Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
  • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
  • C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
  • C07K16/2803—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
  • C07K16/2827—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against B7 molecules, e.g. CD80, CD86
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
  • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
  • A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
  • A61K47/6801—Drug-antibody or immunoglobulin conjugates defined by the pharmacologically or therapeutically active agent
  • A61K47/6803—Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates
  • A61K47/6811—Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates the drug being a protein or peptide, e.g. transferrin or bleomycin
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
  • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
  • A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
  • A61K47/6835—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
  • A61K47/6849—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a receptor, a cell surface antigen or a cell surface determinant
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
  • A61P35/02—Antineoplastic agents specific for leukemia
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
  • A61P35/04—Antineoplastic agents specific for metastasis
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
  • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
  • C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
  • C07K14/71—Receptors; Cell surface antigens; Cell surface determinants for growth factors; for growth regulators
• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
  • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
  • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
  • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
  • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
  • G01N33/574—Immunoassay; Biospecific binding assay; Materials therefor for cancer
  • G01N33/57484—Immunoassay; Biospecific binding assay; Materials therefor for cancer involving compounds serving as markers for tumor, cancer, neoplasia, e.g. cellular determinants, receptors, heat shock/stress proteins, A-protein, oligosaccharides, metabolites
  • G01N33/57492—Immunoassay; Biospecific binding assay; Materials therefor for cancer involving compounds serving as markers for tumor, cancer, neoplasia, e.g. cellular determinants, receptors, heat shock/stress proteins, A-protein, oligosaccharides, metabolites involving compounds localized on the membrane of tumor or cancer cells
• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
  • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
  • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
  • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
  • G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K39/00—Medicinal preparations containing antigens or antibodies
  • A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K38/00—Medicinal preparations containing peptides
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K2317/00—Immunoglobulins specific features
  • C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
  • C07K2317/34—Identification of a linear epitope shorter than 20 amino acid residues or of a conformational epitope defined by amino acid residues
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K2317/00—Immunoglobulins specific features
  • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
  • C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
  • C07K2317/565—Complementarity determining region [CDR]
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K2317/00—Immunoglobulins specific features
  • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
  • C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
  • C07K2317/569—Single domain, e.g. dAb, sdAb, VHH, VNAR or nanobody®
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K2317/00—Immunoglobulins specific features
  • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
  • C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K2317/00—Immunoglobulins specific features
  • C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
  • C07K2317/92—Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K2317/00—Immunoglobulins specific features
  • C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
  • C07K2317/94—Stability, e.g. half-life, pH, temperature or enzyme-resistance
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K2319/00—Fusion polypeptide
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K2319/00—Fusion polypeptide
  • C07K2319/30—Non-immunoglobulin-derived peptide or protein having an immunoglobulin constant or Fc region, or a fragment thereof, attached thereto
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K2319/00—Fusion polypeptide
  • C07K2319/32—Fusion polypeptide fusions with soluble part of a cell surface receptor, "decoy receptors"
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K2319/00—Fusion polypeptide
  • C07K2319/33—Fusion polypeptide fusions for targeting to specific cell types, e.g. tissue specific targeting, targeting of a bacterial subspecies
• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
  • G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
  • G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
  • G01N2333/705—Assays involving receptors, cell surface antigens or cell surface determinants
  • G01N2333/70503—Immunoglobulin superfamily, e.g. VCAMs, PECAM, LFA-3
  • G01N2333/70532—B7 molecules, e.g. CD80, CD86

Definitions

• the present application relates to the technical fields of biomedicine or biopharmacy, and in particular to an anti-PD-Ll single-domain antibody and derivatives and use thereof.
• PD-L1 Programmed death 1 ligand 1
• CD274 is a member of the B7 family and a ligand for PD-1.
• PD-L1 is a type I transmembrane protein consisting a total of 290 amino acids, including one IgV-like region, one IgC-like region, one transmembrane hydrophobic region and one intracellular region composed of 30 amino acids.
• PD-L1 has an effect of negatively regulating immune responses. It is found through studies that PD-L1 is mainly expressed in activated T cells, B cells, macrophages, dendritic cells, and the like. In addition to lymphocytes, PD-L1 is also expressed in endothelial cells of many other tissues such as the thymus, heart, placenta and the like, and various non lymphoid systems such as melanoma, liver cancer, gastric cancer, renal cell carcinoma, ovarian cancer, colon cancer, breast cancer, esophageal cancer, head and neck cancer and the like. PD-L1 has certain versatility in regulating autoreactive T and B cells and immune tolerance, and plays a role in T and B cell response in peripheral tissues. The high expression of PD-L1 on tumor cells is related to the poor prognosis of cancer patients.
• PD-1 Programmed death- 1
• PD-L1 PD-L1
• CD279 is a member of the B7-CD28 superfamily.
• the cytoplasmic region of CD279 contains two tyrosine residues, one near the N-terminal is located in an immunoreceptor tyrosine -based inhibitory motif (ITIM), and the other near the C-terminal is located in an immunoreceptor tyrosine- based switch motif (ITSM).
• ITIM immunoreceptor tyrosine -based inhibitory motif
• ITMS immunoreceptor tyrosine- based switch motif
• PD-1 is mainly expressed on surfaces of activated T lymphocytes, B lymphocytes and macrophages. Under normal circumstances, PD-1 can inhibit the function of T lymphocytes and promote the function of Treg cells, thereby inhibiting autoimmune responses and preventing the occurrence of autoimmune diseases.
• the binding of PD-L1 expressed by tumor cells to PD-1 can promote the immune escape of tumors by inhibiting lymphocytes.
• the binding of PD-L1 to PD-1 may cause a variety of biological changes and immune regulation, such as inhibiting the proliferation and activation of lymphocytes, inhibiting the differentiation of CD4+ T cells into Thl and Thl7 cells and inhibiting the release of inflammatory cytokines.
• monoclonal antibodies in cancer diagnostics and targeted therapy has launched a revolution in tumor therapy.
• Traditional monoclonal antibodies have a high molecular mass that may hinder their propensity to penetrate through tissues, resulting in low effective concentrations in tumors and insufficient therapeutic effects. .
• long development periods, high production costs, insufficient stability and many other factors of traditional antibodies limit their clinical application and popularization.
• Single-domain antibodies are currently the smallest antibody molecules, and the molecular weight (without Fc) is 1/10 of that of ordinary antibodies.
• single-domain antibodies also have unique functional characteristics, such as a low molecular weight, high stability, good solubility, easy expression, high tissue penetrability, simple humanization and low preparation costs, which may overcome the shortcomings of traditional antibodies.
• the objective of the present application is to provide a class of specific single-domain antibodies which are effective against PD-L1.
• a complementarity determining region (CDR) of a VHH chain of an anti-PD-Ll single-domain antibody is provided.
• the CDR of the VHH chain consists of the following:
• CDR1 with an amino acid sequence as shown in SEQ ID NO: 5n+l
• CDR2 with an amino acid sequence as shown in SEQ ID NO: 5n+2, or CDR2 with an amino acid sequence having an sequence identity of greater than 85% with a sequence as shown in SEQ ID NO: 2;
• CDR3 with an amino acid sequence as shown in SEQ ID NO: 5n+3.
• n is independently 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15.
• n is 0 or 1.
• amino acid sequence of CDR2 is shown in SEQ ID NO: 2, 7, 81, 84, 87, 90, 93, or 96.
• CDR1, CDR2 and CDR3 are separated by framework regions FR1, FR2, FR3 and FR4 of the VHH chain.
• a VHH chain of an anti-PD-Ll single domain antibody is provided.
• the VHH chain of the anti-PD-Ll single-domain antibody includes the CDR1, CDR2 and CDR3 according to the first aspect of the present application.
• an amino acid sequence of the VHH chain of the anti- PD-Ll single-domain antibody is shown in SEQ ID NO: 5n+4, 82, 85, 88, 91, 94 or 97.
• n is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15.
• Any one of the amino acid sequences above also includes a derivative sequence which is obtained through addition, deletion, modification and/or substitution of 1-8 (preferably 1- 5, more preferably 1-3) amino acid residues and can retain a PD-L1 binding affinity of the anti-PD-Ll single-domain antibody.
• n is 0 or 1.
• amino acid sequence of the VHH chain of the anti- PD-Ll single-domain antibody is shown in SEQ ID NO: 4, 9, 82, 85, 88, 91, 94 or 97.
• an anti-PD-Ll single-domain antibody is provided.
• the anti-PD-Ll single-domain antibody is a single-domain antibody against a PD- L1 epitope and has the VHH chain of the anti-PD-Ll single-domain antibody according to the second aspect of the present application.
• a polynucleotide encodes a protein selected from the group of proteins including: the CDR region of the VHH chain of the anti-PD-Ll single-domain antibody according to the first aspect of the present application, the VHH chain of the anti-PD-Ll single-domain antibody according to the second aspect of the present application, or the anti-PD-Ll single-domain antibody according to the third aspect of the present application.
• the polynucleotide has an amino acid sequence as shown in SEQ ID NO: 5n, 83, 86, 89, 92, 95 or 98.
• n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 or 16.
• the polynucleotide includes DNA or RNA.
• an expression vector is provided.
• the expression vector contains the polynucleotide according to the fourth aspect of the present application.
• the expression vector also contains a nucleotide sequence encoding an Fc fragment of immunoglobulin.
• the immunoglobulin is IgGl, IgG2, IgG3 or IgG4.
• a host cell contains the expression vector according to the fifth aspect of the present application, or a genome of the host cell is integrated with the polynucleotide according to the fourth aspect of the present application.
• the host cell includes prokaryotic cells or eukaryotic cells.
• the host cell is selected from the group of Escherichia coli, yeast cells and mammalian cells.
• a method of producing an anti-PD-Ll single-domain antibody includes the steps of: (a) culturing the host cell according to the sixth aspect of the present application under conditions suitable for the production of single-domain antibodies, and thereby obtaining a culture containing the anti-PD-Ll single-domain antibody; and
• the anti-PD-Ll single-domain antibody has an amino acid sequence as shown in SEQ ID NO: 5n+4, 82, 85, 88, 91, 94 or 97.
• n is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15.
• a single-domain antibody fusion protein has a structure as shown in formula I from N-terminal to C-terminal:
• Z1 is the VHH chain of the anti-PD-Ll single-domain antibody according to the second aspect of the present application.
• Z2 is an Fc fragment of immunoglobulin
• F is a linker sequence
• Z3 is an immunoregulatory molecule moiety.
• the immunoglobulin is IgGl, IgG2, IgG3 or IgG4.
• an amino acid sequence of Z2 is shown in SEQ ID NO: 99.
• amino acid sequence of Z2 is the same or substantially same as the amino acid sequence as shown in SEQ ID NO: 99.
• F has an amino acid sequence selected from the group including GGGGS, (GGGGS) , (GGGGS) , (GGGGS) 4 , (GGGGS) 5 , or a combination thereof.
• amino acid sequence of F is shown in SEQ ID NO: 100.
• amino acid sequence of L is the same or substantially same as the amino acid sequence as shown in SEQ ID NO: 100.
• the immunoregulatory molecule is a TGFPRII extracellular domain.
• an amino acid sequence of Z3 is shown in SEQ ID NO: 101.
• amino acid sequence of Z3 is the same or substantially same as the amino acid sequence as shown in SEQ ID NO: 101.
• the substantially same indicates that at most 50 (preferably 1-20, more preferably 1-10, more preferably 1-5, most preferably 1-3) amino acids are different, and the difference includes substitution, deletion or addition of amino acids.
• the substantially same indicates that a sequence identity of an amino acid sequence and a corresponding amino acid sequence is at least 70%, at least 75%, at least 80%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98% or at least 99%.
• an amino acid sequence of the single-domain antibody fusion protein is shown in SEQ ID NO: 102.
• an immunoconjugate in a ninth aspect of the present application, includes:
• a coupling moiety selected from the group including a detectable marker, a drug, a toxin, a cytokine, a radionuclide or an enzyme.
• the coupling moiety is a drug or a toxin.
• the coupling moiety is a detectable marker.
• the conjugate is selected from a fluorescent or luminescent marker, a radioactive marker, a MRI (magnetic resonance imaging) or CT (electronic computer X-ray tomography) contrast agent, or an enzymes capable of producing a detectable product, a radionuclide, a biotoxin, a cytokine (such as IL-2 and similar), an antibody, an antibody Fc fragment, an antibody scFv fragment, a gold nanoparticle/nanorod, a viral particle, a liposome, a magnetic nanoparticle, a prodrug activating enzyme (such as DT-diaphorase (DTD) or biphenyl hydrolase-like protein (BPHL)), a chemotherapeutic agent (such as cisplatin) or any form of nanoparticle or similar.
• a fluorescent or luminescent marker such as a radioactive marker, a MRI (magnetic resonance imaging) or CT (electronic computer X-ray tomography) contrast agent
• the immunoconjugate contains a multivalent (such as bivalent) VHH chain of the anti-PD-Ll single-domain antibody according to the second aspect of the present application, the anti-PD-Ll single-domain antibody according to the third aspect of the present application, or the single-domain antibody fusion protein according to the eighth aspect of the present application.
• the multivalent indicates that the amino acid sequence of the immunoconjugate contains multiple repeated VHH chains of the anti-PD-Ll single domain antibody according to the second aspect of the present application, the anti-PD-Ll single-domain antibody according to the third aspect of the present application, or the single domain antibody fusion protein according to the eighth aspect of the present application.
• the anti-PD-Ll single-domain antibody according to the third aspect of the present application or the single-domain antibody fusion protein according to the eighth aspect of the present application is provided, which is used in preparation of (a) reagents used for detecting PD-L1 molecules and (b) drugs used for treating tumors.
• detection includes flow cytometry and cellular immunofluorescence detection.
• a pharmaceutical composition which includes:
• the pharmaceutical composition is in a form of injection.
• the pharmaceutical composition is used for manufacturing a drug for treating tumor, and the tumor is selected from the group including gastric cancer, liver cancer, leukemia, kidney tumor, lung cancer, small intestinal carcinoma, bone cancer, prostate cancer, colorectal cancer, breast cancer, colon cancer, cervical cancer, lymphoma, adrenal gland tumor, bladder tumor, or a combination thereof.
• one or more uses of the anti-PD-Ll single domain antibody according to the third aspect of the present application or the single-domain antibody fusion protein according to the eighth aspect of the present application is provided:
• the use is non-diagnostic and non-therapeutic.
• a recombinant protein in a thirteenth aspect of the present application, includes:
• the tag sequence includes a 6His tag, an HA tag, a Flag tag, an Fc tag, an HSA or anti-HSA antibody or single-domain antibody, or a combination thereof.
• the recombinant protein specifically binds to a PD-L1 protein.
• VHH chain according to the second aspect of the present application use of the VHH chain according to the second aspect of the present application, the single-domain antibody according to the third aspect of the present application, the single-domain antibody fusion protein according to the eighth aspect of the present application, or the immunoconjugate according to the ninth aspect of the present application is provided, which is used in manufacture of a medicament, a regent, a detection plate or a kit.
• the reagent, the detection plate or the kit is used for detecting a PD-L1 protein in a sample.
• the medicament is used for treating or preventing a tumor expressing the PD-L1 protein (namely PD-L1 positive).
• the tumor includes gastric cancer, lymphoma, liver cancer, leukemia, kidney tumor, lung cancer, small intestinal carcinoma, bone cancer, prostate cancer, colorectal cancer, breast cancer, colon cancer, drenal gland tumor, or a combination thereof.
• a method for detecting a PD-L1 protein in a sample which includes the steps: ( 1 ) contacting the sample with the single-domain antibody according to the third aspect of the present application or the single-domain antibody fusion protein according to the eighth aspect of the present application; and
• detection includes qualitative detection and quantitative detection.
• a method for treating a disease includes administering the single-domain antibody according to the third aspect of the present application, the single-domain antibody fusion protein according to the eighth aspect of the present application, or the immunoconjugate according to the ninth aspect of the present application in an effective amount to a subject in need.
• the subject includes a mammal.
• the mammal is a human.
• Figure 1 shows that single-domain antibodies of the present application can bind to a human PD-L1 protein on a cell surface, and the binding effect of a portion of the antibodies is similar to that of a positive control.
• Figure 2 shows that modified single-domain antibodies can still bind to the human PD- L1 protein on the cell surface, and the binding effect of the antibodies is similar to that of a positive control.
• Figure 3 shows that modified single-domain antibodies can still block the binding of the PD-L1 protein to the human PD-1 protein on the cell surface, and the blocking effect of the antibodies is similar to that of a positive control.
• Figure 4 shows that single-domain antibodies of the present application can effectively activate T cells, and the activation effect is similar to or better than that of an antibody of a positive control.
• Figure 5 shows a schematic structural diagram of a fusion protein.
• Figure 6 shows that the fusion protein of the present application can bind to the human PD-L1 protein on the cell surface.
• Figure 7 shows that the fusion protein of the present application can block the binding of the PD-L1 protein to the human PD-1 protein on the cell surface, and the blocking effect of an antibody is similar to that of a positive control.
• Figure 8 shows that the fusion protein of the present application can bind to TGFpi, TGFP2 and TGFP3.
• Figure 9 shows that the fusion protein of the present application can effectively block a TGFp/SMAD signal pathway.
• Figure 10 shows that the fusion protein of the present application can effectively activate T cells, and the activation effect is similar to or better than that of an antibody of a positive control.
• Figure 11 shows that the fusion protein of the present application can effectively inhibit tumor growth in mice.
• Figure 12 shows a photograph of the PD-L1-VHH crystal sample of the present application.
• Figure 13 shows the crystal structure of the PD-L1-VHH complex of the present application (the upper structure is PD-L1 and lower structure is the VHH).
• Figure 14 shows a hydrogen bond interaction interface of PD-L1-VHH of the present application (the upper structure is PD-L1 and the lower structure is VHH).
• Figure 15 shows a hydrophobic interaction interface of PD-L1-VHH of the present application (the upper structure is PD-L1 and the lower structure is VHH).
• Figure 16 shows the effect of different drug groups on the tumor volume of h-PD-Ll knock-in mice implanted with h-PD-Ll knock-in MC38 tumors.
• Figure 17 shows pictures of tumors in different drug groups 27 days after inoculation.
• Figure 18 shows the effect of each group of drugs on tumor weight of h-PD-Fl knock- in mice implanted with h-PD-Fl knock-in MC38 tumors.
• Figure 19 shows the effect of different drug groups on body weight of h-PD-Fl knock - in mice implanted with h-PD-Fl knock-in MC38 tumors.
• Figure 20 shows the effect of different drug groups on tumor volume of h-PD-Fl knock - in mice implanted with h-PD-Fl knock-in MC38 tumors.
• Figure 21 shows pictures of tumors in different drug groups 28 days after inoculation.
• Figure 22 shows the effect of each group of drugs on tumor weight of h-PD-Fl knock- in mice implanted with h-PD-Fl knock-in MC38 tumors.
• Figure 23 shows the effect of different drug groups on body weight of h-PD-Fl knock - in mice implanted with h-PD-Fl knock-in MC38 tumors.
• the present application used a human-derived PD-L1 antigen protein for immunizing llamas to obtain high-quality immune libraries containing single-domain antibody genetic sequences.
• the inventors screened for single-domain antibodies with genetic sequences showing relatively high humanization levels (sequence identity > 85%) from the immune single-domain antibody gene library.
• PD-L1 protein molecules were subjected to biotinylation, and the immune library containing sequence of single-domain antibodies was screened using yeast display technology, and thus genes of the candidate single-domain antibodies specific to PD-L1 were obtained.
• genes and engineered mutants thereof were transferred into Expi-CHO cells and further screened in the aspects of antibody affinity, ability to block the binding of PD-L1 to PD-1, thermal stability and activation of T cell activity to obtain a class and panel of single-domain antibodies, which can be expressed efficiently in vitro with high binding specificity to human PD-L1 antigen.
• a fusion protein produced by fusing a single domain antibody sequence (as a targeting moiety) of the present application with an IgGl Fc fragment (as a linking moiety) and a TGFPRII extracellular domain (as an immunoregulatory molecule moiety) is highly active with PD-L1, and can effectively block the interaction between PD-L1 and PD-1, effectively block the TGF-p/SMAD signal pathway, effectively activate human T lymphocytes and effectively inhibit tumor growth in mice.
• single-domain antibody of the present application As used herein, the terms "single-domain antibody of the present application”, “anti-PD- Ll single-domain antibody of the present application” and “PD-L1 single-domain antibody of the present application” are used interchangeably and all refer to single-domain antibodies with specificity in recognizing and binding to PD-L1 (including human PD-L1). Single domain antibodies with an amino acid sequence of a VHH chain as shown in SEQ ID NO: 4, 9, 82, 85, 88, 91, 94 or 97 are particularly preferred.
• antibody or "immunoglobulin” is a heterotetrameric glycoprotein of about 150,000 daltons with the same structural characteristics, which consists of two identical light chains (L) and two identical heavy chains (H). Each light chain is linked to a heavy chain through a covalent disulfide bond, and the numbers of disulfide bonds between the heavy chains of different immunoglobulin isotypes are different. Each heavy chain and light chain also have regularly spaced intrachain disulfide bonds. Each heavy chain has a variable region (VH) at one end, followed by multiple constant regions.
• VH variable region
• Each light chain has a variable region (VL) at one end and a constant region at the other end; the constant region of each light chain is relative to the first constant region of the corresponding heavy chain, and the variable region of each light chain is relative to the variable region of the corresponding heavy chain.
• Special amino acid residues form an interface between the variable regions of the light chain and the heavy chain.
• single domain antibody VHH
• single domain antibody VHH
• CHI light chain and heavy chain constant region 1
• variable means that certain parts of the variable region of an antibody are different in sequence, so that the binding and specificity of various specific antibodies to specific antigens are formed. However, variability is not evenly distributed in the entire variable region of the antibody. Variability is concentrated in three fragments in the light chain and heavy chain variable regions known as CDRs or hypervariable regions. The more conserved part of the variable region is called a framework region (FR).
• FR framework region
• the variable regions of the natural heavy chain and light chain each contain four FRs, which are roughly in a b-folded configuration and connected by three CDRs forming a connecting loop, and in some cases, a partial b folded structure can be formed.
• the CDRs in each chain are closely joined together by the FR and form an antigen binding site of an antibody together with the CDRs of another chain (see Kabat et ah, NIH Publ. No. 91-3242, Volume I, pp. 647- 669 (1991)). Constant regions are not directly involved in the binding of antibodies to antigens, but they exhibit different effector functions, such as participating in antibody- dependent cytotoxicity of the antibody.
• immunoconjugates and fusion expression products include conjugates formed by binding drugs, toxins, cytokines, radionuclides, enzymes and other diagnostic or therapeutic molecules to the antibody of the present application or fragments thereof.
• the present application also includes a cell surface marker or antigen bound to the anti-PD-Ll protein antibody or fragments thereof.
• variable region and “complementarity determining region (CDR)” are used interchangeably.
• the heavy chain variable region of an antibody includes CDRs being CDR1, CDR2 and CDR3.
• the heavy chain of an antibody includes the above heavy chain variable region and heavy chain constant region.
• antibody of the present application refers to a polypeptide which specifically binds to the PD-L1 protein, such as a protein or polypeptide having a heavy chain variable region, which may or may not contain initiation methionine.
• the present application also provides other proteins or fusion expression products having the antibody of the present application.
• the present application includes any protein or protein conjugate and fusion expression product (namely immunoconjugate and fusion expression product) having a heavy chain containing a variable region, as long as the variable region is identical or at least 90% homologous, preferably at least 95% homologous to the heavy chain variable region of the antibody of the present application.
• antigen-binding properties of an antibody can be described by three specific regions, called variable regions (CDR), located in the heavy chain variable region, separated by four framework regions (FR), and the amino acid sequences of the four FRs are relatively conservative and do not directly participate in a binding reaction.
• CDR variable regions
• FR framework regions
• CDRs form a circular structure and are close to each other in spatial structure due to the b folds formed by the FRs therebetween, and the CDRs on a heavy chain and the CDRs on a corresponding light chain constitute antigen binding sites of an antibody.
• the amino acid sequences of antibodies of the same type can be compared to determine which amino acids constitute the FR or CDR regions.
• variable regions of the heavy chains of the antibody of the present application are of particular interest, because at least some of the variable regions are involve binding to antigens. Therefore, the present application includes molecules which have the heavy chain variable regions of the antibody with CDRs, as long as the CDRs thereof have 90% homology or above (preferably 95% or above, most preferably 98% or above) with the CDRs identified here.
• the present application includes not only intact antibodies, but also fusion proteins formed by fragments of immunologically active antibodies or antibodies and other sequences. Therefore, the present application also includes fragments, derivatives and analogs of the antibodies.
• fragment refers to polypeptides which substantially retain the same biological function or activity as the antibodies of the present application.
• the polypeptide fragments, derivatives or analogs of the present application may be (i) a polypeptide in which one or more conservative or non-conservative amino acid residues (preferably conservative amino acid residues) are substituted, and such substituted amino acid residues may or may not be encoded by genetic codes, (ii) a polypeptide with substitution groups in one or more amino acid residues, (iii) a polypeptide formed by fusing a mature polypeptide to another compound (such as a compound which extends the half-life of polypeptides, such as polyethylene glycol), or (iv) a polypeptide formed by fusing an additional amino acid sequence to the polypeptide sequence (such as a leader sequence, a secretory sequence, a sequence used for purifying the polypeptide or proprotein sequence, or a fusion protein formed with the
• the antibody of the present application refers to a polypeptide having PD-L1 protein binding activity and the CDRs above.
• the term also includes variant forms of polypeptides containing the CDRs above and having the same functions as the antibody of the present application. These variant forms include (but are not limited to) deletion, insertion and/or substitution of one or more (usually 1-50, preferably 1-30, more preferably 1-20, most preferably 1-10) amino acids and the addition of one or more (usually within 20, preferably within 10, and more preferably within 5) amino acids at the C-terminal and/or N-terminal.
• deletion, insertion and/or substitution of one or more (usually 1-50, preferably 1-30, more preferably 1-20, most preferably 1-10) amino acids and the addition of one or more (usually within 20, preferably within 10, and more preferably within 5) amino acids at the C-terminal and/or N-terminal.
• functions of a protein are usually not changed.
• variant forms of the polypeptide include homologous sequences, conservative variants, allelic variants, natural mutants, induced mutants, DNA encoded proteins which can be hybridized with coding DNA of the antibody of the present application under high or low stringency conditions, and polypeptides or proteins obtained by using antiserum against the antibody of the present application.
• the present application also provides other polypeptides, such as a fusion protein containing the single-domain antibody or fragments thereof.
• the present application also includes fragments of the single-domain antibody of the present application.
• the fragments have at least about 50 consecutive amino acids of the antibody of the present application, preferably at least about 60 consecutive amino acids, more preferably at least about 80 consecutive amino acids, and most preferably at least about 100 consecutive amino acids.
• “conservative variants of the antibody of the present application” refer to polypeptides formed by substitution of at most 10, preferably at most 8, more preferably at most 5, and most preferably at most 3 amino acids with amino acids having same or similar properties in comparison with the amino acid sequence of the antibody of the present application. These conservative variant polypeptides are best produced through substitution of amino acids according to Table 1.
• the present application also provides polynucleotide molecules encoding the antibody or fragments thereof or fusion protein thereof.
• the polynucleotides of the present application can be in the form of DNA or RNA.
• DNA forms include cDNA, genomic DNA or artificially synthetic DNA.
• DNA can be single-stranded or double-stranded.
• DNA can be coding strands or non-coding strands.
• Polynucleotides encoding the mature polypeptides of the present application include coding sequences only encoding the mature polypeptides, coding sequences of the mature polypeptides and various additional coding sequences, and the coding sequences of the mature polypeptides (and optional additional coding sequences) as well as non-coding sequences.
• polynucleotides encoding polypeptides may include a polynucleotide encoding the polypeptide, or a polynucleotide which also includes the additional coding and/or non-coding sequence.
• the present application also relates to polynucleotides which are hybridized with the sequences above, and the identity between the two sequences is at least 50%, preferably at least 70%, and more preferably at least 80%.
• the present application particularly relates to polynucleotides which can be hybridized with the polynucleotides of the present application under stringent conditions.
• stringent conditions refer to: (1) hybridization and elution at relatively low ionic strength and relatively high temperature, such as 0.2 x SSC, 0.1% SDS and 60°C; or (2) addition of a denaturing agent during hybridization, such as 50% (v/v) formamide, 0.1% calf serum/0.1% Ficoll, 42°C or similar; or (3) hybridization occurring only when the identity between two sequences is at least 90% or above, and more preferably 95% or above.
• a polypeptide encoded by a hybridizable polynucleotide has the same biological function and activity as a mature polypeptide.
• a full-length nucleotide sequence of the antibody of the present application or fragments thereof can usually be obtained by a PCR amplification method, a recombination method or an artificial synthesis method.
• a feasible method is using artificial synthesis method to synthesize relevant sequences, especially when the fragment length is short.
• a fragment with a very long sequence can be obtained by first synthesizing multiple small fragments and then linking the fragments.
• a coding sequence of a heavy chain and an expression tag (such as 6His) can be fused together to form a fusion protein.
• Biomolecules nucleic acids, proteins, or similar
• Biomolecules involved in the present application include biomolecules which exist in an isolated form.
• DNA sequences encoding the protein (or fragments thereof, or derivatives thereof) of the present application can be obtained completely through chemical synthesis.
• the DNA sequences can then be introduced into various existing DNA molecules (such as vectors) and cells known in the art.
• mutation can also be introduced into the protein sequences of the present application through chemical synthesis.
• the present application also relates to vectors containing the suitable DNA sequences and suitable promoters or control sequences. These vectors can be used to transform appropriate host cells to express proteins.
• the host cells can be prokaryotic cells such as bacterial cells; or lower eukaryotic cells such as yeast cells; or higher eukaryotic cells such as mammalian cells.
• prokaryotic cells such as bacterial cells; or lower eukaryotic cells such as yeast cells; or higher eukaryotic cells such as mammalian cells.
• Representative examples include Escherichia coli, Streptomyces, bacterial cells of Salmonella typhimurium, fungal cells such as yeast, insect cells of Drosophila S2 or Sf9, animal cells of CHO, COS7 and 293 cells or similar.
• Transformation of the host cells with recombinant DNA can be performed by conventional techniques well known to those skilled in the art.
• the host cells are prokaryotes such as Escherichia coli
• competent cells which can absorb DNA can be harvested after an exponential growth phase and treated with a CaCb method, and the steps used are well known in the art. Another way is to use MgCb.
• transformation can also be performed by an electroporation method.
• the host cells are eukaryotes, the following DNA transfection methods can be selected: a calcium phosphate co-precipitation method, conventional mechanical methods such as microinjection, electroporation, liposome packaging or similar.
• Obtained transformants can be cultured by conventional methods to express polypeptides encoded by genes of the present application.
• a culture medium used in culture can be selected from various conventional culture mediums. Culture is carried out under conditions suitable for the growth of the host cells. After the host cells have grown to an appropriate cell density, a selected promoter is induced by a suitable method (such as temperature conversion or chemical induction), and the cells are further cultured for a period of time.
• the recombinant polypeptides in the method above can be expressed in cells or on cell membranes, or secreted out of the cells. If necessary, the recombinant proteins can be separated and purified through various separation methods according to the physical, chemical and other characteristics. These methods are well known to those skilled in the art. Examples of these methods include, but are not limited to conventional renaturation treatment, treatment with a protein precipitation agent (a salting out method), centrifugation, osmotic fungus breaking, ultra-treatment, ultra-centrifugation, molecular sieve chromatography (gel filtration), adsorption chromatography, ion exchange chromatography, high performance liquid chromatography (HPLC) and other various liquid chromatography techniques and combinations of these methods.
• a protein precipitation agent a salting out method
• centrifugation osmotic fungus breaking
• ultra-treatment ultra-treatment
• ultra-centrifugation molecular sieve chromatography
• HPLC high performance liquid chromatography
• the antibody of the present application can be used alone and can be combined or coupled with detectable markers (for diagnostic purposes), therapeutic agents, PK (protein kinase) modified moieties or any combination of these substances.
• Detectable markers for diagnostic purposes include, but are not limited to fluorescent or luminescent markers, radioactive markers, MRI (magnetic resonance imaging) or CT (electronic computer X-ray tomography) contrast agents, or enzymes capable of producing detectable products.
• Therapeutic agents which can be combined or coupled with the antibody of the present application include, but are not limited to: 1. radionuclides; 2. biotoxins; 3. cytokines such as IL-2; 4. gold nanoparticles/nanorods; 5. virus particles; 6. liposomes; 7. magnetic nanoparticles; 8. prodrug activating enzymes (such as DT-diaphorase (DTD) or biphenyl hydrolase-like protein (BPHL)); 9. chemotherapeutics (such as cisplatin) or any form of nanoparticles or similar.
• DTD DT-diaphorase
• BPHL biphenyl hydrolase-like protein
• the "fusion protein of the present application” refers to a bifunctional fusion protein having both the anti-PD-Ll single-domain antibody described in the first aspect of the present application and an immunoregulatory molecule moiety.
• a fusion protein is provided, and the single-domain antibody fusion protein has a structure as shown in formula I from N-terminal to C-terminal:
• Z1 is the VHH chain of the anti-PD-Ll single-domain antibody according to the second aspect of the present application.
• Z2 is an Fc fragment of immunoglobulin
• L is a linker sequence
• Z3 is an immunoregulatory molecule part.
• the immunoglobulin can be IgGl, IgG2, IgG3 or IgG4.
• the immunoglobulin is IgGl
• the amino acid sequence of Z2 is shown in SEQ ID NO: 99.
• the amino acid sequence of Z2 is the same or substantially same as the amino acid sequence as shown in SEQ ID NO: 99.
• L is a flexible amino acid linker.
• L has an amino acid sequence selected from the group including GGGGS, (GGGGS)2, (GGGGS)3, (GGGGS) 4 , (GGGGS) 5 , or a combination thereof.
• amino acid sequence of L is shown in SEQ ID NO: 100. In other embodiments, the amino acid sequence of L is the same or substantially same as the amino acid sequence as shown in SEQ ID NO: 100.
• the immunoregulatory molecule is a TGFPRII extracellular domain.
• the amino acid sequence of Z3 is shown in SEQ ID NO: 101.
• the amino acid sequence of Z3 is the same or substantially same as the amino acid sequence as shown in SEQ ID NO: 101.
• the substantially same indicates that at most 50 (preferably 1- 20, more preferably 1-10, more preferably 1-5, most preferably 1-3) amino acids are different, and the difference includes substitution, deletion or addition of amino acids.
• the substantially same indicates that the sequence identity of an amino acid sequence and a corresponding amino acid sequence is at least 70%, at least 75%, at least 80%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98% or at least 99%.
• amino acid sequence of a single-domain antibody fusion protein is shown in SEQ ID NO: 102.
• TGFP is a key inducer of Epithelial-mesenchymal-transition (EMT). At the same time, TGFP has a strong immunosuppressive effect in a tumor microenvironment, and thus has an important regulatory effect on tumor development, metastasis and drug resistance.
• EMT Epithelial-mesenchymal-transition
• a TGFP receptor II is selected as an immunoregulatory molecule in the fusion protein.
• the fusion protein of the present application has the advantages of high dual target binding affinity and specificity, and thereby further enhancing the anti-tumor immune function.
• the present application also provides a composition.
• the composition is a pharmaceutical composition, which contains the antibody or active fragments thereof or fusion protein thereof and a pharmaceutically acceptable carrier.
• these substances can be formulated in a non-toxic, inert and pharmaceutically acceptable aqueous carrier medium, wherein the pH is usually about 5-8, preferably about 6-8, although the pH can be changed according to properties of the formulated substances and disease conditions to be treated.
• the formulated pharmaceutical composition can be administered by conventional routes, including (but not limited to) intratumoral administration, intraperitoneal administration, intravenous administration, or topical administration.
• the pharmaceutical composition of the present application can be directly used to bind PD-L1 protein molecules, and thus can be used to treat tumors.
• other therapeutic agents can also be used at the same time.
• the pharmaceutical composition of the present application contains a safe and effective amount (such as 0.001-99 wt%, preferably 0.01-90 wt%, more preferably 0.1-80 wt%) of the single-domain antibody (or a conjugate thereof) of the present application and a pharmaceutically acceptable carrier or excipient.
• a pharmaceutically acceptable carrier or excipient includes (but is not limited to) saline, buffer, glucose, water, glycerol, ethanol and combinations thereof.
• a pharmaceutical preparation should be matched with the administration mode.
• the pharmaceutical composition of the present application can be prepared into an injection form, for example, the pharmaceutical composition is prepared by conventional methods with physiological saline or an aqueous solution containing glucose and other adjuvants.
• the pharmaceutical composition such as an injection and a solution should be manufactured under sterile conditions.
• the dosage of active ingredients is a therapeutically effective amount, such as about 10 pg/kg body weight to about 50 mg/kg body weight per day.
• the polypeptides of the present application can also be used with other therapeutic agents.
• a safe and effective amount of the immunoconjugate is administered to a mammal, wherein the safe and effective amount is usually at least about 10 pg/kg body weight, and in most cases not higher than about 50 mg/kg body weight.
• the dosage is about 10 pg/kg body weight to about 10 mg/kg body weight.
• factors such as the administration route and the health conditions of patients should also be considered for the specific dosage, which are within the skill range of a skilled physician.
• the single-domain antibody contains a detectable marker. More preferably, the marker is selected from the following group of isotopes, colloidal gold markers, colored markers or fluorescent markers.
• Colloidal gold labelling can be performed by methods known to those skilled in the art.
• the anti-PD-Ll single-domain antibody is labelled with colloidal gold to obtain a colloidal gold labelled single-domain antibody.
• the anti-PD-Ll single-domain antibody of the present application has high specificity and titer.
• the present application also relates to a method for detecting a PD-L1 protein. Steps of the method are generally as follows: obtaining a cell and/or tissue sample; dissolving the sample in a medium; and detecting the level of the PD-L1 protein in the dissolved sample.
• the sample used is not particularly limited, and a representative example is a sample containing cells in a cell preservation solution.
• the present application also provides a kit containing the antibody (or fragments thereof) of the present application or detection plates.
• the kit further includes a container, an instruction for use, a buffer agent or similar.
• the present application also provides a detection kit for detecting the level of PD-L1.
• the kit includes an antibody for identifying the PD-L1 protein, a lysis medium for dissolving a sample and general reagents and buffers required for detection, such as various buffers, detection markers, detection substrates, or similar.
• the detection kit may be an in-vitro diagnostic device.
• the single-domain antibody of the present application has high values in biological use and clinical use, and use of the single-domain antibody relates to the fields of diagnosis and treatment of PD-L1 related diseases, basic medical research, biological research, or similar. Preferred use is for clinical diagnosis and targeted therapy for PD-L1.
• the single-domain antibody of the present application is highly specific to human PD- L1 protein with a correct spatial structure.
• the single-domain antibody of the present application has high affinity.
• the single-domain antibody can inhibit a PD-1/PD-L1 pathway on the basis of TGF- b in a targeting and tumor microenvironment, restore T cells activity, enhance immune response and more effectively improve the effect of inhibiting tumor occurrence and development.
• the single-domain antibody of the present application has no apparent toxicity.
• Example 1 Construction of a single-domain antibody library
• IgG2 and IgG3 sequences were amplified from cDNA:
• the target fragments were recovered by using a PCR purification kit (purchased from QIAGEN).
• a linearized yeast display vector and products of the third round of PCR were mixed and electrotransformed into saccharomyces cerevisiae (ATCC® 20828) to construct an anti-PD- L1 single-domain antibody library from two animals, and the library size was measured to 4.47 x 10 7 and 4.14 x 10 7 .
• Example 2 Screening of a PD-L1 single-domain antibody
• Biotinylation of human PD-L1 protein A human PD-L1 protein was dissolved in an appropriate volume of double-distilled water, and a biotin was dissolved and mixed with the protein solution according to a product instruction of a biotin labelling kit (purchased from Thermo) and then incubated at 4°C for 2 hours.
• a desalting column purchased from Thermo was used to remove excess biotin, and pretreatment by the desalting column and collection operation of a sample were both carried out according to steps in the product instruction.
• a VHH library constructed in Example 2 was inoculated into an SD-CAA amplification culture medium (1 L of SD-CAA amplification culture medium contained 6.7 g of YNB, 5 g of casamino acids, 13.62 g of Na 2 HP0 4 ⁇ I2H2O, 7.44 g of NaH 2 P0 4 and 2% of glucose), the number of inoculated yeast cells was greater than ten times the library capacity (initial amplification concentration was 0.5 OD 6 oo/ml), and culture was carried out overnight at 30°C and 225 rpm.
• yeast cells were resuspended with an SD-CAA induction culture medium, the initial concentration was adjusted to be 0.5 OD 6 oo/ml, and induction was carried out overnight. The concentration of the library after induction was measured, and ten times the library capacity of the yeast cells were taken and centrifuged to remove the culture medium.
• the yeast cells were resuspended with 50 ml of a washing buffer (PBS + 0.5% BSA + 2 mM EDTA) and centrifuged to remove the supernatant.
• the yeast cells were resuspended with 10 ml of the washing buffer.
• a biotin-labelled PD-L1 protein (final concentration 100 mM) was added, incubated at room temperature for 30 minutes and centrifuged, and the yeast cells were collected and washed 3 times with 50 ml of the washing buffer.
• the yeast cells were resuspended with 5 ml of the washing buffer, 200 m ⁇ of S A magnetic beads (purchased from Miltenyi) were added, and the cells were incubated upside down for 10 minutes.
• a mixture of the yeast and magnetic beads was washed 3 times with the washing buffer and then added into an LS column (purchased from Miltenyi).
• the LS column was placed on a magnetic stand and washed with the washing buffer to remove non-specifically bound yeast cells.
• the column was removed from the magnetic stand, and the washing buffer was added to elute the yeast.
• the eluted yeast was centrifuged and transferred into a 200 ml SD-CAA amplification culture medium for amplification.
• the yeast cells enriched by MACS were inoculated into an SD-CAA amplification culture medium, and the initial amplification concentration was 0.5 OD 6 oo/ml. Shake flask culture was carried out overnight at 30°C and 225 rpm.
• the yeast cell were resuspended with an SD-CAA induction culture medium (1L of SD-CAA induction culture medium contains 6.7 g of YNB, 5 g of casamino acids, 13.62 g of Na 2 HP0 4 ⁇ I2H2O, 7.44 g of NaPbPCF, 2% of galactose, 2% of raffinose and 0.1% of glucose), the initial concentration was 0.5 OD 6 oo/ml, and induction was carried out overnight.
• An anti-c-Myc mouse-derived antibody (purchased from Thermo) diluted by 1:200 and 100 nM of biotin-labelled PD-L1 antigen were added and incubated at room temperature for 10 minutes.
• the yeast was washed 3 times with PBS, a goat anti-mouse IgG (H+L) Alexa Fluor Plus 488 (purchased from Invitrogen) diluted by 1:500 and a streptavidin APC-conjugated fluorescent antibody (purchased from Invitrogen) were added and incubated in the dark at 4°C for 15 minutes. 2 ml of PBS was added to resuspend the cells, and a BD FACSArialll instrument was used for sorting to obtain yeast which has high binding affinity to PD-L1 antigen.
• PBS goat anti-mouse IgG
• Alexa Fluor Plus 488 purchased from Invitrogen
• streptavidin APC-conjugated fluorescent antibody purchased from Invitrogen
• Yeast liquid with high binding ability to the PD-L1 antigen which was obtained by MACS and FACS enrichment, was cultured overnight in an SD-CAA amplification culture medium at 30°C and 225 rpm.
• Yeast plasmids were extracted according to operations of a yeast plasmid extraction kit (purchased from TIANGEN). The plasmids were transformed into Top 10 competent cells (purchased from TIANGEN) by electrotransfer, coated on an ampicillin resistant flat plate and cultured overnight at 37°C. Single clones were taken for sequencing to obtain a VHH gene sequence.
• Example 3 Construction, expression and purification of a heavy chain antibody
• a VHH gene sequence was linked to a human IgGl (LALA mutation) Fc fragment and digested into a linearized pCDNA3.1 vector by using a homologous recombinase (purchased from Vazyme) and an EcoR I/Not I enzyme, and the process was carried out in accordance with a product instruction.
• a homologous recombination product was transformed into Top 10 competent cells, coated on an ampicillin resistant flat plate and cultured overnight at 37°C, and single clones were taken for sequencing.
• An ExpiCHOTM expression system kit (purchased from Thermo) was used for transferring plasmids into Expi-CHO cells, and a transfection method was in accordance with a product instruction; after the cells were cultured for 5 days, the supernatant was collected, and protein A magnetic beads (purchased from GenScript) were used for purifying the target protein according to a sorting method.
• the magnetic beads were resuspended with an appropriate volume of binding buffer (PBS + 0.1% Tween 20, pH 7.4) (1-4 times the volume of magnetic beads) and then added into a sample to be purified, and the mixture was incubated at room temperature for 1 hour and gently shaken during the period.
• the sample was placed on a magnetic stand (purchased from Beaver), the supernatant was removed, and the magnetic beads were washed 3 times with the binding buffer. 3-5 times the volume of the magnetic beads of an elution buffer (0.1M sodium citrate, pH 3.2) was added for shaking at room temperature for 5-10 minutes, the mixture was placed back on the magnetic stand, and the elution buffer was collected and transferred into a collection tube with an added neutralization buffer (1M Tris, pH 8.54) and mixed uniformly.
• an elution buffer 0.1M sodium citrate, pH 3.2
• Example 4 Binding of a purified anti-PD-Ll antibody to human PD-L1
• a pCHOl.O vector (purchased from Invitrogen) of human PD-L1 cDNA (purchased from Sino Biological) was cloned into MCS through transfection to produce CHO cells (CHO-hPD-Ll cells) overexpressing human PD-L1.
• the cell density of the CHO-hPD-Ll cells subjected to enlarge cultivation was adjusted to 2 x 10 6 cells/ml, and 100 m ⁇ of the cells were added into each well of a 96-well flow plate and centrifuged for later use.
• a purified PD-L1 antibody was diluted with PBS, three times dilution was started for a total of 12 points when the concentration was 400 nM, and 100 m ⁇ of the diluted sample was added into each well of the 96-well flow plate with cells, incubated at 4°C for 30 minutes and washed twice with PBS.
• 100 m ⁇ of goat F(ab')2 anti-human IgG-Fc (PE) (purchased from Abeam) diluted 100 times with PBS was added into each well, incubated at 4°C for 30 minutes and washed twice with PBS.
• 100 m ⁇ of PBS was added into each well for resuspending the cells, detection was carried out on a CytoFlex (Bechman) flow cytometer, and corresponding MFI was calculated.
• Example 5 Affinity measurement of a PD-L1 antibody
• a protein construction and expression purification method was the same as that in Example 3, and the purity of an obtained protein was detected by HPLC.
• the mobile phase was 150 mM Na 2 HP0 4 ⁇ 123 ⁇ 40, and the pH was 7.0.
• Chromatographic conditions detection wavelength 280 nm, column temperature 25 °C, flow rate 0.35 ml/min, detection time 20 minutes, and a Zenix-C SEC-300 chromatographic column (SEP AX 4.6 x 300 mm, 3 pm).
• This experiment detected the binding activity of the purified C-Ye-18 mutant samples and CHO-hPD-Ll cells.
• the experimental method was the same as that in Example 4.
• Experimental results are in Figure 2.
• the C-Ye-18 mutant samples and CHO-hPD- LI cells have good binding activity, and the level was comparable to that of C-Ye-18 and a control antibody ATE.
• This experiment detected the binding affinity of the purified C-Ye-18 mutant samples and human PD-L1.
• the experimental method was the same as that in Example 5.
• Experimental results are shown in Table 8.
• the C-Ye-18 mutant samples have very good binding activity with the human PD-L1 protein.
• Example 9 Blocking of binding of PD-L1 to PD-1 by C-Ye-18 mutant samples
• a pCHOl.O vector (purchased from Invitrogen) of human PD-L1 cDNA (purchased from Sino Biological) was cloned into MCS through transfection to produce CHO cells (CHO-hPD -1 cells) overexpressing human PD-L1.
• the cell density of the CHO-hPD-1 cells subjected to enlarge cultivation was adjusted to 2 x 10 6 cells/ml, and 100 m ⁇ of the cells were added into each well of a 96-well flow plate and centrifuged for later use.
• Purified mutant samples were diluted with PBS, three times dilution was started for a total of 12 points when the concentration was 400 nM, 60 m ⁇ of a diluted sample was added into each well of a 96- well sample dilution plate, 60 m ⁇ of biotinylated human PD-L1 protein (purchased from AcroBiosystems) was added into each well at the same time, the final concentration was 500 ng/ml, and the mutant samples were incubated at 4°C for 30 minutes. 100 m ⁇ of a co incubation sample was added into each well of the 96-well flow plate with cells, incubated at 4°C for 30 minutes and washed twice with PBS.
• DSC Different scanning calorimetry
• a temperature -raising program was set as follows: the constant temperature of 25°C was hold for 5 minutes, and the temperature was raised to 99°C at a speed of 0.5°C/min. After the program ends, the temperature values of the lowest points of curves in a "Melt Curve" diagram were read, namely the Tm value of the sample. Specific results are shown in the following Table 9.
• Example 11 A mixed lymphocyte reaction experiment In the present Example, a mixed lymphocyte reaction experiment (MLR) was used to detect the activity of C-Ye-18 mutant samples to activate T cells.
• MLR mixed lymphocyte reaction experiment
• PBMC cells purchased from SAILY BIO, SLB-HPB
• PBMC cells purchased from SAILY BIO, SLB-HPB
• 10 ml of an X-VIVO-15 culture medium purchased from LONZA
• PBMC cells purchased from SAILY BIO, SLB-HPB from another donor were thawed, centrifuged and resuspended with 10 ml of the X-VIVO-15 culture medium.
• CD4 + T cells were enriched with a CD4 + T cell sorting kit (purchased from Stemcell) and resuspended with X-VIVO-15, the cell density was adjusted to be 2 x 10 6 cells/ml, the CD4 + T cells were mixed with the collected mature DC cells at a ratio of 1 : 1 , and 100 m ⁇ of a mixture was added into each well of a 96-well U-shaped bottom plate.
• the C-Ye-18 mutant samples were diluted with the X-VIVO-15 culture medium, three times dilution was started for a total of 9 points when the concentration was 200 nM, 100 m ⁇ of the mixed cells were added into each well and cultured for 5 days, the supernatant was collected, and an ELISA (purchased from eBioscience) method was used to detect the expression amount of IFN-g and IL2.
• Results are shown in Figure 4, the C-Ye-18 mutant samples, C-Ye-18-1, C-Ye-18-5 and C-Ye-18-6 all show relatively good biological activity in the MLR experiment, and the activation level was similar to or superior to that of a control antibody ATE.
• a TGFPRII extracellular domain (SEQ ID NO: 101) was used as an immunoregulatory molecule moiety of a fusion protein, and a PD-L1 antibody (human IgGl Fc, LALA mutation) (C-Ye-18-5, SEQ ID: 94) was used as a targeting moiety of the fusion protein to form a PD-L1 antibody/TGFpRII extracellular region fusion protein (PM8001, SEQ ID: 102).
• a C-terminal amino acid of a PD-L1 single-chain antibody of the present application was linked to the TGFPRII extracellular region through (G4S)4G and routinely expressed through an Expi-CHO expression system.
• An expression and purification method was the same as that in Example 3, and a fusion protein PM8001 with the structure as shown in Figure 5 was obtained.
• a method for detecting the binding activity of a purified PD-L1 antibody (C-Ye-18-5, SEQ ID: 94), a PM8001 molecule, a TGF-PR2-Fc fusion protein, a positive control M7824 (WO2015/118175 A2) and a negative control IgG protein to PD-L1 on a cell surface was the same as that in Example 4.
• experimental results are shown in Figure 6, the PM8001 molecule of the present application and the CHO-hPD-Ll cells have binding activity, and the binding activity was similar to that of the positive control molecule M7824.
• a method for detecting blocking of the binding activity of PD-L1 protein to PD-1 cells by a purified PD-L1 antibody (C-Ye-18-5), a PM8001 molecule, a TGF-PR2-Fc fusion protein, a positive control M7824 and a negative control IgG protein was the same as that in Example 9.
• experimental results are shown in Figure 7, the PM8001 molecule of the present application can block the binding of PD-L1 protein to PD-1 cells, and the blocking level was comparable to that of the positive control molecule M7824.
• Example 15 An ELISA level binding experiment of a PM8001 molecule and human TGF-b family protein
• TGF-bI human TGF-bI (acrobiosystems, TG1-H421), TGF-P2 (PeproTech, 100-35B) andTGF- b3 (PeproTech, 100-36E) protein were diluted with an ELISA coating solution and then added into an ELISA plate for coating overnight at 4°C. The coating solution was removed, 250 m ⁇ of PBST was added into each well for washing 3 times, and the ELISA plate was blocked with 5% BSA for 1 hour at room temperature for later use.
• a purified PD-L1 antibody (C-Ye-18-5), a PM8001 molecule, a TGF ⁇ R2-Fc fusion protein and a positive control M7824 were subjected to gradient dilution and then added into the blocked ELISA plate for incubation at room temperature for 2 hours.
• PBST was added for washing 3 times, goat anti -human Fc-HRP (abeam, ab97225) was added into each well for incubation at room temperature for 1 hour, after PBST was added for washing 3 times, an ELISA color developing solution was added and placed at room temperature for 3 minutes, an ELISA termination solution was added, and a value of absorbance at 450 nm was read.
• the PM8001 molecule of the present application has relatively good binding to human TGF-bI and TGF-P3 proteins at the ELISA level and relatively weak binding activity to human TGF-P2 protein, and the binding level was comparable to that of the positive control molecule M7824.
• Example 16 An experiment of a PM8001 molecule in blocking a TGF-p/SMAD signal pathway
• Example 17 A mixed lymphocyte reaction experiment
• a method of using mixed lymphocytes to detect a purified PD-L1 antibody (C-Ye-18- 5), a PM8001 molecule, a TGF ⁇ R2-Fc fusion protein, a positive control M7824 and a negative control IgG protein in activation of human T lymphocytes was the same as that in Example 9. Results are shown in Figure 10, the PM8001 molecule of the present application shows relatively good biological activity in an MLR experiment, and the activation level was comparable to or superior to that of the positive control molecule M7824.
• mice including half male and half female were used in an experiment, light and dark adjustment was carried out every 12 hours, the temperature was 24+/-2°C, the humidity was 40-70%, and the mice drank water and had a diet freely.
• the mice were purchased from Zhejiang Weitong Lihua Experimental Technology Co., Ltd.
• a PM8001 molecule was injected into the tail veins of the SD mice once at a dosage of 10 mg/Kg.
• Blood collection time points blood was collected from the jugular veins of the mice 3 minutes, 4 hours, 10 hours, 24 hours, 48 hours, 72 hours, 120 hours, 168 hours, 240 hours, 336 hours, 504 hours and 672 hours after administration.
• a whole blood sample was placed at 2-8°C for 30 minutes and centrifuged at 12000 rpm for 5 minutes, serum was collected and centrifuged at 12000 rpm for 5 minutes at 2-8°C and stored at -80°C, and the molecular weight of free PM8001 in the serum was detected by ELISA. Results are shown in Table 10.
• the free state molecule of PM8001 of the present application has a half-life of about 146 hours in the SD mice.
• MC38 cells h-PD-Ll KI MC38 expressing human PD-L1 were used for determining the anti-tumor effect of PM8001 in PD-L1 transgenic mice.
• an h-PD- L1 KI MC38 tumor-bearing mouse model was established by subcutaneous inoculation. Grouping was carried out when the average tumor volume was 80-120 mm 3 , the mice were given with different antibodies and different dosages of treatment during single intraperitoneal injection, the tumor volumes and body weight changes of the mice of each group were monitored twice every week for a total of three weeks, the dosage and mode of administration are shown in Table 11, and the tumor volume changes of the mice are shown in Figure 11.
• Example 20 Identification of the crystal structure of a complex of PD -LI and a single-domain antibody VHH fragment
• a human- derived PD-Fl-His tag (SEQ ID: 109) was expressed by an Escherichia coli prokaryotic system.
• a PD-F1 single-domain antibody fusion protein (SEQ ID: 110) was expressed by a CHO system.
• the PD-L1 single-domain antibody fusion protein was digested and purified with an IdeS enzyme followed by a GingisKHAN enzyme, and finally a PD-L1 single- domain antibody VHH (SEQ ID: 111) was obtained.
• PD-L1 and VHH were mixed at a molar ratio of 1:1 to prepare a complex sample for crystallization.
• the purified complex was digested with carboxypeptidase B to remove the His tag of PD-L1.
• the complex (7.5 mg/mL) was mixed with a crystallization reagent at a ratio of 1:1 and subjected to crystal culture at 18°C. Three days later, crystals were observed under INT kit culture conditions, and the crystal morphology is shown in Figure 12.
• a single crystal was selected for an X-ray diffraction experiment at Shanghai Light Source, and diffraction data with a resolution of 1.6 A was obtained.
• XDS software was used for data processing.
• a molecular replacement method was adopted for crystal phase identification with PD-L1 (PDB ID: 5jds) and VHH (PDB ID: 5m2j) structures as models respectively.
• Refmac5 was used for refining the crystal structure.
• COOT was used for model detection, manual reconstruction and structural verification.
• Example 21 The growth inhibition effect of a PM8001 injection on an h-PD-Ll knock-in MC38 model inoculated subcutaneously in h-PD-Ll knock-in C57BL/6 mice
• h-PD-Fl knock-in MC38 subcutaneous tumor-bearing model was established by subcutaneously inoculating h-PD-Fl knock-in MC38 mouse colon cancer cells into h-PD-Fl knock-in C57BF/6 mice (purchased from GemPharmatech Co, Ftd).
• mice Ten days after inoculation, the mice were divided into 5 groups (6 mice per group) according to the tumor volume and subjected to intraperitoneal injection of PBS, 14.7 mg/kg PM8001, 10 mg/kg PM8001-NSD (anti-human PD-F1 VHH), 10 mg/kg PM800I -TGF-PRII and 24.6 mg/kg M7824 (the corresponding molar dosages of the above administration groups were the same) respectively, and administration was carried out twice at an interval of three days.
• the anti-tumor effect and the safety in the tumor-bearing mice of PM8001, PM8001-NSD, PM 8001 -TGF-PRII and M7824 were investigated.
• Figure 16 shows the effect of different drug groups on the tumor volume of h-PD-Ll knock-in mice implanted with h-PD-Ll knock-in MC38 tumors.
• Figure 17 shows tumor pictures of different drug groups 27 days after inoculation. The tumors of the mice in a negative control PBS group grow rapidly, the tumor volume reaches 1500 mm 3 or above 27 days after inoculation (namely, the 17th day after administration), and it indicates that the tumor model in this experiment was successfully established.
• the same molar dosage of PM8001, PM8001-NSD, PM 8001 -TGF-PRII and M7824 can inhibit tumor growth to different degrees, and TGI of the above groups on the 17th day after administration were 80%, 72%, 15% and 53% respectively; the PM8001 injection group has a higher tumor growth inhibition effect than that of PM8001-NSD, P 8001 -TGF-b R II and a similar molecular group M7824.
• the tumors were taken and weighed.
• the tumor weight in the PM8001 injection group was lower than that of PM8001-NSD, P 8001 -TGF-b R II and the similar molecular group M7824.
• Figure 18 shows the effect of each group of drugs on tumor weight of h-PD-Ll knock-in mice implanted with h-PD-Ll knock-in MC38 tumors.
• Figure 19 shows the effect of different drug groups on body weight of h-PD-Ll knock - in mice implanted with h-PD-Ll knock-in MC38 tumors. There was no abnormality in the state of the mice in each group; compared with the control group, the body weight of the mice in each administration group was not significantly reduced; at the end of the experiment, the gross anatomy of the mice in each group shows no apparent lesions in main organs, and it indicates that the used administration dosages of drugs in each group in this experiment show no apparent toxicity to the mice.
• Example 22 The growth inhibition effect of different dosages of PM8001 on an h- PD-L1 knock-in MC38 model inoculated subcutaneously in h-PD-Ll knock-in C57BL/6 mice
• the h-PD-Ll knock-in MC38 subcutaneous tumor-bearing model was established by subcutaneously inoculating h-PD-Ll knock-in MC38 mouse colon cancer cells into h-PD-Ll knock-in C57BL/6 mice, and this model can be used to evaluate the anti tumor effect related to action mechanisms of test products and safety characteristics in a disease state.
• the mice were divided into 5 groups (6 mice in each group) according to the tumor volume and administered with single intraperitoneal injection of PBS, different dosages (0.3, 2.1, 14.7 mg/kg) of the PM8001 injection or 24.6 mg/kg M7824 respectively.
• the anti-tumor effect of different dosages of PM8001 and the safety in tumor-bearing mice were investigated and compared with the similar molecule M7824.
• Figure 20 shows the effect of different drug groups on tumor volume of h-PD-Ll knock - in mice implanted with h-PD-Ll knock-in MC38 tumors.
• Figure 21 shows tumor pictures of different drug groups 28 days after inoculation. The tumors of the mice in a negative control PBS group grow rapidly, the tumor volume reaches 1300 mm 3 or above 28 days after inoculation, and it indicates that the tumor model in this experiment was successfully established. Compared with the negative control PBS group, PM8001 can inhibit tumor growth in a dosage-dependent manner.
• TGIs at low, medium and high dosages of PM8001 were 31%, 76% and 93% respectively; at the same molar dosage, the tumor growth inhibition effect of the PM8001 group (14.6 mg /kg) was higher than that of the similar molecule M7824 group (24.6 mg/kg). At the end of the experiment, tumors were taken and weighed. PM8001 can reduce tumor weight in a dosage-dependent manner. At the same molar dosage, the tumor inhibition rate of the PM8001 group (14.6 mg/kg) was higher than that of the similar molecule M7824 group (24.6 mg/kg).
• Figure 22 shows the effect of each group of drugs on tumor weight of h-PD-Ll knock-in mice implanted with h-PD-Ll knock-in MC38 tumors.
• Figure 23 shows the effect of different drug groups on body weight of h-PD-Ll knock - in mice implanted with h-PD-Ll knock-in MC38 tumors. There was no abnormality in the state of the mice in each group; compared with the control group, the body weight of the mice in each administration group was not significantly reduced; at the end of the experiment, the gross anatomy of the mice in each group shows no apparent lesions in main organs, and it indicates that the used administration dosages of drugs in each group in this experiment show no apparent toxicity to the mice.
• VKVNAPYHHHHHH SEQ ID NO: 110 PD-L1 single-domain antibody fusion protein amino acid sequence

Landscapes

• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Chemical & Material Sciences (AREA)
• Immunology (AREA)
• General Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Organic Chemistry (AREA)
• Molecular Biology (AREA)
• Cell Biology (AREA)
• Pharmacology & Pharmacy (AREA)
• Veterinary Medicine (AREA)
• Public Health (AREA)
• Animal Behavior & Ethology (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Biochemistry (AREA)
• Oncology (AREA)
• Hematology (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Urology & Nephrology (AREA)
• Biomedical Technology (AREA)
• Proteomics, Peptides & Aminoacids (AREA)
• Biophysics (AREA)
• Genetics & Genomics (AREA)
• Epidemiology (AREA)
• Microbiology (AREA)
• Analytical Chemistry (AREA)
• Biotechnology (AREA)
• Pathology (AREA)
• General Physics & Mathematics (AREA)
• Food Science & Technology (AREA)
• Physics & Mathematics (AREA)
• Hospice & Palliative Care (AREA)
• Toxicology (AREA)
• Zoology (AREA)
• Gastroenterology & Hepatology (AREA)
• Peptides Or Proteins (AREA)
• Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Priority Applications (8)

Applications Claiming Priority (2)

Publications (1)

Family

ID=74866641

Family Applications (1)

Country Status (8)

Cited By (7)

Families Citing this family (16)

Citations (3)

Family Cites Families (20)

• 2019
  • 2019-09-12 CN CN201910863109.0A patent/CN112480253B/zh active Active
  • 2019-09-12 CN CN202211164309.5A patent/CN115947846A/zh active Pending
• 2020
  • 2020-09-07 CN CN202080064136.2A patent/CN114502588B/zh active Active
  • 2020-09-07 WO PCT/IB2020/058303 patent/WO2021048725A1/en not_active Ceased
  • 2020-09-07 EP EP20863990.6A patent/EP4028423A4/en active Pending
  • 2020-09-07 AU AU2020344237A patent/AU2020344237A1/en active Pending
  • 2020-09-07 US US17/642,171 patent/US12409233B2/en active Active
  • 2020-09-07 CA CA3150886A patent/CA3150886A1/en active Pending
  • 2020-09-07 KR KR1020227011569A patent/KR20220064986A/ko active Pending
  • 2020-09-07 JP JP2022516220A patent/JP7773975B2/ja active Active
• 2025
  • 2025-07-16 JP JP2025119680A patent/JP2025163055A/ja active Pending

Patent Citations (3)

Non-Patent Citations (3)

Also Published As

Similar Documents

Legal Events