1C. Other than the features disused hereafter, Figure 1C is quite similar to Figure 1B. First, there are five K residues in the center core 11d, and accordingly, five linking arms 20a-20e are linked thereto, respectively. Second, the linker unit 10C has five first elements 30a-30e linked to each of the linking arms 20a-20e. As disused below, the optional tetrazine group 72 allows for the conjugation with an additional functional element, another molecular construct (see, Part III or Part VII below) .
In order to increase the intended or desired effect (e.g., the therapeutic effect) , the present linker unit may further comprise a second element in addition to the first element. For example, the second element can be either a targeting element or an effector element. In optional embodiments of the present disclosure, the first element is an effector element, while the second element may be another effector element, which works additively or synergistically with or independently of the first element. Still optionally, the first and second elements exhibit different properties； for example, the first element is a targeting element, and the second element is an effector element, and vice versa. Alternatively, the first element is an effector element, and the second element is an element capable of improving the pharmacokinetic property of the linker unit, such as solubility, clearance, half-life, and bioavailability.
According to one embodiment of the present disclosure, the first element is the targeting element that renders the present linker unit specifically target to a lesion site, the second element is the effector element that elicits a therapeutic effect once the present linker unit is delivered to the lesion site. For example, in the treatment of diffused tumor, the present linker unit may comprise a plurality of targeting elements as the first elements and one effector element as the second element. In this case, the targeting element  specifically targets the cell surface antigen expressed on the diffused tumor (e.g., CD5, CD19, CD20, CD22, CD23, CD30, CD37, CD79a, or CD79b) ； while the effector element (e.g., the antibody fragment specific for CD3 or CD16a) recruits T cells or NK cells to kill the tumor cells.
According to an alternative embodiment of the present disclosure, the first element is the effector element and the second element is the targeting element. For example, in the treatment of autoimmune disease, the present linker unit may comprise one targeting element that specifically targets the tissue-associated extracellular matrix protein (e.g., α-aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, and collagen XI) and a plurality of effector elements that produce an therapeutic effect on the lesion site.
Structurally, the second element is linked to the azide, alkyne, tetrazine, or strained alkyne group at the N-or C-terminus of the center core. Specifically, the second element may be optionally conjugated with a short PEG chain (preferably having 2-12 repeats of EG units) and then linked to the N-or C-terminal amino acid residue having an azide group or an alkyne group (e.g., AHA residue or HPG residue) . Alternatively, the second element may be optionally conjugated with the short PEG chain and then linked to the coupling arm of the center core.
According to some embodiments of the present disclosure, the center core comprises an amino acid having an azide group (e.g., the AHA residue) at its N-or C-terminus； and accordingly, a second element having an alkyne group is linked to the N-or C-terminus of the center core via the CuAAC reaction. According to other embodiments of the present disclosure, the center core comprises an amino acid having an alkyne group (e.g., the HPG residue) at its N-or C-terminus； and a second element having an azide group is thus capable of being linked to the N-or C-terminus of the center core via the “Copper (I) -catalyzed alkyne-azide cycloaddition (CuAAC) ” reaction (or the “click” reaction for short) as exemplified in Scheme 1.
《Scheme 1 CuAAC reaction》
Figure PCTCN2016071184-appb-000011
The CuAAC reaction yields 1, 5 di-substituted 1, 2, 3-triazole. The reaction between alkyne and azide is very selective and there are no alkyne and azide groups in natural biomolecules. Furthermore, the reaction is quick and pH-insensitive. It has been suggested that instead of using copper (I) , such as cuprous bromide or cuprous iodide, for catalyzing the click reaction, it is better to use a mixture of copper (II) and a reducing agent, such as sodium ascorbate to produce copper (I) in situ in the reaction mixture. Alternatively, the second element can be linked to the N-or C-terminus of the present center core via a copper-free reaction, in which pentamethylcyclopentadienyl ruthenium chloride complex is used as the catalyst to catalyze the azide-alkyne cycloaddition.
Figure 1D provides an example of the present linker unit carrying a plurality of first elements and one second element. In this example, the center core 11c comprises one HPG (GHP) residue and five lysine (K) residues. Five linking arms 20a-20e are respectively linked to the five K residues of the center core 11c； and five first elements 30a-30e are respectively linked to said five linking arms 20a-20e via the thiol-maleimide reaction. In addition to the first elements, the linker unit 10D further comprises one second element 50 that is linked to one end of a short PEG chain 62. Before being conjugated with the center core 11c, the other end of the short PEG chain 62 has an azide group. In this way, the azide group may reacted with the HPG residue that having an alkyne group via CuAAC reaction, so that the second element 50 is linked to the center core 11c. The solid dot 40 depicted in Figure 1D represents the chemical bond resulted from the CuAAC reaction occurred between the HPG residue and the azide group.
Alternatively, the second element is linked to the center core via a coupling arm. According to certain embodiments of the present disclosure, the coupling arm has a  tetrazine group, which can be efficiently linked to a second element having a TCO group via the inverse electron demand Diels–Alder (iEDDA) reaction (see, scheme 2) . According to other embodiments of the present disclosure, the coupling arm has a TCO group, which is capable of being linked to a second element having a tetrazine group via the iEDDA reaction. In the iEDDA reaction, the strained cyclooctenes that possess a remarkably decreased activation energy in contrast to terminal alkynes is employed, and thus eliminate the need of an exogenous catalyst.
Reference is now made to Figure 1E, in which the center core 11d comprises a terminal cysteine (C) residue and five lysine (K) residues. As depicted in Figure 1E, five linking arms 20a-20e are respectively linked to the five K residue of the center core 11d, and then five first elements 30a-30e are respectively linked to the five linking arms 20a-20e via thiol-maleimide reactions. The cysteine residue is linked to the coupling arm 60, which, before being conjugated with the second element, comprises a tetrazine group or a TCO group at its free-terminus. In this example, a second element 50 linked with a short PEG chain 62 having a corresponding TCO or tetrazine group can be linked to the coupling arm 60 via the iEDDA reaction. The ellipse 70 as depicted in Figure 1E represents the chemical bond resulted from the iEDDA reaction occurred between the coupling arm 60 and the short PEG chain 62.
《Scheme 2 iEDDA Reaction》
Figure PCTCN2016071184-appb-000012
According to other embodiments of the present disclosure, before the conjugation with a second element, the coupling arm has an azide group. As such, the coupling arm can be linked to the second element having a strained alkyne group (e.g., the DBCO, DIFO, BCN, or DICO group) at the free-terminus of a short PEG chain via SPAAC reaction (see, scheme 3) , and vice versa.
Reference is now made to Figure 1F, in which the linker unit 10F has a structure similar to the linker unit 10E of Figure 1E, except that the coupling arm 60 comprises an azide or a strained alkyne group (e.g., the DBCO, DIFO, BCN, or DICO group) , instead of the tetrazine or TCO group. Accordingly, the second element 50 linked with a short PEG chain 62 may have a corresponding strained alkyne (e.g., DBCO, DIFO, BCN, or DICO) or azide group, so that it can be linked to the coupling arm 60 via the SPAAC reaction. The diamond 90 as depicted in Figure 1F represents the chemical bond resulted from the SPAAC reaction occurred between the coupling arm 60 and the short PEG chain 62.
《Scheme 3 SPAAC reaction》
Figure PCTCN2016071184-appb-000013
Scheme 4 is an exemplary illustration of the process of preparing the present linker unit. In step 1, the center core comprising the amino acid sequence of (GSK) 3 and a  L-azidohomoalanine (AHA) residue at the C-terminus thereof is prepared. In step 2, three linking arms are respectively linked to the lysine (K) residues of the center core via forming an amide bond between the NHS group and the amine group； the linking arm linked to the center core has a maleimide (Mal) group at the free-terminus thereof. In step 3, three anti-A antigen scFvs (scFv α A) as the first element are respectively linked to the linking arms via the thiol-maleimide reaction. Meanwhile, in step 4, one anti-B antigen scFv (scFv α B) as the second element is linked with a short PEG chain that has 4 repeats of EG units and a DBCO group at the free terminus. Finally, in step 5, the second element is linked to the AHA residue of the center core via the SPAAC reaction.
《Scheme 4 Preparation of linker unit linked with two different scFvs via linking arm and C-terminal amino acid residue》
Figure PCTCN2016071184-appb-000014
Scheme 5 illustrates another example of the process for preparing the present linker unit. In step 1, the center core comprising the amino acid sequence of (K-Xaa) 3 and a cysteine residue at the C-terminus thereof is prepared. In step 2, a PEG chain (as the coupling arm) that has the maleimide (Mal) group at one terminus and a tetrazine group at the other terminus is linked to the cysteine residue via the thiol-maleimide reaction. Then, in step 3, three linking arm are respectively linked to the lysine (K) residues of the center core. Next, three anti-A antigen scFvs (scFv α A) as the first elements are respectively linked to the linking arms via the thiol-maleimide reaction as described in step 4. Meanwhile, in step 5, one anti-B antigen scFv (scFv α B) as the second element is linked with a short PEG chain that has 3 repeats of EG units and a TCO group at the free terminus. Finally, in step 6, the second element is linked to the coupling arm via the iEDDA reaction.
《Scheme 5 Preparation of linker unit linked with two different scFvs via linking arm and coupling arm》
Figure PCTCN2016071184-appb-000015
PEGylation is a process, in which a PEG chain is attached or linked to a molecule (e.g., a drug or a protein) . It is known that PEGylation imparts several significant pharmacological advantages over the unmodified form, such as improved solubility, increased stability, extended circulating life, and decreased proteolytic degradation. According to one embodiment of the present disclosure, the second element is a PEG chain, which has a molecular weight of about 20,000 to 50,000 daltons.
Figure 1G provides an alternative example of the present linker unit (linker unit 10G) , in which five first elements 30 are respectively linked to the lysine residues via the linking arms 20 and the AHA (AAH) residue of the center core 11e is linked with a PEG chain 80 via the CuAAC reaction. The solid dot 40 depicted in Figure 1G represents the chemical bond  resulted from the CuAAC reaction occurred between the AHA residue and the PEG chain 80.
Figure 1H provides another example of the present disclosure, in which the N-terminus of the center core 13 is a cysteine residue that is linked to a coupling arm 60. A PEG chain 80 can be efficiently linked to the coupling arm 60 via the iEDDA reaction. The ellipse 70 of the linker unit 10H represents the chemical bond resulted from the iEDDA reaction occurred between the coupling arm 60 and the PEG chain 80.
Figure 1I provides an alternative example of the present linker unit, in which the linker unit 10I has a structure similar to the linker unit 10G of Figure 1G, except that the PEG chain 80 is linked to the coupling arm 60 via the SPAAC reaction. The diamond 90 depicted in Figure 1I represents the chemical bond resulted from the SPAAC reaction occurred between the coupling arm 60 and the PEG chain 80.
According to some embodiments of the present disclosure, in addition to the first and second elements, the present linker unit further comprises a third element. In this case, one of the N-and C-terminus of the center core is an amino acid having an azide group or an alkyne group, while the other of the N-and C-terminus of the center core is a cysteine residue. The lysine residues of the center core are respectively linked with the linking arms, each of which has a maleimide group at its free terminus； whereas the cysteine residue of the center core is linked with the coupling arm, which has a tetrazine group or a strained alkyne group at its free terminus. As described above, the first element is therefore linked to the linking arm via the thiol-maleimide reaction, and the second element is linked to the coupling arm via the iEDDA reaction. Further, a third element is linked to the terminal amino acid having an azide group or an alkyne group via the CuAAC reaction or SPAAC reaction.
Optionally, the first, second, and third elements are different. According to one embodiment of the present disclosure, the linker unit may have two different kinds of targeting elements and one kind of effector element, two different kinds of effector elements and one kind of targeting element, or one kind of targeting element, one kind of effector element, and one element capable of improving the pharmacokinetic property of the linker unit, such as solubility, clearance, half-life, and bioavailability.
Reference is now made to the linker unit 10J of Figure 1J, in which the center core 11f has an HPG (GHP) residue at the N-terminus thereof and a cysteine residue at the C-terminus thereof. The linking arms 20 and the coupling arm 60 are respectively linked to the lysine (K) residues and the cysteine (C) residue of the center core 11f. Further, five first elements 30 are respectively linked to the five linking arms 20, the second element (i.e., the PEG chain) 80 is linked to the coupling arm 60 via the short PEG chain 62, and the third element 50 is linked to the HPG residue. The solid dot 40 indicated the chemical bond resulted from the CuAAC reaction occurred between the HPG residue and the short PEG chain 62； while the ellipse 70 represents the chemical bond resulted from the iEDDA reaction occurred between the coupling arm 60 and the PEG chain 80.
Figure 1K provides another embodiment of the present disclosure, in which the linker unit 10K has the similar structure with the linker unit 10J of Figure 1J, except that the short PEG chain 62 is linked with the HPG residue via the SPAAC reaction, instead of the iEDDA reaction. The diamond 90 in Figure 1K represents the chemical bond resulted from the SPAAC reaction occurred between the short PEG chain 62 and the HPG residue.
In the preferred embodiments of this disclosure, the linking arms have a maleimide group in the free terminus for conjugating with first elements having the sulfhydryl group via the thiol-maleimide reaction. Also, there is one cysteine residue or an amino acid residue with an azide or alkyne group at a terminus of the peptide core for attaching a coupling arm for linking a second element.
It is conceivable for those skilled in the arts that variations may be made. A conjugating group, other than maleimide, such as azide, alkyne, tetrazine, or strained alkyne may be used for the free terminus of the linking arms, for linking with first elements with a CuAAC, iEDDA, or SPAAC reaction. Also the cysteine residue (or an amino acid residue with an azide or alkyne group) of the peptide core needs not to be at the N-or C-terminus. Furthermore, two or more of such residues may be incorporated in the peptide core to attach multiple coupling arms for linking a pleural of second elements.
PART II Uses of Peptide Core-Based Multi-Arm Linkers
Compared with previously known therapeutic constructs, the present linker unit discussed in Part I is advantageous in two points:
(1) The number of the functional elements may be adjusted in accordance with the needs and/or applications. The present linker unit may comprise two elements (i.e., the first and second elements) or three elements (i.e., the first, second, and third elements) in accordance with the requirements of the application (e.g., the disease being treated, the route of administration of the present linker unit, and the binding avidity and/or affinity of the antibody carried by the present linker unit) . For example, when the present linker unit is directly delivered into the tissue/organ (e.g., the treatment of eye) , one element acting as the effector element may be enough, thus would eliminate the need of a second element acting as the targeting element. However, when the present linker unit is delivered peripherally (e.g., oral, enteral, nasal, topical, transmucosal, intramuscular, intravenous, or intraperitoneal injection) , it may be necessary for the present linker unit to simultaneously comprise a targeting element that specifically targets the present linker unit to the lesion site； and an effector element that exhibits a therapeutic effect on the lesion site. For the purpose of increasing the targeting or treatment efficacy or increasing the stability of the present linker unit, a third element (e.g., a second targeting element, a second effector element, or a PEG chain) may be further included in the present linker unit.
(2) The first element is provided in the form of a bundle. As described in Part I of the present disclosure, the number of the first element may vary with the number of lysine residue comprised in the center core. If the number of lysine residue in the center core ranges from 2 to 15, then at least two first elements may be comprised in each linker unit. Thus, instead of providing one single molecule (e.g., cytotoxic drug and antibody) as traditional therapeutic construct or method may render, the present linker unit is capable of providing more functional elements (either as targeting elements or as effector elements) at one time, thereby greatly improves the therapeutic effect.
In certain therapeutic applications, it is desirable to have a single copy of a targeting or effector element. For example, in using an scFv for targeting an extracellular matrix protein for delivering a bundle of scFv for neutralizing a pro-inflammatory cytokine, a single copy of the scFv specific for the extracellular protein is desirable, so that unwanted effects due to overly tight binding may be avoided. In another example, in using scFv specific for CD3 or CD16a to recruit T cells or NK cells to kill targeted tumor cells bound by a bundle of  scFv specific for a tumor-associated antigen on the tumor cells, a single copy of the scFv specific for CD3 or CD16a is desirable, so that unwanted effects due to cross-linking of the CD3 or CD16a may be avoided. In still another example, it is desirable to have only one copy of long-chain PEG for enhancing pharmacokinetic properties. Two or more long PEG chains may cause tangling and affect the binding properties of the targeting or effector elements.
Based on the advantages listed above, the second aspect of the present disclosure pertains to a use of the present linker unit. Specifically, the present disclosure provides a method for treating different diseases (including immune disorder, diffused tumor, solid tumor, osteoporosis disease, and age-related macular degeneration) , in which the method comprising administering a subject in need thereof a therapeutically effective amount of the present linker unit.
A first set of diseases treatable by the present linker unit is the immune disorder. Illustrative linker units suitable for treating immune disorders include a first element that is an antibody fragment specific for a pro-inflammatory cytokine or a receptor of the cytokine； or a soluble receptor specific for the cytokine； and a second element that is an antibody fragment specific to the tissue specific extracellular matrix protein.
According to one embodiment, the present linker unit suitable for treating psoriasis comprises a first element of an scFv specific for TNF-α, IL-12/IL-23, or IL-17； or the receptor of IL-17； and a second element of an scFv specific for collagen I or collagen VII.
According to another embodiment, the present linker unit suitable for treating systemic lupus erythematosus (SLE) , cutaneous lupus, or Sjogren’s syndrome comprises an scFv specific for BAFF as the first element； and an scFv specific for collagen I or collagen VII as the second element.
Some skin diseases, such as atopic dermatitis, pemphigus vulgaris, and several types of urticaria, which have obvious inflammatory manifestation in the skin, are not treated with antibodies targeting specific TNF-α, IL-12/IL-23, IL-17, or BAFF, because those antibodies are not found to be sufficiently efficacious. It is rational to expect that if those  anti-inflammatory antibodies are distributed favorable to the skin, they may be able to treat those skin diseases.
According to still another embodiment, the present linker unit is used to treat rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis. In the embodiment, the first element is an scFv specific for TNF-α, IL-1, IL-6, IL-12/IL-23, IL-17, IL-6R, or IL-17E； and the second element is an scFv specific for collagen II, collagen IX, collagen XI, or α-aggrecan.
According to further another embodiment, the present linker unit suitable for treating inflammatory bowel disease (e.g., Crohn’s disease and ulcerative colitis) comprises an scFv specific for TNF-α as the first element； and an scFv specific for collagen III or collagen V as the second element.
In the treatment of diffused tumor (for example, acute lymphocytic leukemia (ALL) , chronic lymphocytic leukemia (CLL) , acute myelogenous leukemia (AML) , chronic myelogenous leukemia (CML) , Hodgkin lymphoma, non-Hodgkin lymphoma, and myeloma) , the first element of the present linker unit is the antibody fragment specific for the cell surface antigen associated with and/or overexpressed on the diffused tumor； and the second element of the present linker unit is the antibody fragment specific for the cell surface antigen CD3 or CD16a. According to the embodiments of the present disclosure, the cell surface antigen associated with and/or overexpressed on the diffused tumor is CD5, CD19, CD20, CD22, CD23, CD27, CD30, CD33, CD34, CD37, CD38, CD43, CD72a, CD78, CD79a, CD79b, CD86, CD134, CD137, CD138, or CD319.
For treating B-lymphocyte-derived lymphoma or leukemia, the first element is an scFv specific for CD5, CD19, CD20, CD22, CD23, CD30, CD37, CD79a, or CD79b； and the second element is an scFv specific for CD3 or CD16a.
In the treatment of plasmacytoma or multiple myeloma, the first element is an scFv specific for CD38, CD78, CD138, or CD319； and the second element is an scFv specific for CD3 or CD16a.
To treat T-cell derived lymphoma or leukemia, the first element is an scFv specific for CD5, CD30, or CD43； and the second element is an scFv specific for CD3 or CD16a.
As to the treatment of myelogenous leukemia, the first element is an scFv specific for CD33 or CD34； and the second element is an scFv specific for CD3 or CD16a.
Another set of diseases treatable by the present linker unit is solid tumors, which can be melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, or head and neck squamous cell carcinoma. According to the embodiment of the present disclosure, the first element of the present linker unit is a peptide hormone, a growth factor, or an scFv specific for a tumor-associated antigen； and the second element is an scFv specific for the cell surface antigen CD3 or CD16a.
According to the embodiments of the present disclosure, the peptide hormone is secretin, cholecystokinin (CCK) , somatostatin, or thyroid-stimulating hormone (TSH) .
In the embodiments of the present disclosure, the growth factor is selected from the group consisting of epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , vascular endothelial growth factor A (VEGF-A) , basic fibroblast growth factor (bFGF) , and hepatocyte growth factor (HGF) .
According to one embodiment, the tumor-associated antigen is selected from the group consisting of human epidermal growth factor receptor (HER1) , HER2, HER3, HER4, carbohydrate antigen 19-9 (CA 19-9) , carbohydrate antigen 125 (CA 125) , carcinoembryonic antigen (CEA) , mucin 1 (MUC 1) , ganglioside GD2, melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) , mesothelin, mucine-related Tn, Sialyl Tn, Globo H, stage-specific embryonic antigen-4 (SSEA-4) , and epithelial cell adhesion molecule (EpCAM) .
In some instances, some tumor-associated antigen may be shed from the solid tumor of a subject and wanders into the circulation system of the subject. In these cases, the present method for treating solid tumor comprises the step of, (a) subjecting the subject to a blood dialysis procedure using an antibody specific for one or more tumor-associated  antigens to remove the tumor-associated antigens that are shed from the tumor and wanders into the circulation of the subject； and (b) administering the present linker unit for treating the solid tumor.
For the purpose of treating osteoporosis disease, the first element of the present disclosure is an scFv specific for receptor activator of nuclear factor κB (RANKL) ； and the second element of the present disclosure is a second scFv specific for collagen I or osteonectin.
According to the embodiments of the present disclosure, the present linker unit is useful in treating age-related macular degeneration (AMD) , in which the first element of the present linker unit is an scFv specific for VEGF-A； and the second element of the present disclosure is a long PEG chain having a molecular weight of about 20,000 to 50,000 daltons.
PART III Molecular Constructs with Targeting and Effector Moieties
Another aspect of the present disclosure pertains to a molecular construct comprising at least two linker units. In addition to the peptide core-based multi-arm linkers discussed above in Part I of the present disclosure, the molecular construct may also use linker unit with a compound core (see, below) as one or both of its linker units. According to certain embodiments of the present disclosure, at least one of the linker units of the present molecular construct comprises the polypeptide core. Preferably, at least two linker units of the present molecular construct comprise the polypeptide cores. More preferably, all the linker units of present molecular construct respectively comprise the polypeptide cores.
III- (i) Linker Units with a Compound Core
In addition to the linker unit described in part I of the present disclosure, also disclosed herein is another linker unit that employs a compound, instead of the polypeptide, as the center core. Specifically, the compound is benzene-1, 3, 5-triamine, 2- (aminomethyl) -2-methylpropane-1, 3-diamine, tris (2-aminoethyl) amine, benzene-1, 2, 4, 5-tetraamine, 3, 3', 5, 5'-tetraamine-1, 1'-biphenyl, tetrakis (2-aminoethyl) methane, tetrakis-(ethylamine) hydrazine, N, N, N', N', -tetrakis (aminoethyl) ethylenediamine, benzene-1,2, 3, 4, 5, 6-hexaamine, 1-N, 1-N, 3-N, 3-N, 5-N, 5-N-hexakis (methylamine) -benzene-1, 3, 5- triamine, 1-N, 1-N, 2-N, 2-N, 4-N, 4-N, 5-N, 5-N, -octakis (methylamine) -benzene-1, 2, 4, 5-triamine, benzene-1, 2, 3, 4, 5, 6-hexaamine, or N, N-bis [ (1-amino-3, 3-diaminoethyl) pentyl] -methanediamine. Each of these compounds has 3 or more amine groups in identical or symmetrical configuration. Therefore, when one of the amine groups of a compound is conjugated with a coupling arm, all of the molecules of the compound have the same configuration.
Similar to the mechanism of linkage described in Part I of the present disclosure, each compound listed above comprises a plurality of amine groups, and thus, a plurality of PEG chains having NHS groups can be linked to the compound via forming an amine linkage between the amine group and the NHS group； the thus-linked PEG chain is designated as linking arm, which has a maleimide group at the free-terminus thereof. Meanwhile, at least one of the amine groups of the compound core is linked to another PEG chain, which has an NHS group at one end, and a functional group (e.g., an azide, alkyne, tetrazine, or strained alkyne group) at the other end； the thus-linked PEG chain is designated as coupling arm, which has a functional group at the free-terminus thereof.
Accordingly, two different elements can be respectively linked to the linking arm and/or coupling arm via the thiol-maleimide reaction (the linkage between the element and the linking arm) and the CuAAC reaction, SPAAC reaction or the iEDDA reaction (the linkage between the element and the coupling arm) .
According to some embodiments of the present disclosure, the linking arm is a PEG chain having 2-20 repeats of EG units； and the coupling arm is a PEG chain having 2-12 repeats of EG unit. In one embodiment, both the linking and coupling arms have 12 repeats of EG unit, in which one terminus of the coupling arm is an NHS group, and the other terminus of the coupling arm is an alkyne group.
<<Scheme 6 Linkage of linking and coupling arms respectively having maleimide group and azide group to center core>>
Figure PCTCN2016071184-appb-000016
Schemes  6 and 7 respectively depict the linkages between the center core, and the linking arm and the coupling arm, in which NHS represents NHS ester, Mal represents maleimide group, azide represents azide group, and alkyne represents alkyne group.
<<Scheme 7 Linkage of linking and coupling arms respectively having maleimide group and alkyne group to center core>>
Figure PCTCN2016071184-appb-000017
The requirement of having multiple NH2 groups exist in a symmetrical and identical orientation in the compound serving as the center core is for the following reason: when one of the NH2 group is used for connecting a bifunctional linker arm with N-hydroxysuccinimide (NHS) ester group and alkyne, azide, tetrazine, or strained alkyne group, the product, namely, a core with a coupling arm having alkyne, azide, tetrazine or strained alkyne, is homogeneous and may be purified. Such a product can then be used to produce multi-arm linker units with all other NH2 groups connected to linking arms with maleimide or  other coupling groups at the other ends. If a compound with multiple NH2 groups in non-symmetrical orientations, the product with one bifunctional linking arm/coupling arms is not homogeneous.
Some of those symmetrical compounds can further be modified to provide center cores with more linking arms/coupling arms. For example, tetrakis (2-aminoethyl) methane, which can be synthesized from common compounds or obtained commercially, may be used as a core for constructing linker units with four linking arms/coupling arms. Tetrakis (2-aminoethyl) methane can react with bis (sulfosuccinimidyl) suberate to yield a condensed product of two tetrakis (2-aminoethyl) methane molecules, which can be used as a core for constructing linker units having six linking arms/coupling arms. The linker units, respectively having 3 linking arms/coupling arms, 4 linking arms/coupling arms and 6 linking arms/coupling arms, can fulfill most of the need for constructing targeting/effector molecules with joint-linker configuration.
As would be appreciated, the numbers of the linking arm and/or the coupling arm and the element linked thereto may vary with the number of amine groups comprised in the center core. In some preferred embodiments, the numbers of the linking arm/coupling arm and the corresponding linking element linked thereto ranges from about 1-7.
Reference is now made to Figure 2, in which benzene-1, 2, 4, 5-tetraamine having 4 amine groups is depicted. Three of the amine groups are respectively linked to the linking arms 20, and one of the amine group is linked to the coupling arm 60, which has an azide group at its free-terminus. Three first elements 30 are then respectively linked to the three linking arms 20 via the thiol-maleimide reactions, and one second element 50 is linked to the coupling arm 60 via the CuAAC reaction. The solid dot 40 as depicted in Figure 2 represents the chemical bond resulted from the CuAAC reaction occurred between the coupling arm 60 and the second element 50.
III- (ii) Molecular Construct with Joint-linker Configuration
According to some embodiments of the present disclosure, the molecular construct comprises two linker units, and the linker units are coupled to each other via either the CuAAC reaction (using copper or pentamethylcyclopentadienyl ruthenium chloride complex  as catalyst) , the SPAAC reaction, or the iEDDA reaction. In the embodiments, one of the linker units is linked with a plurality of first elements, which act as the targeting elements, and the other of the linker units is linked with a plurality of second elements, which act as the effector elements.
According to other embodiments of the present disclosure, the molecular construct comprises three linker units, in which the first and second linker units are coupled to each other via the iEDDA reaction, and then, the third linker unit is coupled to the first or second linker unit via the CuAAC reaction. Alternatively, the first and second linker units are coupled to each other via the iEDDA reaction, and the third linker unit is coupled to the first or second linker unit via the SPAAC reaction. In the embodiments, the first, second, and third linker units respectively carry a plurality of first, second, and third elements, in which the first, second, and third elements are different. According to one embodiment, two of the three elements (i.e., the first, second, and third elements) are targeting elements, and one of the three elements is an effector element. According to another embodiment, two of the three elements are effector elements, and one of the three elements is a targeting element. According to still another embodiment, one of the three elements is a targeting element, another of the three elements is an effector element, and the other of the three elements is an element capable of improving the pharmacokinetic property of the molecular construct, such as solubility, clearance, half-life, and bioavailability.
Reference is first made to Figures 3A-3D, which respectively depict the linkage between the two linker units. Figure 3A depicts a molecular construct comprising two linker units (100A, 200A) , which are coupled to each other via the iEDDA reaction. The first linker unit 100A comprises a first center core 110a, a linking arm 120 (as the first linking arm) , and a coupling arm 130a (as the first coupling arm) , in which the linking and coupling arms are respectively linked to the first center core 110a at one ends. Similarly, the second linker unit 200A comprises a second center core 210a, a linking arm 220 (as the second linking arm) , and a coupling arm 230a (as the second coupling arm) , in which the linking and coupling arms are respectively linked to the second center core 210a at one ends. One of the  coupling arms  130a, 230a has a tetrazine group at its free terminus, while the other of the  coupling arms  130a, 230a has a TCO group. Specifically, if the coupling arm 130a has a tetrazine group 152 at its free terminus (i.e., the terminus not connected to the first center  core 110a) , then the coupling arm 230a would have a TCO group 154 at its free terminus (i.e., the terminus not connected to the second center core 210a) , and vice versa. Accordingly, the two linker units (100A, 200A) are coupled to each other via the iEDDA reaction occurred between the respective free ends of the  coupling arms  130a, 230a. The ellipse 156 as depicted in Figure 3A represents the chemical bond resulted from the iEDDA reaction occurred between the coupling  arms  130a, 230a.
In the depicted embodiment, each of the linking  arms  120, 220 has a maleimide group at its free terminus. Accordingly, a first targeting element 140 and a first effector element 240, each has a thiol group are respectively linked to the linking  arms  120, 220 via the thiol–maleimide reaction.
According to one embodiment, both the first and  second center cores  110a, 210a depicted in Figure 3A are polypeptide cores. According to another embodiment, both the first and  second center cores  110a, 210a depicted in Figure 3A are compound cores. According to still another embodiment, one of the first and  second center cores  110a, 210a depicted in Figure 3A is a polypeptide core, while the other of the first and  second center cores  110a, 210a depicted in Figure 3A is a compound core.
Figure 3B provides an alternative embodiment of the present disclosure, in which both the first and  second center cores  110b, 210b are polypeptide cores, and are respectively linked to a first targeting element 140 and a first effector element 240 via the linking  arms  120, 220. The unique feature in this embodiment is that, one of the  center cores  110b, 210b comprises an amino acid residue having an azide group (e.g., the AHA residue) at it N-or C-terminus, while the other of the  center cores  110b, 210b comprises an amino acid residue having an alkyne group (e.g., the HPG residue) at it N-or C-terminus, such configuration allows the  center cores  110a, 210a to be directly linked to each other, that is, without connecting through any coupling arms as that depicted in Figure 3A.. Specifically, if the center core 110b comprises the amino acid residue having the azide group 162 at its N-or C-terminus, then the center core 210b would comprises the amino acid residue having the alkyne group 164 at its N-or C-terminus, and vice versa. Accordingly, the  linker units  100B, 200B can couple together directly via the CuAAC reaction occurred between the N-or C-terminal amino acid residues of the  center cores   110b, 210b. The solid dot 166 as depicted in Figure 3B represents the chemical bond formed between the N-or C-terminal amino acid residues.
Figure 3C is another embodiment of the present disclosure. The  linker units  100C, 200C have the similar structures as the  linker units  100A, 200A, except that the coupling  arms  130b, 230b respectively have an azide group 162 and a DBCO group 172, instead of the azide group 152 and the alkyne group 154 as depicted in the  linker units  100A, 200A of Figure 3A. Specifically, the center core 110a is linked with a coupling arm 130b (as the first coupling arm) having an azide group 162 at its free-terminus； and the center core 210a is linked with a coupling arm 230b (as the second coupling arm) having a DBCO group 172 at its free-terminus. The  linker units  100C, 200C are then coupled together via the SPAAC reaction occurred between the coupling  arms  130b, 230b； and forming the chemical bond 182, depicted as a diamond.
In one embodiment, both the first and  second center cores  110a, 210a depicted in Figure 3C are polypeptide cores. In another embodiment, both the first and  second center cores  110a, 210a depicted in Figure 3C are compound cores. In still another embodiment, one of the first and  second center cores  110a, 210a depicted in Figure 3C is a polypeptide core, while the other of the first and  second center cores  110a, 210a depicted in Figure 3C is a compound core.
As would be appreciated, two linker units can be coupled to each other via the CuAAC reaction occurred between the center core and the coupling arm. Reference is now made to Figure 3D, in which the center core 110b comprises a N-or C-terminal amino acid residue that has an azide group 162 (e.g., the AHA residue) , and the center core 210a is linked with a coupling arm 230b having a TCO group 172 at its free-terminus. Accordingly, the  linker units  100B and 200C can be coupled together via the SPAAC reaction occurred between the center core 110b and the coupling arm 230b； and forming the chemical bond 182.
According to one embodiment, the  linker units  100B, 200C depicted in Figure 3D respectively comprise polypeptide cores. According to another embodiment, the center core 100B depicted in Figure 3D is a polypeptide core, while the center core 200C depicted in Figure 3D is a compound core.
Alternatively, the linker unit 200B that comprises a N-or C-terminal amino acid residue having an alkyne group 160b (e.g., the HPG residue) , and the linker unit 100C comprising the coupling arm 130b with an azide group 160a at its free-terminus can be coupled together via the azide-alkyne cycloaddition occurred between the center core 210b and the coupling arm 130b.
Compared with other therapeutic construct, the present molecular construct is advantageous in at least the three following aspects:
(1) the linker unit comprising a specified number and/or type of targeting/effector element can be prepared independently, then proceed to be coupled together via the CuAAC reaction, the iEDDA reaction, or the SPAAC reaction；
(2) the number and kind of the targeting and/or effector elements may vary in accordance with the requirements of application (e.g., the disease being treating, and the binding avidity and/or affinity of the targeting and/or effector element) . The combination of the targeting and effector elements may be adjusted according to specific needs and/or applications. Each of the present targeting and effector elements may vary with such factors like particular condition being treated, the physical condition of the patient, and/or the type of disease being treated. The clinical practitioner may combine the most suitable targeting element and the most suitable effector element so as to achieve the best therapeutic effect. According to embodiments of the present disclosure, the targeting element may be a growth factor, a peptide hormone, a cytokine, or an antibody fragment； and the effector element may be an immunomodulant, a chelator complexed with a radioactive nuclide, a cytotoxic drug, a cytokine, a soluble receptor, or an antibody； and
(3) compared with other coupling reactions, the CuAAC reaction, the iEDDA reaction, or the SPAAC reaction is more efficient in terms of coupling any two linker units.
Reference is now made to Figure 4, in which six libraries are illustrated, and are prepared independently. In this embodiment, Libraries 1-6 respectively comprise a plurality of  linker units  300A, 300B, 300C, 400A, 400B, and 400C that are linked with functional elements. Each  linker units  300A, 300B, and 300C are similar in structures； in which each of the  linker units  300A, 300B, and 300C comprises one center core 310, one coupling arm 330 linked thereto and has a tetrazine group 350 at its free terminus, and a specified number of the linking arm 320. For instance, Linker unit 300A comprises four  linking arms 320, and accordingly, four targeting elements 340a can be respectively linked to the four linking arms 320. Similarly, two targeting elements 340b and five targeting elements 340c can be respectively linked to the  linker units  300B and 300C. The targeting  elements  340a, 340b, and 340c can be the same or different. As to the  linker units  400A, 400B and 400C, each of these linker units comprises one center core 410, one coupling arm 430 linked thereto and has a strained alkyne group 450 at its free terminus, and a specified number of the linking arm 420. As depicted, three effector elements 440a, five effector elements 440b, and eight effector elements 440c can be respectively linked to the  linker units  400A, 400B and 400C. The  effector elements  440a, 440b, and 440c can be the same or different. The Libraries 1-6 may be prepared independently. One skilled artisan may select the first linker unit from  Libraries  1, 2 and 3, and the second linker unit from  Libraries  4, 5, and 6, then proceed to couple the first and second linker units via the iEDDA reaction occurred between the tetrazine group 350 and the strained alkyne group 450 so as to produce the molecular construct with the specified number of targeting and effector elements.
Based on the library concept, the present molecular construct can be produced with different configurations depending on the libraries selected. Figure 5A provides an example of the present molecular construct, in which each of the first and second center cores (310, 410) is linked with three linking arms (320, 420) and one coupling arm (330, 340) . Three of the first targeting elements 340 are respectively linked to the linking arms 320； and three of the first effector elements 440 are respectively linked to the linking arms 420. The two linker units are coupled to each other via the iEDDA reaction occurred between two coupling  arms  330, 430, and forming the chemical bond 356. By this configuration, equal numbers of multiple targeting and/or effector elements may be carried in one molecular construct.
Figure 5B provides another example of the present molecular construct, in which the first and second center cores respectively contain different numbers of amine groups (e.g., lysine residues) , and accordingly, the molecular construct contains non-equal numbers of targeting and effector elements. In the depicted example, the first center core 310 is linked to one coupling arm 330, and two linking arms 320. The second center core 410 is linked to one coupling arm 430, and five linking arms 420. Accordingly, two targeting elements  340 are respectively linked to the linking arms 320； and five effector elements 440 are respectively linked to the linking arms 420. The ellipse 356 in Figure 5B represents the linkage between two coupling  arms  330, 430.
In optional embodiments, the present molecular construct may further comprise a relatively long PEG chain connected to either the first or second center core, so that the present molecular construct may be segregated further away from the reticuloendothelial system and attains a longer half-life after being administered to a subject. In the case where a protein is modified by a PEG chain so as to improve its pharmacokinetic properties and/or to decrease immunogenicity, PEG up to 20,000-50,000 daltons in length, is preferred. Accordingly, in one preferred embodiment of the present invention, linking arms of relatively shorter lengths are used to connect the targeting and effector elements, while a PEG chain of 20,000 to 50,000 daltons is connected to any of the linker units with the purpose of increasing in vivo half-life of the present molecular construct.
In some embodiments, multiple scFv fragments are used as the targeting and/or effector elements to construct the present molecular construct. The targeting element/effector element pharmaceuticals based on molecular constructs comprising scFv fragments should have longer in vivo half-lives than individual antibody fragments. For some clinical applications, such as using anti-TNF-α and anti-IL-12/IL-23 in the treatment of rheumatoid arthritis, anti-RANKL in the treatment of osteoporosis, and anti-VEGF-A in the treatment of the eye disease of age-related macular degeneration, much extended half-lives of the pharmaceuticals are desired, so as to eliminate the need of frequent administration of the drugs. For the molecular constructs used in those applications, PEG chains that are 20,000 to 50,000 daltons by weight, may be used as the linking arms to link the scFv fragments that serve as targeting or effector elements. PEGs of these lengths have been used to modify a large number of therapeutic proteins to increase their half-lives.
According to some embodiments of the present disclosure, the linker unit may comprise two linking arms respectively linked to the different functional elements. Reference is now made to Figure 6, in which the molecular construct comprises two linker units 100A and 200D. The first and second functional elements 140, 240 (one serves as the targeting element, and the other serves as the effector element) are respectively linked  to the first center core 110a and the second center core 210c via the linking  arms  120, 220； and the two  center cores  110a, 210c are coupled to each other via the iEDDA reaction occurred between the coupling  arms  130a, 230a, in which the ellipse 156 represents the chemical bond forming therebetween. In addition to the functional element 240, the second center core 210c is further linked to a PEG chain 260. Specifically, the second center core 210c comprises an AHA residue, which can be reacted with and linked to the PEG chain 260 having a stained alkyne group via the SPAAC reaction, in which the diamond 182 represents the chemical bond forming from the SPAAC reaction. Depending on the intended and desired use, the third element can be a second targeting element, a second effector element, or an element capable of improving the pharmaceutical property of the molecular construct. According to one embodiment of the present disclosure, the PEG chain 260 has a molecular weight about 20,000 to 50,000 daltons.
Based on the concept, a linker unit may comprise a plurality of linking arms, which can be linked to a plurality of functional elements. For example, a linker unit may comprises 5-12 linking arms, which can be linked to 5-12 functional elements. This is especially useful when the functional elements are small molecules, such as cytotoxic drugs or toll-like receptor agonists. The linker unit carrying multiple molecules of a cytotoxic drug is herein referred to as a drug bundle.
Further, the polypeptide cores can be employed to prepare the molecular construct comprising three linker units. Accordingly, another aspect of the present disclosure is directed to a molecular construct comprising three linker units. Among the three linker units, two of them may be connected to each other via the iEDDA reaction, while the third linker unit is connected to any of the two linker units by the SPAAC reaction or CuAAC reaction. The rationale for constructing a multi-linker unit (e.g., three linker units) is that two different sets of targeting elements or two different sets of effector elements can be incorporated therein.
Reference is now made to Figure 7, in which the molecular construct comprises three linker units (500, 600, 700A) . The  linker units  500, 600, 700A respectively comprise a center core (510, 610, 710) , and an linking arm (520, 620, 720) with a functional element (540, 640, 740) linked thereto. The linker unit 600 is characterized in comprising a  cysteine residue at one of its N-or C-terminus that is linked with a coupling arm 630； and an amino acid residue having an azide or alkyne group at the other of its N-or C-terminus. One of the coupling  arms  530, 630 has a tetrazine group at its free terminus, and the other of the coupling  arms  530, 630 has a strained alkyne group at its free terminus. Accordingly, the  linker units  500, 600 can be coupled to each other via the iEDDA reaction occurred between the coupling  arms  530, 630 as the linkage manner described in Figure 3A. As to the linkage of the linker unit 300, when the N-or C-terminal amino acid residue of the center core 610 has an azide group (e.g., the AHA residue) , the center core 710 comprises an amino acid having an alkyne group (e.g., the HPG residue) at its N-or C-terminus； or, when the N-or C-terminal amino acid residue of the center core 610 has an alkyne group (e.g., the HPG residue) , then the center core 710 comprises an amino acid having an azide group (e.g., the AHA residue) at its N-or C-terminus. Thus, as the linkage manner described in Figure 3B, the  linker units  600, 700A can be directly coupled to each other via the CuAAC reaction occurred between the N-or C-terminal amino acid residues of the  center cores  610, 710 without the presence of the coupling arms. The ellipse 560 and the solid dot 670 in Figure 7 respectively represent the chemical bonds resulted from the iEDDA reaction and the CuAAC reaction.
Alternatively, two of the three linker units may be connected to each other via the iEDDA reaction, while the third linker unit is connected to any of the two linker units by the SPAAC reaction. Reference is now made to Figure 7B, in which the  linker units  500, 600 are coupled together via the iEDDA reaction as described in Figure 7A, whereas the linker unit 700B is linked to the linker unit 600 via the SPAAC reaction occurred between the center core 610 and the coupling arm 730. The diamond 672 in Figure 7B represents the chemical bond resulted from the SPAAC reaction.
As would be appreciated, each number of the  functional elements  540, 640, 740 respectively linked to the  linker units  100, 200, 300 are different depending on the intended use. With the library concept depicted in Figure 4, the linker units respectively carrying different numbers and/or types of functional elements can be prepared separately as different libraries, and one skilled artisan may select and combine the desired linker units from the libraries in accordance with the various applications.
Basically, the coupling arm of the present molecular construct described in above aspects and/or embodiments of the present disclosure that has an azide, alkyne, tetrazine, or strained alkyne group at the terminus is designed as a PEG chain having 2-12 repeats of EG units. The linking arm is designed as a PEG chain having 2-20 repeats of EG units.
Adopting a polypeptide as the center core provides versatility in the present molecular construct, in which multiple copies or types of targeting/effector elements may be present in one construct, accordingly, enhanced specificity of drug delivery and potency in the intended target sites are achieved. A large number of configurations can be adopted by employing the molecular construct comprising multiple linker units. A few examples are: a first linker unit carrying three scFvs targeting elements, and a second linker unit carrying 5 cytotoxic drugs； a first linker unit carrying three scFvs targeting elements, and a second linker unit carrying three scFvs effector elements； a first linker unit carrying two scFvs of the first set targeting elements, a second linker unit carrying two scFvs of the second set targeting elements, and a third linker unit carrying 5 cytotoxic drugs； a first linker unit carrying 2 bi-scFv targeting elements, and a second linker unit carrying two scFvs effector elements； or a first linker unit carrying three scFvs targeting elements, a second linker unit carrying two scFvs effector elements plus a linking arm attached with a long PEG of 20,000-50,000 daltons for the purpose of increasing pharmacokinetic properties.
In some embodiments of this invention, a bi-functional PEG acting as a linking arm is used to link the antigen-binding fragments of antibodies, which serve as targeting or effector elements, to the amine groups located in the polypeptide core. Each PEG may have NHS group at one end and maleimide group at the other end. The NHS group may couple with amine group in the polypeptide core, while the maleimide group may couple with sulfhydryl group of a cysteine residue of an scFv, bi-scFv, or Fab fragment of an antibody. The scFv and bi-scFv are engineered to have a polypeptide linker with terminal cysteine residue at the C-terminal. Fab may be derived from a whole IgG by pepsin cleavage, and the free sulfhydryl groups are derived from the inter-chain disulfide bond by a mild reduction reaction.
Schemes 8-12 provide several working example respectively depicting the coupling and preparation of specified linker units.
<<Scheme 8 Coupling of linker units via C-terminal amino acid residues>>
Figure PCTCN2016071184-appb-000018
Scheme 8 is a schematic diagram depicting the preparation of the present molecular construct in accordance with one embodiment of the present disclosure, in which NHS represents NHS ester, Mal represents maleimide group, AAH represents L-azidohomoalanine (AHA) residue, AAH represents homopropargylglycine (HPG) residue, Ac represents acetyl group, and scFv represent single-chain variable fragment. In step 1, the first center core comprising the amino acid sequence of (GSK) 3 and a L-azidohomoalanine (AHA) residue at the C-terminus thereof； and the second center core comprising the amino acid sequence of (GSK) 5 and a homopropargylglycine (HPG) residue at the C-terminus thereof, are respectively prepared. For the purpose of stabilizing the polypeptide, the N-terminuses of the first and second center cores are respectively modified with an acetyl group. In step 2, the linking arms are respectively linked to the lysine residues in the first and second center cores via forming an amide linkage there between；  the linked arm linked to the center core has a maleimide group at the free-terminus. In step 3, the first targeting element (i.e., the antibody) having a thiol group (e.g., a cysteine residue) is linked to the linking arm linked with the first center core via the thiol–maleimide reaction； similarly, the effector element (i.e., the drug) having a thiol group is linked to the linking arm linked with the second center core via the thiol–maleimide reaction. In step 4, the two linker units are coupled via a CuAAC reaction occurred between the AHA and HPG residues.
<<Scheme 9 Method of coupling of effector element with polypeptide core through linking to linking arms>>
Figure PCTCN2016071184-appb-000019
Optionally, the targeting/effector element can be linked to the center core in an alternative method. Scheme 9 is a scheme illustrating the coupling of the effector element with the polypeptide core, in which the linking arm is first linked to the center core, and then the effector element (i.e., the drug) is linked to the linking arm via the thiol–maleimide reaction. In the alternative method of scheme 10, the effector element (i.e., the drug) is coupled to the linking arm so as to produce a linking arm-effector conjugate (i.e., PEG-drug) ； next, the linking arm-effector conjugate is linked to the center core via forming an amide linkage between the lysine residues and the NHS esters.
<<Scheme 10 Alternative method of coupling of effector element with polypeptide core by first conjugating with PEG chain and then linking to amino groups of lysine residues>>
Figure PCTCN2016071184-appb-000020
Alternatively, the linking arms for the joint-linker configuration may also be used to link bispecific scFv, which act as targeting elements or effector elements. These configurations will increase the specificity of targeting and/or the potency of the effector mechanisms.
Scheme 11 provides an example of preparing the present molecular construct, which comprises two linker units； both linker units comprises the amino acid sequence of (K-Xaa4) 3 and a cysteine (C) residue at the C-terminus thereof. In step 1, two coupling arms are respectively linked to the C residues of the linker units, in which one of the coupling arms has a maleimide (Mal) group at one terminus and a tetrazine group at the other terminus, while the other coupling arm has a Mal group at one terminus and a TCO group at the other terminus. In step 2, the linking arms are respectively linked to the lysine (K) residues via forming the amide bond between the linking arm and the K residue. Then, in step 3, three anti-A antigen scFvs (scFv α A) and three anti-B antigen scFvs (scFv α B) are respectively linked to the linking arms of the linker units via the thiol-maleimide reaction. Finally, in step 4, the two linker unit are coupled to each other via the iEDDA reaction occurred between the tetrazine and TCO group.
<<Scheme 11 Preparation of molecular construct via iEDDA reaction occurred between coupling arms>>
Figure PCTCN2016071184-appb-000021
Scheme 12 provides an example of preparing a molecular construct comprising three linker units, in which two linker units respectively linked with the scFv α A and scFv α B are coupled to each other via the iEDDA reaction as described in Scheme 11 and a third linker unit couples with the second linker unit via a CuAAC reaction. In this example, the third linker unit is a drug bundle. However, this reaction scheme can be applied to a third linker unit with other elements, such as scFv. In the present example, the center linker unit (that is, the second linker unit) comprises an HPG (GHP) residue at its N-terminus, and accordingly, a drug bundle conjugated with an AHA (AAH) residue can be linked to the second linker unit via the CuAAC reaction occurred between the HPG and AHA residues. Alternatively, the center linker unit may comprise an AHA residue at its N or C-terminus, and can couple with a third linker unit carrying a coupling arm with a DBCO or another strained alkyne group via a SPAAC reaction. The thus-formed molecular construct in scheme 12 has three functional elements: scFv α A, scFv α B, and drug molecule. The molecular  constructs with three linker units can carry three sets of scFv, of which two sets as targeting elements and one set as effector elements, or one set as targeting elements and two sets as effector elements.
<<Scheme 12 Preparation of molecular construct having three linker units with three functional elements>>
Figure PCTCN2016071184-appb-000022
When the targeting and effector elements are all scFv, and linking arms of 600 daltons (12 EG units) are used, a molecular construct with a total of six scFvs has a molecular weight of about 170,000 daltons. A molecular construct with seven scFvs has a molecular weight of about 200,000 daltons, and a molecular construct with eight scFvs has a molecular weight of about 230,000 daltons. Most of the molecular constructs of this invention have molecular weights smaller than 200,000 daltons, and a few molecular constructs have molecular weights in 200,000-250,000 daltons.
When four different sets of scFv are to be carried in one molecular construct, it is preferable to have one linker unit carrying a joined single-chain, bi-specific scFv (bi-scFv) , such as scFv1-scFv2 (e.g., specific for HER2 and HER3) , and the other two linker units each carrying one scFv (i.e., scFv3 and scFv4 respectively) . There are two ways to construct bi-specific scFv1-scFv2. In the “tandem” configuration, VL1-VH1-VL2-V H2 or VH1-VL1-VH2-V L2 is arranged； in the “diabody” configuration, VL2-VL1-VH1-V H2 or VH2-VH1-VL1-V L2 is arranged. Proper linkers with GGGGS (SEQ ID NO: 6) repeats or other sequences are placed between the immunoglobulin domains.
In our experience, a peptide or a PEG linker, which contain maleimide and azide groups may become polymerized upon long-term storage, due to the automatic coupling reaction between the maleimide and azide groups. Therefore, it is preferable that each linker unit is prepared freshly and independently, and processed to connecting the targeting or effector elements onto the linker units, and the coupling of the linker units through click reaction without delay. An alternative preferred embodiment is that the targeting elements and effector elements are both conjugated to linker units with alkyne groups, and the alkyne group in one of the linker units is then converted to azide with a short homo-bifunctional linker with azide at both ends. The linker units, one with alkyne and the other with azide, are then coupled via a click reaction.
The preferred linking arms for this invention are PEG. The length of the linking arms is important for several considerations. It should be long enough to allow flexibility of the linked scFv or other types of functional elements to reach targeted antigenic sites on targeted cell surface without steric constraints； yet not long enough to cause intra-molecular and inter-molecular tangling of the linking arms and their linked scFv fragments or functional elements, or to unnecessarily increase the size of the whole molecular construct for hindering tissue penetration. Linking arms that are too long may also fail to pull antigen molecules to form compacted clusters, if such clusters are required to initiate signal-transducing process for apoptosis or other cellular effects. The optimal length of linking arms for different types of combinations of targeted antigens and their binding agents may be determined by any skilled artisan in the related field without undue experimentation. In our experience with CD20 as a target antigen and anti-CD20 (rituximab) Fab in a 4-arm PEG linker, a PEG arm of about 1, 000-1, 200 daltons (about 25-30 ethylene glycol units) is  effective in causing apoptosis. Therefore, PEG linkers of 100 to 1, 000 daltons are suitable for the purpose of the present invention. A linking arm of NHS- (PEG) 12-Maleimide (approximately 500 daltons) is preferred in a number of molecular construct of this invention. A fully stretched (PEG) 12 has a length of
Figure PCTCN2016071184-appb-000023
Applicable linking arms and coupling arms are not limited by PEG chains. Peptides comprising glycine, serine and other amino acid hydrophilic residues, and polysaccharides, and other biocompatible linear polymers, which are modified to contain NHS and maleimide groups, can be used.
For certain therapeutic applications, it is desirable that the effector elements in the molecular constructs of this disclosure be released from the linking arms, so that they can get into cells in the targeted site, including cells bound by the targeting elements or surrounding cells, to cause pharmacological effects. In those cases, a cleavable bond is engineered in the linking arm. Cleavable bonds, which are susceptible for cleavage by hydrolysis, acid exposure, reduction, and enzymes, have been developed. For example, peptide segments susceptible to matrix metalloproteinases, which are present in inflammatory tissues, have been used in constructing therapeutic constructs. One embodiment of the present invention is to use PEG linkers with S-Sbond adjacent to the maleimide group NHS-PEG2-12-S-S-maleimide, wherein S-S is a disulfide bond, which can be slowly reduced.
According to some embodiments of the present disclosure, the targeting element described in above-mentioned embodiments is selected from the group consisting of a growth factor, a peptide hormone, a cytokine, and an antibody fragment； and the effector element is an immunomodulant, a chelator complexed with a radioactive nuclide, a cytotoxic drug, a cytokine, a soluble receptor, or an antibody.
In the embodiments, the antibody is in the form of an antigen-binding fragment (Fab) , a variable fragment (Fv) , a single-chain variable fragment (scFv) , a single domain antibody (sdAb) , or a bi-specific single-chain variable fragment (bi-scFv) . According to one embodiment, the bi-scFv is a bi-specific tandem scFv or a bi-specific diabody scFv.
In order to retain diffusing ability of the molecular constructs, a molecular size smaller than 250, 000 daltons is preferred. Thus, scFv fragments are preferred for most of the embodiments. At the DNA level, genes are constructed so that the VL and VH are linked as a single polypeptide in either order (VL-VH or VH-VL) by a peptide linker of 10-25 amino acid residues with glycine and serine being the major residues. At the C-terminal, a short stretch with glycine and serine and a terminal residue cysteine is engineered. Recombinant scFv and bi-scFv can be produced in bacteria, such as E. coli and Pseudomonas putida, in yeast, such as Pichia pastoris, or in mammalian cells, such as CHO and HEK293 cell lines.
The inventors’ laboratory have produced a large number of IgG antibodies, Fab, scFv and various antibody fragments, Fc-based proteins, and other recombinant antibodies in HEK293 and CHO cell lines for experimentation in in vitro systems and in animal models. Our laboratory has also developed cell lines for producing antibodies for human clinical trials. The HEK293 transient expression system can be conveniently employed to produce up to 1 g of IgG or antibody fragments using a few flasks of 1-2 liters in the research laboratory. The scFv fragments to be used in the molecular constructs of this invention generally do not have a carbohydrate modification, and carbohydrate modification is not required for the binding activity of the scFv to their antigenic targets. Furthermore, only one disulfide bond and one terminal cysteine are present in the scFv fragment. Therefore, small-scale bacterial expression systems have been developed as a manufacturing alternative for producing scFv. With E. coli, expression systems for recovering scFv in intracellular inclusion bodies, in periplasm, and in secreted form have been employed. The scFv can be purified in most cases with an affinity column with Protein L, which interacts with VH of most κ light chain, or in other cases with ion-exchange columns.
The examples of this invention based on the joint-linker platform employ mainly scFv and Fab as the targeting and/or effector elements. However, specific binding molecules may also be screened from large libraries of binding molecules based on sdAb or other antibody fragments. Libraries of binding molecules, which are not based on immunoglobulin domains but resemble antibodies in having specific binding affinities to selected target molecules, include (1) aptamers, which are oligonucleotides or short peptides selected for binding to target molecules, (2) fynomers, which are small binding  proteins derived from the human Fyn SH3 domain, (3) affimers, which are binding proteins derived from the cysteine protein inhibitor family of cystatins, and (4) DARPins (designed ankyrin repeat proteins) , which are genetically engineered proteins with structures derived from the natural ankyrin proteins and consist of 3, 4, or 5 repeat motifs of these proteins. These antibody-mimetics have molecular weights of about 10K to 20K daltons.
Cytokines, growth factors, peptide hormone or their natural fragments or synthetic analogues may also be used as targeting or effector elements. Small molecule drugs, such as cytotoxic drugs (such as auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin) and immunostimulatory drugs (e.g. motolimod, imiquimod, resiquimod, and gardiquimod) may also be linked as effector elements and carried to diseased target cells or tissues. CpG oligonucleotides, lipopolysaccharides derived from certain Gram-negative bacteria and glucans (such as zymosan and β-D-glucan) derived from fungi of especially Aspergillus and Agaricus species have strong immunostimulatory activities and can also be employed as effector elements. Most of those immunostimulatory substances bind to toll-like receptors on various immunocytes and hence activate the immune system.
In some embodiments of the present disclosure, at least one of the targeting element and the effector element of the present molecular construct is the antibody fragment specific for the cell surface antigen. Specifically, when the targeting element is the antibody fragment specific for the cell surface antigen, the present construct is capable of specifically targeting to the cell/tissue/organ with the cell surface antigen expressed thereon. As for the cell surface antigen-specific antibody that employed as the effector element of the present construct, it may either activate or inhibit the signaling transduction pathway via binding with the cell surface antigen, and accordingly, regulate the growth/survival/function of the cell/tissue/organ with the cell surface antigen expressed thereon. According to the embodiments, the cell surface antigen may be selected from the group consisting of, receptor activator of nuclear factor κB (RANKL) , CD3, CD4, CD5, CD7, CD8, CD10, CD11 c, CD13, CD14, CD15, CD16a, CD19, CD20, CD22, CD23, CD25, CD27, CD28, CD30, CD33, CD34, CD36, CD37, CD38, CD41, CD43, CD52, CD56, CD61, CD64, CD65, CD74, CD78, CD79a, CD79b, CD80, CD86, CD134, CD137, CD138, CD319, cytotoxic T-lymphocyte-associated protein 4 (CTLA-4, or CD152) , programmed cell death 1 (PD-1, or CD279) , and programmed cell death 1 ligand 1 (PD-L1, or CD274) . According to one  working example, the present molecular construct is useful in treating diffused tumors, in which the targeting element is an antibody fragment specific for CD19, CD20, CD38 or CD138； and the effector element is an antibody fragment specific for CD3 or CD16a. According to another working example, the present molecular construct is useful in treating solid tumors, in which the effector element is an antibody fragment specific for PD1. According to still another working example, the present molecular construct is useful in treating diffused tumors, in which the targeting element is an antibody fragment specific for CD79a； and the effector element is an antibody fragment specific for CD79b. According to still another working example, the present molecular construct is useful in treating diffused tumors, and the targeting element is an antibody fragment specific for CD79b； and the effector element is an antibody fragment specific for CD79a.
In some embodiments of the present disclosure, the targeting element of the present molecular construct is the antibody fragment specific for the tumor-associated antigen, which is selected from the group consisting of human epidermal growth factor receptor (HER1) , human epidermal growth factor receptor 2 (HER2) , human epidermal growth factor receptor 3 (HER3) , human epidermal growth factor receptor (HER4) , carbohydrate antigen 19-9 (CA 19-9) , carbohydrate antigen 125 (CA 125) , mucin 1 (MUC 1) , ganglioside GD2, ganglioside GD3, ganglioside GM2, fucosyl GM1, Neu5GcGM3, melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) , mesothelin, mucine-related Tn, Sialyl Tn, LewisY, Sialyl LewisY, LewisA, Lewisx, heparin-binding epidermal growth factor (HB-EGF) , Globo H, stage-specific embryonic antigen-4 (SSEA-4) , and transferring receptor. According to one working example, the present molecular construct is useful in treating the breast tumor/cancer, in which the targeting element is an antibody fragment specific for HER1 or HER2. According to another working example, the present molecular construct is useful in treating the prostate tumor/cancer, in which the targeting element is an antibody fragment specific for PSMA.
In some embodiments of the present disclosure, the targeting element of the present molecular construct is the antibody fragment specific for the tissue specific extracellular matrix protein, which is osteonectin, α-aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, or collagen XI. According to one working example, the present molecular construct is useful in treating rheumatoid arthritis, in which the  targeting element is an antibody fragment specific for collagen IX. According to another working example, the present molecular construct is useful in treating psoriasis, in which the targeting element is an antibody fragment specific for VII. According to still another working example, the present molecular construct is useful in treating ankylosing spondylitis, in which the targeting element is an antibody fragment specific for α-aggrecan.
In some embodiments of the present disclosure, at least one of the targeting element and the effector element of the present disclosure is the cytokine. In other embodiments of the present disclosure, at least one of the targeting element and the effector element of the present disclosure is the antibody fragment specific for the cytokine. In the embodiments, the cytokine is B cell activating factor (BAFF) , interleukin-1 (IL-1) , IL-2, IL-6, IL-12/IL23, IL-17, interferon-α (IFN-α) , IFN-β, interferon-γ (IFN-γ) , tumor necrosis factor-α (TNF-α) , or transforming growth factor-β (TGF-β) . Specifically, when the targeting element is the cytokine (e.g., TGF-β) , the present molecular construct is capable of specifically targeting to the receptor-expressing cell/tissue/organ (e.g., tumor cell with the TGF-β receptor expressed thereon) . In the case of the cytokine that serves as the effector element of the present molecular construct, it may activate the cytokine-associated signaling transduction pathway via binding with the cytokine receptor, and accordingly, generate the therapeutic effect (e.g., IFN-α as the effector element that binds to IFN-α receptor and produce the pro-inflammatory or anti-tumor effect) . As for the effector element being an antibody fragment specific for the cytokine, it may capture and neutralize the cytokine, and thus, inhibit the cytokine-associated signaling transduction pathway (e.g., the antibody neutralizing IL-6 and inhibit IL-6 associated inflammation) . According to one working example, the present molecular construct is useful in treating autoimmune diseases, in which the effector element is an antibody fragment specific for TNF-α or IL-17. According to another working example, the present molecular construct is useful in treating solid tumors, in which the effector element is IFN-γ or IL-2. According to still another working example, the present molecular construct is useful in treating solid tumors, in which the effector element is a non-neutralizing antibody fragment specific for IFN-α or IL-2. According to further another working example, the present molecular construct is useful in treating autoimmune diseases, in which the effector element is an antibody fragment specific for BAFF.
According to some embodiments of the present disclosure, the soluble receptor is specific for TNF-α or IL-1. In the embodiments, the soluble receptor is used to capture and neutralize the cytokine without triggering the associated signaling transduction pathway.
In some embodiments of the present disclosure, the targeting element of the present molecular construct is the growth factor. In other embodiments of the present disclosure, at least one of the targeting element and the effector element of the present disclosure is the antibody fragment specific for the growth factor. In the embodiments, the growth factor is selected from the group consisting of epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , vascular endothelial growth factor A (VEGF-A) , basic fibroblast growth factor (bFGF) , and hepatocyte growth factor (HGF) . With similar concept as described above, when the targeting element is the growth factor (e.g., EGF) , the present molecular construct is capable of specifically targeting to the receptor-expressing cell/tissue/organ (e.g., tumor cell with the EGF receptor expressed thereon) . In the case of the effector element being an antibody fragment specific for the growth factor (e.g., VEGF-A) , it may capture and neutralize the growth factor-associated signaling transduction pathway (e.g., VEGF-A-induced angiogenesis) . According to one working example, the present molecular construct is useful in treating solid tumors, in which the effector element is an antibody fragment specific for VEGF-A.
In some embodiments of the present disclosure, the targeting element of the present molecular construct is the peptide hormone. In other embodiments of the present disclosure, at least one of the targeting element and the effector element of the present molecular construct is the antibody fragment specific for the peptide hormone. In the embodiments, the peptide hormone is selected from the group consisting of secretin, cholecystokinin (CCK) , gastrin, gastrin-releasing polypeptide, glucagon-like polypeptide 1 (GLP-1) , neuromedin, adrenocorticotropic hormone (ACTH) , thyroid-stimulating hormone (TSH) , gonadotropin-releasing hormone (GnRH) , and somatostatin. According to one working example, the present molecular construct is useful in treating solid tumors, in which the targeting element is CCK or somatostatin.
In some embodiments of the present disclosure, the effector element of the present molecular construct is the antibody fragment specific for the hapten, which is selected from  the group consisting of dinitrophenol (DNP) , trinitrophenol (TNP) , dansyl, penicillin, p-aminobenzoic acid, and a short peptide having an amino acid sequence of SEQ ID NO: 20. Specifically, when the effector element is the antibody fragment specific for the hapten, it may be used with an immunoregulatory effector that is tagged with the same hapten.
In some embodiments of the present disclosure, the effector element of the present molecular construct is the immunomodulant. According to the embodiments, the immunomodulant is a toll-like receptor agonist. In the embodiments, the toll-like receptor agonist is selected from the group consisting of lipoteichoic acid, glucan, motolimod, imiquimod, resiquimod, gardiquimod, CpG oligodeoxynucleotide (CpG DON) , lipopolysaccharide (LPS) , monophosphoryl lipid A, and zymosan. According to one working example, the present molecular construct is useful in treating solid tumors, in which the effector element is LPS or imiquimod.
In some embodiments of the present disclosure, the effector element of the present molecular construct is the cytotoxic drug, which is selected from the group consisting of auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin.
According to some embodiments of the present disclosure, the radioactive nuclide is 111In, 131I, or 177Lu. According to other embodiments of the present disclosure, the chelator is selected from the group consisting of 1,4, 7, 10-tetraazacyclododecane-1, 4, 7, 10-tetraacetic acid (DOTA) , 1,4, 7-triazacyclononane-1, 4, 7-triacetic acid (NOTA) , 1, 4, 7-triazacyclononane-1, 4-diacetic acid (NODA) , and diethylenetriaminepentaacetic acid (DTPA) . In one working example, the radioactive nuclide is 90Y or 111In, and the chelator is DOTA. In another working example, the radioactive nuclide is 111In, and the chelator is NOTA. In still another working example, the radioactive nuclide is 111In, and the chelator is NODA. In further another working example, the radioactive nuclide is 90Y, 111In, or 177Lu, and the chelator is DTPA.
In may molecular constructs of this invention, the preferred targeting or effector elements are Fab, Fv, single-chain Fv (scFv) , single-domain antibody (sdAb) , or other antigen-binding fragments of antibodies. For the scFv, a linker with a sequence of (GGGGS) 2-5 is placed between VL and VH, or between VH and VL. Other sequences of flexible nature and without a rigid secondary structure, such as the linking sequences  between CH1 and CH2 domains and CH2 and CH3 domains of some human immunoglobulin isotypes, may also be used. A linker of (GGGGS) 1-3 and a terminal cysteine residue is configured at the C-terminal of the scFv or other antibody fragment, or a growth factor, hormone, or cytokine. The sulfhydryl group is for conjugating with a maleimide group at the end of the linking arms extending from a linker unit.
The antibody drug conjugate (ADC) approach, which has been pursued very actively in recent years, has an underlined rationale of bringing a payload of a cytotoxic drug to the target cells. However, in a typical ADC approach using reduced sulfhydryl groups of inter-chain disulfide bonds, in particular those in the hinge region of antibody molecules, the drug/antibody ratios (DAR) are usually variable and exhibit a distribution of 1-8 among the drug-conjugated antibody molecules. It is also known that for a typical ADC, an average DAR above 4 or 5 may cause instability and hence aggregation or precipitation problems on the antibody molecules. In a typical ADC construct, the targeting part is limited to two Fab or Fv antigen-binding fragments. In the present invention, the targeting element can accommodate growth factors, cytokines, hormones, in addition to various antibody fragments, and the effector element can accommodate a broad array of effector elements, including small molecular drugs, such as cytotoxic drugs, toll-like receptor agonists, chelators for radioactive nuclides, and proteins, such as scFv for various immune factors, cells, and/or cytokines. In the molecular construct of the present invention, the specificity of targeting is enhanced by adjusting the number of a particular targeting element and/or including two different sets of targeting elements.
The linker unit comprising cytotoxic drug payload can be prepared separately and then conjugating with different IgG antibodies for the preparation of antibody-drug conjugates. In one set of preferred embodiments, a linker unit with any of the followings: 3 or more cytotoxic drugs, 2 or more toll-like receptor agonists (e.g., LPS molecules) , 2 or more chelators for radioactive nuclides (which is also referred to as bundles of cytotoxic drugs, LPS molecules, or chelators) , can be conjugated to each of the two C-termini of CH3 domains of IgG molecules specific for certain target antigens. These bundles of cytotoxic drugs, LPS molecules, and chelators may be supplied to academic and industrial laboratories producing antibody drug conjugates for laboratory tests, clinical trials, or commercial distribution.
According to the embodiments of the present disclosure, there is ample flexibility in the numbers of targeting elements and effector elements that can be installed, allowing higher targeting specificity and effector activity. The linker units for a targeting element and for an effector element can be prepared separately before joining. In preparing ADCs, the bundles of cytotoxic drugs, LPS molecules, chelators for radioactive nuclides, or other small molecules can be prepared separately without exposing the antibodies to harsh chemical conditions. In using this approach, the drug to antibody ratios (DAR) can be better controlled than if the drugs are conjugated directly onto antibody molecules. The adoption of the joint-linker platform can accommodate the preparation of various targeting/effector pharmaceutical molecules. Another advantage is that IgG. Fc is not contained in the molecular constructs and can minimize potential Fc-mediated effects, such as complement-mediated activation, when such effects are not desired.
PART IV Uses of Molecular Constructs with Targeting and Effector Moieties
Many of those immunotherapeutic antibodies for treating tumors and the anti-inflammatory antibodies for treating autoimmune diseases are acting on the immune system. While the anticipated pharmacologic effect is to activate the immune system or suppress immune activities at the targeted tumor sites or diseased sites, the effect of the administered antibodies causes immunological enhancing or suppressing effects systemically, which results in a wide range of side effects. Therefore, an overriding principle of this invention is to carry the therapeutic effectors to the disease sites (e.g., a tumor, an inflammation site and the like) while minimizing an overall systemic immune-enhancing or immunosuppressing effect.
The present molecular construct, as discussed in Part III, above, possesses both the targeting and effector elements； hence, drug molecules carried by the effector element are directed to the intended target site by the targeting element. Accordingly, target treatment of any disease, condition, and/or disorder may be achieved by proper selection of the targeting and effector elements. Accordingly, another aspect of the present invention is directed to uses of the present molecular constructs (including those with the joint-linker configuration and the Fc-based ones) in the treatment of various diseases, conditions, and/or disorders. Suitable diseases, conditions and/or disorders that may be treated by  the present methods include autoimmune diseases (rheumatoid arthritis, psoriasis, SLE, 
Figure PCTCN2016071184-appb-000024
syndrome, and Crohn’s disease) , osteoporosis, diffusive tumors (various types of lymphomas and leukemia) , solid tumors, and dry and wet age-related macular degeneration. Specifically, each of these methods comprises administering to the subject or patient a therapeutically effective amount of the molecular construct according to any of the above-mentioned aspect/embodiments.
The targeting elements involved in constructing the targeting/effector pharmaceuticals for treating the above diseases include scFv specific for (1) collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, collagen XI, α-aggrecan, osteonectin, and some other components of extracellular matrix in joints, skin, or bone, (2) CD19, CD20, CD22, CD30, CD52, CD79a, CD79b； CD38, CD56, CD74, CD78, CD138； or CD319, CD5, CD4, CD7, CD8, CD30； or CD13, CD14, CD15, CD33, CD34, CD36, CD37, CD41, CD61, CD64, CD65, CD11 c and other surface antigens of cells of lymphoid and myeloid lineages and of plasma cells, (3) EGFR, HER2/Neu, HER3, TN, Globo H, GD-2, CA125, CA19-9, and CEA overly expressed on solid tumors. The targeting elements may also be antibodies of hormones, growth factors, or cytokines, in which receptors of hormones, growth factors, or cytokines are expressed on tumor cells or other diseased cells. Noted that many autoimmune diseases are diseases of the connective tissues, and hence various collagen types can serve as target antigens for shuffling targeting/effector pharmaceuticals to the targeted connective tissues.
The selections of effector elements for the T-E pharmaceuticals of this invention covers a broad range of molecules, including (1) scFv specific for inflammatory cytokines (such as TNF-α, IL-12/IL-23, IL-17, IL-1, IL-6, BAFF) , (2) scFv specific for RANKL, (3) scFv for CD3, and CD16a, expressed on T cells and NK cells, (4) scFv specific for PD-1, PD-L1, CTLA-4 and other immune checkpoints, (5) immunoenhancing cytokines (IFN-α, IFN-γ, IL-2, TNF-α) , (6) cytotoxic molecules, (7) TLR agonists (LPS, motolimod, imiquimod, resiquimod, gardiquimod, CpG oligonucleotides, β-glucan, zymosan) , and (9) chelating agents for radioactive nuclides.
This invention rationalizes that the requirement for the strength of binding of targeting element to the targeted molecules is not uniformly same. For targeting a tumor-associated  antigen on the surface of targeted tumor cells, e.g., with scFv specific for CD19, CD38, HER2/Neu, EGFR, CA125, it is generally desirable that the binding avidity of the targeting element to the targeted tumor-associated antigen is high. In such way, the specific binding to the targeted cells, in relative to other cells not expressing the antigens, will be enhanced. Furthermore, when the binding affinity and avidity is high, the targeting/effector pharmaceuticals can still bind to those target cells expressing relatively low densities of the targeted antigens. As a result, the payloads of effector elements, such as a payload of cytotoxic drugs, or immune-enhancing effector elements, have enhanced chances to exhibit their effector functions.
For shuffling anti-inflammatory agents, such as anti-TNF-α, anti-IL-17, anti-IL12/IL23, and anti-BAFF to the diseased joints, skin, or bowl, it is not necessary that the targeting element binds to the targeted antigens in the extracellular matrix in the diseased sites, e.g., scFv specific for collagen II, collagen IX, collagen VII, collagen I, or osteonectin, too tightly. It is possible that if the binding is too strong, it will elicit unwanted immune functions or affect the integrity of the extracellular matrix. It is anticipated that the abundance of the extracellular protein can sequester the therapeutic molecules with the targeting moieties； even the avidity of the targeting moieties in binding their targeted molecules is not high. An equilibrium state of the on-and-off binding of the targeting element of the T-E pharmaceutical will bring about a raised local concentration of the T-E pharmaceuticals.
This invention rationalizes that for the targeting with scFv specific for collagen II, collagen I, collagen VII, collagen IX, or osteonectin, the avidity is not too high. In preferred embodiments, if the targeting IgG antibody has an affinity constant, Kd<1x10-9, in binding to the target antigen, only one scFv is incorporated to the pharmaceutical, and for two scFvs to be employed in the pharmaceutical, the affinity of the targeting IgG antibody binding to the target antigen should be lower, 1x10-8>Kd>1x10-9. To achieve increased specificity in targeting anti-TNF-α to the joints, anti-IL17 or anti-BAFF to the skin, two targeting elements each with a different binding antigen can be adopted. This will enhance the binding to the aimed target tissue over normal tissues or cells, which express one of the two target antigens.
IV- (i) Immune disorder
The molecular constructs used for treating autoimmune diseases are designed based on the rationale that if antibodies specific for pro-inflammatory cytokines are carried to the diseased tissues affected by those pro-inflammatory cytokines, the therapeutic efficacy will be enhanced and the side effects decreased. Cytokines, unlike hormones, generally do not circulate in the blood stream and act on remote target cells. Cells of the lymph nodes emigrate via the efferent lymph vessel and enter the lymphatic circulation. The products of lymphocytes do not get out the lymph nodes moving upstream against the blood flow coming into the nodes. In fact, administered antibodies can enter lymph nodes via the blood circulation. However, most of the cytokine molecules do not get out of the lymph nodes via blood circulation. The cytokines secreted by the local lymph nodes act on cells in the microenvironment of the lymph nodes. Therefore, if antibodies targeting pro-inflammatory cytokines are channeled to some degrees to the diseased inflammatory tissues, less of the antibodies will go to the lymph nodes, and hence side effects will be decreased, and more of the antibodies will go to the diseased tissue and therapeutic efficacy can be enhanced.
Using antibody against TNF-α for example, in applying such molecular constructs or pharmaceuticals comprising the same, using the molecular construct with scFv specific for collagen II as the targeting element and scFv specific for TNF-α as the effector element, an amount of the present molecular construct carrying excess amount of effector element (i.e., scFv specific for TNF-α with an amount that exceeds the total amount of TNF-α in the blood circulation) is administered. While a small amount of the therapeutic agent is neutralized by TNF-α in the blood, the remaining amount will be favorably localized to the tissues (including joints) where collagen II is abundant. Like many cytokines (also referred as interleukins or lymphokines) , TNF-α acts mainly in the microenvironment of the immune system. It has a very short half-life, about 1 hour and there is a minute amount of it in the blood circulation. The administered anti-TNF-α of this invention will not be mainly present in lymphoid system and neutralize the TNF-α in the lymphoid system. Therefore, the side effects of anti-TNF-α in causing serious infections should be decreased.
In one embodiment, the present method is useful in treating autoimmunity, in which the first targeting element is an scFv specific for α-aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, and collagen XI； and the first effector element is a an  scFv specific for TNF-α, IL-17, IL-1, IL-6, IL-12/IL-23, BAFF, the receptor of IL-6 (IL-6R) , or the receptor of IL-17 (IL-17R) ； or the soluble receptor of TNF-α or IL-1.
IV- (i) -A Psoriasis
A preferred set of the present inventions is to construct molecular constructs with scFv specific for type I collagen and type VII collagen as the targeting elements and scFv specific for TNF-α, IL-12/IL-23, or IL-17 as the effector elements. In one embodiment of the present disclosure, the various T-E molecules based on the “joint-linker” configuration contain scFv specific for collagen I and/or collagen VII as the targeting elements and scFv specific for IL-17 as the effector elements.
In one preferred embodiment, the present method is employed to treat psoriasis, in which the first targeting element is an scFv specific for collagen I, or collagen VII； and the first effector element is an scFv specific for TNF-α, IL-12/IL-23, IL-17, or IL-17R.
IV- (i) -B SLE, Cutaneous Lupus, or Sjogren’s Syndrome
In the present invention, scFv of antibodies specific for BAFF or IFN-α are to be carried to the skin by targeting elements, scFv specific for collagen I and collagen VII. In one embodiment of the present disclosure, the various T-E molecules based on the “joint-linker” configuration contain scFv specific for collagen I and/or collagen VII as the targeting elements and scFv specific for BAFF as the effector elements.
In another preferred embodiment, the present method is suitable for the treatment of SLE, cutaneous lupus, or Sjogren’s syndrome, in which the first targeting element is an scFv specific for collagen I or collagen VII； and the first effector element is an scFv specific for BAFF.
IV- (i) -C Rheumatoid Arthritis, Psoriatic Arthritis, or Ankylosing Spondylitis
In still another preferred embodiment, the disease treated by the present method is rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis, in which the first targeting element is an scFv specific for collagen II, collagen IX, collagen XI, or α-aggrecan； and the  first effector element is an scFv specific for TNF-α, IL-1, IL-6, IL-12/IL-23, or IL-17； or IL-6R or IL-17R.
IV- (i) -D Inflammatory Bowel Disease
It has been found that the collagen types I, III and V are abundant in the intestine and colon. It is rationalized that since collagen I is widely distributed in various tissues, it is preferable to use scFv specific for collagen III or collagen V as the targeting elements to carry scFv specific for TNF-α to the intestine and colon in patients with Crohn’s disease or ulcerative colitis. In one embodiment of the present disclosure, the various T-E molecules based on the “joint-linker” configuration contain scFv specific for collagen III and/or collagen V as the targeting elements and scFv specific for TNF-α as the effector elements.
In further another preferred embodiment, the present method may be used to treat inflammatory bowel disease, in which the first targeting element is an scFv specific for collagen III or collagen V； and the first effector element is an scFv specific for TNF-α. According to the embodiment, the inflammatory bowel disease is Crohn’s disease or ulcerative colitis.
IV- (ii) Tumor
The present invention rationalizes that a preferred drug targeting approach has two folds of considerations. One is to increase the avidity and specificity of the targeting agents, so that target cells expressing relatively low antigen densities are still bound by the targeting agents. Secondly, the therapeutic agents are brought to diseased tumor tissue, without requiring that the therapeutic agents be internalized into the cells that express a particular tumor-associated antigen. Examples of such therapeutic agents are scFv, which recruit T cells and NK cells for mediating cytolytic effects on the targeted cells. Another set of examples of such therapeutic agents are toll-like receptor agonists, such as LPS molecules, and scFv specific for immune checkpoints, such as scFv specific for PD-1, PD-L1, and CTLA-4, which elicit immune response in the local sites. Still another set of examples is bundles of chelating agents for radioactive nuclides. With many of those therapeutic agents, cytolytic effects on the diseased cells and bystander cells can be elicited in the tissue sites regardless of the levels of tumor-associated antigen expressed by the  tumor cells.
The present invention thus embodies a number of remedies to increase the relative localization of therapeutic agents in the targeted site. Such a rationalization about specific delivery of therapeutic agents to diseased sites is not limited to therapeutic agents targeting cancer but also therapeutic agents targeting tissues affected by other diseases. The target-specific delivery needs not to be absolute. In another word, it is not necessary that all administered drug molecules be delivered to the intended diseased site. As long as the delivery to the diseased target is enhanced, as compared to the same drugs without a targeting element, the therapeutic effects of the drug should be increased and the side effects decreased.
IV- (ii) -ADiffused Tumor
A preferred set of embodiments of T-E pharmaceuticals of the present invention is the employment of cytotoxic drug bundles in the joint-linker configuration. The potent cytotoxic drugs include auristatin, maytansine, doxorubicin, calicheamicin, camptothecin, and others. A preferred embodiment is that 5-10 cytotoxic molecules are carried in a linker unit. For comparison, a typical IgG antibody drug conjugates currently approved or under clinical development carry two Fab fragments for targeting and 3 or 4 molecules on the average of a cytotoxic drug for rendering lysis of the target cells. In a molecular construct of this invention, it contains 3-5 scFv specific for a target antigen as the targeting element and 5-10 cytotoxic molecules as the effector element. Both the targeting specificity and pharmacological effects can be much enhanced in comparison with the typical antibody drug conjugate approach. Furthermore, two sets of scFv for two different antigens on target cells can be employed as the targeting elements, enhancing the specificity of targeting and the uptake or internalization of the bound antibody drug conjugates by the targeted cells. In the molecular constructs of this invention, the cytotoxic molecules are conjugated through a PEG or peptide linking arms to increase solubility. The linker unit with the cytotoxic drug payload is prepared separately before the coupling with the linker unit conjugated with the targeting elements. In such an approach, the solubility of the linker unit and the entire molecular constructs should not pose a problem.
The molecular constructs described in this section bear a larger binding avidity in binding to the surface antigen of targeted cells but also a larger toxic drug payload than typical antibody drug conjugates that have been approved for clinical uses or are in clinical trials. The inclusion of bundles of cytotoxic drug payload essentially amplifies the potency of the molecular constructs and therefore can increase the specificity of the targeting therapeutic agents. It is anticipated that those therapeutic agents can be administered at a lower dose and can achieve an enhanced therapeutic efficacy and reduced toxicity in treating diffusive and solid tumors. This approach is not only suitable for different types of lymphoma and leukemia derived from B cells, T cells, and other leukocytes but also applicable for tumors that bear cell surface molecules for antibody targeting, such as tumors bearing an antigen belonging to the human epidermal growth factor receptor (EGFR) family, which are often overexpressed on many tumors.
The scFv fragments of anti-CD3 antibodies may also be conjugated to linker units as effector elements for those T-E molecules designed to target tumorous cells. The incorporation of scFv specific for CD3 helps the recruitment of T cells and the attachment of tumor target cells with cytotoxic T cells. The binding by scFv of anti-CD3 induces the activation of T cells, which results in the lysis of the contacted or bridged target cells. There are numerous examples, where the bi-specific antibodies combining anti-CD3 with antibody fragments specific for antigens, such as CD20, CD30, and EGFR, can efficiently lyse target cells expressing those antigens.
The above description has specified a number of effector mechanisms that can be employed in molecular constructs that enlist targeting functions. Those effector mechanisms include cytotoxic drug payloads and scFv specific for CD3 or CD16a. The assortment of effectors for B cell-derived tumors, T cell-derived tumors, and some other types of leukemia, some of which are in diffusive forms, is different from that for solid tumors. For example, immune-enhancing agents, such as LPS, can be incorporated as the effector element in a molecular construct for targeting solid tumors. The potent immune enhancing IgG and anti-CD28 may be applied and recruited to local tumor sites for stimulating immune activities. Those potent immune enhancers are not applicable as therapeutic effectors for treating various types of leukemia and diffusive tumors.
For achieving the effect of apoptosis, a binding agent must be able to cross-link and cluster the targeted cell surface molecule, such as B-cell receptors or CD20, effectively. We rationalize that the cross-linking of the surface molecules should achieve a “centrally-focused” cluster of cross-linked molecules, rather than a large number of small aggregates on the targeted cell surface. We further rationalize that a number of factors will affect a binding agent in achieving its apoptotic effect. The multiple valence of a binding agent can enhance the cross-linking ability. However, if the binding arms are too many, it will increase the size of the binding agent and affect its ability to penetrate into tissues. The binding agent should effectively bind to the targeted cell surface on a planar surface of a cell. Therefore, the binding arms, such as PEG-scFv, have a certain degree of flexibility and can reach to the targeted antigenic sites without steric constraints. On the other hand, if the binding arms are too long, the cross-linking and clustering effects may not be optimal, or the binding arms reach to cell surface molecules on an adjacent cell. We also rationalize that if sufficient linking arms are in a multi-arm linker, the Fab or scFv fragments can provide more flexibility than whole IgG or F (ab’ ) 2.
The preferred embodiments in this invention have adopted the above rationales. While our invented methodologies are applicable for antibodies specific for various antigens on various types of cells, our examples employ antibodies specific for the B cells and for the antigens on those cells, namely, CD20, CD79a/CD79b (also known as Igα/β) , and immunoglobulin isotype-specific antigenic epitopes, referred to as migis-α and migis-β, which are represented by the exterior segments of the membrane-anchor peptides extending from the C-termini of the membrane-bound immunoglobulin chains of α and δ.
CD20 is a transmembrane protein that has provided as a therapeutic target for the treatment of B cell malignancies. CD20 is expressed by over 95％of B lymphocytes throughout their differentiation and maturation pathway, from the pre-B cell stage to the terminally differentiated plasma cells, but is absent on the hematopoietic stem cells. CD20 is believed to exist predominantly as a tetramer on the cell surface. Until now, the most widely used B cell-targeting antibody drug is rituximab, which is a chimeric IgG1 monoclonal antibody directed against CD20. Accumulating data indicate that rituximab is effective only for about 50％of the patients with B cell lymphoma. Anti-CD20 antibodies, which are  approved for clinical uses or in human clinical trials, include chimeric ”C2B8” monoclonal antibody (rituximab) , monoclonal antibody 1F5, and chimeric 2H7 antibody.
Antibodies specific for other B cell surface antigens, such as CD19 and CD22, generally do not cause lytic effects on B cell-derived tumor cells. We rationalize that it will be effective to employ scFv specific for a B cell surface antigen, such as CD19, in combination with scFv specific for CD20, to increase the binding specificity and avidity and to result in cell lysis of the targeted cells. In such an application, scFv specific for CD20 can be considered as a targeting element and an effector element. A large number of CD markers on B cells probably can be combined with CD20 under such a rationale, as long as there is some level of CD20 present on the intended target B tumors. In one embodiment of the present disclosure, the various T-E molecules based on the “joint-linker” configuration contain scFv specific for CD20 and CD19 as the targeting elements and scFv specific for CD3 or CD16a, and bundles of cytotoxic drugs as the effector elements.
While there are considerable heterogeneities among multiple myeloma in terms of surface antigen expression, a systematic profiling of the surface markers for individual patients can provide targeting strategies. In recent years, a number of antibody drug conjugates or bispecific antibodies targeting a few CD markers, such as CD38, CD138, CD78, and CD319, and other surface antigens are under development. We rationalize that if the avidity of the targeting antibodies and the effector mechanisms can be enhanced, the treatments can be much more specific and effective. The preferred embodiments of this invention in the treatment of multiple myeloma are molecular constructs employing 3 or more scFv of one or two antibodies specific for CD38, CD78, CD138, or CD319 as the targeting element and a drug payload with 5-10 cytotoxic drug molecules as the effector element. Other effector elements, such as scFv specific for CD3 or CD16a may also be employed. In one embodiment of the present disclosure, the various T-E molecules based on the “joint-linker” configuration contain scFv specific for CD38 and CD138 as the targeting elements and scFv specific for CD3 or CD16a, and bundles of cytotoxic drugs as the effector elements.
In order that a targeted protein on a cell surface can be effectively cross-linked to form a large cluster, the protein must possess two or more antigenic sites for the binding agent to  bind (without the help of a secondary cross-linking agent) . For example, because each Igα/Igβ-BCR complex has only one copy of Igα and one copy of Igβ, a binding agent with even multiple copies of Fab or scFv specific for Igα or Igβ cannot induce productive cross-linking of Igα/Igβ-BCR to form a cluster. In another word, a 4-arm multi-arm linker with 4 Fabs (or scFv) specific for Igα will at best form many small units of 4 BCRs, but cannot form larger cross-linked complexes. Therefore, for cross-linking Igα/Igβ-BCR, a 4-6-arm multi-arm linker should have 2-three scFvs specific for Igα conjugated onto one linker unit and 2-three scFvs specific for Igβ conjugated onto the other linker unit. Alternatively, a 4-arm linker with scFv specific for Igα and a 4-arm linker with scFv specific for Igβ are administered in combination to a patient.
According to some embodiments of the present disclosure T-E molecules, which resemble those designed for treating B-cell derived tumors are designed. For those constructs, scFv specific for CD markers of T cells are employed as targeting elements and the effector elements are the same as those for targeting B cell tumors. This invention also pertains to the development of molecular constructs based on fragments of anti-CD3 antibodies for causing T cell anergy or dysfunction partially without inducing T cell activation and cytokine storm. Such constructs can then be used for treating T cell-mediated autoimmune diseases, including type-I diabetes, SLE, multiple sclerosis, inflammatory bowel diseases, etc. As will be discussed in later sections, in molecular constructs with various scFv specific for tumor-associated antigens as the targeting element, scFv specific for CD3 can also be used as the effector element for recruiting T cells for the elimination of the targeted tumor cells.
According to some embodiments of the present disclosure T-E molecules, which resemble those designed for treating B-cell derived tumors are designed. For those constructs, scFv specific for CD markers of myeloid lineage cells are employed as targeting elements and the effector elements are the same as those for targeting B cell tumors.
According to other embodiments of the present disclosure, the disease treatable with the present method is a tumor, including a diffused tumor or a solid tumor. In these embodiments, the diffused tumor can be acute lymphocytic leukemia (ALL) , chronic  lymphocytic leukemia (CLL) , acute myelogenous leukemia (AML) , chronic myelogenous leukemia (CML) , Hodgkin lymphoma, non-Hodgkin lymphoma, or myeloma.
In one embodiment of the present disclosure, the present method is useful in treating the diffused tumor, in which the first targeting element is an scFv specific for CD4, CD5, CD7, CD8, CD10, CD11c, CD13, CD14, CD15, CD19, CD20, CD22, CD23, CD30, CD33, CD34, CD36, CD37, CD38, CD41, CD43, CD56, CD61, CD64, CD65, CD74, CD78, CD79a, CD79b, CD80, CD138, or CD319； and the first effector element is a cytotoxic drug, or an scFv specific for CD3 or CD16a. in another embodiment of the present disclosure, one of the first targeting element and the first effector element is an scFv specific for CD79a； and the other of the first targeting element and the first effector element is an scFv specific for CD79b. Optionally, the cytotoxic drug is selected from the group consisting of auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin.
In one preferred embodiment, the present method is employed to treat B-lymphocyte-derived lymphoma or leukemia, in which the first targeting element is an scFv specific for CD5, CD19, CD20, CD22, CD23, CD30, CD37, CD79a, or CD79b； and the first effector element is the cytotoxic drug, or an scFv specific for CD3 or CD16a.
In another preferred embodiment, the present method is employed in the treatment of B-lymphocyte-derived lymphoma or leukemia, in which one of the first targeting element and the first effector element is an scFv specific for CD79a； and the other of the first targeting element and the first effector element is an scFv specific for CD79b.
In still another preferred embodiment, the disease treated by the present method is plasmacytoma or multiple myeloma, in which the first targeting element is an scFv specific for CD38, CD78, CD138, or CD319； and the first effector element is a cytotoxic drug, or an scFv specific for CD3 or CD16a.
In further another preferred embodiment, the present method possesses an effect on T-cell derived lymphoma or leukemia, in which the first targeting element is an scFv specific for CD5, CD30, or CD43； and the first effector element is a cytotoxic drug, or an scFv specific for CD3 or CD16a.
In one preferred embodiment, the present method is used to treat myelogenous leukemia, in which the first targeting element is an scFv specific for CD33 or CD34； and the first effector element is a cytotoxic drug, or an scFv specific for CD3 or CD16a.
IV- (ii) -B Solid Tumor
The present invention pertains to multi-arm linkers conjugated with antibody fragments specific for the tumor-associated antigens listed above. Many antibodies specific for tumor-associated antigens, such as anti-HER2/NEU (trastuzumab) , anti-CA19-9 (derived from clone 1116-NS-19-9) , anti-CA125 (derived from clone OC125) , anti-GD2 (ch14.18 monoclonal antibody) , and anti-Globo H (clone VK9) are readily available for application. The present invention pertains to the employment of scFv or bi-scFv of antibodies specific for those tumor-associated antigens in conjunction with multi-arm linkers for carrying therapeutic agents to tumor sites.
In some embodiments of the present invention, T-E molecules in the “joint-linker” configurations are designed to conjugate multiple copies of a ligand, a growth factor, cytokine or hormone, and one or more copies of a therapeutic agent to the tumor site, where the diseased cells express the receptors to which the ligand binds. Such a drug delivery approach will enhance specificity and hence will enable higher therapeutic effects and lower side effects than simply applying the therapeutic agents.
Ligands suitable for such an approach include epidermal growth factor (EGF) and its mutants, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , vascular endothelial growth factor A (VEGF-A) , basic fibroblast growth factors (FGF) , hepatocyte growth factors (HGF) , gastrin, CCK, secretin, gastrin-releasing peptide, glucagon-like peptide 1 (GLP-1) , neuromedin, thyroid-stimulating hormone (TSH, or thyrotropin) , adrenocorticotropic hormone (ACTH) , gonadotropin-releasing hormone (GnRH) and somatostatin.
There are at least four types of VEGF’s (VEGF-A, VEGF-B, VEGF-C and VEGF-D) . Among them, VEGF-A is involved in the angiogenesis of endothelial cells of blood vessels. VEGF-A can bind to both VEGF receptors 1 and 2 (VEGFR1 and VEGFR2) . It has been found that when the Ser2-Asp3 of EGF at the N-terminal is mutated to Trp2-Val3 or  Trp2-Arg3, the mutated EGF can bind to not only HER1, but also HER2 and HER3 (Stortelers C. et al., Biochemistry 41: 8732-8741, 2002) . Thus, the targeting with EGF (W2V3) , EGF (W2R3) , or VEGF-A can reach broader scope of tumor target cells than antibodies specific for the EGF or VEGF-A receptors.
The sizes of most of those peptides or proteins are relatively small: EGF, 53 a.a., somatostatin, 14 and 28 a.a., secretin, 27 a.a., gastrin, 14-34 a.a., CCK, 8-58 a.a., gastrin-releasing peptide, 27a.a., GLP-1, 37 a.a., the receptor-binding β chain of thyroid stimulating hormone, 118 a.a., neuromedin, 10 a.a., ACTH, 39 a.a., and GnRH, 10 a.a. VEGF-A is a dimer with two peptides of 120-188 a.a. in length. In the radioimaging studies, truncated segments of the hormones or factors or artificially designed peptides have been shown to retain comparable or even stronger binding to their respective receptors. For example, an octapeptide has been designed for the imaging of tumors expressing somatostatin receptors.
Some products of bacteria, viruses, and other microorganisms can elicit strong immune response. For example, super antigens, such as staphylococcal enterotoxins, can activate a significant portion of T cells by binding to the MHC class II antigen and T cell receptor at the same time. A large variety of microbial products can bind to toll-like receptors (TLRs) and activate a broad range of immune activities.
Three TLR agonists have been approved by FDA for treatment certain cancer and infectious diseases. Bacillus Calmette-Guérin, which activates TLR2 and TLR4, has long been used as a vaccine against tuberculosis. It is now approved for use in immunotherapy of in situ bladder carcinoma. Imiquimod, a small imidazoquinoline originally developed as a topical antiviral agent, which also binds to TLR7, is approved for actinic keratosis, and superficial basal cell carcinoma. Monophosphoryl lipid A, a derivative of lipopolysaccharide (LPS) from Salmonella minnesota, which binds to TLR2 and TLR4, is approved as an adjuvant for a vaccine against papilloma virus, which causes most cases of cervical carcinoma.
Other TLR agonists that have been studied as potential therapeutic immunostimulatory substances include (1) glucans, include β-D-glucans derived from the cell wall of certain fungi, especially Aspergillus and Agaricus species, and zymosan derived from the cell wall  of certain fungi, such as the yeast Saccharomyces cerevisiae, which bind to TLR2 and other receptors of immunocytes, (2) motolimod, a small molecule, which binds to TLR8, (3) imiquimod as explained above, and (4) CpG oligodeoxynucleotides (CpG DON) , short single-stranded synthetic DNA molecules containing a C followed by a G nucleotide, which binds to TLR9. Those TLR binding agents generally activate dendritic cells, macrophages, natural killer cells, neutrophils, and other immune cells of the native immunity and elicit the production of a large array of inflammatory cytokines, which augment the adaptive immunity. The native and the adaptive immunity act in synergy in the removal of the pathologic elements.
LPS derived from Gram-negative bacteria, also referred to as endotoxin or exogenous pyrogen, is a very strong stimulator of the immune system. LPS binds to CD14/TLR4/MD2 receptor complex on monocytes, dendritic cells, and macrophages, elicits strong responses of the innate immune system, and induces production of inflammatory cytokines. In humans, LPS at 1 μg/kg can induce shock and is a powerful immunostimulatory agent. Systemic administration of unmodified LPS can potentially be very risky.
The present invention rationalize if LPS can be tied to a carrier and carried to tumor site, it can elicit in situ powerful local immune response, cause the release of inflammatory cytokines, increase vascular permeability, and recruit various effector cells to the site. This may help lyse the tumor cells in the inflamed tissue. Since cells in a tumor express tumor-associated antigens at varying density, the present approach elicits immune activities to all cells in a tumor site regardless of the cells’ densities of tumor-associated antigens.
This invention rationalizes that the powerful inflammatory activity of the LPS will be largely limited to the targeted tumor site. Accordingly, a preferred embodiment is that three scFvs specific for a tumor-associated antigen are conjugated to one linker unit as the targeting element and 2-3 LPS or monophosphoryl lipid A molecules are conjugated to the other linker unit as the effector element. Additionally, two sets of scFv specific for two tumor-associated antigens may be separately conjugated to two linker units, which are then joined to form the targeting element.
It is demonstrated that LPS can be conjugated to a protein via a linker. The methodology involves the activation of LPS with 1-cyano-4-dimethylaminopyridinium  tetrafluoroborate (CDAP) and the coupling with a primary amino group of a protein. The experiment also shows that LPS is conjugated to the protein preserving 70％of its endotoxic activity. The conjugation of LPS to a linker unit of this invention can be achieved by following a similar procedure. Activation of the hydroxyl groups in the carbohydrate element of LPS can be performed by the treatment with CDAP under a mild condition in an aqueous solution. Subsequently, the CDAP-activated LPS is reacted with a NH2----SH cross linker and then with the maleimide groups of the linking arms of a linker unit.
The present invention rationalizes that if therapeutic agents can be localized more specifically to diseased sites, larger therapeutic windows can be obtained, and more therapeutic effects can be achieved, and fewer side effects will be caused. In the present invention, T-E molecules are designed for carrying scFv specific for immune checkpoints, such as cytotoxic T-lymphocyte-associated protein 4, or CTLA-4 (CD152) , programmed cell death 1, or PD-1 (CD279) , and programmed cell death 1 ligand 1, or PD-L1 (CD274 or B7-H1) , as effector elements for liberating immunological mechanisms to destroy cancerous cells.
The present invention rationalizes that if those cytokines are recruited to tumor sites, they can elicit strong immune activities or inflammatory activities locally, which then leads to the elimination of the tumors. Therefore, the present invention employs the multi-arm linkers for conjugating scFv or bi-scFv specific for immunoregulatory cytokines rather than the immunoregulatory cytokines themselves. The rationale is to use the scFv to recruit the immunoregulatory cytokines, which are already present in the body and circulating in the blood, and to concentrate them in the tumor site. The cytokine-specific scFv used in these molecular constructs do not neutralize the activities of the cytokines. The scFv also do not have very high binding affinity for the cytokines. For those individual scFv fragments, Kd in the range of 1-5 x10-8 is adequate. In this preferred embodiment, each of the scFv can potentially recruit multiple molecules of an immunoregulatory cytokine, rendering increased therapeutic effects.
Some tumors have two overexpressed tumor-associated markers, e.g., CA19-9 and CCK/gastrin receptors on some gastrointestinal and neuroendocrine tumors, or Globo H and HER2/Neu on some breast tumors. The present invention rationalizes that by  employing two guiding mechanisms, each carrying a different effector agent, e.g., one with a cytotoxic drug payload and the other with LPS, the combined therapeutic effects will be stronger and the side effects will be smaller. In a preferred therapeutic modality, the molecular conjugate with LPS, anti-PD-1, anti-PD-L1, anti-CTLA4, anti-TNF-α, anti-IFN-γ, or anti-IFN-α, is applied first, so that an “in-situ” inflammation or immune activation is induced, permitting increased vascular permeability. If the local inflammation or immune activation cannot lead to the complete cytolytic effects on the tumor or diseased cells, a subsequent administration of a molecular construct carrying cytotoxic drug payload can augment the cytolytic effects on the cells bearing the targeted tumor-associated antigen.
The therapeutic effectors that can be carried to the targeted solid tumor site by the targeting components include the following: (1) cytotoxic drugs, which kill the bound cells； (2) anti-CD16a or anti-CD3, which induces ADCC or cytotoxic activities； (3) LPS or other TLR agonists, anti-IL-2, anti-TNF-α, anti-IFN-γ, or anti-IFN-α, which activate immune activities； (4) anti-PD1, anti-PD-L1, anti-CTLA4, or other immune checkpoint inhibitors, which liberate immune checkpoints and depress inhibitory feedback activities. The therapeutic aim of these agents is to cause the lysis of the tumor cells bearing receptors for the ligand.
As examples, various T-E molecules in joint-linker configuration incorporate scFv specific for HER2/Neu alone or in combination with scFv specific for HER1 as targeting elements and a cytotoxic drug, LPS, or scFv specific for CD3, CD16a, PD1, or VEGF-A as effector elements. Various T-E molecules in joint-linker configuration incorporate scFv specific for GD2 alone or in combination with scFv specific for Globo H as targeting elements and a cytotoxic drug, LPS, or scFv specific for CD3, CD16a, PD1, or VEGF-A as effector elements. Various T-E molecules in joint-linker configuration incorporate cholecystokinin (CCK) alone or in combination with somatostatin as targeting elements and a cytotoxic drug, LPS, or scFv specific for CD3, CD16a, PD1, or VEGF-A as effector elements. Several T-E molecules in joint-linker configuration incorporate scFv specific for prostate-specific membrane antigen (PSMA) as the targeting elements and scFv specific, but non-neutralizing for IL-2, TNF-α, IFN-α, or IFN-γ as the effector elements.
In a previous section, the employment of growth factors, peptide hormone, or cytokines as targeting elements in molecular constructs based on multi-arm linker units was  elucidated and the preferred embodiments were described. Those non-immunoglobulin peptides or proteins can also be configured into IgG-like molecular constructs or 2-chain IgG. Fc fusion proteins. Specifically, growth factors, such as EGF or its mutant, epiregulin, HB-EGF, VEGF-A, FGF, HGF, gastrin, CCK, secretin, gastrin-releasing peptide, GLP-1, neuromedin, the β-chain of TSH, ACTH, GnRH, or somatostatin, can be incorporated as targeting elements. Tumors derived from cells expressing receptors of those growth factors or hormones often express those receptors. In one embodiment of the present disclosure, the molecular constructs enlist EGF as a targeting element in IgG. Fc fusion protein configurations. The effector elements include linker units containing cytotoxic molecules or LPS molecules, which are conjugated to the C-terminal peptide linkers. The effectors may also be scFv specific for CD3, CD16a, PD-1, or VEGF-A. Immunoregulatory cytokines, such as IFN-α, TNF-α, IL-2, and IFN-γ, can be incorporated as effector elements. The scFv or immunoregulatory cytokine can be expressed as part of the recombinant peptide chain.
The invention also pertains to a preferred embodiment of T-E molecules that incorporate scFv specific for tumor-associated antigens as targeting elements and scFv specific for haptens as effector elements. Such haptens include dinitrophenol (DNP) , trinitrophenol (TNP) , dansyl group, penicillin, p-aminobenzoic acid, or short peptides derived from proteins of human cells, viruses, or bacteria, for which antibodies are already available. For example, a peptide WADWPGPP of 8 amino acid residues, which is located in the CεmX domain of membrane-bound IgE on human B lymphocytes is unique in sequence in the entire protein database, is not physically accessible by antibodies on the B cell surface. When a T-E molecule of this design is administered to a patient with a tumor expressing the tumor-associated antigen the drug aims to target, the T-E molecule binds to the tumor cells and serves as the base in the tumor site to recruit subsequently administered immunoregulatory antibodies, cytokines, or other proteins, which are tagged with the hapten.
The hapten tagged on the therapeutic molecule can be engineered via a linker, such as 
Figure PCTCN2016071184-appb-000025
at the C-terminal end of antibodies, such as IgG antibodies specific for PD-1, PD-L1, CTLA4, VEGF-A, CD3, CD28, or immunoregulatory cytokines, such as IL-2, TNF-α, INF-α, or INF-γ. The linker and the peptide hapten can be expressed as part  of an integral recombinant protein. Bundles of cytotoxic drug payload based on a linker unit may also be tagged with the hapten through a linking arm and be recruited to the tumor site. This treatment strategy will increase the relative distribution of the therapeutic agents in favor of the tumor site and achieve enhanced therapeutic effects and decreased toxicity and side effects.
IgG specific for CD3 or CD28 are extremely powerful T cell activators. A systemic application of these antibodies can cause massive cytokine storms. However, if the activation of T cells by anti-CD3 or anti-CD28 antibodies can be administered at much reduced quantities and be concentrated to tumor tissues, their induced effects may be very effective in inducing local immune activities and inflammation and recruiting various immunocytes to counter tumor cells. Thus, a preferred embodiment of the present invention is to tag these antibodies with a hapten. The tagged anti-CD3 or CD28 is then administered at very minute quantities.
Certain tumor-associated antigens, such as CA19-9, CA125, and carcinoembryonic antigen (CEA) , are shed from tumor cells and are present in the blood circulation. The detection and measurements of those antigens in serum samples have become routine assays for the preliminary detection of tumors in people undergoing physical health examination. The assays have also been used to monitor the efficacy of therapy and tumor status post treatments. While tumor-associated antigens of other types in serum are not assayed routinely, they are also known to be present in the blood circulation in varying quantities.
The keys in achieving therapeutic purposes for drug-conjugated tumor-targeting pharmaceuticals is that the therapeutic agents are specifically brought to the targeted tumor sites and that minimal quantities of the toxic therapeutic agents are trapped by other molecules and tissues. The present invention also pertains to the clearance of circulating tumor-associated antigens, such as CA19-9, CA125, or CEA, when such tumor-associated antigens are the antigenic targets of the targeting elements of the T-E pharmaceuticals of this invention. The clearance of the tumor-associated antigen in the blood can be performed by passing the patient’s plasma through affinity columns packed with resins conjugated with the antibodies specific for the intended tumor-associated antigens in a  blood dialysis procedure, prior to the application of the pharmaceuticals of this invention specific for the targeted tumor-associated antigens.
There are several potential mechanisms that cause the lysis of a target cell upon the binding of an antibody to a cell surface antigen on the target cell. These mechanisms include apoptosis, antibody-dependent cellular cytotoxicity (ADCC) , and complement-mediated cytolysis (CMC) . The relative importance of these three mechanisms may depend on the targeted antigens and the antibodies binding to the antigens. In the case of targeting Igα or Igβ by antibodies for causing B cell lysis, IgG antibodies specific for Igα or Igβ do not cause effective lysis, suggesting that the antibodies fail to elicit all three lytic mechanisms. The antibodies do not cross-link Igα or Igβ effectively to cause apoptosis, as explained in an earlier section above. They also seem to fail mediate effective ADCC and CMC. A research group is therefore developing a toxin-conjugated anti-Igβ effectively to cause apoptosis. It is also likely that antibodies specific for tumor associated antigens of peptidoglycan or mucin nature cannot induce internalization of the antibodies and their carried cytotoxic drugs.
The present invention also pertains to the new treatment modality of sequential administrations of a PEG-modified binding agent and a drug-conjugated anti-PEG antibody. The PEG-modified binding agents include protein therapeutics that are conjugated with PEG to improve pharmacokinetic properties and the multi-arm linker-based therapeutics, which employ PEG linking arms, of this invention. In cases when the PEG-modified binding agents do not lead to effective cytolytic mechanisms of the targeted cells, due to low density of the targeted surface antigen, insufficient cross-linking, inability to induce apoptosis, or other reasons, the cytolytic effect is enhanced or induced by the use of drug-conjugated anti-PEG IgG or F (ab’ ) 2. Multiple molecules of anti-PEG IgG or F (ab’ ) 2 can bind to each strand of PEG and multiple molecules of a cytotoxic drug can be carried by each anti-PEG IgG or F (ab’ ) 2 molecule. The use of the divalent anti-PEG IgG or F (ab’ ) 2 can cause cross-linking of the complexes of targeted surface antigen and the PEG-linked binding agent. The binding by divalent anti-PEG IgG or F (ab’ ) 2 can cause the aggregation of the large complexes (targeted surface antigen plus PEG-linked binding agent plus drug-conjugated divalent anti-PEG IgG or F (ab’ ) 2 and lead to the internalization of such complexes by the target cells. The internalized drug will then cause the cytolysis of the  targeted cells. The treatment strategy should be effective in combination with the use of the molecular constructs for targeting tumor-associated antigens.
Such a strategy enables enhanced binding and specificity of the tumor-targeting binders, amplification by the anti-PEG antibody binding, and hence a larger and more specific drug payload. The drug-conjugated anti-PEG IgG can be prepared by engineering the IgG by installing a (GGGGS) 2 linker and a cysteine residue at the C-termini of the γ heavy chains and conjugating to the two sulfhydryl groups with two linker units of cytotoxic dug payloads, each with 3-5 molecules of a cytotoxic drug.
The present invention also pertains to the new treatment modality of sequential administrations of PEG-linked antigen-binding fragments of antibodies specific for a tumor associated antigen, such as CEA, Globo H, or SSEA4, and an LPS-conjugated anti-PEG antibody. The use of LPS-conjugated anti-PEG IgG or F (ab’ ) 2 elicits strong immune response in the targeted tumor site. For example, a 4-arm PEG linker conjugated with 4 scFv fragments is first administered to a patient with cancer expressing Globo H or SSEA4, followed with a lapse of time, by an LPS-conjugated anti-PEG IgG or F (ab’ ) 2.
In certain embodiments of the present disclosure, the present method is useful for treating the solid tumor.
In the embodiment, the first targeting element is a peptide hormone, a growth factor, or an antibody fragment specific for a tumor-associated antigen； and the first effector element is a cytotoxic drug, a toll-like receptor agonist, a chelator complexed with a radioactive nuclide, a cytokine, or an antibody fragment specific for a growth factor, a cell surface antigen, a hapten, or a cytokine.
According to some optional embodiments of the present disclosure, when the effector element is the antibody specific for the hapten, the method further comprises the step of administering to the subject an immunoregulatory effector that is tagged with the same hapten, prior to, concurrent with, or after the administration of the present molecular construct.
According to one example, the solid tumor treatable by the present method may be melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung  cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, or head and neck squamous cell carcinoma.
According to another example, the tumor-associated antigen is selected from the group consisting of human epidermal growth factor receptor (HER1) , human epidermal growth factor receptor 2 (HER2) , human epidermal growth factor receptor 3 (HER3) , human epidermal growth factor receptor (HER4) , carbohydrate antigen 19-9 (CA 19-9) , carbohydrate antigen 125 (CA 125) , mucin 1 (MUC 1) , ganglioside GD2, ganglioside GD3, ganglioside GM2, fucosyl GM1, Neu5GcGM3, melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) , mesothelin, mucine-related Tn, Sialyl Tn, LewisY, Sialyl LewisY, LewisA, Lewisx, heparin-binding epidermal growth factor (HB-EGF) , Globo H, and stage-specific embryonic antigen-4 (SSEA-4) .
According to still another example, the peptide hormone is selected from the group consisting of secretin, gastrin, cholecystokinin (CCK) , gastrin-releasing polypeptide, glucagon-like polypeptide 1 (GLP-1) , neuromedin, thyroid-stimulating hormone (TSH) , adrenocorticotropic hormone (ACTH) , gonadotropin-releasing hormone (GnRH) , and somatostatin.
According to still another example, the growth factor is selected from the group consisting of epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , vascular endothelial growth factor A (VEGF-A) , basic fibroblast growth factor (bFGF) , and hepatocyte growth factor (HGF) . In one working example, the first targeting element is EGF, mutant EGF, HB-EGF, VEGF-A, bFGF, or HGF. In another working example, the first effector element is an scFv specific for EGF, mutant EGF, VEGF-A, bFGF, or HGF.
In one example, the cell surface antigen is PD-1, PD-L1, CTLA-4, CD3, CD16a, CD28, or CD134.
In another example, the hapten is dinitrophenol (DNP) , trinitrophenol (TNP) , dansyl, penicillin, p-aminobenzoic acid, or a short peptide having an amino acid sequence of SEQ ID NO: 20.
In still another example, the cytokine is IL-2, IL-10, IL-12, IFN-α, IFN-γ, TGF-β, or TNF-α. According to one embodiment, the first effector element is a non-neutralizing scFv specific for the cytokine selected from the group consisting of IL-2, IFN-α, IFN-γ, and TNF-α. 
As would be appreciated, the cytotoxic drug exhibiting a cytotoxic effect on tumor cell can be anti-estrogens (e.g., tamoxifen, raloxifene, and megestrol) , LHRH agonists (e.g., goscrclin and leuprolide) , anti-androgens (e.g., flutamide and bicalutamide) , photodynamic therapies (e.g., vertoporfin, phthalocyanine, photosensitizer Pc4, and demethoxy-hypocrellin A) , nitrogen mustards (e.g., cyclophosphamide, ifosfamide, trofosfamide, chlorambucil, estramustine, and melphalan) , nitrosoureas (e.g., carmustine and lomustine) , alkylsulphonates (e.g., busulfan and treosulfan) , triazenes (e.g., dacarbazine, temozolomide) , platinum containing compounds (e.g., cisplatin, carboplatin, oxaliplatin) , vinca alkaloids (e.g., vincristine, vinblastine, vindesine, and vinorelbine) , taxoids (e.g., paclitaxel, docetaxeal, and taxol) , epipodophyllins (e.g., etoposide, etoposide phosphate, teniposide, topotecan, 9-aminocamptothecin, camptoirinotecan, irinotecan, crisnatol, mytomycin C) , anti-metabolites, DHFR inhibitors (e.g., methotrexate, dichloromethotrexate, trimetrexate, edatrexate) , IMP dehydrogenase inhibitors (e.g., mycophenolic acid, tiazofurin, ribavirin, and EICAR) , ribonuclotide reductase inhibitors (e.g., hydroxyurea and deferoxamine) , uracil analogs (e.g., 5-fluorouracil (5-FU) , floxuridine, doxifluridine, ratitrexed, tegafur-uracil, capecitabine) , cytosine analogs (e.g., cytarabine (ara C), cytosine arabinoside, and fludarabine) , purine analogs (e.g., mercaptopurine and Thioguanine) , Vitamin D3 analogs (e.g., EB 1089, CB 1093, and KH 1060) , isoprenylation inhibitors (e.g., lovastatin) , dopaminergic neurotoxins (e.g., 1-methyl-4-phenylpyridinium ion) , cell cycle inhibitors (e.g., staurosporine) , actinomycin (e.g., actinomycin D, dactinomycin) , bleomycin (e.g., bleomycin A2, bleomycin B2, peplomycin) , anthracycline (e.g., daunorubicin, doxorubicin, idarubicin, epirubicin, pirarubicin, zorubicin, mitoxantrone) , MDR inhibitors (e.g., verapamil) , Ca2+ ATPase inhibitors (e.g., thapsigargin) , imatinib, thalidomide, lenalidomide, tyrosine kinase inhibitors (e.g., axitinib, bosutinib, cediranib, dasatinib, erlotinib, gefitinib, imatinib, lapatinib, lestaurtinib, neratinib, nilotinib, semaxanib,  sunitinib, toceranib, vandetanib, vatalanib, rituximab, nilotinib, sorafenib, everolimus, temsirolimus, proteasome inhibitors (e.g., bortezomib) , mTOR inhibitors (e.g., rapamycin, temsirolimus, everolimus, and ridaforolimus) , oblimersen, gemcitabine, carminomycin, leucovorin, pemetrexed, cyclophosphamide, dacarbazine, procarbizine, prednisolone, dexamethasone, campathecin, plicamycin, asparaginase, aminopterin, methopterin, porfiromycin, melphalan, leurosidine, leurosine, chlorambucil, trabectedin, procarbazine, discodermolide, carminomycin, , aminopterin, or hexamethyl melamine. According to one specific embodiment of the present disclosure, the cytotoxic drug is auristatin, maytansine, doxorubicin, calicheamicin, or camptothecin.
According to the embodiment, the toll-like receptor agonist is lipoteichoic acid, glucan, motolimod, imiquimod, resiquimod, gardiquimod, CpG oligodeoxynucleotide (CpG DON) , lipopolysaccharide (LPS) , monophosphoryl lipid A, or zymosan.
IV- (iv) Osteoporosis Disease
In the extracellular matrix network of the bone, the major tissue-specific protein is osteonectin, also referred to as secreted protein acidic and rich in cysteine (SPARC) . Collagen I is a dominant protein in the bone matrix, although it is also present in the connective tissue lining the skin.
In treating osteoporosis, a set of the present inventions is to construct T-E molecules with scFv specific for osteonectin and/or collagen I as the targeting elements and scFv specific for RANKL or sclerostin as the effector elements. We rationalize that if anti-RANKL or anti-sclerostin antibodies can be preferentially localized in the bone, the dosage can be decreased, and the therapeutic efficacy increased. In one embodiment of the present disclosure, the various T-E molecules based on the “joint-linker” configuration contain scFv specific for osteonectin (SPARC) and collagen I as the targeting elements and scFv specific for RANKL as the effector elements.
According to certain embodiments of the present disclosure, the present method is useful in treating osteoporosis disease, in which the first targeting element is an scFv specific for collagen I or osteonectin； and the first effector element is an scFv specific for receptor activator of nuclear factor κB (RANKL) .
PART V Anti-Inflammatory Molecules with Tissue-Targeting Functions
In the broad sense of the Fc-based configuration, immunoglobulin antibody can serve as the base of a targeting or effector element, and its corresponding effector or targeting element can be incorporated at the C-terminal of its two heavy γ chains in the form of scFv domains. For a typical “Fc-based” configuration, two-chain IgG. Fc is used as the base of the molecular platform. Each of the polypeptide chain is fused with one or two targeting and one or two effector elements, for a total of two to three elements on each chain. The T-E molecule with an Fc-based configuration will have a total of four to six elements (e.g., scFv, growth factor, or cytokines) . Optionally, the Fc portion of the molecular constructs also carries Fc-mediated effector functions, ADCC, and/or complement-mediated activation. While in certain other applications, such Fc-mediated effector functions are avoided.
In designing the Fc-based molecular constructs, targeting elements are positioned at the N-or C-terminus. If the effector elements function by binding to a cell surface component, such as CD3, CD16a, PD-1, PD-L1, or CTLA-4, they should also be positioned at the terminus. If the effector elements function by binding to and neutralizing soluble factors, such as VEGF, TNF-α, IL-17, or BAFF, they can be positioned between a terminal targeting or effector element and CH2-CH3.
In some embodiments of the present disclosure, both the effector element and the targeting element carried by the CH2-CH3 segment (or CH2-CH3 chain) are mostly comprised of amino acid residues, and for the sake of discussion, these molecular constructs are referred to anti-inflammatory molecules with tissue-targeting functions or anti-inflammatory Fc-based molecular construct. For example, the effector element may be an antibody fragment or a soluble receptor, while the targeting element is also an antibody fragment. Some illustrative structures of this Fc-based molecular construct are discussed in this section.
Referring to Figure 8A, which is a schematic diagram illustrating an Fc-based molecular construct 800A according to certain embodiments of the present disclosure. As illustrated, the Fc-based molecular construct 800A comprises two identical CH2-CH3 chains 810, a first pair of effector elements E1 linked to the N-termini of the CH2-CH3 chains 810, and a first pair of targeting elements T1 linked to the C-termini of the CH2-CH3 chains 810. In this  illustrative configuration, both the targeting element T1 and effector element E1 are antibody fragments.
In some embodiments, the CH2-CH3 chains are adopted from human immunoglobulins γ1 or γ4. In general, γ1 is chosen, when Fc-mediated functions, such as antibody-dependent cellular cytotoxicity (ADCC) and complement-mediated activity (inflammatory activation or target cell lysis) , are desired. In the case where Fc-mediated functions are avoided, γ4 is chosen for constructing the present Fc-based molecular constructs.
The Fc-based molecular construct 800B illustrated in Figure 8B is quite similar to the Fc-based molecular construct 800A of Figure 8A in structure, except that the two effector elements E1 are respectively linked to the C-termini of the CH2-CH3 chains 810, while the two targeting effectors are respectively linked to the C-termini of the CH2-CH3 chains 810.
According to certain embodiments, both the effector elements and targeting elements are linked to the N-termini of the CH2-CH3 chains. For example, when both the effector element and the targeting element are in the form of single-chain variable fragments (scFvs) , the effector element and the targeting element may be linked in a tandem or diabody configuration, thereby forming a bispecific scFv that is linked to the N-terminus of the CH2-CH3 chain.
The Fc-based molecular construct 800C (Figure 8C) comprises an Fc portion, and accordingly, each CH2-CH3 chain 810 has a T1-E1 bispecific scFv linked to the N-terminus thereof.
As discussed above, the anti-inflammatory Fc-based molecular constructs can also use a soluble receptor (e.g., the soluble receptor of TNF-α or IL-1) as the effector element, according to certain embodiments. In these cases, the Fc-based molecular construct 800D (Figure 8D) may have two effector elements E1 respectively linked to the N-termini of the CH2-CH3 chains 810, and two targeting elements T1 respectively linked to the C-termini of the CH2-CH3 chains 810. It is also possible that the effector elements and the targeting elements are respectively arranged at the C-and N-termini of the CH2-CH3 chains； see, for example, the Fc-based molecular construct 800E of Figure 8E.
In some examples, the first pair of effector elements or the first pair of the targeting elements takes a Fab configuration (i.e., consisting of the VH-CH1 domain and the VL-Cκ domain) ； this Fab fragment is linked to the N-termini of the CH2-CH3 chains, so that the Fc-based molecular construct adopts an IgG configuration. In these cases, the pair of elements that is not in the Fab configuration may be linked to the C-termini of the pair of CH2-CH3 segments.
For example, in the Fc-based molecular construct 800F of Figure 8F, each of the two targeting elements T1 comprises the VH-CH1 domain 820 and the VL-Cκ domain 825, thereby forming a Fab configuration 830 that is linked to the N-termini of the CH2-CH3 chains 810, so that the Fc-based molecular construct 800F adopts the IgG configuration. In this case, the pair of effector elements E1 is linked to the C-termini of the pair of CH2-CH3 chains 810.
As described above, the present Fc-based molecular construct may carry a total of six elements at most. The additional elements may be a second pair of effector elements or a second pair of targeting elements.
According to other embodiment, the Fc-based molecular construct 900A (Figure 9A) comprises a second pair of targeting elements T2. In these cases, the targeting elements T1 and T2 are linked in a tandem or diabody configuration to form a bispecific scFv that is linked to the N-terminus of the CH2-CH3 chain 910, and the effector element E1 is linked to the C-terminus of the CH2-CH3 chain 910.
According to embodiments exemplified in Figure 9B, the Fc-based molecular construct 900B comprises a second pair of effector elements E2. In these cases, the effector element E1 and E2 are linked in a tandem or diabody configuration to form a bispecific scFv that is linked to the N-terminus of the CH2-CH3 chain 910, and the targeting element T1 is linked to the C-terminus of the CH2-CH3 chain 910.
Now that the basic structural arrangements of the anti-inflammatory Fc-based molecular constructs have been discussed above, certain combinations of particular effector element (s) and targeting element (s) are provided below for the illustration purpose.
According to some embodiments, the effector element is an scFv specific for TNF-α, and the targeting element is an scFv specific for collagen II or collagen IX, or α-aggrecan. According to some embodiments, each of the two effector elements is an scFv specific for IL-17, while the targeting element is an scFv specific for collagen I or collagen VII. Still alternatively, each of the two effector elements is an scFv specific for BAFF, and the targeting element is an scFv specific for collagen I or collagen VII. In some embodiments, each of the two effector elements is an scFv specific for TNF-α, and the targeting element is an scFv specific for collagen III or collagen V. In some other embodiments, the two effector elements are in the form of a Fab specific for RANKL, and the targeting element is an scFv specific for collagen I or osteonectin. For example, such molecular construct may take the configuration of any of those depicted in Figures 8A-8C and 8F.
In some embodiments, the first pair of effector elements includes an scFv specific for TNF-α and an scFv specific for IL-17, while the first pair of targeting elements includes an scFv specific for collagen II and an scFv specific for collagen IX. In some alternative embodiments, the first pair of effector elements includes an scFv specific for TNF-α and an scFv specific for IL-17, while the first pair of targeting elements includes an scFv specific for collagen I and an scFv specific for collagen VII. Alternatively, each of the two effector elements is an scFv specific for BAFF, and the targeting element is an scFv specific for collagen I or collagen VII. Still alternatively, each of the two effector elements is an scFv specific for RANKL, and the targeting element is an scFv specific for collagen I or osteonectin. These molecular constructs may take the configuration of any of those depicted in Figures 8B, 8D, and 8F.
In certain embodiments, the two effector elements are in the form of a Fab antibody specific for TNF-α, while the targeting element is an scFv specific for collagen II or collagen IX. In some embodiments, the two effector elements are in the form of a Fab antibody specific for IL-17, and the targeting element is an scFv specific for collagen I or collagen VII. Alternatively, the two effector elements are in the form of a Fab antibody specific for BAFF, and the targeting element is an scFv specific for collagen I or collagen VII. Still alternatively, the two effector elements are in the form of a Fab antibody specific for TNF-α, and the targeting element is an scFv specific for collagen III or collagen V.
The essence of this invention is the rationalization and conception of the specific combination or pairing of the targeting and effector elements. The adoption of Fc-fusion configuration in the molecular constructs is a preferred embodiment. It is conceivable for those skilled in the arts to link the pairs of targeting and effector elements of this invention employing other molecular platforms, such as peptides, proteins (e.g., albumin) , polysaccharides, polyethylene glycol, and other types of polymers, which serve as a structural base for attaching multiple molecular elements.
PART VI Uses Of Anti-Inflammatory Molecules with Tissue-Targeting Functions
Another aspect of the present disclosure is directed to the use of the anti-inflammatory Fc-based molecular constructs discussed above in Part V.
As could be appreciated, the description in Part IV- (i) regarding the rationales underlying the selection of suitable targeting and effector elements is also applicable in this section. For example, anti-inflammatory Fc-based molecular constructs used for treating various immune disorders contain an antibody fragment (e.g., scFv, Fab, and the like) specific for collagen II, collagen XI, or α-aggrecan used as targeting elements and an antibody fragment (e.g., scFv, Fab, and the like) specific for TNF-α and IL-17 as effector elements.
According to various embodiments of the present disclosure, the present treatment method involves the administration of a suitable anti-inflammatory Fc-based molecular construct to a subject in need of such treatment. Specific examples of anti-inflammatory Fc-based molecular constructs for treating various immune disorders, in particular, autoimmune diseases, are discussed below.
According to certain embodiments, the present method is used to treat rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis. In these cases, each effector element of the anti-inflammatory Fc-based molecular construct is an antibody fragment specific for TNF-α, IL-12/IL-23, IL-1, IL-17, or IL-6, while each targeting element is an antibody fragment specific for collagen II, collagen IX, collagen XI, or α-aggrecan. For example, each effector element of the first pair of effector elements is an scFv specific for TNF-α, while each targeting element of the first pair of targeting elements is an antibody fragment  specific for collagen II. In other embodiments, the effector element is an scFv specific for TNF-α, while the targeting element is an antibody fragment specific for collagen IX. Alternatively, the effector element is an scFv specific for TNF-α, while the targeting element is an antibody fragment specific for α-aggrecan. According to various embodiments, the above-mentioned anti-inflammatory Fc-based molecular constructs may have the configuration of 800A, 800B, or 800C discussed above.
Another anti-inflammatory Fc-based molecular construct for treating rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis comprises two effector elements that are in the form of a Fab antibody specific for TNF-α. In these cases, both targeting elements of the first pair of targeting elements is scFvs specific for collagen II or scFvs specific for collagen IX. Configurations of these Fc-based molecular constructs are illustrated in Figure 8F, for example.
The present methods are also applicable in the treatment of psoriasis. For example, the anti-inflammatory Fc-based molecular construct may comprise effector elements of an antibody fragment specific for TNF-α, IL-12/IL-23, or IL-17, and targeting elements of an antibody fragment specific for collagen I or collagen VII. According to some embodiments, the effector elements are scFvs specific for IL-17, while the targeting elements are scFvs specific for collagen I. Alternatively, the effector elements are scFvs specific for IL-17, while the targeting elements are scFvs specific for collagen VII. These anti-inflammatory Fc-based molecular constructs have the configuration of 800A, 800B, or 800C discussed above.
Another anti-inflammatory Fc-based molecular construct for treating psoriasis comprises two effector elements that are in the form of a Fab antibody specific for IL-17. In these cases, both targeting elements of the first pair of targeting elements is scFvs specific for collagen I or scFvs specific for collagen VII. Configurations of these Fc-based molecular constructs are illustrated in Figure 8F, for example.
Another set of diseases treatable by the present method using the anti-inflammatory Fc-based molecular constructs are systemic lupus erythematosus, cutaneous lupus, or 
Figure PCTCN2016071184-appb-000026
Syndrome. In these embodiments, each effector is an antibody fragment specific for BAFF, and each targeting element is an antibody fragment specific for collagen I  or collagen VII. These anti-inflammatory Fc-based molecular constructs may have the configuration illustrated in Figures 8A to 8C. As could be appreciated, the pair of effector elements may also take the form of a Fab antibody specific for BAFF, and the pair of targeting elements may be scFvs specific for collagen I or collagen VII, which takes the configuration of the molecular construct 800F illustrated in Figure 8F.
In other embodiments, the present method is used to treat inflammatory bowel disease, such as Crohn’s disease or ulcerative colitis. In these cases, each effector is an antibody fragment specific for TNF-α, and each targeting element is an antibody fragment specific for collagen III or collagen V. Configurations of these Fc-based molecular constructs are illustrated in Figures 8A to 8C, for example. Of course, the pair of effector elements may also take the form of a Fab antibody specific for TNF-α, while the pair of targeting elements may be scFvs specific for collagen III or collagen V, thereby giving the configuration illustrated in Figure 8F.
The present anti-inflammatory Fc-based molecular constructs are also applicable in the treatment of osteoporosis. For example, the effector elements are antibody fragments specific for RANKL, while the targeting elements are antibody fragments specific for collagen I or osteonectin. As could be appreciated, the antibody fragments specific for RANKL may be scFvs so that the Fc-based molecular construct has the configuration illustrated in Figures 8A to 8C, or they may take the form of a Fab so that the Fc-based molecular construct has the configuration illustrated in Figure 8F.
It should be noted that above-examples are given for the purpose of illustration, and treatments using anti-inflammatory Fc-based molecular constructs with other T-E combinations are within the scope of the present disclosure.
PART VII Molecular Constructs for Treating Tumors
Another aspect of the present disclosure is directed to an Fc-based molecular construct that, like the molecular construct described in Part V above, has at least a pair of targeting elements and at least a pair of effector elements linked, directly or indirectly, to a CH2-CH3 domain of an immunoglobulin. By selecting the T-E elements of the present Fc-based molecular construct, the molecular construct can be used to treat various cellular  proliferative diseases, including diffused tumor and solid tumors. The present disclosure is also advantageous in that, in some embodiments, it utilizes the linker unit according to the first aspect of the present disclosure, which provides a facile means for controlling the amount of the cytotoxic drug payload of the present Fc-based molecular construct may take different configurations, which are discussed below, respectively.
VII- (i) Molecular Constructs with Antibody as Targeting Elements and Drug Bundle as Effector Elements
According to certain embodiments of the present disclosure, each effector element of the first pair of effector elements is a drug bundle, while each targeting element of the first pair of targeting elements is an antibody fragment specific for a cell surface antigen or a tumor associated antigen. In these cases, the Fc-based molecular constructs for treating tumors may have the configuration of molecular construct 1000A of Figure 10A or molecular construct 1000B of Figure 10B. As illustrated in Figure 10A, the effector elements E1 (for example, drug bundles) are linked to the C-termini of the pair of CH2-CH3 segments 1010, whereas the targeting elements T1 (in this case, an scFv) are linked to the N-termini of the pair of CH2-CH3 segments 1010. According to alternative embodiments, the molecular construct 1000B (see, Figure 10B) has a pair of targeting elements T1 that takes the form of a Fab 1030. Specifically, the Fab 1030 configuration comprises the VH-CH1 domain 1020 and the VL-Cκ domain 1025, and is linked to the N-termini of the pair of CH2-CH3 segments 1010, so that the Fc-based molecular construct 1000A adopts the IgG configuration. In this case, the pair of effector elements E1 is linked to the C-termini of the pair of CH2-CH3 chains 1010.
In some embodiments, the CH2-CH3 chains are adopted from human immunoglobulins γ1 or γ4. In general, γ1 is chosen, when Fc-mediated functions, such as antibody-dependent cellular cytotoxicity (ADCC) and complement-mediated activity (inflammatory activation or target cell lysis) , are desired. In the case where Fc-mediated functions are avoided, γ4 is chosen for constructing the present Fc-based molecular constructs. As could be appreciated, the above-mentioned structure of the Fc region is also applicable in other Fc-based molecular construct discussed in Part VII.
The drug bundle may be provided as the linker unit discussed in Part I of the present disclosure (see, for example Figure 1A to Figure 1 C) . Briefly, the drug bundle comprises a center core, a plurality of linking arms, and optionally, a coupling arm. The center core may be a compound having a plurality of amine groups or a polypeptide comprising a plurality of lysine (K) residues, according to various embodiments of the present disclosure. Each of the linking arms has one terminus that is linked to the center core by reacting with the amine groups of the compound core or the amine side chain of the K residues of the polypeptide core. The linking arm also carries a maleimide group at the free terminus thereof, wherein each of the molecules (e.g., molecules of cytotoxic drugs in this case, and/or TLR agonists, or chelator/radioactive nuclide complexes described below) is linked to the center core via connecting through the linking arm by reacting with the maleimide group. According to optional embodiments of the present disclosure, each of the effector elements E1 is a drug bundle with 3-5 cytotoxic molecules.
In the case where the center core is the polypeptide core, then the amino acid residue at the N-or C-terminus of the center core is a cysteine residue or has an azide group or an alkyne group. According to certain embodiments, for polypeptide cores with a terminal amino acid residue having the azide group, the drug bundle is linked to the peptide extension via the SPAAC reaction or CuAAC reaction occurred between said terminal residue and the C-terminus of the peptide extension. Alternatively, when the polypeptide cores has a terminal amino acid residue with the alkyne group, the drug bundle is linked to the peptide extension via the CuAAC reaction occurred between said terminal residue and the C-terminus of the peptide extension. Still alternatively, for polypeptide cores with a terminal residue that is cysteine or for compound cores, the drug bundle further comprises said coupling arm. Specifically, the coupling arm has one terminus linked to the center core by reacting with the cysteine residue of the polypeptide core or one amine group of the compound core. The coupling arm also carries an alkyne group, azide group, tetrazine group, or strained alkyne group at the free terminus thereof, so that the drug bundle is linked to the C-terminus of the peptide extension via the iEDDA reaction (for coupling arms with the tetrazine or cyclooctene group) , SPAAC (for coupling arms with the azide or cyclooctyne group) reaction or CuAAC reaction (for coupling arms with the alkyne or azide group) occurred therebetween.
According to certain embodiments, the present Fc-based molecular construct for treating tumors further comprises a pair of peptide extensions 1050 (see, Figures 10A and 10B) respectively having the sequence of (G2-4S) 2-8C. As illustrated, the pair of peptide extensions 1050 is linked to the C-termini of the pair of CH2-CH3 segments 1010. The cysteine residue at the C-terminus of the peptide extension is linked with a coupling arm 1055 via thiol-maleimide reaction occurred therebetween. Also, before being conjugated with the effector element E1 (in this case, a drug bundle) , the free terminus of the conjugating arm (that is, the terminus that is not linked to the cysteine residue) is modified with an alkyne, azide, strained alkyne, or tetrazine group, so that the drug bundle is linked thereto via iEDDA reaction or the SPAAC or CUAAC reaction occurred therebetween.
For example, in Figure 10A, the coupling arm 1040 of the effector element E1 (in this case, a drug bundle) is linked to the CH2-CH3 segment 1010 via iEDDA reaction. The ellipse 1045 as depicted in Figure 10A represents the chemical bond resulted from the iEDDA reaction occurred between the peptide extension 1050 and the effector element E1. As could be appreciated, an iEDDA reaction is occurred between a tetrazine group and a cyclooctene group, such as a transcyclooctene (TCO) group.
Alternatively, in Figure 10B, the effector element E1 is linked to the CH2-CH3 segment 1010 via SPAAC reaction. The diamond 1045 as depicted in Figure 10B represents the chemical bond resulted from the SPAAC reaction occurred between the peptide extension 1050 and the effector element E1. Specifically, an SPAAC reaction is occurred between an azide group and a strained alkyne group (e.g., a cyclooctyne group, including, dibenzocyclooctyne (DBCO) , difluorinated cyclooctyne (DIFO) , bicyclononyne (BCN) , and dibenzocyclooctyne (DICO) group) .
According to some optional embodiments of the present disclosure, the Fc-based molecular construct for treating tumors may further comprise a second pair of targeting elements. For example, the molecular construct 1000C of Figure 10C comprises a first pair of targeting elements T1 and a second air of targeting elements T2, as well as effector elements E1. Specifically, the second pair of effector elements T2 is inked, in a tandem or diabody configuration, to the N-termini of the pair of elements T1 that is linked to the N-termini of the pair of CH2-CH3 segments 1010, thereby forming a pair of bispecific scFvs  that is linked to the N-termini of the pair of CH2-CH3 segments 1010. Also, the pair of effector elements E1 is linked to the CH2-CH3 segment 1010 via iEDDA reaction by forming a chemical bond 1045 between the peptide extension 1050 and the effector element E1. However, the present disclosure is not limited thereto； rather, the effector elements E1 is linked to the CH2-CH3 segment 1010 via SPAAC reaction or CuAAC reaction in other embodiments.
According to various embodiments of the present disclosure, the Fc-based molecular construct that has the configuration illustrated in any of Figure 10A to Figure 10C is applicable in the treatment of diffused tumors. For example, the drug bundle of such Fc-based molecular construct comprises a plurality of cytotoxic drug molecules, such as, auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin. Also, the targeting elements of such Fc-based molecular construct may be an antibody fragment (e.g., scFv, Fab, or the like) specific for cell surface antigen selected from the group consisting of CD5, CD19, CD20, CD22, CD23, CD30, CD33, CD34, CD37, CD38, CD43, CD78, CD79a, CD79b, CD138, and CD319.
According to other embodiments of the present disclosure, the Fc-based molecular construct that has the configuration illustrated in any of Figure 10A to Figure 10C is applicable in the treatment of solid tumors, including malignant and/or metastatic solid tumors. In some cases, the drug bundle for use as effector elements comprises multiple cytotoxic drug molecules, e.g., auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin. Alternatively, the drug bundle comprises multiple molecules of TLR agonist, such as, LPS, monophosphoryl lipid A, motolimod, imiquimod, resiquimod, gardiquimod, CpG DON, lipoteichoic acid, β-glucan, and zymosan. Still alternatively, the drug bundle comprises multiple molecules of a chelator (e.g., DOTA, NOTA, NODA, and DTPA) complexed with a radioactive nuclide (e.g., 90Y, 111In, and 177Lu) . On the other hand, the targeting elements of such Fc-based molecular construct may be an antibody fragment (e.g., scFv, Fab, or the like) specific for HER1, HER2, HER3, HER4, CA19-9, CA125, CEA, MUC1, MAGE, PSMA, PSCA； mucin-related Tn, Sialyl Tn, Globo H, SSEA-4, ganglioside GD2, or EpCAM.
In the cases where the of Fc-based molecular constructs have a second pair of targeting elements, the effector element of the first pair of effector elements is a drug bundle comprising multiple cytotoxic drug molecules, while the first and second pairs of targeting elements are scFvs specific for HER2 and scFvs specific for HER1, respectively.
VII- (ii) Molecular Constructs with Growth Factor/Peptide Hormone as Targeting Elements and Drug Bundle as Effector Elements
According to certain embodiments of the present disclosure, each effector element of the first pair of effector elements is a drug bundle, while each targeting element of the first pair of targeting elements is a growth factor or a peptide hormone. In these cases, the Fc-based molecular constructs are suitable for treating solid tumors (including malignant and/or metastatic ones) may have the configuration of molecular construct 1100 of Figure 11. As illustrated in Figure 11, the effector elements E1 are linked to the C-termini of the pair of CH2-CH3 segments 1110, whereas the targeting elements T are linked to the N-termini of the pair of CH2-CH3 segments 1110.
Like the Fc-based  molecular construct  1000A or 1000B, the present molecular construct 1100 further comprises a pair of peptide extensions 1150 respectively having the sequence of (G2-4S) 2-8C, which is linked to the C-termini of the pair of CH2-CH3 segments 1110. Similarly, to facilitate the conjugation of the drug bundle, the cysteine residue is linked with a coupling arm 1155, and the drug bundle is linked to the coupling arm 1155 via iEDDA reaction, SPAAC reaction, or CuAAC reaction occurred therebetween (see the above discussion regarding Figure 10A) . For example, in Figure 11, the coupling arm 1140 of the effector element E1 is linked to the coupling arm 1155 via iEDDA reaction, in which the ellipse 1145 represents the chemical bond resulted from the iEDDA reaction occurred between the coupling arm 1155 and the effector element E1. However, the present disclosure is not limited thereto； rather, the effector elements E1 is linked to the CH2-CH3 segment 1110 via SPAAC reaction or CuAAC reaction in other embodiments.
As could be appreciated, the discussions in Part VII- (i) above regarding the Fc region and drug bundle of the Fc-based molecular constructs are also applicable here, and hence, detailed description regarding the same is omitted herein for the sake of brevity.
Since the present molecular construct (e.g., the molecular construct 1100) is applicable in the treatment of solid tumors, the drug bundle for use as effector elements comprises multiple cytotoxic drug molecules, e.g., auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin, according to some embodiments. Alternatively, the drug bundle comprises multiple molecules of TLR agonist, such as, LPS, monophosphoryl lipid A, motolimod, imiquimod, resiquimod, gardiquimod, CpG DON, lipoteichoic acid, β-glucan, and zymosan. Still alternatively, the drug bundle comprises multiple molecules of a chelator (e.g., DOTA, NOTA, NODA, and DTPA) complexed with a radioactive nuclide (e.g., 90Y, 111In, and 177Lu) .
On the other hand, targeting elements suitable for use in combination with the above-mentioned drug bundles are growth factors including, but not limited to EGF, mutant EGF, epiregulin, HB-EGF, VEGF-A, bFGF, and HGF. Other targeting elements combinable with the above-mentioned drug bundles are peptide hormones； illustrative examples of which include CCK, somastatin, and TSH.
VII- (iii) Molecular Constructs with Growth Factor/Peptide Hormone as Targeting Elements and Antibody as Effector Elements
According to other embodiments of the present disclosure, the Fc-based molecular construct comprises an antibody fragment as effector elements and a growth factor or peptide hormone as targeting elements. Such molecular constructs are applicable in the treatment of solid tumors (including malignant and/or metastatic ones) .
Figure 12A illustrate a Fc-based molecular construct 1200A, in which the pair of effector elements E1 (in this case, scFvs) is linked to the N-termini of the pair of CH2-CH3 segments 1210, whereas the pair of targeting elements T1 is linked to the C-termini of the pair of CH2-CH3 segments 1210. As to the Fc-based molecular construct 1200B of Figure 12B, the effector elements E1 and targeting elements T1 are respectively linked to the C-and N-termini of the pair of CH2-CH3 segments 1210.
As could be appreciated, the antibody fragment may also take the form of a Fab, according to certain embodiments of the present disclosure. For example, the Fc-based molecular construct 1200C of Figure 12C comprises a pair of effector elements E1 in the  form of a Fab 1230. Specifically, the Fab 1230 configuration comprises the VH-CH1 domain 1220 and the VL-Cκ domain 1225； the Fab 1230 is linked to the N-termini of the pair of CH2-CH3 segments 1210 so that the Fc-based molecular construct 1200A adopts the IgG configuration. In this case, the pair of targeting elements T1 is linked to the C-termini of the pair of CH2-CH3 chains 1210.
According to various embodiments of the present disclosure, the antibody fragments suitable for use as the effector elements are those specific to cell surface antigens such as PD-1, PD-L1, CTLA-4, CD3, CD16a, CD28, and CD134. Another example of the effector element is the antibody fragment specific for the growth factor like EGF, mutant EGF, epiregulin, HB-EGF, VEGF-A, bFGF, and HGF. Antibody fragments specific for haptens are also suitable for use as effector elements, and illustrative examples of haptens include DNP, TNP, dansyl, penicillin, p-aminobenzoic acid, and a polypeptide having the amino acid sequence of SEQ ID NO: 20.
As to the targeting element suitable for use in this series of Fc-based molecular constructs, the targeting element may be a growth factor such as EGF, mutant EGF, epiregulin, HB-EGF, VEGF-A, bFGF, and HGF. Alternatively, the targeting element may be a peptide hormone like CCK, somastatin, and TSH.
The essence of this invention is the rationalization and conception of the specific combination or pairing of the targeting and effector elements. The adoption of Fc-fusion configuration in the molecular constructs is a preferred embodiment. It is conceivable for those skilled in the arts to link the pairs of targeting and effector elements of this invention employing other molecular platforms, such as peptides, proteins (e.g., albumin) , polysaccharides, polyethylene glycol, and other types of polymers, which serve as a structural base for attaching multiple molecular elements.
PART VIII Uses of Molecular Constructs for Treating Tumors
By selecting the effector element (s) and the targeting element (s) , the Fc-based molecular constructs of Part VII above are also useful in the treatment of various tumors, including diffused tumors and solid tumors. In view of this, the present disclosure also covers method for treating tumors by using the Fc-based molecular construct in Part VII.  According to embodiments of the present disclosure, the method comprises the administration of the present Fc-based molecular construct or a pharmaceutical comprising the same in an effective amount to a subject in need of such treatment.
For a molecular construct targeting tumor cells, such as those targeting EGFR, HER2/neu, or CD20, the pharmacologic purpose is to lyse the targeted cells expressing those antigens. In general, it is desirable that the molecular construct bear Fc-mediated functions, such as ADCC or complement-mediated cytolysis. However, if the molecular construct can be joined with effector elements that elicit strong immune-destruction functions, such as scFv specific for CD3 or CD16a, or immunoregulatory functions, such as scFv specific for PD-1, PD-L1, CTLA-4, the Fc-mediated functions may not be crucial. The IgG molecules may also be linked at the termini of the two heavy chains with bundles of cytotoxic molecules, LPS molecules, or chelating groups for radioactive nuclides.
Fc region (paired CH2-CH3 domains) of human IgG1 mediates antibody-dependent cellular cytotoxicity (ADCC) and complement-mediated cytolysis (CMC) . The present invention rationalizes that those Fc-mediated functions can be maintained, while increasing the binding avidity of an antibody’s binding ability. It is known that some proportions of cells in tumor, which express low densities of targeted antigens, are resistant to the targeting therapeutic antibodies. For example, cells expressing low levels of HER2/Neu in breast tumor or CD20 in B cell lymphoma are not killed by trastuzumab or rituximab, respectively. The molecular conjugates of this invention with much higher binding avidity may bind sufficiently strongly to those cells and mediate cytolytic mechanism on them.
 Different Fc receptors for different subclasses of IgG are on different sets of effector cells, which mediate different sets of immune mechanisms in conjunction with the IgG subclasses. FcγRI (CD64) , FcγRIIa (CD32) , and FcγRIIIb (CD16b) are on macrophages, neutrophils, and eosinophils, and mediate phagocytosis of IgG-coated particles and microbes. FcγRIIIa (CD16a) is mainly on NK cells and macrophages in some tissues and mediates ADCC. When FcγRIIIa on NK cells are bound by IgG1 and clustered, the NK cells secrete cytotoxic granules and death-causing factors that lyse the IgG-bound cells. A preferred embodiment of this invention is to conjugate scFv of antibodies specific for FcγRIIIa to multi-arm linkers, which are conjugated with scFv for various antigenic targets  (e.g., CD20, EGFR) and tumor-associated antigens expressed on various cell targets. It is shown in a recent paper that a bi-specific antibody with one Fab specific for HER2/Neu and one Fab specific for FcγRIIIa is superior to anti-HER2/Neu antibody trastuzumab in lysing tumor cells expressing low density of HER2 antigen. The molecular construct of this invention has higher avidity for both HER2/Neu and should have higher lytic activities toward tumor cells expressing very low HER2/Neu.
To treat diffused tumors, such as B lymphocyte-derived lymphoma or leukemia, plasmacytoma, multiple myeloma, T-cell derived lymphoma or leukemia, and myelogenous leukemia, the present Fc-based molecular construct uses drug bundles comprising multiple cytotoxic drug molecules as effector elements, and antibody fragments specific for a suitable cell surface antigen as targeting elements.
According to certain embodiments, the present method is used to treat B lymphocyte-derived lymphoma or leukemia. In these cases, the cell surface antigens targeted by the present Fc-based molecular construct are cell surface antigens on human B lymphocytes, such as CD5, CD19, CD20, CD22, CD23, CD30, CD37 CD43, CD79a, and CD79b.
In other embodiments, the diffused tumor treatable by the present method is plasmacytoma or multiple myeloma, and the cell surface antigens targeted in these cases are those on human plasma cells, including CD38, CD78, CD138, and CD319.
Alternatively, the present method involves the treatment of T-cell derived lymphoma or leukemia using molecular constructs that target cell surface antigens on human T cells, such as CD5, CD30, and CD43.
When treating myelogenous leukemia according to some embodiments, the cell surface antigens targeted by the molecular construct used are those on human myeloid lineage leukocytes, like CD33 and CD34.
According to certain embodiments, the present Fc-based molecular construct uses drug bundles as effector elements and antibody fragments specific for a suitable tumor-associated antigen as targeting elements to treat solid tumors, such as melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small  cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, and head and neck squamous cell carcinoma. In particular, the molecular constructs discussed above in Part V- (ii) above are preferred in these embodiments.
According to some optional embodiments, the method for treating solid tumors further comprises the step of subjecting the subject to a blood dialysis procedure using an antibody fragment specific for one or more tumor-associated antigens to remove the tumor-associated antigens that are shed from the tumor into the circulation of the subject, prior to the administration of the molecular construct.
Alternatively, the method for treating solid tumors involves the use of Fc-based molecular construct with drug bundles or antibody fragments specific for cell surface antigens, growth factors or haptens as effector elements, and growth factors or peptide hormones as targeting elements. Illustrative examples of such molecular construct include those discussed above in Part VII- (iii) . The solid tumor treatable by these molecular constructs are melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, or head and neck squamous cell carcinoma.
According to some embodiments, the molecular construct uses drug bundles of cytotoxic drug molecules as effector elements and EGF or its mutants as targeting elements.
According to other embodiments, the molecular construct uses scFvs specific for CD3, CD16a, PD-1, or VEGF as effector elements and EGF or its mutants as targeting elements. 
According to some embodiments, the effector elements are antibody fragments specific for hapten. In these cases, the method further comprises the step of administering to the subject an immunoregulatory effector that is tagged with the same hapten after the administration of the molecule construct. For example, the immunoregulatory effector can  be IFN-α, IL-2, TNF-α, and IFN-γ, and an IgG antibody specific for PD-1, PD-L1, CTLA-4, or CD3.
In some embodiments, the pair of CH2-CH3 segments is derived from human IgG heavy chain γ1, and the molecular construct uses drug bundles of cytotoxic drug molecules or LPS molecules as effector elements and EGF or its mutants, epiregulin, HB-EGF, VEGF-A, FGF, HGF, CCK, somastatin, or TSH as targeting elements.
In some embodiments, the pair of CH2-CH3 segments is derived from human IgG heavy chain γ1, and the molecular construct uses scFvs specific for human CD3, CD16a, PD-1, PD-L1, or VEGF-A as effector elements and EGF or its mutants, epiregulin, HB-EGF, VEGF-A, FGF, HGF, CCK, somastatin, or TSH as targeting elements.
EXPERIMENTAL EXAMPLES
Example 1: Synthesis of peptide 1 (SEQ ID NO: 17) , peptide 2 (SEQ ID NO: 18) , and peptide 3 (SEQ ID NO: 19) as peptide cores, and conjugation of SH group of cysteine residue with maleimide-PEG3-transcyclooctene (TCO) as conjugating arm
Peptides 1 to 3 were synthesized by solid-phase peptide synthesis method and purified with reverse phase high-performance liquid chromatography (HPLC) using Shimadzu Nexera-i LC-2040C 3D HPLC system to 95％purity. The reverse phase HPLC used a Kromasil 100-5C18 column (250 mm X 4.6 mm； 5 μm) , with a mobile phase of acetonitrile and 0.1％trifluoroacetic acid, a linear gradient of 10％to 45％acetonitrile over 15 minutes, at a flow rate of 1.0 mL/min and a column temperature of 25℃.
The purified peptide was dissolved in 100 mM sodium phosphate buffer (pH 7.0) containing 50 mM NaCl and 5 mM EDTA at a final concentration of 2 mM. The dissolved peptide was reduced by 1 mM tris (2-carboxyethyl) phosphine (TCEP) at 25℃ for 2 hours. For conjugating the SH group of the cysteine residue with maleimide-PEG3-TCO (Conju-probe Inc., San Diego, USA) to create a functional linking group TCO, the peptide and maleimide-PEG3-TCO were mixed at a 1/10 ratio and incubated at pH 7.0 and 25℃ for 24 hours. TCO-conjugated peptides were purified by reverse phase HPLC on a Supelco C18 column (250 mm X 10 mm； 5 μm) , using a mobile phase of acetonitrile and 0.1％trifluoroacetic acid, a linear gradient of 0％to 100％acetonitrile over 30 minutes, at a flow  rate of 1.0 mL/min and a column temperature of 25℃. Figure 13 showed the reverse phase HPLC elution profile for the purification of TCO-peptide 2； with the peak of the TCO-peptide 2 being indicated with an arrow.
The identification of the three synthesized TCO-peptides (illustrated below) was carried out by mass spectrometry MALDI-TOF. Mass spectrometry analyses were performed by Mass Core Facility of Institute of Molecular Biology (IMB) , Academia Sinica, Taipei, Taiwan. Measurements were performed on a Bruker Autoflex III MALDI-TOF/TOF mass spectrometer (Bruker Daltonics, Bremen, Germany) .
The present TCO-peptide 1, as illustrated below, had a molecular weight (m.w. ) of 1807.0 daltons.
Figure PCTCN2016071184-appb-000027
The present TCO-peptide 2, as illustrated below, had a m.w. of 2078.9 daltons.
Figure PCTCN2016071184-appb-000028
The present TCO-peptide 3, as illustrated below, had a m.w. of 3380.8 daltons.
Figure PCTCN2016071184-appb-000029
Example 2: Synthesis of  peptides  1 and 2 as peptide cores, and conjugation of SH group of cysteine residue with maleimide-PEG4-tetrazine as conjugating arm
Peptides  1 and 2 were prepared as in Example 1, and then dissolved in 100 mM sodium phosphate buffer (pH 7.0) containing 50 mM NaCl and 5 mM EDTA at 2 mM final concentration. The dissolved peptide was reduced by 1 mM TCEP at 25℃ for 2 hours. For conjugating the SH group of cysteine residue with maleimide-PEG4-tetrazine (Conju-probe Inc. ) to create a functional linking group tetrazine, the peptide and maleimide-PEG4-tetrazine were mixed at a 1/5 ratio and incubated at pH 7.0 and 4℃ for 24 hours. Tetrazine-conjugated peptides were purified by reverse phase HPLC on a Supelco C18 column (250 mm X 10 mm； 5 μm) , using a mobile phase of acetonitrile and 0.1％trifluoroacetic acid, a linear gradient of 0％to 100％acetonitrile over 30 minutes, at a flow rate of 1.0 mL/min and a column temperature of 25℃. The identification of said two  synthesized tetrazine-peptides was carried out by mass spectrometry MALDI-TOF set forth in the preceding Example.
The present tetrazine-peptide 1, as illustrated below, had a m.w. of 1912.7 daltons.
Figure PCTCN2016071184-appb-000030
The present tetrazine-peptide 2, as illustrated below, had a m.w. of 2185.2 daltons.
Figure PCTCN2016071184-appb-000031
Example 3: Synthesis of  peptides  1 and 2 as peptide cores, and conjugation of SH group of cysteine residue with maleimide-PEG5-DBCO as conjugating arm
Peptides  1 and 2 were prepared as in the earlier Example. The peptide was dissolved in 100 mM sodium phosphate buffer (pH 7.0) containing 50 mM NaCl and 5 mM EDTA at 2 mM final concentration. The dissolved peptide was reduced by 1 mM TCEP at 25℃ for 2 hours.
For conjugating the SH group of cysteine residue with dibenzylcyclooctyne (DBCO) to create a functional linking group of DBCO, the peptide and maleimide-PEG5-DBCO (Conju-probe Inc. ) were mixed at a 1/5 ratio and incubated at pH 7.0 and the room temperature for 24 hours. DBCO-conjugated peptides were purified by reverse phase HPLC on a Supelco C18 column (250 mm X 10 mm； 5 μm) , using a mobile phase of acetonitrile and 0.1％trifluoroacetic acid, a linear gradient of 0％to 100％acetonitrile over 30 minutes, at a flow rate of 1.0 mL/min and a column temperature of 25℃. The identification of the two synthesized DBCO-peptides was carried out by mass spectrometry MALDI-TOF.
The present DBCO-peptide 1, as illustrated below, had a m.w. of 1941.8 daltons.
Figure PCTCN2016071184-appb-000032
The present DBCO-peptide 2, as illustrated below, had a m.w. of 2213.9 daltons.
Figure PCTCN2016071184-appb-000033
Example 4: Synthesis of peptide 4 (SEQ ID NO: 21) , peptide 5 (SEQ ID NO: 22) , and peptide 6 (SEQ ID NO: 23) as peptide cores
Peptides 4 to 6 were synthesized by solid-phase peptide synthesis method, and then purified by reverse phase HPLC to 95％purity. The unnatural amino acids, homopropagylglycine (GHP) and azidohomoalanine (AAH) contained an alkyne and an azide group, respectively. The reverse phase HPLC used a Supelco C18 column (250 mm X 4.6 mm； 5 μm) , with a mobile phase of acetonitrile and 0.1％trifluoroacetic acid, a linear gradient of 2％to 90％acetonitrile over 30 minutes, at a flow rate of 1.0 mL/min and a column temperature of 25℃.
The identification of said three synthesized peptides was carried out by mass spectrometry MALDI-TOF. The present peptide 4 
Figure PCTCN2016071184-appb-000034
Figure PCTCN2016071184-appb-000035
had a molecular weight of 1317.0 daltons； the present peptide 5 
Figure PCTCN2016071184-appb-000036
had a m.w. of 1589.9 daltons； while the present peptide 6
Figure PCTCN2016071184-appb-000037
had a m.w. of 1634.66 daltons.
Example 5: Synthesis of peptide 7 (SEQ ID NO: 24) as peptide core and conjugation of SH group of cysteine residue with maleimide-PEG3-TCO or maleimide-PEG4-tetrazine as conjugating arm
Peptide 7
Figure PCTCN2016071184-appb-000038
was synthesized, and the conjugation of the crosslinkers was performed as described in above examples. The synthesized TCO-peptide 7 and tetrazine-peptide 7 were examined using MALDI-TOF.
The present TCO-peptide 7, as illustrated below, had a m.w. of 1736.78 daltons.
Figure PCTCN2016071184-appb-000039
The present tetrazine-peptide 7, as illustrated below, had a m.w. of 1820.62 daltons.
Figure PCTCN2016071184-appb-000040
Example 6: Synthesis of peptide 8 (SEQ ID NO: 25) as peptide core, and conjugation of SH group of cysteine residue with maleimide-PEG3-TCO, maleimide-PEG4-tetrazine or maleimide-PEG5-DBCO as conjugating arm
Peptide 8 (Ac-C-Xaa-K-Xaa-K-Xaa-K； wherein Xaa was a PEGylated amino acid with 2 EG units； SEQ ID NO: 25) was synthesized by solid-phase peptide synthesis method and then purified using reverse phase HPLC to 95％purity. The reversed phase HPLC was conducted using a Kromasil 100-5C18 column (250 mm X 4.6 mm； 5 μm) , with a mobile phase of water and 0.1％TFA, a linear gradient of 10 ％to 40 ％acetonitrile over 12 minutes, at a flow rate of 1.0 mL/min and a column temperature of 25℃.
The identification of the synthesized peptide 8 was carried out by mass spectrometry ESI-MS. High resolution and high mass accuracy experiments were done on a LTQ Orbitrap XL ETD mass spectrometer (Thermo Fisher Scientific, San Jose, CA) equipped with standard ESI ion source. Mass ESI-TOF analyses were performed by GRC Mass Core Facility of Genomics Research Center, Academia Sinica, Taipei, Taiwan. The sample of the synthesized peptide showed a strong molecular ion at 981.9, corresponding to [M-H] -, indicating that the actual molecular weight of the PEGylated peptide was 983.0 daltons.
The conjugation of the crosslinkers was performed as described in above examples, and mass spectrometry ESI-MS was used to examine the products (illustrated below, in which the Xaa2 denotes a PEGylated amino acid with two EG units) .
The present TCO-peptide 8, as illustrated below, had a m.w. of 1478.87 daltons.
TCO-PEG3-C- (Xaa2-K) 3
The present tetrazine-peptide 8, as illustrated below, had a m.w. of 1584.92 daltons.
Tetrazine-PEG4-C- (Xaa2-K) 3
The present DBCO-peptide 8, as illustrated below, had a m.w. of 1613.8 daltons
DBCO-PEG5-C- (Xaa2-K) 3
Example 7: Synthesis of peptide 9 (SEQ ID NO: 26) as peptide core, and conjugation of SH group of cysteine residue with maleimide-PEG3-TCO as conjugating arm
Peptide 9 (Ac-C-Xaa-K-Xaa-K-Xaa-K-Xaa-K-Xaa-K； wherein Xaa was a PEGylated amino acid with 6 EG units； SEQ ID NO: 26) was prepared as set forth in an earlier Example. The identification of the synthesized peptide 9 was carried out by mass spectrometry ESI-MS. The sample of the synthesized peptide showed a strong molecular ion at 828.0,  corresponding to [M+3H] 3+, indicating that the actual molecular weight of the PEGylated peptide was 2480.7 daltons.
The conjugation of the crosslinker was performed as set forth in above examples, and then examined with mass spectrometry ESI-MS. The present TCO-peptide 9, as illustrated below, had a m.w. of 2975 daltons.
TCO-PEG3-C- (Xaa6-K) 5
Example 8: Synthesis of linker unit by conjugating NHS-PEG12-maleimide to NH2 groups of TCO- peptides  1 and 2
Two linking arms of PEG12-maleimide were attached to the peptide core TCO-peptide 1； while three linking arms of PEG12-maleimide were attached to the peptide core TCO-peptide 2. The crosslinker, NHS-PEG12-maleimide (succinimidyl- [ (N-maleimido-propionamido) -dodecaethyleneglycol]ester, was purchased from Thermo Fisher Scientific Inc. (Waltham, USA) . The conjugation procedure was performed per the manufacturer’s instruction； the peptide with lysine residues was dissolved in the conjugation buffer, phosphate buffered saline (PBS, pH 7.5) at 100 mM. NHS-PEG12-maleimide crosslinker was added to the dissolved peptide at 1 mM final concentration (20-fold molar excess over 0.1 mM peptide solution) . The reaction mixtures were incubated for 18 hours at room temperature. PEG12-maleimide-conjugated TCO-peptide 1 and peptide 2 were purified by reverse phase HPLC on a Supelco C18 column (250 mm X 4.6 mm； 5 μm) , using a mobile phase of acetonitrile and 0.1％trifluoroacetic acid, a linear gradient of 0％to 100％acetonitrile over 30 minutes, at a flow rate of 1.0 mL/min and a column temperature of 25℃. Figure 14 showed the reverse phase HPLC profile for the purification of PEG12-maleimide-conjugated TCO-peptide 2, with the peak being indicated with an arrow. 
The identification of the PEG12-maleimide-conjugated TCO-peptide 1 and peptide 2 was carried out by mass spectrometry MALDI-TOF.
 The present PEG12-maleimide-conjugated TCO-peptide 1, as illustrated below, was a peptide core-based linker unit carrying one coupling arm with a TCO group and two PEG linking arms with maleimide groups. The result of mass spectrometry MALDI-TOF indicated that the present molecular construct had a m.w. of 3330.7 daltons.
Figure PCTCN2016071184-appb-000041
]The present PEG12-maleimide-conjugated TCO-peptide 2, as illustrated below, was a peptide core-based linker unit carrying one coupling arm with a TCO group and three PEG linking arms with maleimide groups. Figure 15 showed the mass spectrometry MALDI-TOF result, indicating that the present molecular construct had a m.w. of 4332 daltons； (ESI-TOF) m/z (z＝4) : [M + 4H] +； calculated for C185H313N31O83S1 1083.7829； found 1083.7833) , corresponding to [M+Na] +.
Figure PCTCN2016071184-appb-000042
Example 9: Synthesis of linker unit by conjugating NHS-PEG12-maleimide to NH2 groups of tetrazine-peptide 2 and DBCO-peptide 1
Three linking arms of PEG12-maleimide were attached to tetrazine-peptide 2, while two linking arms were attached to DBCO-peptide 1. The conjugation of NHS-PEG12-maleimide to the NH2 groups of the lysine residues of the peptide cores was performed as described in the earlier Examples, and the products were identified using mass spectrometry MALDI-TOF.
As illustrated below, the present PEG12-maleimide-conjugated tetrazine-peptide 2 carried one coupling arm with a tetrazine group and three PEG linking arms with maleimide groups. Figure 16A showed the mass spectrometry MALDI-TOF result, indicating that the construct had a m.w. of 4461 daltons.
Figure PCTCN2016071184-appb-000043
As illustrated below, the present PEG12-maleimide-conjugated DBCO-peptide 1 carried one linking arm with a DBCO group and two PEG linking arms with maleimide groups. Figure 16B showed the mass spectrometry MALDI-TOF result, indicating that the construct had had a m.w. of 3445 daltons.
Figure PCTCN2016071184-appb-000044
Example 10: Synthesis of linker unit by conjugating NHS-PEG12-maleimide to NH2 groups of peptides 4 to 6
Two linking arms of PEG12-maleimide were attached to the peptide 4； while three linking arms of PEG12-maleimide were attached to the peptide 5 and peptide 6. The conjugation of NHS-PEG12-maleimide to the NH2 groups of the lysine residues of the peptide cores was performed as in the earlier Example, and the products were identified using mass spectrometry MALDI-TOF.
The present PEG12-maleimide-conjugated peptide 4, as illustrated below, had a m.w. of 2817.3 daltons； it was a peptide core-based linker unit carrying one alkyne group and two PEG linking arms with maleimide groups.
Figure PCTCN2016071184-appb-000045
The present PEG12-maleimide-conjugated peptide 5 (illustrated below) had a m.w. of 3839.2 daltons； it was a peptide core-based linker unit carrying one alkyne group and three PEG linking arms with maleimide groups.
Figure PCTCN2016071184-appb-000046
PEG12-maleimide-conjugated peptide 6 (illustrated below) had a m.w. of 3811.5 daltons； it was a peptide core-based linker unit carrying one azide group and three PEG linking arms with maleimide groups.
Figure PCTCN2016071184-appb-000047
Example 11: Synthesis of linker unit by conjugating NHS-PEG12-maleimide to NH2 groups of TCO-peptide 7 and tetrazine-peptide 7
Two linking arms of PEG12-maleimide were attached to a peptide core, the peptide 7 from the preceding Examples. The conjugation of NHS-PEG12-maleimide to the NH2  groups of the lysine residues of the peptide core was performed as described above, and the identification was carried out by mass spectrometry MALDI-TOF.
The present PEG12-maleimide-conjugated TCO-peptide 7, as illustrated below, had a m.w. of 3237.63 daltons； it was a peptide core-based linker unit carrying one an alkyne group, one coupling arm with a TCO group, and two PEG linking arms with maleimide groups.
Figure PCTCN2016071184-appb-000048
The present PEG12-maleimide-conjugated tetrazine-peptide 7, as illustrated below, had a m.w. of 3342.98 daltons； it was a peptide core-based linker unit carrying one alkyne group, one coupling arm with a tetrazine group, and two PEG linking arms with maleimide groups.
Figure PCTCN2016071184-appb-000049
Example 12: Synthesis of linker unit by conjugating NHS-PEG12-maleimide to NH2 groups of TCO-peptide 8 and tetrazine-peptide 8
Three linking arms of PEG12-maleimide were attached to the peptide cores, TCO-peptide 8 and tetrazine-peptide 8. The conjugation of NHS-PEG12-maleimide to the NH2 groups of the lysine residues of the peptide core was performed as in Example 8, and the identification was carried out by mass spectrometry MALDI-TOF.
The present PEG12-maleimide-conjugated TCO-peptide 8 (illustrated below) had a m.w. of 3774.9 daltons； it was a linker unit based on PEGylated amino acid and lysine； it carried one coupling arm with a TCO group and three PEG linking arms with maleimide groups.
Figure PCTCN2016071184-appb-000050
The present PEG12-maleimide-conjugated tetrazine-peptide 8 (illustrated below) had a m.w. of 3856.94 daltons (Figure 17； (ESI-TOF) m/z (z＝4) : [M + 4H] + Calculated for C171H287N23O71S1H3Na 964.7363； Found 964.7324) ； it was a linker unit based on PEGylated amino acid and lysine； it carried one coupling arm with a tetrazine group and three PEG linking arms with maleimide groups.
Figure PCTCN2016071184-appb-000051
Example 13: Synthesis of linker unit by conjugating NHS-PEG6-maleimide to NH2 groups of TCO-peptide 9
Five linking arms of PEG6-maleimide were attached to the peptide cores, TCO-peptide 9. The conjugation of NHS-PEG6-maleimide to the NH2 groups of the lysine residues of the peptide core was performed as in Example 8, the identification was carried out by mass spectrometry MALDI-TOF.
PEG6-maleimide-conjugated TCO-peptide 9 (illustrated below) had a m.w. of 5543.78 daltons (Figure 18； (ESI-TOF) m/z (z＝6) : [M + 6H] + Calculated for C244H421N29O101S1Na 924.297； Found 924.299) ； it was a linker unit based on PEGylated amino acid and lysine； it carried one coupling arm with a TCO group and five PEG linking arms with maleimide groups.
Figure PCTCN2016071184-appb-000052
Example 14: Synthesis of linker unit with 1, 3, 5-triaminobenzene conjugated with 1 NHS-PEG12-alkyne linking arm and 2 NHS-PEG12-maleimide linking arms
1, 3, 5-triaminobenzene was purchased from BOC Sciences, Creative Dynamics Inc., NY, USA, and NHS-PEG12-alkyne linking arm and NHS-PEG12-maleimide from Thermo Fisher Scientific Inc. Waltham, MA, USA. The conjugation of the linking arms employed a two-step procedure as shown in scheme 13. In step (i) , 1, 3, 5-triaminobenzene was dissolved in the conjugation buffer (phosphate buffered saline, PBS, PH 7.2) at 1 mM and NHS-PEG12-alkyne crosslinker was added to 1, 3, 5-triaminobenzene solution at 1 mM final concentration (1:1 molar ratio) . Thereafter, 4 μl of the 250 mM NHS-PEG12-alkyne stock solution was added to 1 ml of 1, 3, 5-triaminobenzene solution. The reaction mixtures were incubated for 1 hour at room temperature. In step (ii) , NHS-PEG12-maleimide crosslinker was added to the incubated solution in the step (i) at 10 mM final concentration (1:30 molar ratio) . Next, 30 μl of the 250 mM NHS-PEG12-maleimide stock solution was added to 125 μl of incubated solution； then 845 μl of the conjugation buffer was added to make the final solution 1 ml. The reaction mixtures were incubated for 2 hours at room temperature.
<<Scheme 13 Two-step synthesis of 1, 3, 5-triaminobenzene conjugated with one NHS-PEG12-alkyne linking arm and two NHS-PEG12-maleimide linking arms>>
Figure PCTCN2016071184-appb-000053
The product, 1, 3, 5-triaminobenzene conjugated with one NHS-PEG12-alkyne coupling arm and two NHS-PEG12-maleimide linking arms, was purified by subjecting the reaction mixture through reverse phase HPLC column and collecting the fractions containing the  linker unit. The product was analyzed by mass spectroscopy ESI (Figure 19) . The data showed (ESI-TOF) m/z: [M+H] + -calculated for C104H180N7O46 2263.1955； found 2263.1920. The three isotopic peaks were also visible in the MS spectrum at 2264.1934, 2265.1938 and 2266.1927, corresponding to [M+H+1] +, [M+H+2] + and [M+H+3] +.
Example 15: Conjugation of five DM1-SMCC molecules to TCO-peptide 9
DM1-SMCC, which was N2’-Deacetyl-N2’- (3-mercapto-1-oxopropyl) -maytansine (DM1) modified by a linker, succinimidyl-4- (N-maleimidom-ethyl) cyclohexan-1-carboxylate (SMCC) , was purchased from ALB Technology Inc., Hong Kong, China. TCO-peptide 9 with free amine groups was dissolved in 100 mM sodium phosphate buffered at pH 7.5. DM1-SMCC was added to the TCO-peptide 9 solution at 1 mM final concentration (25-fold molar excess over the 0.04 mM TCO-peptide 9 solution) by adding 4 μl of the 250 mM DM1-SMCC solution per milliliter of NH2-containing TCO-peptide 9 solution. The reaction mixtures were incubated for 24 hours at room temperature. The reaction product was separated by HPLC and then lyophilized. The TCO-peptide 9 with five DM1-SMCC molecules was purified by reverse phase HPLC on a Supelco C18 column (250 mm X 4.6 mm； 5 μm) , using a mobile phase of acetonitrile and 0.1％trifluoroacetic acid, a linear gradient of 30％to 100％acetonitrile over 30 minutes, at a flow rate of 1.0 mL/min and a column temperature of 25℃.
Figure 20 showed the reverse phase HPLC profile for the purification of TCO-peptide 9 with five DM1-SMCC molecules (also referred to as a drug bundle) ； the peak being indicated with an arrow. The mass spectroscopic analysis of the thus-synthesized drug bundle, as provided in Figure 21, indicated that the molecular construct had a m.w. of 7803 daltons.
The present drug bundle, as illustrated below, was composed of a linker unit with a free TCO functional group and a set of five DM1 molecules as effector elements.
Figure PCTCN2016071184-appb-000054
Example 16: Conjugation of LPS molecules to TCO-peptide 1
LPS from Salmonella enterica sv. Minnesota (Cat No. L2137, Sigma) was chromatographically purified on the Superdex 200 10/300 Tricon column (HR, GE Healthcare) in an
Figure PCTCN2016071184-appb-000055
Explorer FPLC system. The elution buffer, 50 mM HEPES, pH7.5, was used. The sample was injected and eluted isocratically at 0.5 mL/min and collected in 1-mL fractions. The fractions containing LPS were then dialyzed against MilliQ water using a 3500 MWCO membrane at 4℃overnight. The dialyzed LPS were lyophilized for subsequent conjugation.
Before the conjugation, the purified LPS was activated as follows. An amount of 1 ml of 2 mg/ml of an aqueous LPS solution was vortexed for 3 min and sonicated for 15 min at 25℃. Then, 1 ml of 4.5 mM sodium deoxycholate (NaDC) was added； 100 μl of 2.5 mM EDTA solution was added. The mixture was stirred for 30 minutes at 37℃, sonicated for 15 minutes, and stirred for another 30 minutes at 37℃. 40 μl of 100 mg/ml 1-cyano-4-dimethylaminopyridinium tetrafluoroborate (CDAP) in acetonitrile was added. After 30 seconds, 40 μl of 0.2M aqueous triethylamine (TEA) was added. The mixture was kept at 25℃for further 150 seconds with stirring to allow activation of LPS by CDAP
LPS derived from Salmonella enterica sv. Minnesota was reacted with dansyl hydrazine to introduce a hydrazine group for subsequent coupling with amine group on a linker unit. Briefly, 1 ml of 2.0 mg/ml dansyl hydrazine in 0.1 M sodium borate buffer, pH 9.3, was added to the CDAP-activated LPS. The mixture was left to react overnight in the dark at 25℃under stirring. The reaction was quenched by adding 100 μl of ethanolamine. The unreacted dansyl hydrazine was removed by dialysis against Milli-Q water using a 3, 500 MWCO dialysis membrane for 24 hours at 4℃in the dark. The sample was characterized using fluorescence spectroscopy by measuring the emission spectra under the excitation at 325 nm. Figure 22 showed that LPS, upon the reaction with dansyl hydrazine, exhibited an emission maximum at 495 nm in fluorescence spectrophotometric analysis.
The identification of the purified LPS and the dansyl-activated LPS was carried out by mass spectrometry MALDI-TOF. The purified LPS had a m.w. of 3143 daltons； the dansyl-activated LPS had a m.w. of 3651 daltons, indicating one LPS conjugated with two dansyl hydrazine molecules； one dansyl hydrazine molecule had a m.w. of 265 daltons.
The conjugation of LPS molecules to the NH2 groups of the lysine residues of TCO-peptide 1 was performed. Briefly, 0.67 mole of the dansyl-activated LPS was mixed with 0.067 mole of TCO-peptide 1 in 0.1 M sodium bicarbonate buffer, pH 9.5, at room temperature overnight.
The present drug bundle, as illustrated below, was composed of a linker unit with a free TCO functional group and a set of two LPS molecules as effector elements.
Figure PCTCN2016071184-appb-000056
Example 17: Conjugation of a imiquimod molecule with NHS-PEG6-maleimide-conjugated TCO-peptide 9
The NH2 group of the imiquimod molecule was reacted with a homo-bifunctional crosslinker, NHS-PEG5-NHS (Conju-probe Inc. ) at a 1:3.5 molar ratio. Mass spectrometric analysis showed that PEG5-NHS conjugated with imiquimod had a m.w. of 658.36 daltons (Figure 23) .
The product, imiquimod-PEG5-NHS, was purified by HPLC to remove the excess, unreacted crosslinkers. TCO-peptide 9 and imiquimod-PEG5-NHS were then mixed in 100 mM sodium phosphate buffer at pH 7.5 at 25℃for 18 hours. Mass spectrometric analysis showed that the drug bundle with imiquimod had a m.w. of 5135 daltons.
The present drug bundle, as illustrated below, was composed of a linker unit with a free TCO functional group and a set of five imiquimod molecules as effector elements.
Figure PCTCN2016071184-appb-000057
Example 18: Conjugation of DOTA-NHS to TCO-peptide 9
DOTA-NHS (1, 4, 7, 10-tetraazacyclododecane-1, 4, 7, 10-tetraacetic acid N-hydroxy-succinimide ester) was purchased from Macrocyclics, Inc. Dallas, USA. Conjugation of DOTA-NHS to TCO-peptide 9 employed a two-step procedure as illustrated in Scheme 14. In the first step, TCO-peptide 9 was dissolved in the conjugation buffer (phosphate buffered saline, PBS, with 5 mM EDTA pH 7.0) at 1 mM. The reaction mixtures were incubated for overnight at room temperature. In the second step, the DOTA-NHS ester was added to the incubated solution at 100 mM final concentration (1:100 molar ratio or 1:20 equivalent ratio) . Since the DOTA-NHS ester was acidic because of containing TFA, the pH of the solution was adjusted to 8.0 in order to activate the NHS ester-NH2 coupling reaction. The reaction mixtures were incubated overnight at room temperature.
<<Scheme 14 Two-step procedure for conjugation of DOTA-NHS to TCO-peptide 9>>
Figure PCTCN2016071184-appb-000058
According to the data in Figure 24A, the present molecular construct had a m.w. of 4907.685； (ESI-TOF) m/z (z＝5) : [M + 3H] +； calculated for C214H38N39O86S1 982.5358； found 982.5370.
Example 19: Chelation of Yttrium atoms by DOTA-conjugated linker unit based on TCO-peptide 9
Scheme 15 showed the chelation of five Y3+ ions by DOTA-conjugated TCO-peptide 9. Herein, Y (NO3) 3 solution was added to the reaction mixtures at a 1:100 molar ratio,  incubated for 2 hours at room temperature. Free DOTA-NHS and Y3+ ions were removed from reaction mixtures by using NAP-10 Sephadex G-25 column.
<<Scheme 15 Chelation of Yttrium atom by DOTA-conjugated TCO-peptide 9>>
Figure PCTCN2016071184-appb-000059
DOTA-conjugated TCO-peptide 9 with bound Y3+ ions was analyzed by mass spectroscopy MALDI-TOF. Mass spectrometric analysis showed that the sample of DOTA-conjugated TCO-peptide 9 with bound Y3+ ions had a m.w. of 5355 daltons (Figure 24B) .
Illustrated below is the present drug bundle, which was composed of a linker unit with a free TCO functional group and a set of five DOTA groups respectively chelating an Y3+ ion as effector elements.
Figure PCTCN2016071184-appb-000060
Example 20: Isolation of VH and VL sequences from hybridoma cell lines producing monoclonal antibodies respectively specific for human CD79a, CD79b, and collagen VII for the preparation of scFv
Mouse B cell hybridoma 24C10 producing anti-CD79a antibody and hybridoma 1F10 producing anti-CD79b antibody were generated in our laboratory employing standard hybridoma methodology. The mouse hybridoma line LH7.2 specific for human collagen VII was a gift from Prof. Irene M. Leigh, University of Dundee, U. K. Poly (A) + RNA was reverse-transcribed with a SuperScript III RT-PCR system (Invitrogen, Carlsbad, USA) , and the first strand cDNA was synthesized. To determine the sequence of variable region of 24C10, 1F10, and LH7.2, cDNA of VH and VL were amplified by PCR using a set of DNA primers provided by Ig-primer Sets (Novagen, Madison, USA) according to the manufacturer’s instructions. The sequences of VH and VL for all clones were determined.
The cDNA sequences of VH and of VL of mouse anti-human CD79a monoclonal antibody clone 24C10 are indicated in SEQ ID NO: 27 and SEQ ID NO: 28, respectively； the cDNA sequences of VH and of VL of mouse anti-human CD79b monoclonal antibody clone 1F10 are indicated in SEQ ID NO: 29 and SEQ ID NO: 30, respectively； the cDNA sequences of VH and of VL of mouse anti-human collagen VII monoclonal antibody clone LH7.2 are indicated in SEQ ID NO: 31 and SEQ ID NO: 32, respectively.
Example 21: Preparation of scFv specific for human CD79b and collagen VII
To produce the scFv of anti-CD79b antibody 1F10 (SEQ ID NO: 33) and scFv of anti-human collagen VII antibody LH7.2 (SEQ ID NO: 34) , DNA sequences encoding VL-GSTSGSGKPGSGEGSTKG-VH- (GGGGS) 2-C were synthesized. A flexible linker GGGGSGGGGS and a cysteine residue were installed at the C-terminus of the scFv, so that the modified scFv could be subsequently linked to the maleimide group of linking arms in various linker units of this invention.
The scFv-encoding sequence was placed in pG1K expression cassette. Expi293F cells were seeded at a density of 2.0×106 viable cells/ml in Expi293F expression medium and maintained for 18–24 hours prior to transfection to ensure that cells were actively dividing at the time of transfection. On the day of transfection, 7.5×108 cells in 255 ml medium in a 2-liter Erlenmeyer shaker flask were transfected by ExpiFectamineTM 293 transfection reagent. The transfected cells were incubated at 37℃for 16 to 18 hours post-transfection in an orbital shaker (125 rpm) and the cells were added ExpiFectamineTM 293 transfection enhancer 1 and enhancer 2 to the shaker flask, and incubated for another  6 days. Culture supernatants were harvested and scFv proteins in the media were purified using Protein L affinity chromatography. Figures 25A and 25B respectively showed SDS-PAGE and ELISA analysis of purified scFv proteins of anti-CD79b antibody 1F10. Figures 25C and Figure 25D respectively showed SDS-PAGE and ELISA analysis of purified scFv proteins of anti-collagen VII antibody LH7.2.
Example 22: Production of scFv of trastuzumab, rituximab, centuximab, nivolumab, ipilimumab, ranibizumab, adalimumab, and mutated teplizumab by HEK293 overexpression system
The scFv derived from those antibodies were designed to contain a flexible linker of GGGGSGGGGS and a terminal cysteine residue at the C-terminus. The cysteine residue provides a sulfhydryl group for conjugation with maleimide group present at the free ends of liking arms in various linker units. To produce the scFv of trastuzumab, rituximab, centuximab, nivolumab, ranibizumab, adalimumab, and a mutated teplizumab, we used the VH and VL DNA sequences of those humanized antibodies without further codon optimization. DNA sequences encoding VL-GSTSGSGKPGSGEGSTKG-VH- (GGGGS) 2-C were synthesized. The teplizumab antibody molecule contains a cysteine residue in CDR3 of VH, which interferes with SH-maleimide conjugation explained above. We therefore prepared a mutated teplizumab substituting the cysteine residue with a serine residue. The amino acid sequences of the scFv of trastuzumab, rituximab, centuximab, nivolumab, ranibizumab, adalimumab, and the mutated teplizumab, prepared for the experiments of this invention are set forth in SEQ ID NOs: 35 to 42, respectively.
For preparing scFv proteins using mammalian expression systems, we used the overexpression system based on Expi293FTM cell line for preparing 10-500 mg of scFv for experimentation. The yields were sufficient for preparing various constructs involving a specific scFv for in vitro tests and rodent animal models. The system employed ExpiFectamineTM 293 transfection kit (Life Technologies, Carlsbad, USA) consisting of the Expi293FTM cell line, the cationic lipid-based ExpiFectamineTM 293 Reagent and ExpiFectamineTM 293  transfection Enhancers  1 and 2, and the medium (Gibco, New York, USA) .
The scFv-encoding sequence was placed in pG1 K expression cassette. Expi293F cells were seeded at a density of 2.0×106 viable cells/ml in Expi293F expression medium and maintained for 18 to 24 hours prior to transfection to ensure that the cells were actively dividing at the time of transfection. On the day of transfection, 7.5×108 cells in 255ml medium in a 2-liter Erlenmeyer shaker flask were transfected by ExpiFectamineTM 293 transfection reagent. The transfected cells were incubated at 37℃for 16 to 18 hours post-transfection in an orbital shaker (125 rpm) and the cells were added ExpiFectamineTM 293 transfection enhancer 1 and enhancer 2 to the shaker flask, and incubated for another 5 to 6 days. Culture supernatants were harvested and scFv proteins in the media were purified using Protein L affinity chromatography. In our experience with adalimumab and trastuzumab scFv proteins, over 300 mg of purified scFv could be obtained from the 1 liter culture. Figure 26A showed SDS-PAGE (10％) analysis of purified scFv of trastuzumab (lane 1) and adalimumab (lane 2) , while Figures 26B and 26C respectively showed ELISA analyses of purified scFv of trastuzumab and adalimumab. Figures 26D and 26E respectively showed SDS-PAGE and ELISA analyses of purified scFv of centuximab, in which the trastuzumab scFv (anti-HER2 scFv) was used as a negative control.
Example 23: Production of scFv of adalimumab by an yeast Pichia expression system
The intended scFv constructs were the same as in the preceding Example, while the signal peptides used were different.
DNA sequence of scFv of adalimumab was synthesized and subcloned using primers (forward 5’-GTATCTCTCGAGAAAAGAGATATTCAGATGACGCAATCCCC-3’ (SEQ ID NO: 43) and reverse 5’-GTATCTGCGGCCGCTTAACAGGAGCCACCGCCAC-3’ (SEQ ID NO: 44) ) containing XhoI and NotI restriction sites into pPICZα expression vector, in which the Kex2 signal peptide allowed for extracellular secretion of scFv of adalimumab. The expression plasmid was then transformed into Pichia pastoris by electroporation. To screen for high yield clones, ELISA was performed to measure the expression levels of scFv of adalimumab. Out of 480 transformants, five were selected for further protein induction and examination by SDS-PAGE. The clone scFv_1-A2 was selected for subsequent large-scale fermentation.
The high-yield clone scFv_1-A2 was inoculated in 100 mL of buffered glycerol-complex medium (BMGY, containing 1％yeast extract, 2％peptone, 100 mM K3PO4, 1.34 YNB, 0.4 mg/L biotin and 1％glycerol, pH 6.0) and cultured at 30℃, 200 rpm for 24 hours. On the next day, the culture was changed to a fermentation condition maintaining at 30℃, 30％of dissolved oxygen and pH 6.0. After being fermented for 24 hours, nitrogen source (YE, peptone) and methanol (0.5％, v/v) was added to induce protein expression. The culture supernatant was harvested for protein purification.
A mass spectrometric analysis showed that the scFv had a m.w. of 27296.28 daltons. Figure 27A showed SDS-PAGE analysis of the purified scFv of adalimumab, and Figure 27B showed ELISA analysis of the purified scFvs of adalimumab. The size of the scFv was as expected and the yeast-produced scFv of adalizumab bound to human TNF-α equally well as Expi-293F-produced scFv of adalizumab.
Example 24: Preparation of CCK analogue
The peptide analogue of CCK (CGGGGSDY (SO4H) L (N) GWL (N) DF-NH2； SEQ ID NO: 45) was designed to be composed of an 8-amino acid segment of CCK with three unusual amino acid residues and a consecutive N-terminal extension of six amino acid residues (CGGGGS) with a cysteine residue at the terminal. The tyrosine residue (Y) was sulfated at its OH group on the aromatic ring and X was a norleucine residue. The cysteine residue provided an SH group for conjugation with PEG-maleimide linking arms of the linker unit according to the present disclosure. The peptide was custom-synthesized by Kelowna Inc., Taipei, Taiwan.
Example 25: Preparation of TCO-and DBCO-scFv specific for CD3
The DNA sequence encoding SEQ ID NO: 42 was synthesized and expressed as in the above Examples. The sequences of VL and VH of scFv specific for CD3 were those of VL and VH of mutated Teplizumab. For the conjugation with Mal-PEG3-TCO and Mal-PEG5-DBCO (Conju-probe, Inc. ) , the cysteine residue at the C-terminal end of the purified scFv of the mutated teplizumab was reduced by incubating 5 mM DTT at room temperature for 4 hours with gentle shaking. The buffer of reduced anti-CDthree scFvs was exchanged to sodium phosphate buffer (100 mM sodium phosphate, pH7.0, 50 mM  NaCl, and 5 mM EDTA) by using NAP-10 Sephadex G-25 column. After the reduction reaction and buffer exchange, conjugation was conducted overnight at room temperature in a reaction molar ratio of 1:1 ( [Mal-PEG3-TCO or Mal-PEG5-DBCO: [scFv] ] . The excess crosslinker was removed by a desalting column and the TCO-conjugated and DBCO-conjugated scFv products were analyzed.
The results of mass spectroscopy MALDI-TOF analysis indicated that the sample of TCO-conjugated scFv specific for CD3 had a m.w. of 28053 daltons； while the sample of DBCO-conjugated scFv specific for CD3 had a m.w. of 28178 daltons. The purity of TCO-conjugated scFvs specific for CD3 was identified through Coomassie staining of 12％SDS-PAGE (data not shown) . Figure 28A and Figure 28B show, respectively, the ELISA analysis of TCO-conjugated scFv and DBCO-conjugated scFv specific for CD3, in which anti-PD1 scFv and anti-CDthree scFvs were used as a negative control and positive control, respectively. According to the ELISA results, both TCO-conjugated scFv and DBCO-conjugated scFv specific for CD3 bound to CD3-Fc-fusion protein.
Example 26: Conjugation of three scFvs specific for CD79b to three PEG12-maleimide linking arms based on tetrazine-peptide 2
This example aimed to demonstrate that three scFvs could be conjugated to the three PEG12-maleimide linking arms based on tetrazine-peptide 2. Prior to conjugation with the tetrazine-peptide 2 that had three PEG12-maleimide linking arms, 1F10 scFv was incubated with DTT at a molar ratio of 2:1 ( [DTT] : [scFv] ) at 25℃for 4 hours with gentle shaking to keep its C-terminal cysteine in reduced form. Subsequently, the buffer of reduced 1F10 scFv was exchanged to maleimide-SH coupling reaction buffer (100 mM sodium phosphate, pH 7.0, 50 mM NaCl and 5 mM EDTA) by using an NAP-10 Sephadex G-25 column (GE Healthcare) . After the reduction and buffer exchange, the conjugation to the tetrazine-peptide 2 having three PEG12-maleimide linking arms was conducted overnight at 4℃at a molar ratio of 1:4 ( [linker] : [Protein] ) .
Example 27: Purification of the targeting linker unit containing three scFvs specific for CD79b linked to the three PEG12-maleimide linking arms based on tetrazine-peptide 2
The reaction mixture of the preceding example was applied to a size exclusion chromatography column S75. The PEG12-maleimide-conjugated tetrazine-peptide 2 conjugated with three scFvs specific for CD79b was separated from the free scFv, free PEG12-maleimide-conjugated tetrazine-peptide 2 and the PEG12-maleimide-conjugated tetrazine-peptide 2 conjugated with 1 and two scFvs specific for CD79b by size exclusion chromatography column S75. Figure 29A was the FPLC elution profile on a synthesized targeting linker unit composed of a linker unit with a free tetrazine functional group and a set of three scFvs specific for human CD79b as targeting elements. The product (i.e., the PEG12-maleimide-conjugated tetrazine-peptide 2 having a free tetrazine functional group and being conjugated with a set of three scFvs specific for CD79b) was purified in the elution fractions and shown in lane 5 to 7 of the 10％SDS-PAGE analysis shown in Figure 29B. .
Example 28: Analysis of targeting linker unit containing three scFvs specific for CD79b linked to the three PEG12-maleimide linking arms based on tetrazine-peptide 2 by mass spectrometry MALDI-TOF
The sample of the targeting linker unit of three scFvs specific for CD79b linked to the three PEG12-maleimide linking arms based on tetrazine-peptide 2 was confirmed by using mass spectrometry MALDI-TOF. The median of experimental molecular weight was consistent with the median of theoretical molecular weight of three 1 F10 scFv conjugated to tetrazine-peptide 2 with three PEG12-maleimide linking arms. According to the mass spectrometric profile in Figure 29C, the present targeting linker unit had the median molecular weight of 85996 daltons. Illustrated below is the present targeting linker unit that was composed of a linker unit with a free tetrazine functional group and a set of three scFvs specific for human CD79b as targeting elements.
Figure PCTCN2016071184-appb-000061
Example 29: Preparation of targeting linker unit based on tetrazine-peptide 2 with three scFvs specific for HER2/neu
The conjugation of scFv to the linker unit of prepared in an earlier Example and the purification and analysis of the product were the same as described in the preceding Examples. Figure 30A showed the SDS-PAGE analysis of the synthesized product, indicating that the preparation was relatively pure. However, molecules with substantial PEG component generally migrate slowly in SDS-PAGE than proteins with the same molecular weight. Figure 30B showed the mass spectrometric analysis, indicating that the purified linker unit had a m.w. of 86120 daltons. Illustrated below is the present targeting linker unit, which was composed of a linker unit with one free tetrazine functional group and a set of three scFvs specific for human HER2/neu as targeting elements.
Figure PCTCN2016071184-appb-000062
Example 30: Preparation of effector linker units based on TCO-peptide 2 with three scFvs specific for TNF-α or PD-1
The conjugation of scFv to the linker unit prepared and the purification and analysis of the product were the same as the preceding Examples.
Shown in Figure 30C was the mass spectrometric analysis of the present effector linker unit that was composed of a linker unit with a free TCO functional group and a set of three scFv specific for human TNF-α as effector elements (illustrated below) . As indicated in Figure 30C, this effector linker unit had a molecular weight of 86134 daltons.
Figure PCTCN2016071184-appb-000063
Figure 30D and Figure 30E respectively showed SDS-PAGE and mass spectrometric analyses of another effector linker unit that had one free TCO functional group and a set of three scFvs specific for human PD-1 as effector elements (illustrated below) . As indicated  in Figure 30E, this effector linker unit had a molecular weight of 88431 daltons.
Figure PCTCN2016071184-appb-000064
Example 31: Preparation of targeting linker unit based on tetrazine-peptide 2 with three CCK peptide molecules
The CCK peptide was prepared in an earlier Example. The conjugation of the peptide to the 3-arm linker was performed as described in the preceding Examples. Mass spectrometric analysis showed that the linker-unit with three CCK peptides had a m.w. of 8801 daltons (Figure 31) . Specifically, this targeting linker unit was composed of a linker unit with a free tetrazine functional group and a set of three CCK peptides as targeting elements.
Figure PCTCN2016071184-appb-000065
Example 32: Preparation of targeting linker unit based on TCO-peptide 7 with two scFvs specific for CD20
In this example, a linker unit with two functional groups for conjugating with different linker units was prepared. This targeting linker unit served as the center linker unit in a molecular construct with three linker units, which comprised two targeting linker units and one effector linker unit. In our design, the two targeting linker units were joined via iEDDA reaction between the tetrazine and TCO groups, while the center linker unit and the effector linker unit were joined via CuAAC reaction between the alkyne and azide groups.
The conjugation of scFvs to the linker unit prepared in an earlier Example and the purification and analysis of the product were the same as described in preceding Examples. The resultant targeting linker-unit (illustrated below) was composed of a linker-unit with a  free TCO functional group, a free alkyne group, and a set of two scFvs specific for human CD20 as targeting elements. The mass spectrometric analysis provided in Figure 32 indicated that such targeting linker unit had m.w. of 56949 daltons (indicated with an arrow) .
Figure PCTCN2016071184-appb-000066
Example 33: Conjugation of two scFvs specific for VEGF-A to linker unit with one free TCO group and two PEG linking arms with maleimide groups
The conjugation of scFv to the linker unit prepared in an earlier Example and the purification and analysis of the product were the same as described in preceding Examples.
Illustrated below is the resultant linker unit, an effector linker-unit being composed of a linker unit with a free TCO functional group and a set of two scFvs specific for human VEGF-A as effector elements. The mass spectrometric analysis indicated that this linker unit had a m.w. of 59187 daltons (Figure 33) .
Figure PCTCN2016071184-appb-000067
Example 34: Preparation of molecular construct with three scFv specific for CD79b as targeting element and one scFv specific for CD3 as effector element
In this example, the targeting linker unit of the preceding examples and a TCO-scFv specific for CD3 were coupled via tetrazine-TCO iEDDA reaction. Specifically, the targeting linker unit had three scFv specific for CD79b and one free tetrazine group.
The procedure for tetrazine-TCO ligation was performed per the manufacturer’s instructions (Jena Bioscience GmbH, Jena, Germany) . Briefly, 113 μl of the targeting linker unit (12.4 mg/ml) was added to the solution containing the effector unit at a molar ratio of 1:2 ( [tetrazine] : [TCO] ) . The reaction mixture was incubated for 3 hours at room temperature.
The product was subjected to mass spectrometric analysis, and the result indicated a molecular weight of 114025 daltons (Figure 34A) .
The product, a single linker unit molecular construct with three scFvs specific for CD79b as targeting elements and one scFv specific for CD3 as an effector element, is illustrated below.
Figure PCTCN2016071184-appb-000068
Example 35: Preparation of molecular construct with three scFvs specific for HER2/neu as targeting element and one scFv specific for CD3 as effector element
The targeting linker unit prepared in an earlier Example and the TCO-scFv specific for CD3 were coupled via the tetrazine-TCO iEDDA reaction.
The procedure for tetrazine-TCO ligation was performed as described in the previous Example. The product, as illustrated below, was a single linker unit molecular construct with three scFvs specific for HER2/neu as targeting elements and one scFv specific for CD3 as an effector element. The mass spectrometric analysis shown in Figure 34B indicated that this molecular construct had a molecular weight of 112046 daltons.
Figure PCTCN2016071184-appb-000069
Example 36: Preparation of molecular construct with effector linker unit with two scFvs specific for VEGF-A and long-chain PEG
The long-chain PEG (linear, 20kDa) with a tetrazine group at one end was purchased from Click Chemistry Tools (Scoottsdale, PA, USA) . The coupling of the effector linker unit  and tetrazine-long-chain PEG were coupled by an iEDDA reaction using a protocol similar to that described in the above Example. Figure 35 showed the SDS-PAGE analysis of the reaction mixtures of TCO-peptide 1 after the conjugation with scFv of anti-VEGF-A (lane 2) and further with tetrazine-20 kDa PEG (Lane 2) . Arrow #1 and #2 were respectively TCO-peptide 1 conjugated with one and two scFvs of anti-VEGF-A； arrow #3 and #4 were respectively TCO-peptide 1 conjugated with one and two scFvs of anti-VEGF-A, as well as one tetrazine-20 kDa PEG chain.
Illustrated below is the present molecular construct with two scFvs of anti-VEGF-A and one 20 kDa PEG chain.
Figure PCTCN2016071184-appb-000070
Example 37: Preparation of joint-linker molecular construct composed of targeting linker unit with three scFvs specific for CD79b and effector linker unit with five DM1 molecules
In this example, a joint-linker molecular construct with three scFvs specific for CD79b and a drug bundle of PEG- (SMCC-DM1) 5 was constructed. The molecular construct was made by a TCO-tetrazine iEDDA reaction as described in the preceding Examples. The product, as illustrated below, was a joint-linker molecular construct with three scFvs specific for CD79b and one drug bundle having five DM1 molecules. Figure 36A, Figure 36B, and Figure 37 respectively showed the SDS-PAGE, mass spectrometric (indicating a molecular weight of 91144 daltons) , and ELISA analyses of the present joint-linker molecular construct. Arrow #1 was a linker unit with three scFvs of anti-CD79b； Arrow 2 was a joint-linker molecular construct with three scFvs of anti-CD79b and a drug bundle with five DM1 molecules. The ELISA results showed that the linker unit with three scFvs of anti-CD79b and the joint-linker molecular construct with three scFvs of anti-CD79b and a drug bundle of five DM1 molecules bound specifically to CD79b-Fc fusion protein.
Figure PCTCN2016071184-appb-000071
Example 38: Preparation of joint-linker molecular construct composed of targeting linker unit with three scFvs specific for HER2/neu and effector linker unit with five DM1 molecules
In this example, a joint-linker molecular construct (illustrated below) with three scFvs specific for HER2/neu and a drug bundle having five DM1 molecules. Figure 38 showed SDS-PAGE analysis of this product. The SDS-PAGE pattern of the linker unit with three scFvs of anti-HER2/neu (without the drug bundle) was placed on the left side for comparison. The conjugation with a drug bundle of five DM1 molecules had made the molecular construct larger.
Figure PCTCN2016071184-appb-000072
Example 39: Preparation of joint-linker molecular construct composed of targeting linker unit with three molecules of CCK8 analogue and effector linker unit with five DM1 molecules
In this example, a targeting linker unit with three CCK peptide analogue molecules and one free tetrazine group and an effector linker unit (adrug bundle) with five DM1 molecules and one free TCO group were coupled via an iEDDA reaction as set forth in the preceding Example. Illustrated below was the resultant joint-linker molecular constructs that had three CCK8 peptides and one drug bundle having five DM1 molecules. Figure 39 showed the mass spectrometric analysis of the molecular construct, indicating a m.w. of 16381 daltons.
Figure PCTCN2016071184-appb-000073
Example 40: Preparation of joint-linker molecular construct composed of targeting linker unit with three molecules of CCK8 analogue and effector linker unit with five DOTA chelating groups
In this example, a targeting linker unit with three CCK peptide analogue molecules and one free tetrazine group, and an effector linker unit (adrug bundle) with five DOTA groups and chelated Y+3 and one free TCO group were coupled via an iEDDA reaction as set forth in the preceding Example. Illustrated below was the resultant joint-linker molecular construct that had three CCK8 peptides and one drug bundle having five DOTA groups and chelated Y+3. Figure 40 showed the mass spectrometric analysis of the molecular construct, indicating a m. w. of 12654 daltons.
Figure PCTCN2016071184-appb-000074
Example 41: Preparation of joint-linker molecular construct composed of targeting linker unit with three scFvs specific for HER2/neu and effector linker unit with three scFvs specific for CTLA-4
In this example, a targeting linker unit with three scFvs specific for HER2/neu and one free tetrazine group and an effector linker unit with three scFvs specific for CTLA-4 and one free TCO group were coupled via iEDDA reaction as performed in the preceding Examples. The resultant joint-linker molecular construct, as illustrated below, had three scFvs specific for HER2/neu and three scFvs specific for CTLA-4. In SDS-PAGE anlaysis of the reaction mixture, a band of about 230 kDa. in size was observed.
Figure PCTCN2016071184-appb-000075
Example 42: Preparation of joint-linker molecular construct composed of targeting linker unit 1 with three scFvs specific for CD79b, targeting linker unit 2 with two scFvs specific for CD20, and effector linker unit with five DM1 molecules
In this example, the targeting linker unit (targeting linker unit 2) with two scFvs specific for CD20 from the preceding Example was used as the center linking unit, which was linked with the first targeting unit (targeting linker unit 1) via the via iEDDA reaction between the tetrazine group of the first targeting linker unit and the TCO group of the center linker unit. Also, the center linker unit and the effector linker unit were joined via CuAAC reaction between the alkyne group of the center linker unit and the azide group of the effector linker unit. Figure 41 showed the analysis of the reactants and reaction mixture at different reaction points. The dense band in lane 1 was purified scFv of anti-CD20； arrow 1 in lane 2 was the linker unit with two scFvs of anti-CD20, one TCO group and one alkyne group (targeting linker unit 2) ； arrow #2 in lane 3 was the linker unit with three scFvs of anti-CD79b and one tetrazine group (targeting linker unit 1) ； arrow #3 was the joint-linker comprising the targeting  linker units  1 and 2.
The present joint-linker molecular construct, as illustrated below, comprised three scFvs specific for CD79b (from the first targeting linker unit) , two scFvs specific for CD20 (from the center or the second targeting linker unit) , and five DM1 molecules (from the effector linker unit) .
Figure PCTCN2016071184-appb-000076
Example 43: Assay of biological activity of LPS upon the conjugation to peptide core through linking arm
To test the LPS biological activity of linker unit conjugated with LPS, TLR 4 stimulation cell-based assay was performed using HEK-blueTM detection kit (InvivoGen, San Diego, USA) according to manufacturer’s instruction. HEK-blueTM hTLR4 cells express two human genes, TLR4 and MD-2/CD14 co-receptor genes, and contain the secreted embryonic alkaline phosphatase (SEAP) reporter gene for monitoring nuclear factor (NF) -κB activation. Upon interaction with the TLR4 agonist, TLR4 transduces a signal to trigger the activation of NF-κB and to express secreted alkaline phosphatase, which can be detected by using detection medium (HEK-blueTM detection, a medium used for the quantification of secreted alkaline phosphatase； InvivoGen) and measured with a spectrophotometer.
Briefly, HEK-hTLR4 cells were cultured at a density of 2.5 × 104 cells in 96-well plates and maintained in complete DMEM with selective antibiotics, normocin. Cells were stimulated with different concentrations (2-fold dilutions from 100 μg/ml) of crude LPS, purified LPS, dansyl hydrazine modified LPS, and the LPS conjugated to peptide core for 18 hours. The activation of TLR4 was analyzed by measuring SEAP from the culture medium using a spectrophotometer at 620 nm.
Figure 42 showed the assay results of the biological activity of LPS, before and after modification. The LPS fraction suitable for the modification with dansyl hydrazine was purified, which had a biological activity that was similar to the crude LPS. Dansyl hydrazine-modified LPS and the LPS conjugated to peptide core had comparable partial activities.
Example 44: Assay of biological activity imiquimod upon the conjugation to peptide core through linking arm
To test the biological activity of PEG5-NHS conjugated with imiquimod, TLR 7 stimulation cell-based assay was performed using HEK-blueTM detection kit (InvivoGen, San Diego, USA) per the manufacturer’s instruction. HEK-blueTM hTLR7 cells express two human genes, TLR7 receptor gene and an secreted embryonic alkaline phosphatase  (SEAP) reporter gene. Upon interaction with the TLR7 agonist, TLR7 transduces a signal to trigger the activation of NF-κB and to express secreted alkaline phosphatase, which can be detected by using detection medium (HEK-blueTM detection, a medium used for the quantification of secreted alkaline phosphatase； InvivoGen) and measured with a spectrophotometer.
Briefly, HEK-hTLR7 cells were cultured at a density of 4 × 104 cells in 96-well plates and maintained in complete DMEM with selective antibiotics, normocin. Cells were stimulated with different concentrations (2-fold dilutions from 20 μg/ml) of imiquimod and the PEG5-NHS conjugated with imiquimod for 18 hours. The activation of TLR7 was analyzed by measuring SEAP from the culture medium using a spectrophotometer at 620 nm.
Figure 43 showed the assay results of the biological activity of imiquimod upon the conjugation with linking arm, indicating that the imiquimod molecule conjugated with a linking arm had similar biological activity as the unmodified imiquimod.
Example 45: Pharmacokinetic properties of molecular construct with two scFv of anti-VEGF-A and one 20kDa PEG in Balb/c mice
Balb/c mice, female, 10-week old, were used for this study. The scFv comprised in the molecular constructs was derived from ranibizumab, as prepared in an earlier example. Briefly, 100 μg of scFv of anti-VEGF-A and a linker unit with two scFvs anti-VEGF-A and one 20kDa PEG in 100 ml PBS were respectively injected into the mice via a tail vein. Blood samples were collected via orbital sinus bleeding at 2, 4, 24, 48, and 72 hours after the injection. The blood was allowed to clot, and the sera were collected. The concentration of anti-VEGF-A activity was assayed by ELISA using a 96-well plate coated with huVEGF-A recombinant protein in 2 μg/ml concentration, 50 μl per well. 100 μl aliquots of serum diluted in PBS containing 1％BSA and 1％skim milk were added into the wells and incubated at 37℃ for 2 hours. 100 μl HRP-conjugated protein L diluted in PBS at a ratio of 1:2000 was then added and incubated at 37℃ for 1hour. Next, 50 μl of TMB substrate was added for color development. The reaction was stopped by 50 μl of 1M HCl. Absorbance at 450 nm was measured with a plate reader.
The results, as summarized in Figure 44 showed that the molecular construct with 3scFv specific for VEGF-A and a 20kDa PEG chain maintained substantial serum concentrations even at 72 hours after the administration.
Example 46: Cytotoxic activities of joint-linker molecular construct with 3 scFvs CD79b and five DM1 molecules on Ramos cells
Ramos cells (2x104/well) were seeded into wells of 96-well plates in RPMI1640 medium containing 10％fecal bovine serum. After 2 hours, cells were treated with different concentrations (2-fold dilutions from 20 nM) of scFv of anti-CD79, a linker unit with three scFvs of anti-CD79b (without a drug bundle) , a linker unit with five DM1 molecules (adrug bundle) , and a molecular construct with three scFvs of anti-CD79b and five DM1 molecules. After being incubated for 6 hours, the culture medium was removed by centrifuging at 300 g for 5 minutes and replaced by a fresh medium, and the cells were further incubated for another 24 hours. Cell viability was then determined by alamarBlue cell viability reagent kit (Invitrogen) in accordance with the manufacturer’s instruction.
Figure 45 showed the results of the viability of Ramos cells of the four treatments groups. The molecular construct with three scFvs specific for CD79b and a drug bundle of five DM1 molecules caused approximately 50％of cytolysis of RAMOS cells.
Example 47: Construction of gene segments encoding 2-chain IgG4. Fc fusion protein containing scFv specific for human collagen II and scFv specific for TNF-α
Mouse B cell hybridoma II-II6B3 producing anti-collagen II antibody was purchased from Developmental Studies Hybridoma Bank at the University of Iowa. Poly (A) + RNA was reverse-transcribed with a SuperScript III RT-PCR system (Invitrogen, Waltham, USA) , and first strand cDNA was synthesized. The VH and VL nucleotide and amino acid sequences of II-II6B3 had not been published. To determine the sequences of variable regions of II-II6B3, cDNA of VH and VL were amplified by PCR using a set of DNA primers provided by Ig-primer Sets (Novagen, Madison, USA) per the manufacturer’s instructions. The amino acid sequence of VH and VL of II6B3 monoclonal antibody specific for collagen type II (CII, or COL2) are described in SEQ ID NOs: 46 and 47. The sequences of VL and VH of scFv specific for TNF-α were those of VL and VH of adalizumab.
Illustrated below is the configuration of 2-chain IgG4. Fc fusion protein molecular construct. The scFv1-scFv2-CH2-CH3 (human γ4) recombinant chain was configured by fusing two scFvs, one specific for human collagen II and the other specific for human TNF-α, to the N-terminal of CH2 domain of IgG4. Fc through a flexible hinge region. The first scFv (specific for collagen II) had an orientation of VL-linker-VH and the second scFv (specific for TNF-α) was in VH-linker-VL. The VL and VH in each of the two scFv were connected by a hydrophilic linker, GSTSGSGKPGSGEGSTKG. The two scFvs were connected via a flexible linker, (GGGGS) 3. The sequence of the recombinant chain in the IgG4. Fc fusion protein molecular construct illustrated below is described in SEQ ID NO: 48.
Illustrated below is the configuration of the present 2-chain (scFv α collagen II) - (scFv α TNF-α) -hIgG4. Fc molecular construct.
Figure PCTCN2016071184-appb-000077
Example 48: Expression and purification of recombinant 2-chain (scFv α CII) - (scFv α TNF-α) -hIgG4. Fc fusion protein
In this Example, the gene-encoding sequence was placed in pcDNA3 expression cassette. Expi293F cells were seeded at a density of 2.0 × 106 viable cells/ml in Expi293F expression medium and maintained for 18 to 24 hours prior to transfection to ensure that the cells were actively dividing at the time of transfection. On the day of transfection, 7.5×108 cells in 255-ml medium in a 2-liter Erlenmeyer shaker flask were transfected by ExpiFectamineTM 293 transfection reagent. The transfected cells were incubated at 37℃ for 16 to 18 hours post-transfection in an orbital shaker (125 rpm) and the cells were added ExpiFectamineTM 293 transfection enhancer 1 and enhancer 2 to the shaker flask, and incubated for another 7 days. Culture supernatants were harvested and recombinant  2-chain (scFv α CII) - (scFv α TNF-α) -hIgG4. Fc fusion proteins in the media were purified using Protein A chromatography. Following buffer exchange to PBS, the concentration of (scFv α CII) - (scFv α TNF-α) -hIgG4Fc proteins was determined and analyzed by SDS-PAGE； see, Figure 46； II-II6B3 (lane 1) and (scFv α CII) - (scFv α TNF-α) -hIgG4Fc (lane 2) were analyzed in 10％SDS-PAGE. The Fc-fusion molecular construct was revealed as the major band at about 80 kDa, consistent with the expected size.
Example 49: ELISA analysis of the binding of recombinant 2-chain (scFv α CII) - (scFv α TNF-α) -hIgG4. Fc fusion protein
To examine the binding ability of recombinant 2-chain (scFv α CII) - (scFv α TNF-α) -hIgG4. Fc fusion protein to type II collagen, ELISA assay was performed, using adalimumab and mouse parental monoclonal antibody II-II6B3 for comparison. ELISA plates were coated with 5 μg/mL of human type II collagen (human COL2) , mouse type II collagen (mouse COL2) , and chicken type II collagen (chick COL2) . 1D11 was a human IgG1 antibody against mite allergen as an isotype control. Recombinant 2-chain (scFv α CII) - (scFv α TNF-α) -hIgG4. Fc fusion protein, purified anti-collagen II antibody (II-II6B3) and adalimumab were detected by HRP-conjugated goat anti-human IgG4. Fc, goat anti-mouse IgG. Fc, and goat anti-human IgG1. Fc, respectively. The ELISA results were summarized in Figure 47A.
To examine the binding ability of 2-chain (scFv α CII) - (scFv α TNF-α) -hIgG4. Fc fusion protein to human TNF-α, ELISA assay was performed, along with adalimumab and mouse parental monoclonal antibody II-II6B3. ELISA plates were coated with 1 μg/mL of human TNF-α and 1 μg/mL of human serum albumin as a control. Recombinant 2-chain (scFv α CII) - (scFv α TNF-α) -hIgG4. Fc fusion protein, purified anti-collagen II antibody (II-II6B3) and Adalimumab were detected by HRP-conjugated goat anti-human IgG4. Fc, goat anti-mouse IgG. Fc, and goat anti-human IgG1. Fc, respectively. The results, as summarized in Figure 47B, showed that recombinant 2-chain (scFv α CII) - (scFv α TNF-α) -hIgG4. Fc fusion protein displayed significant binding activity toward human TNF-α； HSA (human serum albumin) was used as control.
Example 50: Preparation of 2-chain IgG4. Fc fusion protein containing scFv specific for human collagen II, scFv specific for TNF-α and scFv specific for human IL-17
The scFv1-scFv2-CH2-CH3-scFv3 (human γ4) recombinant chain was configured by fusing three scFvs, in which the first one specific for human collagen II and the second one specific for TNF-α were fused to the N-terminal of CH2 domain of IgG4. Fc through a flexible hinge region, while the third one specific for IL-17 was fused to the C-terminal of CH3 domain.
The VH and VL of the scFv specific for collagen II were from monoclonal antibody II-II6B3； the VH and VL of the scFv specific for TNF-α were from monoclonal antibody adalimumab； VH and VL of the scFv specific for IL-17 were from secukinumab. The first scFv (specific for collagen II) had an orientation of VL-linker-VH, the second scFv (specific for TNF-α) was in the orientation of VH-linker-VL, and the third scFv (specific for IL-17) was in the orientation of VL-linker-VH. The VL and VH in each of the three scFv were connected by a hydrophilic linker, GSTSGSGKPGSGEGSTKG. The three scFv were fused via a flexible linker, (GGGGS) 3.
The sequence of the recombinant chain in the IgG4. Fc fusion protein molecular construct of the construct illustrated below is shown in SEQ ID NO: 49. The expression of the constructed genes in Expi293F cells and the purification of the expressed fusion protein were performed as in preceding Examples. Characterization of the new construct was performed with SDS-PAGE and ELISA. The antibody Secukinumab (Cosentyx) was purchased from Chang Gung Hospital (Taipei, Taiwan) ； human IL-17 was from Peprotech (NJ, USA) . Figure 48A showed the SDA-PAGE results, indicating that the recombinant chain of the new construct had a size of about 110kDa, consistent with the expected size. Figure 48B showed the ELISA results, indicating that the present recombinant Fc-fusion protein had the binding activity to human collagen II, human TNF-α, and human IL-17.
Illustrated below is the configuration of the present 2-chain (scFv α CII) - (scFv α TNF-α) -hIgG4. Fc- (scFv α IL-17) molecular construct.
Figure PCTCN2016071184-appb-000078
Example 51: Preparation of 2-chain IgG1. Fc fusion protein containing TNF-α soluble receptor and scFv specific for collagen II
The (TNF-α receptor) -CH2-CH3-scFv α collagen II (human γ1) recombinant chain was configured by fusing human TNF-α receptor, IgG1. Fc, and scFv specific for collagen II. The sequences of TNF-α receptor and IgG1. Fc were those of etanercept. Etanercept and scFv were fused via a flexible linker, (GGGGS) 3. The sequence of the recombinant chain in the IgG4. Fc fusion protein molecular construct is shown in SEQ ID NO: 50.
The expression of the constructed genes in Expi293F cells and the purification of the expressed fusion protein were performed as in the preceding Examples. Characterization of the new construct was performed with SDS-PAGE and ELISA. Etanercept (Enbrel) was purchased from Chang Gung Hospital (Taipei, Taiwan) . Figure 49A showed the SDS-PAGE results, indicating that the recombinant chain in the new molecular construct had a size of about 100 kDa, consistent with the expected size (an Etanercept molecule had a molecular weight of 150 kDa and one chain of it was about 75 kDa in size； an scFv was about 27 kDa in size) . Figure 49B showed the ELISA results, indicating the present molecular construct bound to human TNF-α, human collagen II, and mouse collagen II.
Illustrated below is the configuration of the present 2-chain (soluble TNF-α receptor) -IgG1. CH2-CH3-scFv α collagen II molecular construct.
Figure PCTCN2016071184-appb-000079
Example 52: Preparation of 2-chain fusion protein containing intact antibody for human TNF-α and scFv specific for collagen II
The IgG-scFv (human γ1) recombinant chain was configured by fusing the intact antibody specific for human TNF-α and scFv specific for collagen II (illustrated below) . The sequences of intact antibody were those of adalimumab. Adalimumab and scFv were fused via a flexible linker, (GGGGS) 3.
The construction of the heavy and light chains of recombinant genes was built by inserting the two genes into a pG1K expression cassette with the multiple cloning site. To prepare the 2-chain fusion protein containing intact antibody for human TNF-α and scFv specific for collagen type II, transfection of the expression vectors into Expi293F cells was performed as in preceding Examples. The amino acid sequence of the heavy chain of 2-chain fusion protein containing intact antibody for human TNF-α and scFv specific for collagen type II is indicated in SEQ ID NO: 51, and the amino acid sequence of the light chain of the 2-chain fusion protein is indicated in SEQ ID NO: 52.
Figure 50 showed the SDS-PAGE result, indicating that the heavy recombinant chain in the present extended IgG molecular construct had a size of about 75 kDa, consistent with the expected size.
Illustrated below is the configuration of the present anti-human TNF-α in extended IgG configuration with scFv specific for human collagen II at the C-terminal.
Figure PCTCN2016071184-appb-000080
Example 53: Preparation of 2-chain fusion protein containing intact antibody for human IL-17 and scFv specific for collagen VII
The IgG-scFv (human γ1) recombinant chain was configured by fusing the intact antibody specific for human IL-17 and scFv specific for collagen type VII. The sequences of the intact antibody were those of secukinumab. Secukinumab and the scFv were fused via a flexible linker, (GGGGS) 3.
The construction of the heavy and light chains of recombinant genes was built by inserting the two genes into a pG1 K expression cassette with the multiple cloning site. To prepare the 2-chain fusion protein containing intact antibody for human IL-17 and scFv specific for collagen type VII, transfection of the expression vectors into Expi293F cells was performed as in the preceding Example. The amino acid sequence of the heavy chain of 2-chain fusion protein containing intact antibody for human IL-17 and scFv specific for collagen type VII is indicated in SEQ ID NO: 53, and the amino acid sequence of the light chain of the 2-chain fusion protein is indicated in SEQ ID NO: 54.
Figure 51A showed the SDS-PAGE results indicating that the recombinant heavy chain of the new molecular construct had a size of 75 kDa, consistent with the expected size. Figure 51 B showed the ELISA results, indicating that the present molecular construct bound to human IL17 and human collagen VII. The relatively low binding to collagen VII was due to a low concentration the antigen used for coating the ELISA plates
Illustrated below is the present anti-human IL-17 in extended IgG configuration with scFv specific for human collagen VII at the C-terminal.
Figure PCTCN2016071184-appb-000081
Example 54: Preparation of 2-chain IgG4. Fc fusion protein containing scFv specific for human collagen VII and scFv specific for BAFF
cDNA of Mouse B cell hybridoma LH7.2 mAb producing anti-collagen VII antibody was a gift from Dr. Purdie, cancer research UK skin tumor laboratory at Queen Mary University of London. The VH and VL sequences of LH7.2 monoclonal antibody (SEQ ID NOs: 29 and 30) were determined in an earlier Example. The sequences of VL and VH of scFv specific for BAFF were those of VL and VH of belimumab.
The scFv1-CH2-CH3-scFv2 (human γ4) recombinant chain (SEQ ID NO: 55) was configured by fusing two scFv, spaced with IgG4. Fc, one specific for collagen VII and the other specific for BAFF, to the C-terminal of CH3 domain of IgG4. Fc through a flexible linker, (GGGGS) 3 (illustrated below) . The first scFv (specific for collagen VII) had an orientation of VL-linker-VH and the second scFv (specific for BAFF) was in VH-linker-VL. The VL and VH in each of the two scFv were connected by a hydrophilic linker, GSTSGSGKPGSGEGSTKG.
The expression of the constructed genes in Expi293F cells and the purification of the expressed fusion protein were performed as in an earlier Example. Characterization of the new construct was performed with SDS-PAGE and ELISA. The antibody Belimumab  (Belynsta) was purchased from Chang Gung Hospital (Taipei) ； human BAFF was from GenScript (NJ, USA) . Figure 52A showed the SDA-PAGE results, indicating that the recombinant chain in the new molecular construct had a size of about 80-90 kDa, consistent with or somewhat larger than the expected size. Figure 52B showed the ELISA results, indicating that the new construct bound specifically to human BAFF and human collagen VII.
Illustrated below is the configuration of the present 2-chain Fc-fusion molecular construct with scFv α collagen VII-IgG4. CH2-CH3-scFv α BAFF.
Figure PCTCN2016071184-appb-000082
Example 55: Preparation of 2-chain fusion protein containing intact antibody for human BAFF and scFv specific for collagen VII
The IgG-scFv (human γ1) recombinant chain was configured by fusing the intact antibody specific for human BAFF and scFv specific for collagen type VII. The sequences of intact antibody were those of belimumab. Belimumab and the scFv were fused via a flexible linker, (GGGGS) 3.
The construction of the heavy and light chains of recombinant genes was built by inserting the two genes into a pG1 K expression cassette with the multiple cloning site. To prepare the 2-chain fusion protein containing intact antibody for human BAFF and scFv specific for collagen type VII, transfection of the expression vectors into Expi293F cells was performed as in preceding Examples.
The amino acid sequence of the heavy chain of 2-chain fusion protein containing intact antibody for human BAFF and scFv specific for collagen type VII is indicated in SEQ ID NO: 56, and the amino acid sequence of the light chain of the 2-chain fusion protein is indicated in SEQ ID NO: 57. Figure 53A showed the SDS-PAGE results, indicating that the recombinant heavy chain of the new molecular construct had a size of about 80 kDa, consistent with the expected size. Figure 53B showed the ELISA results, indicating that the new extended IgG construct bound specifically to human BAFF and human collagen VII.
Illustrated below is the configuration of the present anti-human BAFF extended IgG configuration with scFv specific for human collagen VII at the C-terminal.
Figure PCTCN2016071184-appb-000083
Example 56: Preparation of 2-chain IgG4. Fc fusion protein containing scFv specific for human osteonectin and scFv specific for RANKL
Mouse B cell hybridoma AON-1 producing anti-osteonectin (SPARC) antibody was purchased from Developmental Studies Hybridoma Bank at the University of Iowa. Poly (A) + RNA was reverse-transcribed with a SuperScript III RT-PCR system (Invitrogen) , and the first strand cDNA was synthesized. The VH and VL nucleotide and amino acid sequences of AON-1 had not been published. To determine the sequences of variable regions of AON-1, cDNA of VH and VL were amplified by PCR using a set of DNA primers provided by Ig-primer Sets (Novagen) according to the manufacturer’s instructions. The VH and VL sequences of AON-1 monoclonal antibody specific for osteonectin are shown in  SEQ ID NOs: 58 and 59. The sequences of VL and VH of scFv specific for RANKL were those of VL and VH of denosumab.
The scFv1-scFv2-CH2-CH3 (human γ4) recombinant chain (SEQ ID NO: 60) was configured by fusing two scFv, one specific for human osteonectin and the other specific for RANKL, to the N-terminal of CH2 domain of IgG4. Fc through a flexible hinge region (illustrated below) . The first scFv (specific for osteonectin) had an orientation of VL-linker-VH and the second scFv (specific for RANKL) was in VH-linker-VL. The VL and VH in each of the two scFv were connected by a hydrophilic linker, GSTSGSGKPGSGEGSTKG. The two scFv were fused via a flexible linker, (GGGGS) 3.
The expression of the constructed genes in Expi293F cells and the purification of the expressed fusion protein were performed as in an earlier Example. The characterization of the binding of the fusion protein to human osteonectin and RANKL by ELISA was performed as in a preceding Example. Characterization of the new construct was performed with SDS-PAGE and ELISA. The antibody Denosumab (Prolia) was purchased from Chang Gung Hospital； human RANKL and human osteonectin (SPARC) were from GenScript. Figure 54A showed the SDS-PAGE results, indicating that the recombinant chain in the new molecular construct had a size of about 80 kDa. Figure 54B showed the ELISA results, indicating that the new Fc-fusion construct bound specifically to human SPARC and human RANKL.
Illustrated below is the configuration of the present 2-chain (scFv α SPARC) - (scFv αRANKL) -hIgG4. Fc molecular construct.
Figure PCTCN2016071184-appb-000084
Example 57: Preparation of 2-chain fusion protein containing intact antibody for human RANKL and scFv specific for human osteonectin
The IgG-scFv (human γ1) recombinant chain was configured by fusing the intact antibody specific for human RANKL and scFv specific for human osteonectin. The sequences of intact antibody were those of denosumab. Denosumab and the scFv were fused via a flexible linker, (GGGGS) 3.
The construction of the heavy and light chains of recombinant genes was built by inserting the two genes into a pG1 K expression cassette with the multiple cloning site. To prepare the 2-chain fusion protein containing the intact antibody for human RANKL and scFv specific for human osteonectin, transfection of the expression vectors into Expi293F cells was performed as in preceding Examples.
The amino acid sequence of the heavy chain of 2-chain fusion protein containing intact antibody for human RANKL and the scFv specific for human osteonectin is indicated in SEQ ID NO: 61 and the amino acid sequence of the light chain of the 2-chain fusion protein is indicated in SEQ ID NO: 62. Figure 55A showed the SAS-PAGE results, indicating that the recombinant heavy chain in the extended IgG molecular construct had a size of about 80 kDa. Figure 55B showed the ELISA results, indicating that the new Fc-fusion construct bound specifically to human SPARC and human RANKL.
Illustrated below is the configuration of the present anti-human RANKL in extended IgG configuration with scFv specific for human osteonectin at the C-terminal.
Figure PCTCN2016071184-appb-000085
Example 58: Immunohistologic chemical analysis of 2-chain IgG4. Fc fusion protein containing scFv specific for human collagen II and scFv specific for TNF-α in binding to joint cartilage
Immunohistologic analysis was performed in the histology core facility of Genomics Research Center, Academia Sinica to examine whether the molecular construct, 2-chain (scFv α collagen II) - (scFv α TNF-α) -hIgG4. Fc (the configuration illustrated in an earlier Example) , had affinity for binding to cartilage. Mouse bone and cartilage samples were obtained from FVB/N mice sacrificed by using CO2. Femur connected with tibia and knee femoral ends were harvested and fixed with 10％neutral buffered formaldehyde at room temperature for 48 hours. Samples were then decalcified in 10％EDTA, pH 7.4, for 7 days, with daily renewal of the solution. After decalcification, samples were post-fixed in 10％neutral buffered formaldehyde at room temperature for 24 hours and stored in 70％ethanol at 4℃ until dehydration by ASP6025 Tissue Processor (Leica) and paraffin embedding.
Safranin O staining was performed according to the protocol described in Schmitz et al., 2010. For immunostaining, 3-μm-thick sections were deparaffinized and rehydrated using Leica AutoStainer XL, followed by staining procedures described in the Tyramide Signal Amplification Biotin kit (PerkinElmer) . In brief, sections were quenched for endogenous peroxidase activity in 3％H2O2 for 15 minutes, followed by antigen retrieval with 1 mg/mL hyaluronidase (Sigma Aldrich) in 37℃ for 20 minutes and 20 μg/mL proteinase k (TOOLS) at room temperature for 10 minutes. Sections were next blocked in TNB buffer of the TSA  kit. For staining with mouse II-II6B3 antibody, additional mouse IgG blocking reagent (Vector Laboratories) was added preceding TNB blocking. Both primary antibodies II-II6B3 and (scFv α CII) - (scFv α TNF-α) -hIgG4Fc were used at 50 μg/mL. Goat anti-mouse IgG Fc and goat anti-human IgG Fc (Jackson ImmunoResearch) were use at 1.6 μg/mL for incorporating HRP, which reacted with the subsequently added biotin-tyramide. The biotin labels were then probed with streptavidin-HRP and chromogenically visualized with diaminobenzidine substrate (BioGenex) . Sections were counterstained using hematoxylin and mounted with Leica CV5030 Coverslipper.
Figures 56A to 56C showed the immunostaining of mouse epiphyseal bone with monoclonal antibodies II-II6B3 (Figure 56 panel A) , adalimumab (Figure 56 panel B) , and (scFv α CII) - (scFv α TNF-α) -hIgG4Fc, i.e., the configuration illustrated in an earlier Example (Figure 56 panel C) , followed by HRP-labeled goat anti-mouse or goat anti-human secondary antibodies and tyramide amplification. Type II collagen was revealed at epiphyseal articular cartilage (AC) and growth plate (GP) in Figure 56 panel A and Figure 56 panel C. The results showed that the anti-collagen II monoclonal antibody II-II6B3 stained the AC and GP parts prominently (Figure 56 panel A) , while adalimumab had no significant staining (Figure 56 panel B) . The present construct also stained positively (Figure 56 panel C) . The positive staining originally revealed in brown color was converted to black/gray. The scale bar represents 250 μm.
Example 59: Immunohistologic chemical analysis of 2-chain IgG1. Fc fusion protein containing scFv specific for collagen II and scFv specific for TNF-α and scFv specific for IL-17 in binding to joint cartilage
The preparation of tissue thin sections, staining with the molecular construct, 2-chain (scFv α CII) - (scFv α TNF-α) -hIgG4. Fc- (scFv α IL-17) (the configuration illustrated in an earlier Example) and controls were performed as in the preceding Examples.
Figures 56D to 56E showed the immunostaining of collagen II in mouse epiphyseal bone. 3-μm thick sections of the femoral end of mouse knee were stained with monoclonal antibodies, an anti-IL17a mouse antibody (purchased from PeproTech, NJ, USA) (Figure 56 panel D) , and the present construct 2-chain (scFv α CII) - (scFv α TNF-α) -hIgG4. Fc- (scFv αIL-17) (Figure 56 panel E) , followed by HRP-labeled goat anti-mouse or goat anti-human  secondary antibodies and tyramide amplification. The results showed that anti-IL17 monoclonal antibody had no significant staining, while the present construct had moderately positive staining.
Example 60: Immunohistologic chemical analysis of 2-chain IgG1. Fc fusion protein containing TNF-α soluble receptor and scFv specific for collagen II in binding to joint cartilage
The preparation of tissue thin sections, staining with the molecular construct, 2-chain (soluble TNF-α receptor) -IgG1. CH2-CH3-scFv α collagen II (the configuration illustrated in an earlier Example) and controls were performed as in the preceding Example.
The staining procedure was the same as in preceding examples. The mouse epiphyseal bone tissue section samples were from the same batch. The results showed that the positive control II-II6B3 stained strongly (Figure 57 panel A) , etanercept had no significant staining (Figure 57 panel B) , and the present construct stained collagen II-containing components AC and GP positively (Figure 57 panel C) .
Example 61: Bio-distribution of recombinant 2-chain IgG4. Fc fusion protein containing scFv specific for human osteonectin (SPARC) and scFv specific for RANKL using in vivo imaging system
A Dylight 680 Antibody Labeling Kit (Thermo Scientific) was used to conjugate denosumab and (scFv α SPARC) - (scFv α RANKL) -hIgG4Fc (scheme 67 of Example 60) , according to the manufacturer’s instructions. 8 to 10-week-old BALB/c mice were injected intravenously with PBS or 40 μg labeled antibodies. At various time points, mice were anaesthetized with isoflurane in O2 and placed in the IVIS Spectrum In Vivo Imaging System (PerkinElmer) with a supine position. Fluorescent images were captured with ex/em ＝675/720, using the Living Image Software V3.2.
To investigate the targeting effect of (scFv α SPARC) - (scFv α RANKL) -hIgG4Fc, tissue distribution of antibodies in mice was compared, through observing fluorescent signals from the abdominal aspect. Fluorescent images from BALB/c mice were acquired and analyzed at 30 minutes, 3 hours, and 28 hours after the administration of DyLight 680-conjugated antibodies. 30 minutes after the injection, the penetration of anti-SPARC, (scFv α SPARC) - (scFv α RANKL) -hIgG4Fc, and BoneTag into limbs was greater than that observed with denosumab. In addition to bladder accumulation, the distribution of denosumab, anti-SPARC, and (scFv α SPARC) - (scFv α RANKL) -hIgG4Fc was more dispersed after 3 hours, while BoneTag was restricted to the head and the limbs. Bone structures were clearly resolved with remaining anti-SPARC 28 hours after the antibody administration.
Figure 58 showed bio-distribution of fluorescence-labeled antibodies in vivo. BALB/c mice were intravenously injected with PBS (1) , denosumab (2) , anti-SPARC mAb (3) , (scFv α SPARC) - (scFv α RANKL) -hIgG4Fc (4) , and BoneTag (5) . Images were captured at indicated time points using IVIS Spectrum imager and analyzed with Living Image software. Spectral unmixing was performed to distinguish tissue autofluorescence from DyLight 680 signals. The results showed that in comparison to denosumab, the present construct was distributed more similarly to anti-SPARC monoclonal antibody at 30 minutes after treatment. At longer time points, the distribution was influenced by half-lives of the reagents. Anti-SPARC and denosumab were both antibodies and had similar serum half-lives.
Example 62: Preparation of 2-chain IgG1. Fc fusion protein molecular construct containing EGF as targeting element and bundles of cytotoxic molecules as effector elements
The configuration illustrated below showed that 2-chain IgG1. Fc fusion protein was prepared by configuring EGF-CH2-CH3 (human γ1) in a recombinant chain. The C-terminal of the 53 a. a. EGF was linked to the N-terminal of CH2 via a linker, ASGGGGSGGGGS. The C-terminal of the CH3 was extended with GGGDC. The cysteine residue at the C-terminal was for coupling with the linker unit carrying a bundle of cytotoxic payload. The sequence of the recombinant peptide chain is shown in SEQ ID NO: 63. The purification of recombinant proteins were performed at 4℃ by protein A chromatography, and the purity of proteins was analyzed through Coomassie staining of 12％SDS-PAGE. Figure 59A showed the SDS-PAGE analysis of the 2-chain EGF-CH2-CH3 with a C-terminal extension and a cysteine residue and a 2-chain EGF-CH2-CH3-scFv of anti-PD1, indicating EGF-CH2-CH3 with a C-terminal extension had a size of about 38 kDa and EGF-CH2-CH3- (scFv of anti-PD1) had a size of about 60-65 kDa, consistent with the expected sizes.
Illustrated below is the configuration of the present 2-chain EGF-hIgG1. Fc with a C-terminal extension and a cysteine residue.
Figure PCTCN2016071184-appb-000086
Example 63: The coupling of a 2-chain EGF-CH2-CH3 fusion protein with two drug bundles of LPS molecules via SPACC reaction
The conjugation of tetrazine-PEG4-Mal to the C-terminal cysteine residue of 2-chain EGF-CH2-CH3 was performed. An aliquot of 0.6 mole of the linker unit conjugated with LPS was mixed with 0.06 mole of 2-chain EGF-IgG1. Fc fusion protein in 0.1 M sodium phosphate buffer, pH 7.0, at room temperature overnight at 10: 1 molar ratio ( [linker] : [protein] ) . The SH group of the terminal cysteine was conjugated with maleimide-PEG4-tetrazine. Mass MALDI-TOF analysis was performed for the identification of the formation of tetrazine-conjugated 2-chain IgG1. Fc fusion protein via SH-maleimide reaction. A mass spectrometric analysis showed that the tetrazine-conjugated 2-chain IgG1. Fc fusion protein had a m. w. of 68852.
The conjugation of a drug bundle (linker unit) with a free TCO group and 2 LPS molecules to the free tetrazine group of the 2-chain EGF-CH2-CH3 was further performed. An amount of 100 μl of 1 mg/ml of the drug bundle was added to the solution containing tetrazine-conjugated 2-chain EGF-CH2-CH3 at a molar ratio of 2: 1 ( [tetrazine] : [TCO] ) . The reaction mixtures were incubated for 16 hours at room temperature.
Figure 59B showed SDS-PAGE analysis of 2-chain IgG1. Fc fusion protein conjugated with a linker unit with two LPS molecules. The band in lane 1 was EGF-CH2-CH3 with a C-terminal linker and cysteine residue, and the arrow in lane 2 was EGF-CH2-CH3 conjugated with a drug bundle with two LPS molecules.
Illustrated below is 2-chain IgG1. Fc fusion protein conjugated with a linker unit with LPS.
Figure PCTCN2016071184-appb-000087
Example 64: Preparation of 2-chain IgG1. Fc fusion molecular constructs containing EGF as targeting element and scFv specific for PD1 as effector element
The configuration illustrated below showed the configuration of 2-chain IgG1. Fc fusion protein molecular construct containing EGF as targeting element and scFv specific for PD-1 as effector element. The 2-chain IgG1. Fc fusion protein, 2-chain EGF-hIgG1. Fc- (scFv αPD1) (SEQ ID NO: 64) , was prepared by configuring EGF-CH2-CH3- (scFv α PD1) (human γ1) in a recombinant chain. The CH2-CH3 was part of human γ1 and the scFv was specific for human PD1. The VL and VH of the scFv specific for PD1 were those of VL and VH of nivolumab. The C-terminal of CH3 was connected with the anti-PD1 scFv with a flexible linker, (GGGGS) 3. The purification of recombinant proteins were performed at 4℃by protein A chromatography.
Figure PCTCN2016071184-appb-000088
To examine the binding ability of the recombinant 2-chain EGF-IgG1. Fc- (scFv α PD1) fusion protein to ERBB1, ELISA analysis was performed on the recombinant 2-chain EGF-IgG1. Fc fusion protein and EGF-IgG1 Fc- (scFv α PD1) fusion protein. ELISA plates were coated with 1 μg/mL, 2 μg/mL, and 4μg/mL of recombinant ERBB1 protein. Cetuximab was a human IgG1 antibody against human EGFR, and cetuximab scFv was used as a positive control. ELISA results summarized in Figure 60A showed that both EGF-IgG1. Fc fusion protein and EGF-IgG1. Fc- (scFv α PD1) fusion protein bound to ERBB1 ecto domain, and had a comparable binding ability with Cetuximab scFv. Each bar represented the mean OD450 value of duplicate samples.
To examine the binding ability of recombinant 2-chain EGF-IgG1. Fc- (scFv α PD1) fusion protein to PD-1, ELISA plates were coated with 1 μg/mL of recombinant human PD-1 protein. Herceptin was a human IgG1 antibody against ERBB2, and Herceptin scFv was used as a negative control. Each bar represented the mean OD450 value of duplicate samples. ELISA results in Figure 60B showed the positive binding of EGF-IgG1. Fc- (scFv α PD1) fusion protein to human PD-1 protein.
Example 65: Preparation of 2-chain IgG1. Fc fusion molecular constructs containing EGF as targeting element and scFv specific for CD3 as effector element
In this example, the 2-chain IgG. Fc fusion protein was prepared by configuring EGF-CH2-CH3- (scFv α CD3) in a recombinant chain (SEQ ID NO: 65) . The CH2-CH3 was part of human γ1 and the scFv was specific for human CD3. The VL and VH of the scFv specific for CD3 were those of VL and VH of teplizumab. The C-terminal of CH3 was connected with the anti-CD3 scFvs with a flexible linker, (GGGGS) 3. Figure 61A showed the SDS-PAGE analysis of the 2-chain EGF-hIgG1. Fc- (scFv α CD3) molecular construct (illustrated in preceding Examples) .
To examine the binding ability of recombinant 2-chain EGF-hIgG1. Fc- (scFv α CD3) fusion protein to ERBB1, ERBB2 and ERBB3, ELISA analysis was performed. ELISA plates were coated with 1 μg/mL, 2 μg/mL and 4μg/mL of recombinant ERBB1, ERBB2, or ERBB3 protein. ELISA results, as summarized in Figure 61 B, showed that the EGF-IgG1. Fc fusion protein and EGF-IgG1. Fc- (scFv α CD3) fusion protein bound to ERBB1 ecto domain, and had a comparable binding ability with Cetuximab scFv. Each bar  represents the mean OD450 value of duplicate samples.
Illustrated below is the configuration of the present 2-chain EGF-hIgG1. Fc- (scFv αCD3) .
Figure PCTCN2016071184-appb-000089
Example 66: Preparation of 2-chain EGF (S2W/D3V) -IgG1. Fc, EGF(S2W/D3V) -IgG1. Fc- (scFv α PD1) and EGF (S2W/D3V) -IgG1. Fc- (scFv α CD3) containing EGF mutant, EGF (S2W/D3V) as targeting element
It has been shown that replacement of only two amino acids in the linear N-terminal region of EGF (Ser-2 to Trp and Asp-3 to Val) was sufficient to make EGF binding for ERBB2/ERBB3 heterodimer and ERBB3 homodimer. EGF (S2W/D3V) represented the replacement of two amino acids (Ser-2 to Trp and Asp-3 to Val) in the N-terminal region of EGF. The 2-chain EGF (S2W/D3V) -IgG1. Fc, EGF (S2W/D3V) -IgG1. Fc- (scFv α PD1) and EGF(S2W/D3V) -IgG1. Fc- (scFv α CD3) fusion proteins containing EGF mutant EGF(S2W/D3V) were prepared and their binding to ERBB1 homodimer, ERBB2/ERBB3 heterodimer and ERBB3 homodimer was studied.
The sequence of the recombinant 2-chain EGF (S2W/D3V) -IgG1. Fc is shown in SEQ ID NO: 66. The C-terminal of CH3 of EGF (S2W/D3V) -IgG1. Fc- (scFv α PD1) (SEQ ID NO: 67) and EGF (S2W/D3V) -IgG1. Fc- (scFv α CD3) (SEQ ID NO: 68) were connected with anti-PD-1 and anti-CDthree scFvs with a flexible linker, (GGGGS) 3, respectively. Figure 62A showed SDS-PAGE analysis of EGF (S2W/D3V) -IgG1. Fc with C-terminal extension (lane 1 and 3) , EGF (S2W/D3V) -IgG1. Fc- (scFv α PD1) (lane 2) , and EGF(S2W/D3V) -IgG1. Fc- (scFv α CD3) (lane 4) . The sizes of the products were consistent with expected sizes. Figures 62B and 62C were results of ELISA analyses of  EGF(S2W/D3V) -IgG1. Fc- (scFv α PD1) , while Figures 62D and 62E were results of ELISA analyses of EGF (S2W/D3V) -IgG1. Fc- (scFv α CD3) in binding to recombinant PD-1 or recombinant CD3-Fc fusion protein, and their binding to ERBB1, ERBB2, and ERBB3. The results showed that EGF (S2W/D3V) -IgG1. Fc- (scFv α PD1) could bind to recombinant PD-1, ERBB！, and ERBB3, and that EGF (S2W/D3V) -IgG1. Fc- (scFv α CD3) could bind to recombinant CD3, ERBB1, and ERBB3.
Illustrated below is the configuration of the present 2-chain EGF (S2W/D3V) -hIgG1. Fc- (scFv α PD-1) .
Figure PCTCN2016071184-appb-000090
Illustrated below is the configuration of the present 2-chain EGF (S2W/D3V) -hIgG1. Fc- (scFv α CD3) .
Figure PCTCN2016071184-appb-000091
Example 67: Preparation of 2-chain IgG1. Fc fusion protein molecular construct containing somatostatin as targeting element
The 2-chain IgG. Fc fusion protein was prepared by configuring somatostatin-CH2-CH3 (human γ1) in a recombinant chain. The C-terminal of the 14 a. a. somatostatin was linked  to the N-terminal of CH2 via a linker, ASGGGGSGGGGS. The C-terminal of the CH3 was extended with GGGDC. The cysteine residue at the C-terminal was for coupling with a bundle of drug. The sequence of the recombinant peptide chain containing somatostatin and IgG. Fc is shown in SEQ ID NO: 69. The two molecular constructs with scFv α PD-1 and scFv α CD3 were also prepared. Figure 63 showed SDS-PAGE (10％) of somatostatin-hIgG1. Fc (lane 1) , somatostatin-hIgG1. Fc- (scFv α CD3) (lane 2) , and somatostatin-hIgG1. Fc- (scFv α PD-1) (lane 3) . The results showed that the sizes of the three constructs were consistent with the expected sizes.
Because of the very small size of somatostatin, SDS-PAGE analysis was not suitable to determine that somatostatin was incorporated into the Fc-fusion protein. Tandem mass spectrometric analysis of trypsin-digested 2-chain somatostatin-hIgG1. Fc- (scFv α PD-1) and 2-chain somatostatin-hIgG1. Fc- (scFv α CD3) was performed for the identification of somatostatin in the molecular constructs. All mass spectrometry experiments were done using a Bruker Autoflex III MALDI TOF/TOF mass spectrometer (Bremen, Germany) equipped with a 200 Hz SmartBean Laser in positive ion mode with delayed extraction in the reflectron mode. Data acquisition was done manually with FlexControl 3.4, and data processing was performed with Flex-Analysis 3.4 (both Bruker Daltonik) .
To identify the peptide by molecular mass searching of protein fragment in protein database using Mascot search engine, the m/z value of a protein fragment in MS/MS spectrum, corresponding to 741.37 daltons, was matched to the amino acid sequence of somatostatin fragment (NFFWK) . The m/z values of two protein fragments in MS/MS spectrum, corresponding to 835.45 and 1286.69 daltons, were matched to the amino acid sequence of two peptide fragments in the human IgG Fc region, DTLMISR and EPQVYTLPPSR.
Illustrated below is the configuration of the present 2-chain somatostatin-hIgG1. Fc- (scFv α PD-1) (SEQ ID NO: 70) .
Figure PCTCN2016071184-appb-000092
Illustrated below is the configuration of the present 2-chain somatostatin-hIgG1. Fc- (scFv α CD3) (SEQ ID NO: 71) .
Figure PCTCN2016071184-appb-000093
Example 68: Staining analysis to examine the binding of 2-chain EGF-IgG1. Fc, 2-chain EGF-IgG1. Fc- (scFv α PD1) , 2-chain EGF-IgG1. Fc- (scFv α CD3) , 2-chain EGF(S2W/D3V) -IgG1. Fc- (scFv α PD1) and 2-chain EGF (S2W/D3V) -IgG1. Fc- (scFv α CD3) fusion proteins to EGFR-expressing tumor cell line
Five molecular constructs were analyzed for their ability to bind to EGFR on tumor cell line A431. A431 was a human epidermoid carcinoma cell line, expressing high levels of EGFR. The assay was performed by incubating 1 x105 EGFR-expressing A431 cells with 10 μg/ml of each construct in PBS, 1 ％BSA on ice for 30 min, using Cetuximab scFv-FITC as a positive control. Cells were washed and incubated with FITC-conjugated goat anti-human IgG. Fc (Caltag, Buckingham, UK) , diluted 1: 200 in PBS/BSA, at 4℃ for 20 minutes in the dark. The a20, a mouse monoclonal antibody specific for a membrane-anchoring segment of human membrane-bound IgE, and OKT3, a mouse  monoclonal antibody specific for human CD3, were used as negative controls. The staining of cells was analyzed by FACS (FACSCanto II； BD Biosciences) using FITC-conjugated rabbit anti-mouse IgG or goat anti-human IgG. Fc.
Figure 64 showed results of the cell staining analysis of EGF-IgG1. Fc, EGF-IgG1. Fc- (scFv α PD1) , EGF-IgG1. Fc- (scFv α CD3) , EGF (S2W/D3V) -IgG1. Fc, and EGF(S2W/D3V) -IgG1. Fc- (scFv α CD3) on EGFR-expressing A431 cells. All those five constructs bound to A431 cells positively in a substantial level.
Example 69: Staining analysis showing binding of 2-chain EGF-IgG1. Fc, 2-chain EGF-IgG1. Fc- (scFv α PD1) , 2-chain EGF-IgG1. Fc- (scFv α CD3) , 2-chain EGF(S2W/D3V) -IgG1. Fc- (scFv α PD1) and 2-chain EGF (S2W/D3V) -IgG1. Fc- (scFv αCD3) to human T-lymphocytes
The ability of the various EGF-IgG. Fc-scFv constructs to bind to human T lymphocytes expressing CD3 and PD-1 was studied with fractionated human peripheral blood T lymphocytes. Peripheral blood mononuclear cells (PBMCs) were isolated from buffy coats from healthy donors (Taiwan Blood Service Foundation) by centrifugation over a Ficoll-Paque PLUS (GE Healthcare) density gradient and cryopreserved in 90％FBS/10％DMSO. Human T cells were prepared from PBMCs by depletion of non-T cells (negative selection) using the human Pan T cell Isolation kit (Miltenyl Biotech, Auburn, CA, USA) . 10 μg/ml of EGF-IgG1. Fc and EGF-IgG1. Fc- (scFv α PD1) , EGF-IgG1. Fc- (scFv α CD3) , EGF(S2W/D3V) -IgG1. Fc- (scFv α PD1) and EGF (S2W/D3V) -IgG1. Fc- (scFv α CD3) were incubated with 1 x 105 T cells in PBS, 1 ％BSA on ice for 20 minutes. Anti-PD-1 and OKT3 were used as positive controls and EGF-IgG1. Fc and EGF (S2W/D3V) -IgG1. Fc as negative controls. Cells were washed and incubated with FITC-conjugated goat anti-human IgG. Fc (Caltag) or rabbit anti-mouse IgG. Fc (AbD Serotec) , diluted 1: 200 in PBS/BSA, at 4℃ for 20 minutes in the dark. Samples were analyzed by FACS analysis (FACSCanto II； BD Biosciences) . Figure 65, panels A to C showed that EGF-IgG1. Fc- (scFv α PD1) and EGF(S2W/D3V) -IgG1. Fc- (scFv α PD1) bound to T cells as anti-PD-1 antibody did. Figure 65 panels D to F showed that EGF-IgG1. Fc- (scFv α CD3) and EGF (S2W/D3V) -IgG1. Fc- (scFv α CD3) also bound to T cells as OKT3 antibody.
Example 70: T cell-mediated cytotoxicity assay of 2-chain EGF (S2W/D3V) - IgG1. Fc- (scFv α CD3) on MDA-MB-231 and A431 tumor cell lines
Human peripheral blood T cells were used as the source of T cells. The T cells were prepared as in the preceding example. T cells were cultured in the presence of 10 μ/ml of recombinant human IL-2 (PeproTech, Rocky Hill, USA) . Anti-DNP AN02 mAb was used as an isotype-matched control.
Aliquots of 5, 000 A431 target cells in 100 μl complete RPMI medium were coated with recombinant EGF-hIgG. Fc-Cys, EGF-hIgG. Fc-scFv α CD3, EGF (S2W/D3V) -IgG1. Fc- (scFv α CD3) , or isotype-matched controls for 30 minutes at 37℃ in a 5％CO2 atmosphere, and then combined with human T cells at different E: T ratios of 20, 10 or 5. After 24 hours of incubation, the cytotoxicity was assayed by a luminescent method using the aCella-Tox kit (Cell Technology, Mountain View, CA) according to the manufacturer’s instructions. The plate was read by a luminometer (multi-detection microplate reader, DS Pharma, Osaka, Japan) .
T cell mediated cytolysis of EGFR-expressing tumor cells by EGF (S2W/D3V) -hIgG1. Fc-scFv α CD3 was studied using MDA-MB-231 tumor cells and A431 tumor cells. MDA-MB-231 was originally derived from a primary invasive ductal carcinoma with pleural effusive metastasis and broadly used in tumor model studies. For this cytotoxicity effects, the source of T cells was important. Isolated human T lymphocytes from donor #56 and #59 were selected to examine the T-cell mediated cytotoxicity. MDA-MB-231 cells were incubated with 10 μg/mL of EGF (S2W/D3V) -hIgG1. Fc or EGF (S2W/D3V) -hIgG1. Fc-scFv α CD3 at 37℃ for 1 hour, and then mixed with human T lymphocytes at different E: T ratios of, 20, 10 or 5, and incubated for 24 hours. Cetuximab mAb was used as a control. Cytolysis was analyzed by using an aCella-Tox kit. The data shown here indicated that scFv α CD3-carrying EGF (S2W/D3V) -hIgG1. Fc recruited effector cells more efficiently to manifest the cytolytic activity.
Figures 66A and 66B showed the degree of cytolysis of EGFR-expressing of A431 cells upon the incubation with EGF-hIgG1. Fc-Cys, EGF-hIgG1. Fc-scFv α CD3, and EGF(S2W/D3V) -IgG1. Fc- (scFv α CD3) ； Figures 66C and 66D showed the degree of cytolysis on MDA-MB-231 by human T lymphocytes from donor #56 (Figure 66C) and #59 (Figure 66D) upon the incubation with EGF (S2W/D3V) -IgG1. Fc- (scFv α CD3) . These  result indicated that EGF (S2W/D3V) -hIgG1. Fc-scFvαCD3 mediated EGFR-expressing MDA-MB-231 cells lysis by ADCC in vitro.
To investigate the time-dependency of cytolysis on A431 cells by human T lymphocytes upon the incubation with EGF (S2W/D3V) -IgG1. Fc- (scFv α CD3) , A431 cells were incubated with 10 μg/mL EGF (S2W/D3V) -hIgG1. Fc, EGF (S2W/D3V) -hIgG1. Fc- (scFv α CD3) , or anti-HER1 mAb (control) at 37℃ for 1 hour, and then mixed with human T lymphocytes isolated from human PBMC at different E: T ratios of 20, 10 or 5, and incubated for 2 (Figure 67A) , 9 (Figure 67B) , or 24 (Figure 67C) hours. The results, as summarized in Figures 67A to 67C, indicated that degree of cytolysis on human T lymphocyte upon the incubation with EGF(S2W/D3V) -IgG1. Fc- (scFv α CD3) was time-dependent.
Example 71: T cell-mediated cytotoxicity assay of 2-chain EGF (S2W/D3V) -IgG1. Fc- (scFv α PD-1) fusion protein on A431 tumor cells
EGF (S2W/D3V) -hIgG1. Fc and EGF (S2W/D3V) -hIgG1. Fc-scFv α PD-1 mediated EGFR-expressing A431 cells lysis by ADCC in vitro. The assay was performed as described in the preceding Example. A431 cells were incubated with 10 μg/mL EGF (S2W/D3V) -hIgG1. Fc, EGF (S2W/D3V) -hIgG1. Fc-scFv α PD-1, or anti-HER1 mAb (control) at 37℃ for 1 hour, and then mixed with human T lymphocytes isolated from human PBMC at different E: T ratios of 20, 10 or 5, and incubated for 24 hours. ADCC were analyzed by using an aCella-TOX kit (Cell Technology Inc. )
Figure 68 showed the degree of cytolysis on A431 by human PBMC upon the incubation with 2-chain EGFw2v3-IgG1. Fc- (scFv α PD-1) .
Example 72: In vivo tumor model of recombinant 2-chain EGFw2v3-IgG1. Fc- (scFv α PD-1) and EGFw2v3-IgG1. Fc- (scFv α CD3) fusion proteins
Three-to four-week old NOD-SCID mice, NOD. CB17-Prkdcscid/IcrCrlBltw are obtained from BioLasco, Taipei, Taiwan. The mice are injected intraperitoneally with 1×106 A431 cells per mouse 2 weeks before the treatment of EGF (S2W/D3V) -hIgG. Fc-Cys, EGF (S2W/D3V) -hIgG. Fc-scFv α PD-1 (scheme 72) , EGF (S2W/D3V) -hIgG. Fc-scFv α CD3, or isotype-matched control recombinant proteins. Mice are grouped into five mice per group, and administrated, intraperitoneally, with the respective protein at 5 mg/kg in 50 mL  of PBS 3 times a week. At the first protein treatment, each mouse is also given 2×107 cells of the human PBMCs intraperitoneally. PBMCs are purified from buffy coats of blood samples from healthy donors (Taiwan Blood Service Foundation) by centrifugation over a Ficoll-Paque PLUS (GE Healthcare) density gradient and cryopreserved in 90％FBS/10％DMSO. Prior to use, the PBMCs are thawed and cultured at 2x106 cells/ml overnight in IMDM medium (Invitrogen) supplemented with10％heat-inactivated FBS, 4 mM L-glutamine, 25 mM HEPES, 50 mg/ml penicillin, and 100 mg/ml streptomycin (complete IMDM medium) . Tumor growth is recorded every 3 to 4 days by caliper. Mice is sacrificed on day 35 and s. c. tumors were removed, weighed, and examined.
It will be understood that the above description of embodiments is given by way of example only and that various modifications may be made by those with ordinary skill in the art. The above specification, examples and data provide a complete description of the structure and use of exemplary embodiments of the invention. Although various embodiments of the invention have been described above with a certain degree of particularity, or with reference to one or more individual embodiments, those with ordinary skill in the art could make numerous alterations to the disclosed embodiments without departing from the spirit or scope of this invention.

Claims (214)

  1. A linker unit comprising, a center core, a plurality of linking arms, and optionally a coupling arm, wherein,
    the center core comprises, (1) a first polypeptide comprising a plurality of lysine (K) residues, wherein each K residue and its next K residue are separated by a filler sequence comprising glycine (G) and serine (S) residues, and the number of K residues ranges from 2 to 15； or (2) a second polypeptide comprising the sequence of (Xaa-K) n, where Xaa is a PEGylated amino acid having 2 to 12 repeats of ethylene glycol (EG) unit, and n is an integral from 2 to 15；
    the plurality of linking arms are respectively linked to the K residues of the center core,
    each of the plurality of linking arms has a maleimide group at its free terminus； and
    the amino acid residue at the N- or C-terminus of the center core has an azide or an alkyne group； or the amino acid residue at the N- or C-terminus of the center core is a cysteine residue, and the thiol group of the cysteine residue is linked with the coupling arm having the azide, the alkyne, a tetrazine or a strained alkyne group at the free terminus of the coupling arm.
  2. The linker unit of claim 1, wherein the filler sequence has the sequence of GS, GGS, GSG, or SEQ ID NOs: 1-16.
  3. The linker unit of claim 1, wherein the first polypeptide comprises 2-15 units of the sequence of G1-5SK.
  4. The linker unit of claim 3, wherein the first polypeptide comprises the sequence of (GSK) 2-15.
  5. The linker unit of claim 1, wherein each of the linking arms is a PEG chain having 2-20 repeats of EG units.
  6. The linker unit of claim 1, wherein the coupling arm is a PEG chain having 2-12 repeats of EG units.
  7. The linker unit of claim 1, wherein the amino acid residue having the azide group is L-azidohomoalanine (AHA) , 4-azido-L-phenylalanine, 4-azido-D-phenylalanine, 3-azido-L-alanine, 3-azido-D-alanine, 4-azido-L-homoalanine, 4-azido-D-homoalanine, 5-azido-L-ornithine, 5-azido-d-ornithine, 6-azido-L-lysine, or 6-azido-D-lysine.
  8. The linker unit of claim 1, wherein the amino acid residue having the alkyne group is L-homopropargylglycine (L-HPG) , D-homopropargylglycine (D-HPG) , or beta-homopropargylglycine (β-HPG) .
  9. The linker unit of claim 1, wherein the strained alkyne group is trans-cyclooctene (TCO) , dibenzocyclooctyne (DBCO) , difluorinated cyclooctyne (DIFO) , bicyclononyne (BCN) , or dibenzocyclooctyne (DICO) .
  10. The linker unit of claim 1, wherein the tetrazine group is 1, 2, 3, 4-tetrazine, 1, 2, 3, 5-tetrazine or 1, 2, 4, 5-tetrazine, or derivatives thereof.
  11. The linker unit of claim 1, further comprising a plurality of first elements that are respectively linked to the plurality of linking arms via thiol–maleimide reaction.
  12. The linker unit of claim 11, further comprising a second element that is,
    linked to the azide group via copper catalyzed azide-alkyne cycloaddition (CuAAC) reaction or strained-promoted azide-alkyne click chemistry (SPAAC) reaction；
    linked to the alkyne group via CuAAC reaction；
    linked to the strained alkyne group via inverse electron demand Diels–Alder (iEDDA) reaction or SPAAC reaction； or
    linked to the tetrazine group via iEDDA reaction.
  13. The linker unit of claim 12, wherein the second element is linked to the azide or alkyne group at the N- or C- terminus of the center core via CuAAC reaction.
  14. The linker unit of claim 13, further comprising a third element that is linked to the coupling arm via iEDDA reaction.
  15. The linker unit of claim 14, wherein the third element is a long PEG chain having a molecular weight of about 20,000 to 50,000 daltons.
  16. The linker unit of claim 12, wherein the second element is linked to the azide group at the N- or C- terminus of the center core via SPAAC reaction.
  17. The linker unit of claim 16, further comprising a third element that is linked to the coupling arm via iEDDA reaction.
  18. The linker unit of claim 17, wherein the third element is a long PEG chain having a molecular weight of about 20,000 to 50,000 daltons.
  19. The linker unit of claim 12, wherein,
    the first element is a first single-chain variable fragment (scFv) specific for a cytokine or a receptor of the cytokine； or a soluble receptor of the cytokine； and
    the second element is a second scFv specific for a tissue-associated extracellular matrix protein.
  20. The linker unit of claim 19, wherein the tissue-associated extracellular matrix protein is selected from the group consisting of α-aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, and collagen XI.
  21. The linker unit of claim 19, wherein the cytokine is selected from the group consisting of tumor necrosis factor-α (TNF-α) , interleukin-17 (IL-17) , IL-1, IL-6, IL-12/IL-23, and B cell activating factor (BAFF) .
  22. The linker unit of claim 19, wherein the receptor of the cytokine is specific for IL-6 or IL-17.
  23. The linker unit of claim 19, wherein the soluble receptor of the cytokine is specific for TNF-α or IL-1.
  24. The linker unit of claim 12, wherein,
    the first element is a first scFv specific for a first cell surface antigen； and
    the second element is a second scFv specific for a second cell surface antigen.
  25. The linker unit of claim 24, wherein the first cell surface antigen is selected from the group consisting of, CD5, CD19, CD20, CD22, CD23, CD27, CD30, CD33, CD34, CD37, CD38, CD43, CD72a, CD78, CD79a, CD79b, CD86, CD134, CD137, CD138, and CD319.
  26. The linker unit of claim 24, wherein the second cell surface antigen is CD3 or CD16a.
  27. The linker unit of claim 12, wherein,
    the first element is a peptide hormone, a growth factor, or a first scFv specific for a tumor-associated antigen； and
    the second element is a second scFv specific for a cell surface antigen.
  28. The linker unit of claim 27, wherein the peptide hormone is secretin, cholecystokinin (CCK) , somatostatin, or thyroid-stimulating hormone (TSH) .
  29. The linker unit of claim 27, wherein the growth factor is selected from the group consisting of epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , vascular endothelial growth factor A (VEGF-A) , basic fibroblast growth factor (bFGF) , and hepatocyte growth factor (HGF) .
  30. The linker unit of claim 27, wherein the tumor-associated antigen is selected from the group consisting of human epidermal growth factor receptor (HER1) , HER2, HER3, HER4, carbohydrate antigen 19-9 (CA 19-9) , carbohydrate antigen 125 (CA 125) , carcinoembryonic antigen (CEA) , mucin 1 (MUC 1) , ganglioside GD2, melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) , mesothelin, mucine-related Tn, Sialyl Tn, Globo H, stage-specific embryonic antigen-4 (SSEA-4) , and epithelial cell adhesion molecule (EpCAM) .
  31. The linker unit of claim 27, wherein the cell surface antigen is CD3 or CD16a.
  32. The linker unit of claim 12, wherein,
    the first element is a first scFv specific for receptor activator of nuclear factor κB (RANKL) ； and
    the second element is a second scFv specific for collagen I or osteonectin.
  33. The linker unit of claim 12, wherein,
    the first element is an scfv specific for VEGF-A； and
    the second element is a long PEG chain having a molecular weight of about 20,000 to 50,000 daltons.
  34. A method of treating a subject having or suspected of having an immune disorder, comprising administering to the subject in need thereof a therapeutically effective amount of the linker unit of claim 19.
  35. The method of claim 34, wherein,
    the immune disorder is psoriasis；
    the first element is an scfv specific for TNF-α, IL-12/IL-23, IL-17, or IL-17R； and
    the second element is an scfv specific for collagen I or collagen VII.
  36. The method of claim 34, wherein,
    the immune disorder is systemic lupus erythematosus (SLE) , cutaneous lupus, or Sjogren’s syndrome；
    the first element is an scfv specific for BAFF； and
    the second element is an scfv specific for collagen I or collagen VII.
  37. The method of claim 34, wherein,
    the immune disorder is rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis；
    the first element is an scfv specific for TNF-α, IL-1, IL-6, IL-12/IL-23, IL-17, IL-6R, or IL-17R； and
    the second element is an scfv specific for collagen II, collagen IX, collagen XI, or α-aggrecan.
  38. The method of claim 34, wherein,
    the immune disorder is inflammatory bowel disease；
    the first element is an scfv specific for TNF-α； and
    the second element is an scfv specific for collagen III or collagen V.
  39. The method of claim 38, wherein the inflammatory bowel disease is Crohn’s disease or ulcerative colitis.
  40. A method of treating a subject having or suspected of having a diffused tumor, comprising administering to the subject in need thereof a therapeutically effective amount of the linker unit of claim 24.
  41. The method of claim 40, wherein the diffused tumor is acute lymphocytic leukemia  (ALL) , chronic lymphocytic leukemia (CLL) , acute myelogenous leukemia (AML) , chronic myelogenous leukemia (CML) , Hodgkin lymphoma, non-Hodgkin lymphoma, or myeloma.
  42. The method of claim 40, wherein,
    the diffused tumor is B-lymphocyte-derived lymphoma or leukemia；
    the first element is an scfv specific for CD5, CD19, CD20, CD22, CD23, CD30, CD37, CD79a, or CD79b； and
    the second element is an scfv specific for CD3 or CD16a.
  43. The method of claim 40, wherein,
    the diffused tumor is plasmacytoma or multiple myeloma；
    the first element is an scfv specific for CD38, CD78, CD138, or CD319； and
    the second element is an scfv specific for CD3 or CD16a.
  44. The method of claim 40, wherein,
    the diffused tumor is T-cell derived lymphoma or leukemia；
    the first element is an scfv specific for CD5, CD30, or CD43； and
    the second element is an scfv specific for CD3 or CD16a.
  45. The method of claim 40, wherein,
    the diffused tumor is myelogenous leukemia；
    the first element is an scfv specific for CD33 or CD34； and
    the second element is an scfv specific for CD3 or CD16a.
  46. A method of treating a subject having or suspected of having a solid tumor, comprising administering to the subject in need thereof a therapeutically effective amount of the linker unit of claim 27.
  47. The method of claim 46, wherein the solid tumor is melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, or head and neck squamous cell carcinoma.
  48. The method of claim 46, wherein the tumor-associated antigen is selected from the  group consisting of human epidermal growth factor receptor (HER1) , HER2, HER3, HER4, carbohydrate antigen 19-9 (CA 19-9) , carbohydrate antigen 125 (CA 125) , carcinoembryonic antigen (CEA) , mucin 1 (MUC 1) , ganglioside GD2, melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) , mesothelin, mucine-related Tn, Sialyl Tn, Globo H, stage-specific embryonic antigen-4 (SSEA-4) , and epithelial cell adhesion molecule (EpCAM) .
  49. The method of claim 46, wherein the peptide hormone is secretin, cholecystokinin (CCK) , somatostatin, or thyroid-stimulating hormone (TSH) .
  50. The method of claim 46, wherein the growth factor is selected from the group consisting of epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , vascular endothelial growth factor A (VEGF-A) , basic fibroblast growth factor (bFGF) , and hepatocyte growth factor (HGF) .
  51. The method of claim 46, wherein the cell surface antigen is selected from the group consisting of CD3 or CD16a.
  52. A method of treating a subject having or suspected of having an osteoporosis disease, comprising administering to the subject in need thereof a therapeutically effective amount of the linker unit of claim 32.
  53. A method of treating a subject suffering from an age-related macular degeneration (AMD) , comprising administering to the subject in need thereof a therapeutically effective amount of the linker unit of claim 33.
  54. A molecular construct comprising a first linker unit and a second linker unit, wherein,
    the first linker unit comprises a first center core comprising a plurality of amine groups, and a first linking arm and optionally a first coupling arm that are respectively linked to the first center core；
    the second linker unit comprises a second center core comprising a plurality of amine groups, and a second linking arm and optionally a second coupling arm that are respectively linked to the second center core； and
    the first and second linker units are coupled to each other via copper catalyzed  azide-alkyne cycloaddition (CuAAC) reaction, strained-promoted azide-alkyne click chemistry (SPAAC) reaction or inverse electron demand Diels–Alder (iEDDA) reaction occurred between any of the followings: the first and second center cores, the first coupling arm and the second center core, the first and second coupling arms, or the first center core and the second coupling arm.
  55. The molecular construct of claim 54, wherein the first and second linker units respectively comprise a plurality of the first and second linking arms linked thereto, and each of the first and second linking arms is linked to the amine groups of the first and second linker units.
  56. The molecular construct of claim 54, wherein each of the first and second linking arms has a maleimide group at the free terminus thereof.
  57. The molecular construct of claim 56, further comprising a first targeting element and a first effector element respectively linked to the first and second linking arms via thiol–maleimide reaction.
  58. The molecular construct of claim 54, wherein,
    each of the first and second linking arms is a PEG chain having 2-20 repeats of ethylene glycol (EG) units； and
    each of the first and second coupling arms is a PEG chain having 2-12 repeats of EG units.
  59. The molecular construct of claim 54, wherein,
    one of the first and second coupling arms has an azide group at the free-terminus thereof, and the other of the first and second coupling arms has an alkyne or a strained alkyne group at the free-terminus thereof； and
    the first and second center cores are coupled to each other via copper catalyzed azide-alkyne cycloaddition (CuAAC) reaction or strained-promoted azide-alkyne click chemistry (SPAAC) reaction occurred between the first and second coupling arms.
  60. The molecular construct of claim 59, wherein the strained alkyne group is dibenzocyclooctyne (DBCO) , difluorinated cyclooctyne (DIFO) , bicyclononyne (BCN) , or dibenzocyclooctyne (DICO) .
  61. The molecular construct of claim 54, wherein,
    one of the first and second coupling arms has a tetrazine group at the free-terminus thereof, and the other of the first and second coupling arms has a trans-cyclooctene (TCO) at the free-terminus thereof； and
    the first and second center cores are coupled to each other via iEDDA reaction occurred between the first and second coupling arms.
  62. The molecular construct of claim 61, wherein the tetrazine group is 1, 2, 3, 4-tetrazine, 1, 2, 3, 5-tetrazine or 1, 2, 4, 5-tetrazine, or derivatives thereof.
  63. The molecular construct of claim 54, wherein at least one of the first and the second center cores is a compound, and the coupling arm is linked to one of the plurality of amine groups of the center core via forming an amide bond therebetween, wherein the coupling arm has an azide, an alkyne, a strained alkyne or a tetrazine group at the free-terminus thereof.
  64. The molecular construct of claim 63, wherein the compound is selected from the group consisting of, benzene-1, 3, 5-triamine, 2- (aminomethyl) -2-methylpropane-1, 3-diamine, tris (2-aminoethyl) amine, benzene-1, 2, 4, 5-tetraamine, 3, 3’, 5, 5’-tetraamine-1, 1’-biphenyl, tetrakis (2-aminoethyl) methane, tetrakis- (ethylamine) hydrazine, N,N, N’, N’, -tetrakis (aminoethyl) ethylenediamine, benzene-1, 2, 3, 4, 5, 6-hexaamine, 1-N, 1-N, 3-N, 3-N, 5-N, 5-N-hexakis (methylamine) -benzene-1, 3, 5-triamine, 1-N, 1-N, 2-N, 2-N, 4-N, 4-N, 5-N, 5-N, -octakis (methylamine) -benzene-1, 2, 4, 5-triamine, and N, N-bis [ (1-amino-3, 3-diaminoethyl) pentyl] methanediamine.
  65. The molecular construct of claim 63, wherein,
    one of the first and the second center cores is the compound, and the coupling arm is linked to one of the plurality of amine groups of the center core via forming an amide bond therebetween, wherein the coupling arm has a DBCO, a DIFO, a BCN, or a DICO group at the free-terminus thereof；
    the other of the first and the second center cores is a polypeptide comprising an amino acid residue at the N-or C-terminal thereof, wherein the amino acid residue is L-azidohomoalanine (AHA) , 4-azido-L-phenylalanine, 4-azido-D-phenylalanine, 3-azido-L-alanine, 3-azido-D-alanine, 4-azido-L-homoalanine, 4-azido-D-homoalanine,  5-azido-L-ornithine, 5-azido-d-ornithine, 6-azido-L-lysine, or 6-azido-D-lysine； and
    the first and second center cores are coupled to each other via SPAAC reaction occurred between the coupling arm and the amino acid residue.
  66. The molecular construct of claim 54, wherein at least one of the first and second center cores is a polypeptide comprising a plurality of lysine (K) residues.
  67. The molecular construct of claim 66, wherein the number of K residues ranges from 2 to 15, and each K residue and its next K residue are separated by a filler sequence comprising glycine (G) and serine (S) residues.
  68. The molecular construct of claim 67, wherein the filler sequence has the sequence of GS, GGS, GSG, or SEQ ID NOs: 1-16.
  69. The molecular construct of claim 67, wherein the polypeptide comprises 2-15 units of the sequence of G1-5SK.
  70. The molecular construct of claim 69, wherein the polypeptide comprises the sequence of (GSK) 2-15.
  71. The molecular construct of claim 66, wherein the polypeptide comprises the sequence of (Xaa-K) n, where Xaa is a PEGylated amino acid having 2 to 12 repeats of ethylene glycol (EG) unit, and n is an integral from 2 to 15.
  72. The molecular construct of claim 66, wherein both the first and second center cores are the polypeptides.
  73. The molecular construct of claim 72, wherein the N-terminus of each of the first and second center cores is modified with an acetyl group.
  74. The molecular construct of claim 72, wherein,
    the first amino acid residue at the N- or C-terminus of one of the first and second center cores is AHA, 4-azido-L-phenylalanine, 4-azido-D-phenylalanine, 3-azido-L-alanine, 3-azido-D-alanine, 4-azido-L-homoalanine, 4-azido-D-homoalanine, 5-azido-L-ornithine, 5-azido-d-ornithine, 6-azido-L-lysine, or 6-azido-D-lysine；
    the first amino acid residue at the N- or C-terminus of the other of the first and second  center cores is L-homopropargylglycine (L-HPG) , D-homopropargylglycine (D-HPG) , or beta-homopropargylglycine (β-HPG) ； and
    the first and second cores are coupled to each other via copper catalyzed azide-alkyne cycloaddition (CuAAC) reaction occurred between the first amino acid residues.
  75. The molecular construct of claim 72, wherein each of the first and second center cores comprises a cysteine residue at the N- or C-terminus thereof； and the first and second coupling arms are respectively linked to the cysteine residues of the first and second center cores via thio–maleimide reaction.
  76. The molecular construct of claim 72, wherein,
    one of the first and second center cores comprises an amino acid residue at the N-or C-terminal thereof, wherein the amino acid reside is selected from the group consisting of L-azidohomoalanine (AHA) , 4-azido-L-phenylalanine, 4-azido-D-phenylalanine, 3-azido-L-alanine, 3-azido-D-alanine, 4-azido-L-homoalanine, 4-azido-D-homoalanine, 5-azido-L-ornithine, 5-azido-d-ornithine, 6-azido-L-lysine, or 6-azido-D-lysine；
    the other of the first and second center cores comprises a cysteine residue at the N- or C-terminus thereof, and the first or the second coupling arm is linked to the cysteine residue via thio–maleimide reaction, wherein the first or the second coupling arm has a DBCO, a DIFO, a BCN, or a DICO group at the free-terminus thereof； and
    the first and second center cores are coupled to each other via SPAAC reaction occurred between the first center core and the second coupling arm, or between the second center core and the first coupling arm.
  77. The molecular construct of claim 54, further comprising a third linking arm linked to the first or the second linker unit.
  78. The molecular construct of claim 77, further comprising a long PEG chain having a molecular weight of about 20,000 to 50,000 daltons linked to the third linking arm via thiol–maleimide reaction.
  79. The molecular construct of claim 57, further comprising a third linker unit comprising a third center core and a third linking arm and a third coupling arm that are respectively linked  to the third center core, wherein the third linker unit is linked to the first or the second linker unit via CuAAC reaction, iEDDA reaction, or SPAAC reaction occurred between any of the followings: the first or the second coupling arm and the third coupling arm, the first or the second center core and the third coupling arm, the first or the second coupling arm and the third center core, or the first or the second center core and the third center core.
  80. The molecular construct of claim 79, wherein the first, second, and third center cores are different.
  81. The molecular construct of claim 79, wherein the third linking arm has a maleimide group at the free terminus thereof, and a second targeting element or a second effector element is linked to the third linking arm via thio-maleimide reaction.
  82. The molecular construct of claim 81, wherein the second targeting element and the second effector element are respectively different from the first targeting element and the first effector element.
  83. The molecular construct of claim 57, wherein,
    the first targeting element is a first single-chain variable fragment (scFv) specific for a tissue-associated extracellular matrix protein； and
    the first effector element is a second scFv specific for a cytokine or a receptor of the cytokine； or a soluble receptor of the cytokine.
  84. The molecular construct of claim 83, wherein the tissue-associated extracellular matrix protein is selected from the group consisting of α-aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, and collagen XI.
  85. The molecular construct of claim 83, wherein the cytokine is selected from the group consisting of tumor necrosis factor-α (TNF-α) , interleukin-17 (IL-17) , IL-1, IL-6, IL-12/IL-23, and B cell activating factor (BAFF) .
  86. The molecular construct of claim 83, wherein the receptor of the cytokine is specific for IL-6 or IL-17.
  87. The molecular construct of claim 83, wherein the soluble receptor of the cytokine is specific for TNF-α or IL-1.
  88. The molecular construct of claim 57, wherein,
    the first targeting element is a first scFv specific for a first cell surface antigen； and
    the first effector element is a cytotoxic drug or a second scFv specific for a second cell surface antigen.
  89. The molecular construct of claim 88, wherein the first cell surface antigen is selected from the group consisting of, CD5, CD19, CD20, CD22, CD23, CD27, CD30, CD33, CD34, CD37, CD38, CD43, CD72a, CD78, CD79a, CD79b, CD86, CD134, CD137, CD138, and CD319.
  90. The molecular construct of claim 88, wherein the cytotoxic drug is selected from the group consisting of auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin.
  91. The molecular construct of claim 88, wherein the second cell surface antigen is CD3 or CD16a.
  92. The molecular construct of claim 88, wherein,
    one of the first and second cell surface antigens is CD79a； and
    the other one of the first and second cell surface antigens is CD79b.
  93. The molecular construct of claim 57, wherein,
    the first targeting element is a peptide hormone, a first growth factor, or a first scFv specific for a tumor-associated antigen； and
    the first effector element is a cytotoxic drug, a toll-like receptor agonist, a chelator complexed with a radioactive nuclide, a cytokine, or a second scFv specific for a second growth factor, a cell surface antigen, a hapten, or the cytokine.
  94. The molecular construct of claim 93, wherein the peptide hormone is secretin, cholecystokinin (CCK) , somatostatin, or thyroid-stimulating hormone (TSH) .
  95. The molecular construct of claim 93, wherein the first growth factor is selected from the group consisting of epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding  epidermal growth factor (HB-EGF) , vascular endothelial growth factor A (VEGF-A) , basic fibroblast growth factor (bFGF) , and hepatocyte growth factor (HGF) .
  96. The molecular construct of claim 93, wherein the tumor-associated antigen is selected from the group consisting of human epidermal growth factor receptor (HER1) , HER2, HER3, HER4, carbohydrate antigen 19-9 (CA 19-9) , carbohydrate antigen 125 (CA 125) , carcinoembryonic antigen (CEA) , mucin 1 (MUC 1) , ganglioside GD2, melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) , mesothelin, mucine-related Tn, Sialyl Tn, Globo H, stage-specific embryonic antigen-4 (SSEA-4) , and epithelial cell adhesion molecule (EpCAM) .
  97. The molecular construct of claim 93, wherein the cytotoxic drug is selected from the group consisting of auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin.
  98. The molecular construct of claim 93, wherein the toll-like receptor agonist is selected from the group consisting of lipopolysaccharide (LPS) , monophosphoryl lipid A, motolimod, imiquimod, resiquimod, gardiquimod, CpG oligodeoxynucleotide (CpG DON) , lipoteichoic acid, β-glucan, and zymosan.
  99. The molecular construct of claim 93, wherein the chelator is selected from the group consisting of 1, 4, 7, 10-tetraazacyclododecane-1, 4, 7, 10-tetraacetic acid (DOTA) , 1, 4, 7-triazacyclononane-1, 4, 7-triacetic acid (NOTA) , 1, 4, 7-triazacyclononane-1, 4-diacetic acid (NODA) , and diethylenetriaminepentaacetic acid (DTPA) .
  100. The molecular construct of claim 93, wherein the radioactive nuclide is 111In, 131I, or 177Lu.
  101. The molecular construct of claim 93, wherein the cytokine is selected from the group consisting of IL-2, IFN-α, IFN-γ, and TNF-α.
  102. The molecular construct of claim 93, wherein the second growth factor is EGF, mutant EGF, VEGF-A, bFGF, or HGF.
  103. The molecular construct of claim 93, wherein the cell surface antigen is selected from the group consisting of CD3, CD16a, CD28, CD134, cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) , programmed cell death 1 (PD-1) , and programmed cell death 1 ligand 1 (PD-L1) .
  104. The molecular construct of claim 93, wherein the hapten is selected from the group consisting of dinitrophenol (DNP) , trinitrophenol (TNP) , and a short peptide having an amino acid sequence of SEQ ID NO: 20.
  105. The molecular construct of claim 93, wherein the second scFv is a non-neutralizing scFv specific for the cytokine selected from the group consisting of IL-2, IFN-α, IFN-γ, and TNF-α.
  106. The molecular construct of claim 57, wherein,
    the first targeting element is an scfv specific for collagen I or osteonectin； and
    the first effector element is an scfv specific for receptor activator of nuclear factor κB (RANKL) .
  107. A method of treating a subject having or suspected of having an immune disorder, comprising administering to the subject in need thereof a therapeutically effective amount of the molecular construct of claim 83.
  108. The method of claim 107, wherein,
    the immune disorder is an autoimmune disorder；
    the first targeting element is an scfv specific for α-aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, and collagen XI； and
    the first effector element is an scfv specific for TNF-α, IL-17, IL-1, IL-6, IL-12/IL-23, BAFF, the receptor of IL-6 (IL-6R) , or the receptor of IL-17 (IL-17R) ； or the soluble receptor of TNF-α or IL-1.
  109. The method of claim 107, wherein,
    the autoimmune disorder is psoriasis；
    the first targeting element is an scfv specific for collagen I, or collagen VII； and
    the first effector element is an scfv specific for TNF-α, IL-12/IL-23, IL-17, or IL-17R.
  110. The method of claim 107, wherein,
    the autoimmune disorder is systemic lupus erythematosus (SLE) , cutaneous lupus, or Sjogren’s syndrome；
    the first targeting element is an scfv specific for collagen I or collagen VII； and
    the first effector element is an scfv specific for BAFF.
  111. The method of claim 107, wherein,
    the autoimmune disorder is rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis；
    the first targeting element is an scfv specific for collagen II, collagen IX, collagen XI, or α-aggrecan； and
    the first effector element is an scfv specific for TNF-α, IL-1, IL-6, IL-12/IL-23, IL-17, IL-6R, or IL-17R.
  112. The method of claim 107, wherein,
    the autoimmune disorder is inflammatory bowel disease；
    the first targeting element is an scfv specific for collagen III or collagen V； and
    the first effector element is an scfv specific for TNF-α.
  113. The method of claim 112, wherein the inflammatory bowel disease is Crohn’s disease or ulcerative colitis.
  114. A method of treating a subject having or suspected of having a diffused tumor, comprising administering to the subject in need thereof a therapeutically effective amount of the molecular construct of claim 88.
  115. The method of claim 114, wherein the diffused tumor is acute lymphocytic leukemia (ALL) , chronic lymphocytic leukemia (CLL) , acute myelogenous leukemia (AML) , chronic myelogenous leukemia (CML) , Hodgkin lymphoma, non-Hodgkin lymphoma, or myeloma.
  116. The method of claim 114, wherein,
    one of the first targeting element and the first effector element is an scfv specific for CD79a； and
    the other of the first targeting element and the first effector element is an scfv specific for CD79b.
  117. The method of claim 114, wherein,
    the first targeting element is an scfv specific for CD5, CD19, CD20, CD22, CD23, CD27, CD30, CD33, CD34, CD37, CD38, CD43, CD72a, CD78, CD79a, CD79b, CD86, CD134, CD137, CD138, and CD319； and
    the first effector element is the cytotoxic drug, or an scfv specific for CD3 or CD16a.
  118. The method of claim 117, wherein the cytotoxic drug is selected from the group consisting of auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin.
  119. The method of claim 117, wherein,
    the diffused tumor is B-lymphocyte-derived lymphoma or leukemia；
    the first targeting element is an scfv specific for CD5, CD19, CD20, CD22, CD23, CD30, CD37, CD79a, or CD79b； and
    the first effector element is the cytotoxic drug, or an scfv specific for CD3 or CD16a.
  120. The method of claim 117, wherein,
    the diffused tumor is B-lymphocyte-derived lymphoma or leukemia；
    one of the first targeting element and the first effector element is an scfv specific for CD79a； and
    the other of the first targeting element and the first effector element is an scfv specific for CD79b.
  121. The method of claim 117, wherein,
    the diffused tumor is plasmacytoma or multiple myeloma；
    the first targeting element is an scfv specific for CD38, CD78, CD138, or CD319； and
    the first effector element is the cytotoxic drug, or an scfv specific for CD3 or CD16a.
  122. The method of claim 117, wherein,
    the diffused tumor is T-cell derived lymphoma or leukemia；
    the first targeting element is an scfv specific for CD5, CD30, or CD43； and
    the first effector element is the cytotoxic drug, or an scfv specific for CD3 or CD16a.
  123. The method of claim 117, wherein,
    the diffused tumor is myelogenous leukemia；
    the first targeting element is an scfv specific for CD33 or CD34； and
    the first effector element is the cytotoxic drug, or an scfv specific for CD3 or CD16a.
  124. A method of treating a subject having or suspected of having a solid tumor, comprising administering to the subject in need thereof a therapeutically effective amount of the molecular construct of claim 93.
  125. The method of claim 124, wherein the solid tumor is melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, or head and neck squamous cell carcinoma.
  126. The method of claim 124, wherein the peptide hormone is secretin, cholecystokinin (CCK) , somatostatin, or thyroid-stimulating hormone (TSH) .
  127. The method of claim 124, wherein the first growth factor is selected from the group consisting of epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , vascular endothelial growth factor A (VEGF-A) , basic fibroblast growth factor (bFGF) , and hepatocyte growth factor (HGF) .
  128. The method of claim 124, wherein the tumor-associated antigen is selected from the group consisting of human epidermal growth factor receptor (HER1) , HER2, HER3, HER4, carbohydrate antigen 19-9 (CA 19-9) , carbohydrate antigen 125 (CA 125) , carcinoembryonic antigen (CEA) , mucin 1 (MUC 1) , ganglioside GD2, melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) , mesothelin, mucine-related Tn, Sialyl Tn, Globo H, stage-specific embryonic antigen-4 (SSEA-4) , and epithelial cell adhesion molecule (EpCAM) .
  129. The method of claim 124, wherein the cytotoxic drug is selected from the group consisting of auristatin, maytansine, doxorubicin, calicheamicin, and camptothecin.
  130. The method of claim 124, wherein the toll-like receptor agonist is selected from the group consisting of lipopolysaccharide (LPS) , monophosphoryl lipid A, motolimod,  imiquimod, resiquimod, gardiquimod, CpG oligodeoxynucleotide (CpG DON) , lipoteichoic acid, β-glucan, and zymosan.
  131. The method of claim 124, wherein the chelator is selected from the group consisting of 1, 4, 7, 10-tetraazacyclododecane-1, 4, 7, 10-tetraacetic acid (DOTA) , 1, 4, 7-triazacyclononane-1, 4, 7-triacetic acid (NOTA) , 1, 4, 7-triazacyclononane-1, 4-diacetic acid (NODA) , and diethylenetriaminepentaacetic acid (DTPA) .
  132. The method of claim 124, wherein the radioactive nuclide is 111In, 131I, or 177Lu.
  133. The method of claim 124, wherein the cytokine is selected from the group consisting of IL-2, IFN-α, IFN-γ, and TNF-α.
  134. The method of claim 124, wherein the second growth factor is EGF, mutant EGF, VEGF-A, bFGF, or HGF.
  135. The method of claim 124, wherein the cell surface antigen is selected from the group consisting of CD3, CD16a, CD28, CD134, cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) , programmed cell death 1 (PD-1) , and programmed cell death 1 ligand 1 (PD-L1) .
  136. The method of claim 124, wherein the first effector element is the scFv specific for the hapten, and the method further comprises the step of administering to the subject an immunoregulatory effector that is tagged with the same hapten.
  137. The method of claim 136, wherein,
    the hapten is selected from the group consisting of dinitrophenol (DNP) , trinitrophenol (TNP) , and a short peptide having an amino acid sequence of SEQ ID NO: 20； and
    the immunoregulatory effector is IFN-α, IL-2, TNF-α, and IFN-γ, and an IgG antibody specific for PD-1, PD-L1, CTLA-4, or CD3.
  138. The method of claim 124, wherein the second scFv is a non-neutralizing scFv specific for the cytokine selected from the group consisting of IL-2, IFN-α, IFN-γ, and TNF-α.
  139. A method of treating a subject having or suspected of having an osteoporosis disease, comprising administering to the subject in need thereof a therapeutically effective amount of the molecular construct of claim 106.
  140. A molecular construct comprising,
    a pair of CH2-CH3 segments of an IgG. Fc；
    a first pair of effector elements, wherein the effector element is an antibody fragment specific for tumor necrosis factor-α (TNF-α) , interleukin-17 (IL-17) , IL-17 receptor (IL-17R) , IL-1, IL-6, IL-6R, IL-12, IL-23, B cell activating factor (BAFF) , or receptor activator of nuclear factor kappa-B ligand (RANKL) ； or a soluble receptor of TNF-α or IL-1； and
    a first pair of targeting elements, wherein the targeting element is an antibody fragment specific for α-aggrecan, collagen I, collagen II, collagen III, collagen V, collagen VII, collagen IX, collagen XI, or osteonectin, wherein,
    when the first pair of effector elements is linked to the N-termini of the pair of CH2-CH3 segments, then the first pair of targeting elements is linked to the C-termini of the pair of CH2-CH3 segments, and vice versa, or
    when the first pair of effectors elements and the first pair of targeting elements are both in the form of single-chain variable fragments (scFvs) , then the first pair of targeting elements is linked to the N-termini of the first pair of effector elements in a tandem or diabody configuration, thereby forming a pair of bispecific scFvs that are linked to the N-termini of the pair of CH2-CH3 segments.
  141. The molecular construct of claim 140, wherein the pair of CH2-CH3 segments is derived from human γ4 or γ1 immunoglobulin.
  142. The molecular construct of claim 140, wherein when the first pair of effector elements is in the form of an antigen-binding fragment (Fab) , and the first pair of targeting elements is in the form of scFvs, and vice versa； then the Fab and scFvs are respectively linked to the N-termini and C-termini of the CH2-CH3 segments, so that molecular construct adopts an extended IgG configuration.
  143. The molecular construct of claim 140, further comprising a second pair of effector elements or a second pair of targeting elements, wherein the second pair of effector or targeting elements is linked to the free C-termini of the CH2-CH3 segments.
  144. The molecular construct of claim 140, wherein,
    the effector element is an scFv specific for TNF-α； and
    the targeting element is an scFv specific for collagen II, collagen IX, or α-aggrecan.
  145. The molecular construct of claim 140, wherein,
    the two effector elements are in the form of a Fab antibody specific for TNF-α； and
    the targeting element is an scFv specific for collagen II or collagen IX.
  146. The molecular construct of claim 140, wherein,
    the effector element is an scFv specific for IL-17； and
    the targeting element is an scFv specific for collagen I or collagen VII.
  147. The molecular construct of claim 140, wherein,
    the two effector elements are in the form of a Fab antibody specific for IL-17； and
    the targeting element is an scFv specific for collagen I or collagen VII.
  148. The molecular construct of claim 140, wherein,
    the effector element is an scFv specific for BAFF； and
    the targeting element is an scFv specific for collagen I or collagen VII.
  149. The molecular construct of claim 140, wherein,
    the two effector elements are in the form of a Fab antibody specific for BAFF； and
    the targeting element is an scFv specific for collagen I or collagen VII.
  150. The molecular construct of claim 140, wherein,
    the effector element is an scFv specific for TNF-α； and
    the targeting element is an scFv specific for collagen III or collagen V.
  151. The molecular construct of claim 140, wherein,
    the two effector elements are in the form of a Fab antibody specific for TNF-α； and
    the targeting element is an scFv specific for collagen III or collagen V.
  152. The molecular construct of claim 140, wherein,
    the effector element is an scFv specific for RANKL； and
    the targeting element is an scFv specific for collagen I or osteonectin.
  153. The molecular construct of claim 140, wherein,
    the two effector elements are in the form of a Fab specific for RANKL； and
    the targeting element is an scFv specific for collagen I or osteonectin.
  154. A method for treating an immune disorder, comprising the step of administering to a subject in need thereof an effective amount of the molecular construct according to claim 140.
  155. The method of claim 154, wherein the immune disorder is an autoimmune disease.
  156. The method of claim 155, wherein,
    the autoimmune disease is rheumatoid arthritis, psoriatic arthritis, or ankylosing spondylitis；
    the effector element is an antibody fragment specific for TNF-α, IL-12/IL-23, IL-1, IL-17, or IL-6； and
    the targeting element is an antibody fragment specific for collagen II, collagen IX, collagen XI, or α-aggrecan.
  157. The method of claim 155, wherein,
    the autoimmune disease is psoriasis；
    the effector element is an antibody fragment specific for TNF-α, IL-12/IL-23, or IL-17； and
    the targeting element is an antibody fragment specific for collagen I or collagen VII.
  158. The method of claim 155, wherein,
    the autoimmune disease is systemic lupus erythematosus, cutaneous lupus, or 
    Figure PCTCN2016071184-appb-100001
    Syndrome；
    the effector element is an antibody fragment specific for BAFF； and
    the targeting element is an antibody fragment specific for collagen I or collagen VII.
  159. The method of claim 155, wherein,
    the autoimmune disease is an inflammatory bowel disease；
    the effector element is an antibody fragment specific for TNF-α； and
    the targeting element is an antibody fragment specific for collagen III or collagen V.
  160. The method of claim 159, wherein the inflammatory bowel disease is Crohn’s disease or ulcerative colitis.
  161. A method for treating osteoporosis, comprising the step of administering to a subject in need thereof an effective amount of the molecular construct according to claim 140.
  162. The method of claim 161, wherein,
    of the effector element is an antibody fragment specific for RANKL； and
    the targeting element is an antibody fragment specific for collagen I or osteonectin.
  163. A molecular construct comprising,
    a pair of CH2-CH3 segments of an IgG. Fc；
    a first pair of effector elements, wherein the effector element is a drug bundle comprising a plurality of cytotoxic drug molecules, and the first pair of effector elements is linked to the C-termini of the pair of CH2-CH3 segments； and
    a first pair of targeting elements, wherein the targeting element is an antibody fragment specific for a cell surface antigen selected from the group consisting of CD5, CD19, CD20, CD22, CD23, CD30, CD33, CD34, CD37, CD38, CD43, CD78, CD79a, CD79b, CD138, and CD319, and the first pair of targeting elements is linked to the N-termini of the pair of CH2-CH3 segments.
  164. The molecular construct of claim 163, wherein the pair of CH2-CH3 segments is derived from human γ4 or γ1 immunoglobulin.
  165. The molecular construct of claim 163, wherein the first pair of targeting elements is in the form of an antigen-binding fragment (Fab) so that the molecular construct adopts an IgG configuration.
  166. The molecular construct of claim 163, wherein the cytotoxic drug is auristatin, maytansine, doxorubicin, calicheamicin, or camptothecin.
  167. The molecular construct of claim 163, further comprising a peptide extension having the sequence of (G2-4S) 2-8C and a coupling arm, wherein,
    the peptide extensions is linked to the C-terminus of one of the pair of CH2-CH3 segments；
    the coupling arm is linked to the C-terminus of the peptide extension via thiol-maleimide reaction occurred therebetween； and
    the drug bundle is linked to the coupling arm via inverse electron demand Diels-Alder  (iEDDA) reaction, strain-promoted azide-alkyne click chemistry (SPAAC) reaction, or Copper (I) -catalyzed alkyne-azide cycloaddition (CuAAC) reaction occurred therebetween.
  168. The molecular construct of claim 167, wherein the drug bundle comprises,
    a center core that is a compound having a plurality of amine groups or a polypeptide comprising a plurality of lysine (K) residues； and
    a plurality of linking arms, each having one terminus linked to the center core by reacting with one of the amine groups or one of the K residues, and carrying a maleimide group at the free terminus thereof, wherein each of the cytotoxic drug molecules is linked to the center core via connecting through the linking arm by reacting with the maleimide group.
  169. A method for the treatment of a diffused tumor, comprising the step of administering to a subject in need thereof an effective amount of the molecular construct according to claim 163.
  170. The method of claim 169, wherein,
    the diffused tumor is B lymphocyte-derived lymphoma or leukemia； and
    the cell surface antigens are cell surface antigens on human B lymphocytes.
  171. The method of claim 170, wherein the cell surface antigens on human B lymphocytes are CD5, CD19, CD20, CD22, CD23, CD30, CD37 CD43, CD79a, or CD79b.
  172. The method of claim 169, wherein,
    the diffused tumor is plasmacytoma or multiple myeloma； and
    the cell surface antigens are cell surface antigens on human plasma cells.
  173. The method of claim 172, wherein the cell surface antigens on human plasma cells are CD38, CD78, CD138, or CD319.
  174. The method of claim 169, wherein,
    the diffused tumor is T-cell derived lymphoma or leukemia； and
    the cell surface antigens are cell surface antigens on human T cells.
  175. The method of claim 174, wherein the cell surface antigens on human T cells are CD5, CD30, or CD43.
  176. The method of claim 169, wherein,
    the diffused tumor is myelogenous leukemia； and
    the cell surface antigens are cell surface antigens on human myeloid lineage leukocytes.
  177. The method of claim 176, wherein the cell surface antigens on human myeloid lineage leukocytes are CD33 or CD34.
  178. A molecular construct comprising,
    a pair of CH2-CH3 segments of an IgG. Fc；
    a first pair of effector elements, wherein the effector element is a drug bundle comprising a plurality of molecules of, a cytotoxic drug, a toll-like receptor (TLR) agonist, or a chelator complexed with a radioactive nuclide, and the first pair of effector elements is linked to the C-termini of the pair of CH2-CH3 segments； and
    a first pair of targeting elements, wherein the targeting element is an antibody fragment specific for a tumor-associated antigen, and the first pair of targeting elements is linked to the N-termini of the pair of CH2-CH3 segments.
  179. The molecular construct of claim 178, wherein the pair of CH2-CH3 segments is derived from human γ4 or γ1 immunoglobulin.
  180. The molecular construct of claim 178, wherein the first pair of targeting elements is in the form of an antigen-binding fragment (Fab) so that the molecular construct adopts an IgG configuration.
  181. The molecular construct of claim 178, further comprising a peptide extension having the sequence of (G2-4S) 2-8C and a coupling arm, wherein,
    the peptide extensions is linked to the C-terminus of one of the pair of CH2-CH3 segments；
    the coupling arm is linked to the C-terminus of the peptide extension via thiol-maleimide reaction occurred therebetween； and
    the drug bundle is linked to the coupling arm via inverse electron demand Diels-Alder (iEDDA) reaction, strain-promoted azide-alkyne click chemistry (SPAAC) reaction, or Copper (I) -catalyzed alkyne-azide cycloaddition (CuAAC) reaction occurred therebetween.
  182. The molecular construct of claim 181, wherein the drug bundle comprises,
    a center core that is a compound having a plurality of amine groups or a polypeptide comprising a plurality of lysine (K) residues； and
    a plurality of linking arms, each having one terminus linked to the center core by reacting with one of the amine groups or one of the K residues, and carrying a maleimide group at the free terminus thereof, wherein each of the molecules is linked to the center core via connecting through the linking arm by reacting with the maleimide group.
  183. The molecular construct of claim 178, further comprising a second pair of targeting elements respectively linked to the N-termini of the first pair of targeting elements in a tandem or diabody configuration, thereby forming a pair of bispecific scFvs that is linked to the N-termini of the pair of CH2-CH3 segments.
  184. The molecular construct of claim 178, wherein the cytotoxic drug is auristatin, maytansine, doxorubicin, calicheamicin, or camptothecin.
  185. The molecular construct of claim 178, wherein the TLR agonist is lipopolysaccharide (LPS) , monophosphoryl lipid A, motolimod, imiquimod, resiquimod, gardiquimod, CpG oligodeoxynucleotide (CpG DON) , lipoteichoic acid, β-glucan, or zymosan.
  186. The molecular construct of claim 178, wherein the chelator is 1, 4, 7, 10-Tetraazacyclododecane-N, 
    Figure PCTCN2016071184-appb-100002
    Figure PCTCN2016071184-appb-100003
    Figure PCTCN2016071184-appb-100004
    -tetraacetic acid (DOTA) , 1, 4, 7-Triaza-cyclononane-1, 4, 7-triacetic acid (NOTA) , 1, 4, 7-triazacyclooctane-1, 4-diacetic acid-7-p-isothiocyanobenzyl (NODA) , or diethylene triamine pentaacetic acid (DTPA) .
  187. The molecular construct of claim 178, wherein the radioactive nuclide is 90Y, 111In, or 177Lu.
  188. The molecular construct of claim 178, wherein the tumor-associated antigen is human epidermal growth factor receptor-1 (HER1) , HER2, HER3, HER4, CA19-9, CA125, carcinoembryonic antigen (CEA) , cell surface-associated mucin 1 (MUC1) , melanoma-associated antigen (MAGE) , prostate-specific membrane antigen (PSMA) , prostate stem cell antigen (PSCA) ； mucin-related Tn, Sialyl Tn, Globo H, stage-specific  embryonic antigen-4 (SSEA-4) , ganglioside GD2, or epithelial cell adhesion molecule (EpCAM) .
  189. The molecular construct of claim 178, wherein,
    the effector element is a drug bundle comprising the plurality of molecules of the cytotoxic drug； and
    the targeting element is an scFv specific for HER2.
  190. The molecular construct of claim 178, further comprising a second pair of targeting elements respectively linked to the first pair of targeting elements, wherein,
    each of the two effector elements of the first pair of effector elements is a drug bundle comprising the plurality of molecules of the cytotoxic drug；
    each of the two targeting elements of the first pair of targeting elements is an scFv specific for HER2； and
    each of the two targeting elements of the second pair of targeting elements is an scFv specific for HER1.
  191. A method for the treatment of a solid tumor, comprising the step of administering to a subject in need thereof an effective amount of the molecular construct according to claim 178.
  192. The method of claim 191, wherein the solid tumor is melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, or head and neck squamous cell carcinoma.
  193. The method of claim 191, further comprising the step of subjecting the subject to a blood dialysis procedure using an antibody fragment specific for one or more tumor-associated antigens to remove the tumor-associated antigens that are shed from the tumor and into the circulation of the subject, prior to the administration of the molecular construct.
  194. A molecular construct comprising,
    a pair of CH2-CH3 segments of an IgG. Fc；
    a first pair of effector elements, wherein the effector element is a drug bundle comprising a plurality of molecules of, a cytotoxic drug, a toll-like receptor (TLR) agonist, or a chelator complexed with a radioactive nuclide； or an antibody fragment specific for a cell surface antigen, a growth factor, or a hapten； and
    a first pair of targeting elements, wherein the targeting element is the growth factor or a peptide hormone, wherein,
    when the effector elements are the drug bundles, then the first pair of effector elements is respectively linked to the C-termini of the pair of CH2-CH3 segments, and the targeting elements is respectively linked to the N-termini of the pair of CH2-CH3 segments； and
    when the effector elements are the antibody fragments, then the effector elements is respectively linked to the N-termini of the pair of CH2-CH3 segments, and the targeting elements is respectively linked to the C-termini of the pair of CH2-CH3 segments, and vice versa.
  195. The molecular construct of claim 194, wherein the pair of CH2-CH3 segments is derived from human γ4 or γ1 immunoglobulin.
  196. The molecular construct of claim 194, wherein, the first pair of effector elements is in the form of an antigen-binding fragment (Fab) so that the molecular construct adopts an IgG configuration.
  197. The molecular construct of claim 194, further comprising a peptide extension having the sequence of (G2-4S) 2-8C and a coupling arm, wherein,
    the peptide extensions is linked to the C-terminus of one of the pair of CH2-CH3 segments；
    the coupling arm is linked to the C-terminus of the peptide extension via thiol-maleimide reaction occurred therebetween； and
    the drug bundle is linked to the coupling arm via inverse electron demand Diels-Alder (iEDDA) reaction, strain-promoted azide-alkyne click chemistry (SPAAC) reaction, or Copper (I) -catalyzed alkyne-azide cycloaddition (CuAAC) reaction occurred therebetween.
  198. The molecular construct of claim 197, wherein the drug bundle comprises,
    a center core that is a compound having a plurality of amine groups or a polypeptide comprising a plurality of lysine (K) residues； and
    a plurality of linking arms, each having one terminus linked to the center core by reacting with one of the amine groups or one of the K residues, and carrying a maleimide group at the free terminus thereof, wherein each of the molecules is linked to the center core via connecting through the linking arm by reacting with the maleimide group.
  199. The molecular construct of claim 194, further comprising a second pair of effector elements or a second pair of targeting elements, wherein the second pair of effector or targeting elements is linked, in a tandem or diabody configuration, to the N-termini of the pair of elements that is linked to the N-termini of the pair of CH2-CH3 segments, thereby forming a pair of bispecific scFvs that is linked to the N-termini of the pair of CH2-CH3 segments.
  200. The molecular construct of claim 194, wherein the cytotoxic drug is auristatin, maytansine, doxorubicin, calicheamicin, or camptothecin.
  201. The molecular construct of claim 194, wherein the TLR agonist is LPS, monophosphoryl lipid A, motolimod, imiquimod, resiquimod, gardiquimod, CpG DON, lipoteichoic acid, β-glucan, or zymosan.
  202. The molecular construct of claim 194, wherein the chelator is DOTA, NOTA, NODA, or DTPA.
  203. The molecular construct of claim 194, wherein the radioactive nuclide is 90Y, 111In, or 177Lu.
  204. The molecular construct of claim 194, wherein the cell surface antigen is PD-1, PD-L1, CTLA-4, CD3, CD16a, CD28, or CD134.
  205. The molecular construct of claim 194, wherein the growth factor is epidermal growth factor (EGF) , mutant EGF, epiregulin, heparin-binding epidermal growth factor (HB-EGF) , VEGF-A, basic fibroblast growth factor (bFGF) , or hepatocyte growth factor (HGF) .
  206. The molecular construct of claim 194, wherein the hapten is dinitrophenol (DNP) , trinitrophenol (TNP) , dansyl, penicillin, p-aminobenzoic acid, or a polypeptide having the amino acid sequence of SEQ ID No: 20.
  207. The molecular construct of claim 194, wherein the peptide hormone is cholecystokinin (CCK) , somastatin, or thyroid-stimulating hormone (TSH) .
  208. The molecular construct of claim 194, wherein,
    the effector element is the drug bundle comprising the plurality of molecules of the cytotoxic drug； and
    the targeting element is EGF.
  209. The molecular construct of claim 194, wherein,
    the effector element is an scFv specific for CD3, CD16a, PD-1 or VEGF； and
    the targeting element is EGF.
  210. A method for the treatment of a solid tumor, comprising the step of administering to a subject in need thereof an effective amount of the molecular construct according to claim 194.
  211. The method of claim 210, wherein the solid tumor is melanomas, esophageal carcinomas, gastric carcinomas, brain tumor, small cell lung cancer, non-small cell lung cancer, bladder cancer, breast cancer, pancreatic cancer, colon cancer, rectal cancer, colorectal cancer, renal cancer, hepatocellular carcinoma, ovary cancer, prostate cancer, thyroid cancer, testis cancer, or head and neck squamous cell carcinoma.
  212. The method of claim 210, wherein when the effector element is the antibody fragment specific for hapten, then the method further comprises the step of administering to the subject an immunoregulatory effector that is tagged with the same hapten after the administration of the molecule construct, wherein the immunoregulatory effector is IFN-α, IL-2, TNF-α, and IFN-γ, and an IgG antibody specific for PD-1, PD-L1, CTLA-4, or CD3.
  213. The method of claim 210, wherein the solid tumor is a malignant tumor, wherein,
    the pair of CH2-CH3 segments is derived from human IgG heavy chain γ1；
    the effector element is the drug bundle comprising the plurality of molecules of the cytotoxic drug or the plurality of molecules of LPS； and
    the targeting element is EGF, mutant EGF, epiregulin, HB-EGF, VEGF-A, FGF, HGF, CCK, somastatin, or TSH.
  214. The method of claim 210, wherein the solid tumor is a malignant tumor, wherein,
    the pair of CH2-CH3 segments is derived from human IgG heavy chain γ1；
    the effector element is an scFv specific for human CD3, CD16a, PD-1, PD-L1, or VEGF-A, and the first pair of effector elements is linked to the C-termini of the pair of CH2-CH3 segments； and
    the targeting element is EGF, mutant EGF, epiregulin, HB-EGF, VEGF-A, FGF, HGF, CCK, somatostatin, or TSH, and the first pair of targeting elements is linked to the N-termini of the pair of CH2-CH3 segments.
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