WO2022174451A1 - 一种具有抗癌活性的多结构域融合蛋白 - Google Patents

一种具有抗癌活性的多结构域融合蛋白 Download PDF

Info

Publication number
WO2022174451A1
WO2022174451A1 PCT/CN2021/077282 CN2021077282W WO2022174451A1 WO 2022174451 A1 WO2022174451 A1 WO 2022174451A1 CN 2021077282 W CN2021077282 W CN 2021077282W WO 2022174451 A1 WO2022174451 A1 WO 2022174451A1
Authority
WO
WIPO (PCT)
Prior art keywords
seq
fragment
fusion protein
amino acid
acid sequence
Prior art date
Application number
PCT/CN2021/077282
Other languages
English (en)
French (fr)
Inventor
黄岩山
Original Assignee
浙江道尔生物科技有限公司
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 浙江道尔生物科技有限公司 filed Critical 浙江道尔生物科技有限公司
Priority to PCT/CN2021/077282 priority Critical patent/WO2022174451A1/zh
Priority to CN202180003793.0A priority patent/CN116917334A/zh
Priority to KR1020237031894A priority patent/KR20230147675A/ko
Priority to PCT/CN2022/076610 priority patent/WO2022174781A1/zh
Priority to US18/277,996 priority patent/US20240124587A1/en
Priority to CA3211427A priority patent/CA3211427A1/en
Priority to JP2023550320A priority patent/JP2024507856A/ja
Priority to CN202280007712.9A priority patent/CN116761814B/zh
Priority to AU2022221660A priority patent/AU2022221660A1/en
Priority to EP22755554.7A priority patent/EP4282884A4/en
Publication of WO2022174451A1 publication Critical patent/WO2022174451A1/zh

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2803Immunoglobulins [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
    • C07K16/2827Immunoglobulins [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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2803Immunoglobulins [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
    • C07K16/2818Immunoglobulins [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 CD28 or CD152
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/395Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A61K39/39533Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
    • A61K39/39558Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against tumor tissues, cells, antigens
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/475Growth factors; Growth regulators
    • C07K14/495Transforming growth factor [TGF]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705Receptors; Cell surface antigens; Cell surface determinants
    • C07K14/71Receptors; Cell surface antigens; Cell surface determinants for growth factors; for growth regulators
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/22Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against growth factors ; against growth regulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K2039/505Medicinal preparations containing antigens or antibodies comprising antibodies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K2039/505Medicinal preparations containing antigens or antibodies comprising antibodies
    • A61K2039/507Comprising a combination of two or more separate antibodies
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/20Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/24Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/30Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/31Immunoglobulins specific features characterized by aspects of specificity or valency multispecific
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/50Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/52Constant or Fc region; Isotype
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/50Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C07K2317/567Framework region [FR]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/50Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C07K2317/569Single domain, e.g. dAb, sdAb, VHH, VNAR or nanobody®
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/60Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
    • C07K2317/62Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising only variable region components
    • C07K2317/622Single chain antibody (scFv)
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/60Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
    • C07K2317/64Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising a combination of variable region and constant region components
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/70Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/73Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/70Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/76Antagonist effect on antigen, e.g. neutralization or inhibition of binding
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2317/00Immunoglobulins specific features
    • C07K2317/90Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
    • C07K2317/94Stability, e.g. half-life, pH, temperature or enzyme-resistance
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2319/00Fusion polypeptide

Definitions

  • the present invention relates to the field of biotechnology, in particular to a multi-domain fusion protein with anticancer activity and a preparation method and use thereof.
  • VEGF vascular endothelial growth factor
  • Bevacizumab trade name
  • Bevacizumab a humanized anti-VEGF monoclonal antibody that binds to VEGF and prevents VEGF from interacting with endothelial cell surface VEGF receptors (Flt-1 and KDR).
  • Bevacizumab is currently FDA-approved for the treatment of metastatic colorectal cancer, advanced, metastatic or recurrent non-small cell lung cancer, and recurrent glioblastoma.
  • Transforming growth factor TGF- ⁇ is a cytokine that maintains tissue homeostasis by regulating cell growth, differentiation, proliferation and survival.
  • TGF- ⁇ pathway can control tumors by promoting cell cycle arrest and apoptosis in the early stages of tumors; but in the late stages of tumors, TGF- ⁇ can also inhibit cytotoxic T cells and promote cancer cell proliferation and invasion. and metastasis ultimately allows tumor escape, a functional switch known as the "TGF- ⁇ paradox".
  • TGF ⁇ signaling induces TH1 cell differentiation into Tregs, attenuates the activation of CD8 + effector cells, and restricts the development of central memory cells, fundamentally affecting tumor-infiltrating T cell function.
  • TGF- ⁇ In mammals, TGF- ⁇ mainly has three subtypes: TGF- ⁇ 1, TGF- ⁇ 2, and TGF- ⁇ 3.
  • TGF- ⁇ By expressing TGF- ⁇ at high levels, tumors are protected from immune surveillance. Consistent with this, non-small cell lung cancer (NSCLC), renal cell carcinoma (CRC), gastric and prostate cancers with high TGF- ⁇ expression are associated with tumor progression and poor prognosis (Marin-Acevedo et al., Journal of Hematology & Oncology). , 11:39, 2018). This shows that TGF- ⁇ antagonism will be a potential new direction for tumor therapy.
  • NSCLC non-small cell lung cancer
  • CRC renal cell carcinoma
  • gastric and prostate cancers with high TGF- ⁇ expression are associated with tumor progression and poor prognosis (Marin-Acevedo et al., Journal of Hematology & Oncology). , 11:39, 2018). This shows that TGF- ⁇ antagonism will
  • anti-PD-1/PD-L1 monoclonal antibodies as immune checkpoint inhibitors have been widely used in tumor therapy.
  • the anti-PD-L1 monoclonal antibody Avelumab fused to TGF- ⁇ receptor II (TGF- ⁇ Trap) has entered the clinical stage of M7824.
  • TGF- ⁇ Trap TGF- ⁇ receptor II
  • the combination of anti-PD-1/PD-L1 mAb, TGF- ⁇ antagonist and anti-VEGF mAb has not yet been reported.
  • the purpose of the present invention is to provide a multi-domain fusion protein with anti-cancer activity and a preparation method and use thereof, so as to solve the problems in the prior art.
  • one aspect of the present invention provides a fusion protein, which includes an anti-PD-L1 single-domain antibody fragment, an antagonistic VEGF fragment, and a TGF- ⁇ binding fragment.
  • Another aspect of the present invention provides an isolated polynucleotide encoding the above-mentioned fusion protein.
  • Another aspect of the present invention provides a construct comprising the isolated polynucleotide described above.
  • Another aspect of the present invention provides an expression system comprising the above-mentioned construct or the above-mentioned exogenous polynucleotide integrated into the genome.
  • Another aspect of the present invention provides a method for preparing the above fusion protein, comprising: culturing the expression system according to claim 15 under suitable conditions to express the fusion protein, and isolating and purifying to provide the fusion protein.
  • Another aspect of the present invention provides the use of the above-mentioned fusion protein or the culture of the above-mentioned expression system in the preparation of medicine.
  • Another aspect of the present invention provides a pharmaceutical composition comprising the above-mentioned fusion protein, or a culture of the above-mentioned expression system.
  • FIG. 1 is a schematic diagram showing the tumor-inhibiting effect of the multi-domain fusion protein in Example 4 of the present invention in M-NSG mice.
  • the inventor of the present invention unexpectedly found a fusion protein molecule, which can block PD-L1/PD-1 interaction by anti-PD-L1 monoclonal antibody, and antagonize VEGF monoclonal antibody to reduce microvascular growth. Combined with the inhibition of metastatic disease, and TGF- ⁇ receptors to improve T cell dysfunction caused by TGF- ⁇ in the tumor microenvironment and enhance the immune response, it has excellent tumor suppressive effect. invention.
  • the first aspect of the present invention provides a fusion protein, the fusion protein includes an anti-PD-L1 single domain antibody fragment, an antagonistic VEGF fragment, and a TGF- ⁇ binding fragment.
  • anti-PD-L1 single-domain antibody fragments can usually be used to block the PD-L1/PD-1 interaction and increase the expression of IFN- ⁇ and/or IL-2 in T lymphocytes, thereby inhibiting tumor growth.
  • Antagonistic VEGF fragments can generally include an Fc portion that can bind to FcRn receptors, thereby prolonging half-life in vivo, and can also bind to effector cells expressing Fc receptors to kill cancer cells.
  • TGF- ⁇ -binding fragments can improve the killing function of tumor-infiltrating T cells on tumor cells by removing over-expressed TGF- ⁇ in the tumor microenvironment.
  • an anti-PD-L1 single domain antibody fragment can be included.
  • the above-mentioned anti-PD-L1 single-domain antibody fragment can generally be a polypeptide or protein fragment that can specifically bind to PD-L1.
  • the corresponding antibody light chain is usually deleted, and only the fragment corresponding to the variable region of the heavy chain is present.
  • the binding properties of anti-PD-L1 single-domain antibody fragments can usually be determined by the three complementarity determining regions (CDRs, complementarity determining regions) included.
  • the CDR regions can be arranged in order with the framework regions (FR, framework regions), and the FR regions Not directly involved in the binding reaction.
  • the complementarity determining region (CDR) of the above-mentioned anti-PD-L1 single-domain antibody fragment can include CDR1 whose amino acid sequence is shown in one of SEQ ID NO. 1-5, and one of SEQ ID NO. 6-9 CDR2, CDR3 shown in one of SEQ ID NO.10 ⁇ 15.
  • the complementarity determining region of the anti-PD-L1 single-domain antibody fragment includes: CDR1 with amino acid sequence shown in SEQ ID NO.1, CDR2 shown in SEQ ID NO.6, SEQ ID NO. CDR3 shown in 10.
  • the complementarity determining region of the anti-PD-L1 single domain antibody fragment includes: CDR1 with amino acid sequence shown in SEQ ID NO.2, CDR2 shown in SEQ ID NO.7, SEQ ID NO. .11 shown CDR3.
  • the complementarity determining region of the anti-PD-L1 single-domain antibody fragment includes: CDR1 whose amino acid sequence is shown in SEQ ID NO.3, CDR2 shown in SEQ ID NO.7, and SEQ ID NO. CDR3 shown in .12.
  • the complementarity determining region of the anti-PD-L1 single domain antibody fragment includes: CDR1 with amino acid sequence shown in SEQ ID NO.4, CDR2 shown in SEQ ID NO.8, SEQ ID NO. CDR3 shown in .13.
  • the complementarity determining region of the anti-PD-L1 single domain antibody fragment includes: CDR1 with amino acid sequence shown in SEQ ID NO.2, CDR2 shown in SEQ ID NO.7, SEQ ID NO. .14 CDR3 shown.
  • the complementarity determining region of the anti-PD-L1 single domain antibody fragment includes: CDR1 with amino acid sequence shown in SEQ ID NO.5, CDR2 shown in SEQ ID NO.9, SEQ ID NO. CDR3 shown in .15.
  • the above-mentioned anti-PD-L1 single-domain antibody fragment may also include a framework region (FR, framework region).
  • the CDR regions can be arranged in order with the FR regions, for example, the anti-PD-L1 single domain antibody fragment can include FR1, CDR1, FR2, CDR2, FR3, CDR3, FR4 in order from N-terminus to C-terminus.
  • the framework region FR includes FR1 whose amino acid sequence can be shown in SEQ ID No. 49, FR2 whose amino acid sequence is shown in one of SEQ ID No. 50-52, and FR2 whose amino acid sequence is shown in one of SEQ ID No. 53-55. FR3 is shown, and FR4 whose amino acid sequence is shown in SEQ ID No. 56.
  • the frame region FR includes:
  • the amino acid sequence is FR1 shown in SEQ ID NO.49, FR2 shown in SEQ ID NO.50, FR3 shown in SEQ ID NO.53; FR4 shown in SEQ ID NO.56, or
  • the amino acid sequence is FR1 shown in SEQ ID NO.49, FR2 shown in SEQ ID NO.51, FR3 shown in SEQ ID NO.54; FR4 shown in SEQ ID NO.56, or
  • the amino acid sequence is FR1 shown in SEQ ID NO.49, FR2 shown in SEQ ID NO.52, FR3 shown in SEQ ID NO.54; FR4 shown in SEQ ID NO.56, or
  • the amino acid sequence is FR1 shown in SEQ ID NO.49, FR2 shown in SEQ ID NO.52, FR3 shown in SEQ ID NO.55; FR4 shown in SEQ ID NO.56.
  • the anti-PD-L1 single domain antibody fragment may include: a) a polypeptide fragment whose amino acid sequence is as shown in one of SEQ ID Nos. 16 to 21; One of ID Nos. 16 to 21 has more than 80% sequence identity and has the function of the polypeptide fragment as defined in a).
  • the polypeptide fragment in the above b) specifically refers to: the amino acid sequence shown in one of SEQ ID No.
  • 16 to 21 has undergone substitution, deletion or addition of one or more (specifically, 1-50, 1 -30, 1-20, 1-10, 1-5, or 1-3) amino acids, or by adding one or more (specifically can be N-terminal and/or C-terminal) amino acids 1-50, 1-30, 1-20, 1-10, 1-5, or 1-3) amino acids, and have an amino acid sequence such as one of SEQ ID No.16-21
  • the function of the polypeptide fragment shown in a polypeptide fragment for example, can be the ability to specifically bind to PD-L1, or it can be the blocking of PD-L1/PD-1 interaction, which can block PD-L1
  • the /PD1 pathway can also be a function of increasing the expression of IFN- ⁇ and/or IL-2 in T lymphocytes, and it can also be a function of inhibiting tumor growth.
  • the amino acid sequence of the anti-PD-L1 single domain antibody fragment in the above b) can be 80%, 85%, 90%, 93%, 95%, 97%, or 99% with one of SEQ ID No. 16 to 21 consistency of the above.
  • the above-mentioned anti-PD-L1 single domain antibody fragment can usually be derived from alpaca (Vicugna pacos), for example, its CDR region can be derived from alpaca.
  • the above-mentioned anti-PD-L1 single-domain antibody fragments may generally be humanized, for example, the framework regions thereof may be derived from humans.
  • sequence identity refers to the percentage of identical residues in the sequences participating in the alignment. Sequence identity of two or more entry sequences can be calculated using computational software well known in the art, such software available from NCBI, for example.
  • an antagonistic VEGF fragment can be included.
  • the above-mentioned VEGF-antagonizing fragment can generally be a polypeptide or protein fragment capable of antagonizing VEGF.
  • the above-mentioned VEGF antagonistic fragment may be a monoclonal antibody or the like.
  • the above-mentioned VEGF antagonistic fragment may be bevacizumab and the like.
  • the antagonistic VEGF fragment may include:
  • the amino acid sequence in the above d) specifically refers to: the amino acid sequence shown in one of SEQ ID No.
  • the amino acid sequence in d) can be more than 80%, 85%, 90%, 93%, 95%, 97%, or 99% identical to one of SEQ ID Nos. 22 to 23.
  • the above-mentioned VEGF antagonistic fragment can usually be derived from a mouse (Mus musculus), for example, the CDR region thereof can be derived from a mouse.
  • the VEGF-antagonizing fragments described above can generally be humanized, eg, their framework regions can be derived from humans.
  • a TGF- ⁇ binding fragment can be included.
  • the above-mentioned TGF- ⁇ -binding fragments can usually specifically bind to each TGF- ⁇ isoform (for example, TGF- ⁇ 1, TGF- ⁇ 2, and TGF- ⁇ 3, etc.), and TGF- ⁇ isoforms are usually highly expressed in various malignant tumors. , is likely to be one of the important factors leading to poor clinical treatment effect.
  • the TGF-beta binding fragment can be a TGF-beta RII (TGF-beta receptor II) extracellular domain structural fragment.
  • the TGF- ⁇ binding fragment may comprise:
  • polypeptide fragment whose amino acid sequence has more than 80% sequence identity with SEQ ID No. 24 and has the function of the polypeptide fragment defined in e).
  • amino acid sequence in the above f) specifically refers to: the amino acid sequence shown in SEQ ID No. 24 is substituted, deleted or added one or more (specifically, 1-50, 1-30, 1-20 1, 1-10, 1-5, 1-3, 1, 2, or 3) amino acids, or adding one or more (specifically, N-terminal and/or C-terminal) amino acids It can be obtained from 1-50, 1-30, 1-20, 1-10, 1-5, 1-3, 1, 2, or 3) amino acids, and has amino acids The function of the polypeptide fragment shown in SEQ ID No.
  • the polypeptide fragment for example, can bind to each TGF- ⁇ isoform (eg, TGF- ⁇ 1, TGF- ⁇ 2, and TGF- ⁇ 3, etc.), thereby eliminating tumor microbes.
  • TGF- ⁇ in the environment can also enhance the killing function of tumor-infiltrating T cells against tumor cells.
  • Said amino acid sequence in f) can be more than 80%, 85%, 90%, 93%, 95%, 97%, or 99% identical to SEQ ID No. 24.
  • the above-mentioned TGF-beta binding fragments can generally be derived from humans (homo sapiens).
  • a linker peptide fragment can also be included.
  • a plurality of linker peptide fragments may be generally included, and at least some of the domains or between each of the domains may be provided with linker peptide fragments.
  • a linker peptide may be provided between the anti-PD-L1 single domain antibody fragment and the VEGF antagonistic fragment.
  • a linker peptide may be provided between the antagonistic VEGF fragment and the TGF- ⁇ binding fragment.
  • the above-mentioned linker peptide fragment can usually be a flexible polypeptide rich in G, S and/or A (mainly composed of glycine (G), serine (S) and/or alanine (A)) of suitable length, so that the Neighboring protein domains are free to move relative to each other.
  • the amino acid sequence of the linker peptide fragment may include, for example, (GS)n, (GGS)n, (GGSG)n, (GGGS)nA, (GGGGS)nA, (GGGGS)nG, (GGGGA)nA, (GGGGG) )nA etc. sequence, wherein n is selected from integers between 1-10.
  • the length of the amino acid sequence of the connecting peptide fragment can be 3-30, 3-4, 4-6, 6-8, 8-10, 10-12, 12-14, 14 -16, 16-18, 18-20, 20-22, 22-24, 24-26, 26-28, or 28-30.
  • the connecting peptide fragment may comprise a polypeptide fragment whose amino acid sequence is shown in one of SEQ ID NO. 34-36.
  • the fusion protein can be linear, for example, the fusion protein can sequentially include anti-PD-L1 single domain antibody fragment, antagonistic VEGF fragment, and TGF- ⁇ binding fragment from the N-terminus to the C-terminus.
  • the fusion protein can also have a structure similar to that of a monoclonal antibody.
  • an anti-PD-L1 single-domain antibody fragment can be located at the N-terminus of the heavy chain of the VEGF fragment, and for another example, an anti-PD-L1 single-domain antibody fragment can be located at the antagonism VEGF.
  • the N-terminus of the light chain of the fragment for another example, the TGF-beta binding fragment can be located at the C-terminus of the heavy chain of the antagonizing VEGF fragment, specifically the C-terminus.
  • the amino acid sequence of the fusion protein may include the sequence shown in one of SEQ ID NO. 23 and SEQ ID NO.
  • the amino acid sequence of the fusion protein may include SEQ ID NO.25 and SEQ ID NO.26, SEQ ID NO.25 and SEQ ID NO.27, SEQ ID NO.25 and SEQ ID NO.28, SEQ ID NO.28
  • SEQ ID NO.28 The sequences shown in NO.25 and SEQ ID NO.29, the sequences shown in SEQ ID NO.30 and SEQ ID NO.27, the sequences shown in SEQ ID NO.30 and SEQ ID NO.29, the sequences shown in SEQ ID NO. 31 and the sequence shown in SEQ ID NO.23, the sequence shown in SEQ ID NO.32 and SEQ ID NO.23, the sequence shown in SEQ ID NO.33 and SEQ ID NO.23.
  • the second aspect of the present invention provides an isolated polynucleotide encoding the fusion protein provided by the first aspect of the present invention.
  • the above-mentioned polynucleotide may be RNA, DNA, cDNA, or the like.
  • Methods of providing such isolated polynucleotides should be known to those skilled in the art. For example, they can be prepared by methods such as automated DNA synthesis and/or recombinant DNA technology, or they can be isolated from suitable natural sources.
  • a third aspect of the present invention provides a construct comprising the isolated polynucleotide provided by the second aspect of the present invention.
  • Appropriate methods of constructing such constructs should be known to those skilled in the art.
  • the construct can be constructed by in vitro recombinant DNA technology, DNA synthesis technology, in vivo recombinant technology, etc., and more specifically, it can be constructed by inserting the above-mentioned isolated polynucleotide into the multiple cloning site of the expression vector. .
  • the expression vector in the present invention generally refers to various commercially available expression vectors well known in the art, such as bacterial plasmids, bacteriophages, yeast plasmids, plant cell viruses, mammalian cell viruses such as adenovirus, retrovirus or other vectors.
  • a suitable vector may contain an origin of replication functional in at least one organism, a promoter sequence, convenient restriction enzyme sites, and one or more selectable markers.
  • these promoters may be lac or trp promoters including but not limited to E.
  • Marker genes can be used to provide a phenotypic trait for selection of transformed host cells, for example, can include, but are not limited to, dihydrofolate reductase for eukaryotic cell culture, neomycin resistance, and green fluorescent protein (GFP), Or for tetracycline or ampicillin resistance in E. coli etc.
  • the expression vector may also include an enhancer sequence. If an enhancer sequence is inserted into the vector, transcription will be enhanced.
  • An enhancer is a cis-acting factor of DNA, usually about There are 10 to 300 base pairs and act on the promoter to enhance transcription of the gene.
  • the fourth aspect of the present invention provides an expression system comprising the construct provided by the third aspect of the present invention or the exogenous polynucleotide provided by the second aspect of the present invention integrated into the genome, so as to express the above-mentioned fusion protein.
  • the above-mentioned expression system can be a host cell, and any cell suitable for the expression vector can be used as a host cell, for example, the host cell can be a prokaryotic cell, such as a bacterial cell; or a lower eukaryotic cell, such as a yeast cell; Fungal cells, or higher eukaryotic cells such as mammalian cells.
  • Escherichia coli, Streptomyces bacterial cells of Salmonella typhimurium
  • fungal cells such as yeast, filamentous fungi, plant cells
  • insect cells of Drosophila S2 or Sf9 CHO, COS, 293 cells, or Bowes Animal cells of melanoma cells, etc.
  • Methods for introducing constructs into host cells should be known to those skilled in the art, for example, microinjection, biolistic, electroporation, virus-mediated transformation, electron bombardment, calcium phosphate precipitation can be used method, etc.
  • the fifth aspect of the present invention provides a method for preparing the fusion protein provided in the first aspect of the present invention.
  • a suitable method to prepare the fusion protein may include: under suitable conditions
  • the expression system provided by the fourth aspect of the present invention is cultured to express the fusion protein, the culture containing the fusion protein is collected, and then separated and purified to provide the fusion protein.
  • the sixth aspect of the present invention provides the use of the fusion protein provided by the first aspect of the present invention and the culture of the expression system provided by the fourth aspect of the present invention in preparing medicine.
  • the above-mentioned drug can be a drug used for the treatment of tumors, for example, can be cancer or solid tumor, specifically can be lung cancer, melanoma, gastric cancer, ovarian cancer, colon cancer, liver cancer, kidney cancer, bladder cancer, breast cancer, classic Hodge Gold lymphoma, hematological malignancies, head and neck cancer and nasopharyngeal cancer, etc.
  • These cancers can be early, intermediate or advanced stage, such as metastatic cancer.
  • the seventh aspect of the present invention provides a pharmaceutical composition comprising the culture of the fusion protein provided by the first aspect of the present invention or the expression system provided by the fourth aspect of the present invention.
  • the content of fusion protein or culture is usually a therapeutically effective amount.
  • a "therapeutically effective amount” generally refers to an amount that, after an appropriate period of administration, can result in a reduction in the severity of symptoms of a disease, an increase in the frequency and duration of asymptomatic periods of the disease, or in the prevention of symptoms caused by the suffering of the disease. injury or disability.
  • the ability to inhibit tumor growth can be evaluated in animal model systems that predict efficacy against human tumors.
  • a therapeutically effective amount of the fusion protein, pharmaceutical composition is generally capable of reducing tumor size, or otherwise alleviating symptoms in a subject.
  • Those skilled in the art can select an appropriate therapeutically effective amount according to the actual situation, for example, it can be the size of the subject, the severity of the subject's symptoms and the selected specific composition or route of administration.
  • the prescription of treatment eg, determination of dosage, etc.
  • a pharmaceutically acceptable carrier may also be included.
  • the above-mentioned carriers may include various excipients and diluents which are not themselves essential to the active ingredient and which are not unduly toxic after administration. Suitable carriers will be well known to those skilled in the art, for example, a thorough discussion of pharmaceutically acceptable carriers can be found in Remington's Pharmaceutical Sciences (Mack Pub. Co., N.J., 1991).
  • the eighth aspect of the present invention provides a method of treatment, comprising: administering to an individual a therapeutically effective amount of the fusion protein provided by the first aspect of the present invention, the culture of the expression system provided by the fourth aspect of the present invention, or the seventh aspect of the present invention
  • the pharmaceutical composition provided by the aspect comprising: administering to an individual a therapeutically effective amount of the fusion protein provided by the first aspect of the present invention, the culture of the expression system provided by the fourth aspect of the present invention, or the seventh aspect of the present invention
  • the pharmaceutical composition provided by the aspect comprising: administering to an individual a therapeutically effective amount of the fusion protein provided by the first aspect of the present invention, the culture of the expression system provided by the fourth aspect of the present invention, or the seventh aspect of the present invention
  • the pharmaceutical composition provided by the aspect comprising: administering to an individual a therapeutically effective amount of the fusion protein provided by the first aspect of the present invention, the culture of the expression system provided by the fourth aspect of the present invention, or the seventh aspect of the present invention
  • the term "treatment” includes prophylactic, curative or palliative treatment that results in the desired pharmaceutical and/or physiological effect.
  • the effect refers to medically reducing one or more symptoms of the disease or completely eliminating the disease, or retarding, delaying the onset of the disease and/or reducing the risk of developing or worsening the disease.
  • “individual” generally includes humans, non-human primates, or other mammals (such as dogs, cats, horses, sheep, pigs, cattle, etc.), which can be obtained by utilizing the formulation, kit or combination benefit from treatment.
  • the fusion protein, the culture of the expression system, or the pharmaceutical composition can be used as a single active ingredient, or can be used in combination with other agents, so as to be administered in combination therapy.
  • the above-mentioned multi-domain fusion protein with anticancer activity, the culture of the expression system, or the pharmaceutical composition can be combined with at least one other antitumor drug.
  • the above-described multi-domain fusion proteins with anticancer activity, cultures of expression systems, or pharmaceutical compositions can be used in combination with antibodies targeting other tumor-specific antigens.
  • the multi-domain fusion protein with anti-cancer activity provided by the present invention can block the PD-L1/PD-1 interaction with anti-PD-L1 monoclonal antibody, and the anti-VEGF monoclonal antibody can reduce microvessel in one antibody fusion protein molecule.
  • Growth and inhibition of metastatic disease, and the function of TGF- ⁇ receptors to relieve cancer cells' tolerance to TGF- ⁇ signals and enhance immune response are organically combined, so that they can be used for tumor treatment and have good industrialization prospects.
  • the experimental methods, detection methods and preparation methods disclosed in the present invention all adopt the conventional molecular biology, biochemistry, chromatin structure and analysis, analytical chemistry, cell culture, recombinant DNA technology and related fields in the technical field. conventional technology. These techniques have been well described in the existing literature. For details, see Sambrook et al.
  • MOLECULAR CLONING A LABORATORY MANUAL, Second edition, Cold Spring Harbor Laboratory Press, 1989 and Third edition, 2001; Ausubel et al., CURRENT PROTOCOLS IN MOLECULAR BIOLOGY, John Wiley & Sons , New York, 1987 and periodic updates; the series METHODS IN ENZYMOLOGY, Academic Press, San Diego; Wolfe, CHROMATIN STRUCTURE AND FUNCTION, Third edition, Academic Press, San Diego, 1998; METHODS IN ENZYMOLOGY, Vol.304, Chromatin (P.M. Wassarman and A.P. Wolfe, eds.), Academic Press, San Diego, 1999; and METHODS IN MOLECULAR BIOLOGY, Vol. 119, Chromatin Protocols (P.B. Becker, ed.) Humana Press, Totowa, 1999, et al.
  • the amino acid sequences of the multi-domain fusion protein, PD-L1-Fc fusion protein (SEQ ID NO. 47) and Fc-TGF ⁇ RII fusion protein (SEQ ID NO. 48) in Table 1 were respectively converted into Base sequence, and introduced HindIII restriction site and Kozak sequence (GCCACC) at the 5' end of the heavy chain and light chain coding sequences respectively, and introduced a stop codon and EcoRI restriction site at the 3' end by gene synthesis (general Biosystems (Anhui) Co., Ltd.) obtained full-length DNA.
  • GCCACC HindIII restriction site and Kozak sequence
  • the synthetic heavy chain and light chain coding genes were double digested by HindIII-HF (purchased from NEB, R3104V) and EcoRI-HF (purchased from NEB, R3101V), and the reagents were recovered in small amounts with agarose gel DNA/PCR products
  • the cassette purchased from Biomiga
  • the clones were picked for identification and confirmed by sequencing, and the heavy chain and light chain expression plasmids based on pCDNA3.1(+) were constructed respectively.
  • the heavy chain and light chain expression plasmids were extracted separately with endotoxin-removing plasmid large-scale kit (purchased from Biomiga, BW-PD3511-02), and the two were mixed 1:1.
  • the anti-PD-L1 single domain antibody is located at the N-terminus of the heavy chain of the anti-VEGF mAb
  • the 100% eluate was diluted to conductance ⁇ 3ms/cm, and the supernatant was adjusted to pH 7.0 and loaded onto a DSP column (Borgron Biotechnology Co., Ltd.), with 15% and 100% elution (20mM PB, 0.5 M NaCl, pH 7.0). 15% of the elution fraction was obtained, which was the target protein.
  • the protein concentration was determined by UV280 method.
  • the anti-PD-L1 single domain antibody is located at the N-terminus of the light chain of the anti-VEGF monoclonal antibody
  • the 100% eluate was diluted to a conductivity of 4ms/cm, and the sample was loaded on a Super Q (TOSOH) column.
  • the protein concentration was determined by UV280 method.
  • Detector Agilent 1100 LC; detection wavelength: 214nm; mobile phase: 150mM pH7.0 PB+5% isopropanol; chromatographic column: Superdex 200 Increase 5/150 GL; running time: 15 minutes; column temperature 25°C. Test results show that the purity is greater than 95%.
  • CD5L-OKT3scFv-CD14 (GenBank: ADN42857.1) was synthesized, digested with HindIII-EcoRI (Takara), and inserted into the vector pCDNA3.1 to construct pCDNA3.1-antiCD3TM.
  • human PD-L1 (GenBank: NM_014143.2) as the template, high-fidelity amplification was used to obtain the PD-L1 fragment by recombinant ligation and inserted into pCDNA3.1-antiCD3TM to construct pCDNA3.1-antiCD3TM-PDL1.
  • CHO cells (Thermo) were transfected and then selected with G418 for 10-14d to generate the stable cell line CHO-antiCD3TM-PDL1.
  • the obtained fragment was amplified with human PD1 (GenBank: NP_005009.2) as the template, and then recombined with the PB513B1-dual-puro vector (Youbao Bio) digested by HindIII-BamHI (Takara) to construct plasmid pB-PD1.
  • High-fidelity amplification was carried out with pGL4.30 (Youbao Bio) as the template, and the obtained fragment was recovered and recombined with the pB-PD1 vector digested by SfiI-XbaI (Takara) to construct the pB-NFAT-Luc2p-PD1 plasmid.
  • the plasmid was extracted with endotoxin-removing plasmid extraction kit (Biomiga) and used to transfect Jurkat cells (Stem Cell Bank of Chinese Academy of Sciences).
  • endotoxin-removing plasmid extraction kit Biomiga
  • Jurkat cells were treated to a relatively adherent state by using 0.1 mg/ml of poly-D-lysine, and then according to the lipofection kit (Lipofectamine 3000; invitrogen)
  • the transfection instructions for transfection of Jurkat cells were carried out; on the third day, pressurized selection was carried out with RPMI1640 medium (Thermo) containing 10% FBS and 2.5 ⁇ g/ml puromycin; After the recovery of cell viability, the content of puromycin was gradually increased to 4 ⁇ g/ml.
  • the monoclonal Jurkat-NFAT-Luc2p-PD1 cell line was obtained.
  • CHO-antiCD3TM-PDL1 and Jurkat-NFAT-Luc2p-PD1 cells Take CHO-antiCD3TM-PDL1 and Jurkat-NFAT-Luc2p-PD1 cells and count them, adjust the cell density to 4 ⁇ 10 6 /ml, and add 25 ⁇ l to each well of each cell in a 96-well plate; use 1% BSA for gradient dilution respectively.
  • the fusion protein sample prepared in Example 2 was added to the cells in 50 ⁇ l; after co-cultivation at 37°C and 5% CO 2 for 6 h, 10 ⁇ l of luciferase substrate (Promega, E2620) was added to each well, shaken on a shaker for 2 min, and read . The operation is as described in the kit.
  • HEK293 cells were plated in 6-well cell culture plates, 1.0 x 10 6 cells per well, and cultured overnight in a 37°C, 5% CO 2 incubator. according to The transfection reagent instructions were used to prepare a transfection system, including 1.0 ⁇ g of pcDNA-KDR plasmid and 4 ⁇ g of pGL4.30 plasmid. 48 hours after transfection, cells were expanded into 10 cm cell culture dishes, and G418 200 ⁇ g/ml and Hygromycin 100 ⁇ g/ml were added. The pressurized medium was replaced with fresh pressurized medium every 3 days until a clear colony of colonies emerged. The cells were digested and plated in a 96-well cell culture plate.
  • the chemiluminescence was detected after stimulation with 0.1 ⁇ g/ml VEGF for 6 hours, and the clones with obvious signal response were selected to continue to expand and cultivate.
  • the monoclonal HEK293-NFAT-KDR was finally obtained.
  • HEK293-NFAT-KDR cells were plated at a density of 40,000 cells/well and digested with Accutase; the digested cells were collected and centrifuged at 1000 rpm for 5 minutes; the supernatant was discarded and the cells were resuspended by adding assay medium (DMEM+5% FBS) ; cell count, adjust the cell density to 1.6 ⁇ 10 6 /ml; lay 96-well cell culture plate, 25ul per well; use assay medium to prepare VEGF solution, the concentration is 60ng/ml; add to the cell culture plate, 25ul per well ; Use the analytical medium to prepare the fusion protein prepared in Example 2, add it to the cell culture plate, 25ul per well; incubate at 37°C, 5% CO 2 for 6h; add 10ul Bright-Glo luciferase detection reagent to each well (Promega, E2620), shake for 2 minutes, transfer 80ul of lysate to an enzyme-labeled white plate, and read
  • Mouse breast cancer cell 4T1 cells were cultured to about 90% confluence (10 cm round dish), digested with trypsin, and plated at 4 ⁇ 10 5 cells/well in a 6-well plate, and cultured overnight.
  • the pGL4.48[luc2P SBE Hygro] plasmid sample obtained by extraction was 4T1 cells were transfected. 24h after transfection, the resulting TGF ⁇ -4T1 cells were trypsinized and transferred to a 10cm dish, cultured with 10% FBS and 150ug/ml hygromycin (InvivoGen, Cat no.: ant-hg-1) in RPMI 1640 Pressurized screening of cells.
  • TGF ⁇ -4T1 cells after pressure screening for 10-15 days were plated at 2 cells/well for monoclonal screening, and TGF ⁇ 1 (Novoprotein, 10ug, Cat no.: CA59) was used to stimulate monoclonal cells to verify monoclonal transfection Finally, TGF ⁇ -4T1 monoclonal cells were obtained.
  • TGF ⁇ -4T1 cells were confluent to about 90%, add about 2.5ml of 0.25% trypsin for digestion, and digest at room temperature for 2 minutes; the cells adhered to the culture dish were pipetted and dispersed in the trypsin solution. The whole digestion process takes ⁇ 5min.
  • MDA-MB-231 human breast cancer cells were used to model huPBMC immune system humanized mice (M-NSG mice) in vivo to determine the in vivo efficacy of the multi-domain fusion proteins of the present invention.
  • PD-L1-Fc fusion protein (SEQ ID NO. 47) is a fusion protein of anti-PD-L1 single domain antibody and human IgG Fc (anti-PD-L1 single domain antibody is located at the N-terminus of Fc), Fc-TGF ⁇ RII fusion protein ( SEQ ID NO. 48) is a fusion protein of human IgG Fc and TGF ⁇ RII (TGF ⁇ RII is located at the C-terminus of Fc).
  • the present invention effectively overcomes various shortcomings in the prior art and has high industrial utilization value.

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Immunology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Toxicology (AREA)
  • Zoology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Oncology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Microbiology (AREA)
  • Mycology (AREA)
  • Epidemiology (AREA)
  • Cell Biology (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

一种具有抗癌活性的多结构域融合蛋白及其制备方法和用途。一种融合蛋白,包括抗PD-L1单域抗体片段、拮抗VEGF片段、TGF-β结合片段。具有抗癌活性的多结构域融合蛋白,能够在一个抗体融合蛋白分子中,将抗PD-L1单抗阻断PD-L1/PD-1相互作用、抗VEGF单抗减少微血管生长和抑制转移性疾病,以及TGF-β受体解除癌细胞对TGF-β信号的耐受、增强免疫应答的功能有机地结合在一起,从而可以用于治疗肿瘤,具有良好的产业化前景。

Description

一种具有抗癌活性的多结构域融合蛋白 技术领域
本发明涉及生物技术领域,特别是涉及一种具有抗癌活性的多结构域融合蛋白及其制备方法和用途。
背景技术
肿瘤细胞和正常细胞不同的地方之一,在其生长的高代谢需求。肿瘤细胞依赖血管提供营养物质和氧气,处理代谢产物,并在现有血管上,促进新生血管的生成。在肿瘤分泌的促血管生成因子中,人血管内皮生长因子(VEGF),特别是VEGF-A是导致肿瘤血管生成的一个重要因素(Josep Garcia等人,2020,Cancer Treatment Reviews 86:1-2)。因此,对VEGF信号通路的抑制可限制多种肿瘤的进展。比如贝伐珠单抗(Bevacizumab,商品名
Figure PCTCN2021077282-appb-000001
),一种人源化抗-VEGF单克隆抗体,可与VEGF结合,阻止VEGF与内皮细胞表面VEGF受体(Flt-1和KDR)相互作用。目前贝伐珠单抗被FDA批准用于转移性结直肠癌,晚期、转移性或复发性非小细胞肺癌和复发性胶质母细胞瘤等的治疗。
转化生长因子TGF-β是一种细胞因子,可通过调节细胞的生长、分化、增殖和生存来维持组织稳态。尽管TGF-β通路在肿瘤的早期阶段,可通过促进细胞周期停滞和凋亡来控制肿瘤;但在肿瘤的晚期阶段,TGF-β也能通过抑制细胞毒性T细胞并促进癌细胞的增殖、侵袭和转移最终使得肿瘤逃逸,这种功能转换被称为“TGF-β悖论”。TGFβ信号通路诱导T H1细胞向Tregs分化,削弱CD8+效应细胞的激活,并限制中央记忆细胞的发育,从根本上影响肿瘤浸润T细胞功能。哺乳动物中,TGF-β主要有TGF-β1、TGF-β2、TGF-β3三种亚型。通过高水平表达TGF-β,肿瘤得以免受免疫监视。与此相一致的是,高表达TGF-β的非小细胞肺癌(NSCLC)、肾细胞癌(CRC),胃癌和前列腺癌均与肿瘤进展和不良预后相关(Marin-Acevedo等人,Journal of Hematology&Oncology,11:39,2018)。这说明,TGF-β拮抗将是肿瘤治疗的一个潜在新方向。
目前,作为免疫检查点抑制剂的抗PD-1/PD-L1单抗已广泛应用于肿瘤治疗。抗PD-L1单抗Avelumab与TGF-β受体II(TGF-βTrap)融合而成的M7824已经进入临床阶段。而抗PD-1/PD-L1单抗、TGF-β拮抗剂和抗VEGF单抗的组合却仍未见报道。
发明内容
鉴于以上所述现有技术的缺点,本发明的目的在于提供一种具有抗癌活性的多结构域融合蛋白及其制备方法和用途,用于解决现有技术中的问题。
为实现上述目的及其他相关目的,本发明一方面提供一种融合蛋白,所述融合蛋白包括抗PD-L1单域抗体片段、拮抗VEGF片段、TGF-β结合片段。
本发明另一方面提供一种分离的多核苷酸,编码上述的融合蛋白。
本发明另一方面提供一种构建体,所述构建体含有上述的分离的多核苷酸。
本发明另一方面提供一种表达系统,所述表达系统含有上述的构建体或基因组中整合有外源的上述的多核苷酸。
本发明另一方面提供上述的融合蛋白的制备方法,包括:在合适的条件下培养如权利要求15所述的表达系统,使之表达所述融合蛋白,分离、纯化以提供所述融合蛋白。
本发明另一方面提供上述的融合蛋白、或上述的表达系统的培养物在制备药物中的用途。
本发明另一方面提供一种药物组合物,包括上述的融合蛋白、或上述的表达系统的培养物。
附图说明
图1显示为本发明实施例4中多结构域融合蛋白在M-NSG小鼠中的抑瘤效果示意图。
具体实施方式
本发明发明人经过大量探索研究,意外地发现了一种融合蛋白分子,该融合蛋白分子可以将抗PD-L1单抗阻断PD-L1/PD-1相互作用、拮抗VEGF单抗减少微血管生长和抑制转移性疾病、以及TGF-β受体改善肿瘤微环境中TGF-β引起的T细胞功能异常和增强免疫应答的功能结合在一起,具有优良的肿瘤抑制效果,在此基础上完成了本发明。
本发明第一方面提供一种融合蛋白,所述融合蛋白包括抗PD-L1单域抗体片段、拮抗VEGF片段、TGF-β结合片段。上述融合蛋白中,抗PD-L1单域抗体片段通常可以用于阻断PD-L1/PD-1相互作用,提高T淋巴细胞中IFN-γ和/或IL-2表达,从而抑制肿瘤生长。拮抗VEGF片段通常可以包括可以与FcRn受体结合的Fc部分,从而可以延长体内半衰期,同时也可与表达Fc受体的效应细胞结合起到杀伤癌细胞的作用。TGF-β结合片段可以通过清除肿瘤微环境中过量表达的TGF-β,提高肿瘤浸润T细胞对肿瘤细胞的杀伤功能。
本发明所提供的融合蛋白中,可以包括抗PD-L1单域抗体片段。上述抗PD-L1单域抗体片段通常可以是能够特异性与PD-L1结合的多肽或蛋白片段。抗PD-L1单域抗体片段中,通常缺失对应的抗体轻链,而只有重链可变区对应的片段。抗PD-L1单域抗体片段的结合特性通常可以由其包括的3个互补决定区(CDR,complementarity determining region)来决定,CDR区可以与框架区(FR,framework region)有序排列,FR区不直接参与结合反应。这些CDR可以形成环状结构,通过其间的FR形成的β折叠在空间结构上相互靠近,构成了抗体的抗原结合位点。例如,上述抗PD-L1单域抗体片段的互补决定区(CDR)可以包括氨基酸序列如SEQ ID NO.1~5其中之一所示的CDR1,SEQ ID NO.6~9其中之一所示的CDR2,SEQ ID NO.10~15其中之一所示的CDR3。
在本发明一具体实施例中,抗PD-L1单域抗体片段的互补决定区包括:氨基酸序列如SEQ ID NO.1所示的CDR1,SEQ ID NO.6所示的CDR2,SEQ ID NO.10所示的CDR3。
在本发明另一具体实施例中,抗PD-L1单域抗体片段的互补决定区包括:氨基酸序列如SEQ ID NO.2所示的CDR1,SEQ ID NO.7所示的CDR2,SEQ ID NO.11所示的CDR3。
在本发明另一具体实施例中,抗PD-L1单域抗体片段的互补决定区包括:氨基酸序列如SEQ ID NO.3所示的CDR1,SEQ ID NO.7所示的CDR2,SEQ ID NO.12所示的CDR3。
在本发明另一具体实施例中,抗PD-L1单域抗体片段的互补决定区包括:氨基酸序列如SEQ ID NO.4所示的CDR1,SEQ ID NO.8所示的CDR2,SEQ ID NO.13所示的CDR3。
在本发明另一具体实施例中,抗PD-L1单域抗体片段的互补决定区包括:氨基酸序列如SEQ ID NO.2所示的CDR1,SEQ ID NO.7所示的CDR2,SEQ ID NO.14所示的CDR3。
在本发明另一具体实施例中,抗PD-L1单域抗体片段的互补决定区包括:氨基酸序列如SEQ ID NO.5所示的CDR1,SEQ ID NO.9所示的CDR2,SEQ ID NO.15所示的CDR3。
上述抗PD-L1单域抗体片段中,还可以包括框架区(FR,framework region)。如上所述,CDR区可以与FR区有序排列,例如,抗PD-L1单域抗体片段自N端至C端可以依次包括FR1、CDR1、FR2、CDR2、FR3、CDR3、FR4。框架区FR包括氨基酸序列可以如SEQ ID No.49所示的FR1、氨基酸序列如SEQ ID No.50~52其中之一所示的FR2、氨基酸序列如SEQ ID No.53~55其中之一所示的FR3、和氨基酸序列如SEQ ID No.56所示的FR4。
在本发明一具体实施例中,所述框架区FR包括:
氨基酸序列如SEQ ID NO.49所示的FR1,SEQ ID NO.50所示的FR2,SEQ ID NO.53所示的FR3;SEQ ID NO.56所示的FR4,或
氨基酸序列如SEQ ID NO.49所示的FR1,SEQ ID NO.51所示的FR2,SEQ ID NO.54所示的FR3;SEQ ID NO.56所示的FR4,或
氨基酸序列如SEQ ID NO.49所示的FR1,SEQ ID NO.52所示的FR2,SEQ ID NO.54所示的FR3;SEQ ID NO.56所示的FR4,或
氨基酸序列如SEQ ID NO.49所示的FR1,SEQ ID NO.52所示的FR2,SEQ ID NO.55所示的FR3;SEQ ID NO.56所示的FR4。
在本发明另一具体实施例中,抗PD-L1单域抗体片段可以包括:a)氨基酸序列如SEQ ID No.16~21其中之一所示的多肽片段;或,b)氨基酸序列与SEQ ID No.16~21其中之一具有80%以上序列一致性且具有a)限定的多肽片段的功能的多肽片段。具体的,上述b)中的多肽片段具体指:氨基酸序列如SEQ ID No.16~21其中之一所示的氨基酸序列经过取代、缺失或者添加一个或多个(具体可以是1-50、1-30个、1-20个、1-10个、1-5个、或1-3个)氨基酸而得到的,或者在N-末端和/或C-末端添加一个或多个(具体可以是1-50个、1-30个、1-20个、1-10个、1-5个、或1-3个)氨基酸而得到的,且具有氨基酸序列如SEQ ID No.16~21其中之一所示的多肽片段的功能的多肽片段,例如,可以是与PD-L1特异性结合的能力,也可以是对PD-L1/PD-1相互作用的阻断,从而可以阻断PD-L1/PD1通路,也可以是提高T淋巴细胞中IFN-γ和/或IL-2表达的功能,还可以是抑制肿瘤生长的功能。上述b)中的抗PD-L1单域抗体片段的氨基酸序列可以与SEQ ID No.16~21其中之一具有80%、85%、90%、93%、95%、97%、或99%以上的一致性。上述抗PD-L1单域抗体片段通常可以来源于羊驼(Vicugna pacos),例如,其CDR区可以来源于羊驼。上述抗PD-L1单域抗体片段通常可以是人源化的,例如,其框架区可以来源于人。
本文中,序列一致性(sequence identity)指参与对比的序列中相同残基的百分比。可采用本领域周知的计算软件计算两条或多条目的序列的序列一致性,这些软件可获自如NCBI。
本发明所提供的融合蛋白中,可以包括拮抗VEGF片段。上述拮抗VEGF片段通常可以是能够拮抗VEGF的多肽或蛋白片段。例如,上述拮抗VEGF片段可以是单克隆抗体等。再例如,上述拮抗VEGF片段可以是贝伐珠单抗等。
在本发明一具体实施例中,拮抗VEGF片段可以包括:
c)氨基酸序列如SEQ ID No.22~23其中之一所示的多肽片段;
d)氨基酸序列与SEQ ID No.22~23其中之一具有80%以上序列一致性且具有c)限定的 多肽片段的功能的多肽片段。具体的,上述d)中的氨基酸序列具体指:如SEQ ID No.22~23其中之一所示的氨基酸序列经过取代、缺失或者添加一个或多个(具体可以是1-50、1-30个、1-20个、1-10个、1-5个、1-3个、1个、2个、或3个)氨基酸而得到的,或者在N-末端和/或C-末端添加一个或多个(具体可以是1-50个、1-30个、1-20个、1-10个、1-5个、1-3个、1个、2个、或3个)氨基酸而得到的,且具有氨基酸如SEQ ID No.22~23其中之一所示的多肽片段的功能的多肽片段,例如,可以是拮抗VEGF的功能,还可以是与FcRn受体结合的Fc部分的功能,从而可以延长体内半衰期,同时也可与表达Fc受体的效应细胞结合起到杀伤癌细胞的作用。所述d)中的氨基酸序列可与SEQ ID No.22~23其中之一具有80%、85%、90%、93%、95%、97%、或99%以上的一致性。上述拮抗VEGF片段通常可以来源于小鼠(Mus musculus),例如,其CDR区可以来源于小鼠。上述拮抗VEGF片段通常可以是人源化的,例如,其框架区可以来源于人。
本发明所提供的融合蛋白中,可以包括TGF-β结合片段。上述TGF-β结合片段通常可以特异性地结合各TGF-β异构体(例如,TGF-β1、TGF-β2和TGF-β3等),TGF-β异构体通常在多种恶性肿瘤中高表达,很可能是导致临床治疗效果不佳的重要因素之一。例如,TGF-β结合片段可以是TGF-βRⅡ(TGF-β受体II)胞外区结构片段。
在本发明一具体实施例中,TGF-β结合片段可以包括:
e)氨基酸序列如SEQ ID No.24所示的多肽片段;
f)氨基酸序列与SEQ ID No.24具有80%以上序列一致性且具有e)限定的多肽片段的功能的多肽片段。具体的,上述f)中的氨基酸序列具体指:如SEQ ID No.24所示的氨基酸序列经过取代、缺失或者添加一个或多个(具体可以是1-50、1-30个、1-20个、1-10个、1-5个、1-3个、1个、2个、或3个)氨基酸而得到的,或者在N-末端和/或C-末端添加一个或多个(具体可以是1-50个、1-30个、1-20个、1-10个、1-5个、1-3个、1个、2个、或3个)氨基酸而得到的,且具有氨基酸如SEQ ID No.24所示的多肽片段的功能的多肽片段,例如,可以结合各TGF-β异构体(例如,TGF-β1、TGF-β2和TGF-β3等),从而可以清除肿瘤微环境中过量表达的TGF-β,还可以提高肿瘤浸润T细胞对肿瘤细胞的杀伤功能。所述f)中的氨基酸序列可与SEQ ID No.24具有80%、85%、90%、93%、95%、97%、或99%以上的一致性。上述TGF-β结合片段通常可以来源于人(homo sapiens)。
本发明所提供的融合蛋白中,还可以包括连接肽片段。所述融合蛋白中,通常可以包括多个连接肽片段,至少部分的结构域或各结构域之间均可以设有连接肽片段。例如,抗PD-L1单域抗体片段、拮抗VEGF片段之间可以设有连接肽。再例如,拮抗VEGF片段、 TGF-β结合片段之间可以设有连接肽。上述连接肽片段通常可以为一段长度合适的富含G、S和/或A(主要由甘氨酸(G)、丝氨酸(S)和/或丙氨酸(A)构成)的柔性多肽,从而使相邻的蛋白质结构域可相对于彼此自由移动。例如,所述连接肽片段的氨基酸序列可以包括如(GS)n、(GGS)n、(GGSG)n、(GGGS)nA、(GGGGS)nA、(GGGGS)nG、(GGGGA)nA、(GGGGG)nA等序列,其中,n选自1-10之间的整数。在本发明一具体实施例中,所述连接肽片段的氨基酸序列的长度可以为3-30、3-4、4-6、6-8、8-10、10-12、12-14、14-16、16-18、18-20、20-22、22-24、24-26、26-28、或28-30。在本发明一更优选的具体实施例中,所述连接肽片段可以包括氨基酸序列如SEQ ID NO.34-36其中之一所示的多肽片段。
本发明所提供的融合蛋白中,融合蛋白可以是线性的,例如,融合蛋白可以自N端至C端可以依次包括抗PD-L1单域抗体片段、拮抗VEGF片段、TGF-β结合片段。融合蛋白也可以具有类似于单克隆抗体的结构,例如,抗PD-L1单域抗体片段可以位于拮抗VEGF片段的重链的N端,再例如,抗PD-L1单域抗体片段可以位于拮抗VEGF片段的轻链的N端,再例如,TGF-β结合片段可以位于拮抗VEGF片段的重链的C端,具体可以为C末端。在本发明一具体实施例中,所述融合蛋白的氨基酸序列可以包括SEQ ID NO.23、SEQ ID NO.25-33其中之一所示的序列,例如,所述融合蛋白的氨基酸序列可以包括SEQ ID NO.25和SEQ ID NO.26所示的序列、SEQ ID NO.25和SEQ ID NO.27所示的序列、SEQ ID NO.25和SEQ ID NO.28所示的序列、SEQ ID NO.25和SEQ ID NO.29所示的序列、SEQ ID NO.30和SEQ ID NO.27所示的序列、SEQ ID NO.30和SEQ ID NO.29所示的序列、SEQ ID NO.31和SEQ ID NO.23所示的序列、SEQ ID NO.32和SEQ ID NO.23所示的序列、SEQ ID NO.33和SEQ ID NO.23所示的序列。
本发明第二方面提供一种分离的多核苷酸,编码本发明第一方面所提供的融合蛋白。上述多核苷酸可以是RNA、DNA或cDNA等。提供所述分离的多核苷酸的方法对于本领域技术人员来说应该是已知的。例如,可以通过自动DNA合成和/或重组DNA技术等方法制备获得,也可以从适合的天然来源加以分离。
本发明第三方面提供一种构建体,上述构建体含有本发明第二方面所提供的分离的多核苷酸。合适的构建上述构建体的方法对于本领域技术人员来说应该是已知的。例如,所述构建体可以通过体外重组DNA技术、DNA合成技术、体内重组技术等方法构建获得,更具体的,可以由上述的分离的多核苷酸插入到表达载体的多克隆位点构建而成。本发明中的表达载体通常指本领域熟知的各种市售表达载体等,例如可以是细菌质粒、噬菌体、酵母质粒、植物细胞病毒、哺乳动物细胞病毒如腺病毒、逆转录病毒或其他载体。通常来说,合适的载 体可以包含在至少一种有机体中起作用的复制起点、启动子序列、方便的限制酶位点和一个或多个可选择的标记。例如,这些启动子可以是包括但不限于大肠杆菌的lac或trp启动子;λ噬菌体PL启动子;真核启动子包括CMV立即早期启动子、HSV胸苷激酶启动子、早期和晚期SV40启动子、毕赤酵母的甲醇氧化酶启动子和其它一些已知的可控制基因在原核或真核细胞或其病毒中表达的启动子。标记基因可用于提供用于选择转化的宿主细胞的表型性状,例如,可以是包括但不限于真核细胞培养用的二氢叶酸还原酶、新霉素抗性以及绿色荧光蛋白(GFP),或用于大肠杆菌的四环素或氨苄青霉素抗性等。当所述的多核苷酸被表达时,表达载体中还可以包括增强子序列,如果在载体中插入增强子序列,则将会使转录得到增强,增强子是DNA的顺式作用因子,通常大约有10到300个碱基对,作用于启动子以增强基因的转录。
本发明第四方面提供一种表达系统,所述表达系统含有本发明第三方面所提供的构建体或基因组中整合有外源的本发明第二方面所提供的多核苷酸,从而可表达上述的融合蛋白。上述表达系统可以是宿主细胞,任何适用于表达载体进行表达的细胞都可以作为宿主细胞,例如,宿主细胞可以是原核细胞,如细菌细胞;或是低等真核细胞,如酵母细胞;丝状真菌细胞、或是高等真核细胞,如哺乳动物细胞。代表性的例子有:大肠杆菌,链霉菌属;鼠伤寒沙门氏菌的细菌细胞;真菌细胞如酵母、丝状真菌、植物细胞;果蝇S2或Sf9的昆虫细胞;CHO、COS、293细胞、或Bowes黑素瘤细胞的动物细胞等。将构建体导入宿主细胞的方法对于本领域技术人员来说应该是已知的,例如,可以显微注射法、基因枪法、电穿孔法、病毒介导的转化法、电子轰击法、磷酸钙沉淀法等方法。
本发明第五方面提供本发明第一方面所提供的融合蛋白的制备方法,本领域技术人员可选择合适的方法以制备所述融合蛋白,例如,所述制备方法可以包括:在合适的条件下培养本发明第四方面所提供的表达系统,使之表达所述融合蛋白,收集含有所述融合蛋白的培养物,而后分离及纯化以提供所述融合蛋白。
本发明第六方面提供本发明第一方面所提供的融合蛋白、本发明第四方面所提供的表达系统的培养物在制备药物中的用途。上述药物可以是用于治疗肿瘤的药物,例如,可以是癌症或实体肿瘤,具体可以是肺癌、黑色素瘤、胃癌、卵巢癌、结肠癌、肝癌、肾癌、膀胱癌、乳腺癌、经典霍奇金淋巴瘤、血液恶性肿瘤、头颈癌和鼻咽癌等,这些癌症可以为早期、中期或晚期,例如转移癌等。
本发明第七方面提供一种药物组合物,包括本发明第一方面所提供的融合蛋白或本发明第四方面所提供的表达系统的培养物。上述药物组合物中,融合蛋白或培养物的含量通常为 治疗有效量的。本发明中,“治疗有效量”通常指一用量在经过适当的给药期间后,能够导致疾病症状的严重性降低,疾病无症状期的频率和持续时间增加,或者防止因疾病痛苦而引起的损伤或失能。抑制肿瘤生长的能力可以在预测对人类肿瘤的疗效的动物模型系统中评价。或者,也可以通过检查抑制细胞生长的能力来评价,这种抑制可以通过本领域技术人员公知的试验在体外测定。治疗有效量的融合蛋白、药物组合物通常能够减小肿瘤大小,或者以其他方式缓解对象的症状。本领域技术人员可以根据实际情况选择合适的治疗有效量,例如,可以是对象的大小、对象症状的严重性和选择的特定组合物或给药途径。治疗的处方(例如,对剂量的决定等)可以是由医生确定的,通常考虑的因素包括但不限于所治疗的疾病、患者个体的情况、递送部位、施用方法以及其它因素等。
本发明所提供的药物组合物中,还可以包括药学上可接受的载体。上述载体可以包括各种赋形剂和稀释剂,这些载体本身并不是必要的活性成分,且施用后没有过分的毒性。合适的载体对于本领域技术人员来说应该是熟知的,例如,在Remington's Pharmaceutical Sciences(Mack Pub.Co.,N.J.,1991)中可找到关于药学上可接受的载体的充分讨论。
本发明第八方面提供一种治疗方法,包括:向个体施用治疗有效量的本发明第一方面所提供的融合蛋白、本发明第四方面所提供的表达系统的培养物、或本发明第七方面所提供的药物组合物。
本发明中,“治疗”一词包括可导致欲求的药学和/或生理效果的预防性、治愈性或缓和性处置。该效果较佳是指医疗上可减少疾病的一种或多种症状或者完全消除疾病,或阻滞、延迟疾病的发生和/或降低疾病发展或恶化的风险。
本发明中,“个体”通常包括人类、非人类的灵长类,或其他哺乳动物(如狗、猫、马、羊、猪、牛等),其可因利用所述制剂、试剂盒或联合制剂进行治疗而获益。
本发明中,上述融合蛋白、表达系统的培养物、或药物组合物可以作为是单一有效成分,也可以与其他药剂联用,从而在联合治疗中施用。例如,可以将上述具有抗癌活性的多结构域融合蛋白、表达系统的培养物、或药物组合物联合其他至少一种抗肿瘤药物。再例如,可以将上述具有抗癌活性的多结构域融合蛋白、表达系统的培养物、或药物组合物与靶向其它肿瘤特异性抗原的抗体联合使用。
本发明所提供的具有抗癌活性的多结构域融合蛋白,能够在一个抗体融合蛋白分子中,将抗PD-L1单抗阻断PD-L1/PD-1相互作用、抗VEGF单抗减少微血管生长和抑制转移性疾病,以及TGF-β受体解除癌细胞对TGF-β信号的耐受、增强免疫应答的功能有机地结合在一起,从而可以用于治疗肿瘤,具有良好的产业化前景。
以下通过特定的具体实例说明本发明的实施方式,本领域技术人员可由本说明书所揭露的内容轻易地了解本发明的其他优点与功效。本发明还可以通过另外不同的具体实施方式加以实施或应用,本说明书中的各项细节也可以基于不同观点与应用,在没有背离本发明的精神下进行各种修饰或改变。
在进一步描述本发明具体实施方式之前,应理解,本发明的保护范围不局限于下述特定的具体实施方案;还应当理解,本发明实施例中使用的术语是为了描述特定的具体实施方案,而不是为了限制本发明的保护范围。
当实施例给出数值范围时,应理解,除非本发明另有说明,每个数值范围的两个端点以及两个端点之间任何一个数值均可选用。除非另外定义,本发明中使用的所有技术和科学术语与本技术领域技术人员通常理解的意义相同。除实施例中使用的具体方法、设备、材料外,根据本技术领域的技术人员对现有技术的掌握及本发明的记载,还可以使用与本发明实施例中所述的方法、设备、材料相似或等同的现有技术的任何方法、设备和材料来实现本发明。
除非另外说明,本发明中所公开的实验方法、检测方法、制备方法均采用本技术领域常规的分子生物学、生物化学、染色质结构和分析、分析化学、细胞培养、重组DNA技术及相关领域的常规技术。这些技术在现有文献中已有完善说明,具体可参见Sambrook等MOLECULAR CLONING:A LABORATORY MANUAL,Second edition,Cold Spring Harbor Laboratory Press,1989and Third edition,2001;Ausubel等,CURRENT PROTOCOLS IN MOLECULAR BIOLOGY,John Wiley&Sons,New York,1987 and periodic updates;the series METHODS IN ENZYMOLOGY,Academic Press,San Diego;Wolffe,CHROMATIN STRUCTURE AND FUNCTION,Third edition,Academic Press,San Diego,1998;METHODS IN ENZYMOLOGY,Vol.304,Chromatin(P.M.Wassarman and A.P.Wolffe,eds.),Academic Press,San Diego,1999;和METHODS IN MOLECULAR BIOLOGY,Vol.119,Chromatin Protocols(P.B.Becker,ed.)Humana Press,Totowa,1999等。
实施例1
融合蛋白的构建和重组表达制备
根据CHO细胞密码子偏好性分别将表1中多结构域融合蛋白氨基酸序列、PD-L1-Fc融合蛋白(SEQ ID NO.47)及Fc-TGFβRII融合蛋白(SEQ ID NO.48)各自转换成碱基序列,并分别在重链和轻链编码序列的5’端引入HindIII酶切位点和 Kozak序列(GCCACC),在3’端引入终止密码子及EcoRI酶切位点通过基因合成(通用生物系统(安徽)有限公司)获得全长DNA。将合成的重链和轻链编码基因分别进行HindIII-HF(购自NEB,R3104V)和EcoRI-HF(购自NEB,R3101V)双酶切,并用琼脂糖凝胶DNA/PCR产物小量回收试剂盒(购自Biomiga)进行切胶回收,与同样进行HindIII和EcoRI双酶切的pCDNA3.1(+)载体用T4连接酶(购自NEB,M0202V)进行连接,转化Top10感受态,涂布在LB氨苄青霉素抗性平板上培养。挑取克隆进行鉴定,并测序确认,分别构建了基于pCDNA3.1(+)的重链和轻链表达质粒。用去内毒素质粒大抽试剂盒(购自Biomiga,BW-PD3511-02)分别提取重链和轻链表达质粒,并将两者1:1混合。取1.0mg混合质粒,使用Wayne293表达培养基(购自中山康晟,A21501)稀释至25mL;取3.0mg PEI(线性,25KD,Polysciences,Inc.),使用Wayne293表达培养基稀释至25mL后加入到质粒溶液中,混匀,室温孵育30分钟。取对数期生长的Hek293F细胞(活率>95%),计数;1100rpm,离心10分钟,弃上清,用450mL Wayne293表达培养基重悬细胞。将上述质粒-PEI混合物,加入到细胞悬液中,37℃,5%CO 2摇床培养箱中培养7天后,离心取上清,用于后续蛋白纯化。
表1多结构域融合蛋白氨基酸序列和编码序列
Figure PCTCN2021077282-appb-000002
实施例2
多结构域融合蛋白的纯化
2.1抗PD-L1单域抗体位于抗VEGF单抗的重链N端
将细胞发酵上清调至pH7.0后上样到Protein A亲和层析柱(博格隆生物技术有限公司),平衡液为20mM PB,0.15M NaCl(pH=7.0),100%0.1M Gly-HCl(pH=3.0)洗脱;洗脱液预先加入10%1M Tris-HCl(pH=8.5)。100%洗脱液稀释至电导 <3ms/cm,上清液调pH7.0上样至DSP层析柱(博格隆生物技术有限公司),分别15%和100%洗脱(20mM PB,0.5M NaCl,pH7.0)。得到15%洗脱组分,即为目的蛋白。采用UV280法测定蛋白浓度。
2.2抗PD-L1单域抗体位于抗VEGF单抗的轻链N端
将细胞发酵上清调至pH7.0后上样到Protein A亲和层析柱(博格隆生物技术有限公司),平衡液为20mM PB,0.15M NaCl(pH=7.0),100%0.1M Gly-HCl(pH=3.0)洗脱;洗脱液预先加入10%1M Tris-HCl(pH=8.5)。100%洗脱液稀释至电导4ms/cm,上样于Super Q(TOSOH)层析柱,平衡液为20mM Tris,pH8,洗脱液为500mM NaCl+20mM Tris(pH=8.0),分别35%和100%洗脱,通过流穿去除过量轻链,得到35%洗脱组分,即为目的蛋白。采用UV280法测定蛋白浓度。
纯度检测使用SEC-HPLC-UV分析。检测器:Agilent 1100 LC;检测波长:214nm;流动相:150mM pH7.0 PB+5%异丙醇;色谱柱:Superdex 200 Increase 5/150 GL;运行时间:15分钟;柱温25℃。检测结果显示纯度都大于95%。
PD-L1-Fc融合蛋白(SEQ ID NO.47)及Fc-TGFβRII融合蛋白(SEQ ID NO.48)的纯化:将细胞发酵上清调至pH7.0后上样到Protein A亲和层析柱(博格隆生物技术有限公司),平衡液为20mM PB,0.15M NaCl(pH=7.0),100%0.1M Gly-HCl(pH=3.0)洗脱;洗脱液预先加入10%1M Tris-HCl(pH=8.5)。
实施例3
鉴定多结构域融合蛋白在体外的功能
3.1抗PD-L1单域抗体片段的体外活性检测:
合成CD5L-OKT3scFv-CD14(GenBank:ADN42857.1),并用HindIII-EcoRI(Takara)酶切,插入载体pCDNA3.1,构建pCDNA3.1-antiCD3TM。以人PD-L1(GenBank:NM_014143.2)为模板,高保真扩增得到PD-L1片段重组连接插入pCDNA3.1-antiCD3TM,构建pCDNA3.1-antiCD3TM-PDL1。转染CHO细胞(Thermo),然后用G418选择10-14d来产生稳定细胞系CHO-antiCD3TM-PDL1。
以人PD1(GenBank:NP_005009.2)为模板扩增所得片段,与经HindIII-BamHI(Takara)酶切的PB513B1-dual-puro载体(优宝生物)重组连接,构建质粒pB-PD1。以pGL4.30(优宝生物)为模板进行高保真扩增,回收所得片段,与经SfiI-XbaI(Takara)酶切的pB-PD1载体重组连接,构建pB-NFAT-Luc2p-PD1质粒。质粒成功 构建后用去内毒素质粒大抽试剂盒(Biomiga)提取质粒用于转染Jurkat细胞(中国科学院干细胞库)。参考专利CN 107022571A中的方法,通过使用0.1mg/ml的多聚-D-赖氨酸将Jurkat细胞处理成相对贴壁的状态,然后根据脂质体转染试剂盒(Lipofectamine 3000;invitrogen)中的转染说明对Jurkat细胞进行转染;第三天用含有10%FBS和2.5μg/ml嘌呤霉素的RPMI1640培养基(Thermo)进行加压筛选;此后每隔一段时间补加培养基,待细胞活率恢复后逐渐增加嘌呤霉素的含量至4μg/ml。最终获得单克隆Jurkat-NFAT-Luc2p-PD1细胞株。
取CHO-antiCD3TM-PDL1、Jurkat-NFAT-Luc2p-PD1细胞并计数,调整细胞密度为4×10 6/ml,96孔板中每孔每个细胞各加入25μl;分别用1%BSA梯度稀释实施例2中制备的融合蛋白样品,并加入50μl至细胞中;37℃、5%CO 2共培养6h后,每孔加入10μl荧光素酶底物(Promega,E2620),振荡器上震荡2min,读数。操作如试剂盒说明。
3.2拮抗VEGF片段的体外活性检测:
HEK293细胞铺6孔细胞培养板,每孔1.0×10 6细胞,37℃,5%CO 2培养箱中过夜培养。按照
Figure PCTCN2021077282-appb-000003
转染试剂说明书配制转染体系,其中pcDNA-KDR质粒1.0μg、pGL4.30质粒4μg。转染48小时后,细胞放大到10cm细胞培养皿,添加G418 200μg/ml、Hygromycin 100μg/ml。每3天更换一次新鲜加压培养基,至有明显的克隆团长出。消化细胞,铺96孔细胞培养板,待单克隆长出后,使用0.1μg/ml VEGF刺激6小时后检测化学发光情况,挑选信号响应明显的克隆继续放大培养。最终获得单克隆HEK293-NFAT-KDR。HEK293-NFAT-KDR细胞按照4万个/每孔密度铺板,使用Accutase进行消化;收集消化后的细胞,1000rpm离心5分钟;弃上清,加入分析培养液(DMEM+5%FBS)重悬细胞;细胞计数,调整细胞密度至1.6×10 6/ml;铺96孔细胞培养板,每孔25ul;使用分析培养液配制VEGF溶液,浓度为60ng/ml;加入到细胞培养板中,每孔25ul;使用分析培养液配制实施例2中制备获得的融合蛋白,加入到细胞培养板中,每孔25ul;37℃,5%CO 2孵育培养6h;每孔加入10ul Bright-Glo荧光素酶检测试剂(Promega,E2620),震荡2分钟转移80ul裂解液至酶标白板中,酶标仪读数。
3.3 TGF-β结合片段的体外细胞活性检测:
小鼠乳腺癌细胞4T1细胞培养长满至90%左右(10cm圆皿),胰酶消化,按照4×10 5个/孔将细胞铺板至6孔板中,培养过夜。抽提得到的pGL4.48[luc2P SBE Hygro] 质粒样品采用
Figure PCTCN2021077282-appb-000004
对4T1细胞转染。转染24h后,得到的TGFβ-4T1细胞采用胰酶消化并转移至10cm培养皿,采用10%FBS和150ug/ml潮霉素(InvivoGen,Cat no.:ant-hg-1)的RPMI 1640培养基对细胞进行加压筛选。加压筛选10~15d后的TGFβ-4T1细胞按照2个/孔进行铺板以进行单克隆筛选,采用TGFβ1(Novoprotein,10ug,Cat no.:CA59)对单克隆细胞进行刺激验证单克隆的转染效果,最终获得TGFβ-4T1单克隆细胞。
TGFβ-4T1细胞长满至90%左右,加入2.5ml左右0.25%胰酶进行消化,室温消化2min;将贴壁在培养皿上的细胞吹打下来,并在胰酶溶液中吹打使分散开来,整个消化过程使用时间~5min,加入完全培养基(RPMI 1640+10%FBS)终止消化,并继续吹打细胞至细胞分散均匀;细胞转移至50m离心管中,1000rpm离心5min;弃上清,加入2ml完全培养基使细胞重悬,采用细胞计数仪测量细胞密度;采用完全培养基(RPMI 1640+10%FBS)稀释细胞,使细胞密度为2×105个/ml;将稀释好的细胞(密度为2×105个/ml)铺板(96孔板),每孔100ul,细胞密度为2×10 4个/孔,96孔板置于37℃培养箱中进行培养过夜;实施例2中制备的融合蛋白样品采用RPMI1640+0.2%FBS培养基(含2ng/ml TGFβ1)稀释至指定浓度(各蛋白样品稀释后室温放置1h);37℃培养箱过夜培养的TGFβ-4T1细胞弃去上清,加入50ul RPMI1640+0.2%FBS培养基,然后加入50μl不同浓度的蛋白溶液;96孔板置于37℃培养箱中继续孵育3h后加入10ul Bright-Glo荧光素酶检测试剂(Promega,E2620),震荡3min;酶标仪读数。
各多结构域融合蛋白的抗PD-L1活性、抗VEGF活性、抗TGFβ活性的测量结果如表2所示。由表2可知,各多结构域融合蛋白均具有良好的体外细胞活性。
表2多结构域融合蛋白的体外细胞活性
Figure PCTCN2021077282-appb-000005
实施例4
多结构域融合蛋白在人源化小鼠体内的肿瘤抑制活性
利用MDA-MB-231(人乳腺癌)细胞在huPBMC免疫系统人源化小鼠(M-NSG小鼠)体内建模来测定本发明的多结构域融合蛋白体内药效。筛选6-8周龄雌性M-NSG小鼠,小鼠接种MDA-MB-231细胞(10*10E6+基质胶25%),于第7天尾静脉注射PBMC(5*10E6/0.2ml),后观察瘤体积及体重,选择肿瘤体积均在140-260mm 3之间的小鼠,依据其肿瘤体积和体重随机分为6组,每组7只,分组当天开始给药。荷瘤小鼠肿瘤体积过大/过小淘汰。每周2次腹腔注射:PBS、同型对照IgG1、阳性对照Tecentriq(Roche)、TAF-6、TAF-7及联合给药(方案详见表3),共给药3周左右。PD-L1-Fc融合蛋白(SEQ ID NO.47)为抗PD-L1单域抗体与人IgG Fc的融合蛋白(抗PD-L1单域抗体位于Fc的N端)、Fc-TGFβRII融合蛋白(SEQ ID NO.48)为人IgG Fc与TGFβRII的融合蛋白(TGFβRII位于Fc的C端)。
在分组前以及实验结束前,从眼眶采血。实验过程中动物体重(每周两次测量),肿瘤体积(每周两次测量)。结果如图1所示。
表3
Figure PCTCN2021077282-appb-000006
综上所述,本发明有效克服了现有技术中的种种缺点而具高度产业利用价值。
上述实施例仅例示性说明本发明的原理及其功效,而非用于限制本发明。任何熟悉此技术的人士皆可在不违背本发明的精神及范畴下,对上述实施例进行修饰或改变。因此,举凡所属技术领域中具有通常知识者在未脱离本发明所揭示的精神与技术思想下所完成的一切等效修饰或改变,仍应由本发明的权利要求所涵盖。

Claims (19)

  1. 一种融合蛋白,所述融合蛋白包括抗PD-L1单域抗体片段、拮抗VEGF片段、TGF-β结合片段。
  2. 如权利要求1所述的融合蛋白,其特征在于,所述抗PD-L1单域抗体片段的互补决定区包括:氨基酸序列如SEQ ID NO.1~5其中之一所示的CDR1,SEQ ID NO.6~9其中之一所示的CDR2,SEQ ID NO.10~15其中之一所示的CDR3。
  3. 如权利要求2所述的融合蛋白,其特征在于,所述抗PD-L1单域抗体片段的互补决定区包括:
    氨基酸序列如SEQ ID NO.1所示的CDR1,SEQ ID NO.6所示的CDR2,SEQ ID NO.10所示的CDR3;或
    氨基酸序列如SEQ ID NO.2所示的CDR1,SEQ ID NO.7所示的CDR2,SEQ ID NO.11所示的CDR3;或
    氨基酸序列如SEQ ID NO.3所示的CDR1,SEQ ID NO.7所示的CDR2,SEQ ID NO.12所示的CDR3;或
    氨基酸序列如SEQ ID NO.4所示的CDR1,SEQ ID NO.8所示的CDR2,SEQ ID NO.13所示的CDR3;或
    氨基酸序列如SEQ ID NO.2所示的CDR1,SEQ ID NO.7所示的CDR2,SEQ ID NO.14所示的CDR3;或
    氨基酸序列如SEQ ID NO.5所示的CDR1,SEQ ID NO.9所示的CDR2,SEQ ID NO.15所示的CDR3。
  4. 如权利要求2所述的融合蛋白,其特征在于,所述抗PD-L1单域抗体片段还包括框架区,所述框架区FR包括氨基酸序列如SEQ ID No.49所示的FR1、氨基酸序列如SEQ ID No.50~52其中之一所示的FR2、氨基酸序列如SEQ ID No.53~55其中之一所示的FR3、和氨基酸序列如SEQ ID No.56所示的FR4。
  5. 如权利要求4所述的融合蛋白,其特征在于,所述框架区FR包括氨基酸序列如下所示的FR1~FR4:
    氨基酸序列如SEQ ID NO.49所示的FR1,SEQ ID NO.50所示的FR2,SEQ ID NO.53所示的FR3;SEQ ID NO.56所示的FR4,或
    氨基酸序列如SEQ ID NO.49所示的FR1,SEQ ID NO.51所示的FR2,SEQ ID NO.54所示的FR3;SEQ ID NO.56所示的FR4,或
    氨基酸序列如SEQ ID NO.49所示的FR1,SEQ ID NO.52所示的FR2,SEQ ID  NO.54所示的FR3;SEQ ID NO.56所示的FR4,或
    氨基酸序列如SEQ ID NO.49所示的FR1,SEQ ID NO.52所示的FR2,SEQ ID NO.55所示的FR3;SEQ ID NO.56所示的FR4。
  6. 如权利要求2所述的融合蛋白,其特征在于,所述抗PD-L1单域抗体片段包括:
    a)氨基酸序列如SEQ ID No.16~21其中之一所示的多肽片段;
    或,b)氨基酸序列与SEQ ID No.16~21其中之一具有90%以上序列一致性且具有a)限定的多肽片段的功能的多肽片段;
    和/或,所述抗PD-L1单域抗体片段来源于羊驼;
    和/或,所述抗PD-L1单域抗体片段是人源化的。
  7. 如权利要求1所述的融合蛋白,其特征在于,所述拮抗VEGF片段为贝伐珠单抗,优选的,所述拮抗VEGF片段包括:
    c)氨基酸序列如SEQ ID No.22~23其中之一所示的多肽片段;或,
    d)氨基酸序列与SEQ ID No.22~23其中之一具有90%以上序列一致性且具有c)限定的多肽片段的功能的多肽片段;
    和/或,所述拮抗VEGF片段来源于鼠;
    和/或,所述拮抗VEGF片段是人源化的。
  8. 如权利要求1所述的融合蛋白,其特征在于,所述TGF-β结合片段为TGF-βRⅡ胞外区结构域片段,优选的,所述TGF-β结合片段包括:
    e)氨基酸序列如SEQ ID No.24所示的多肽片段;或,
    f)氨基酸序列与SEQ ID No.24具有90%以上序列一致性且具有e)限定的多肽片段的功能的多肽片段;
    和/或,所述TGF-β结合片段来源于人。
  9. 如权利要求1所述的融合蛋白,其特征在于,所述融合蛋白还包括连接肽片段,优选的,所述连接肽片段富含G、S和/或A,更优选的,所述连接肽选自由G甘氨酸和/或S丝氨酸和/或A丙氨酸组成的柔性多肽链,所述连接肽的长度为3~30个氨基酸。
  10. 如权利要求9所述的融合蛋白,其特征在于,所述连接肽片段包括氨基酸序列如SEQ ID NO.34-36其中之一所示的多肽片段;
    和/或,所述抗PD-L1单域抗体片段、拮抗VEGF片段之间设有连接肽;
    和/或,所述拮抗VEGF片段、TGF-β结合片段之间设有连接肽。
  11. 如权利要求1~10任一权利要求所述的融合蛋白,其特征在于,所述融合蛋白自N端 至C端依次包括抗PD-L1单域抗体片段、拮抗VEGF片段、TGF-β结合片段;
    和/或,所述抗PD-L1单域抗体片段位于拮抗VEGF片段的重链的N端;
    和/或,所述抗PD-L1单域抗体片段位于拮抗VEGF片段的轻链的N端;
    和/或,所述TGF-β结合片段位于拮抗VEGF片段的重链的C端。
  12. 如权利要求1所述的融合蛋白,其特征在于,所述融合蛋白的氨基酸序列包括SEQ ID NO.23、SEQ ID NO.25-33其中之一所示的序列;
    或,所述融合蛋白的氨基酸序列包括SEQ ID NO.25和SEQ ID NO.26所示的序列、SEQ ID NO.25和SEQ ID NO.27所示的序列、SEQ ID NO.25和SEQ ID NO.28所示的序列、SEQ ID NO.25和SEQ ID NO.29所示的序列、SEQ ID NO.30和SEQ ID NO.27所示的序列、SEQ ID NO.30和SEQ ID NO.29所示的序列、SEQ ID NO.31和SEQ ID NO.23所示的序列、SEQ ID NO.32和SEQ ID NO.23所示的序列、SEQ ID NO.33和SEQ ID NO.23所示的序列。
  13. 一种分离的多核苷酸,编码如权利要求1~12任一权利要求所述的融合蛋白。
  14. 一种构建体,所述构建体含有如权利要求13所述的分离的多核苷酸。
  15. 一种表达系统,所述表达系统含有如权利要求14所述的构建体或基因组中整合有外源的如权利要求13所述的多核苷酸。
  16. 如权利要求1-12任一权利要求所述的融合蛋白的制备方法,包括:在合适的条件下培养如权利要求15所述的表达系统,使之表达所述融合蛋白,分离、纯化以提供所述融合蛋白。
  17. 如权利要求1-12任一权利要求所述的融合蛋白、或如权利要求15所述的表达系统的培养物在制备药物中的用途。
  18. 如权利要求17所述的用途,其特征在于,所述药物选自用于治疗肿瘤的药物。
  19. 一种药物组合物,包括如权利要求1-12之任一权利要求所述的融合蛋白、或如权利要求15所述的表达系统的培养物。
PCT/CN2021/077282 2021-02-22 2021-02-22 一种具有抗癌活性的多结构域融合蛋白 WO2022174451A1 (zh)

Priority Applications (10)

Application Number Priority Date Filing Date Title
PCT/CN2021/077282 WO2022174451A1 (zh) 2021-02-22 2021-02-22 一种具有抗癌活性的多结构域融合蛋白
CN202180003793.0A CN116917334A (zh) 2021-02-22 2021-02-22 一种具有抗癌活性的多结构域融合蛋白
KR1020237031894A KR20230147675A (ko) 2021-02-22 2022-02-17 다중 도메인 융합 단백질 및 이의 응용
PCT/CN2022/076610 WO2022174781A1 (zh) 2021-02-22 2022-02-17 多结构域融合蛋白及其应用
US18/277,996 US20240124587A1 (en) 2021-02-22 2022-02-17 Multi-domain fusion protein and use thereof
CA3211427A CA3211427A1 (en) 2021-02-22 2022-02-17 Multi-domain fusion protein and use thereof
JP2023550320A JP2024507856A (ja) 2021-02-22 2022-02-17 マルチドメイン融合タンパク質及びその応用
CN202280007712.9A CN116761814B (zh) 2021-02-22 2022-02-17 多结构域融合蛋白及其应用
AU2022221660A AU2022221660A1 (en) 2021-02-22 2022-02-17 Multi-domain fusion protein and use thereof
EP22755554.7A EP4282884A4 (en) 2021-02-22 2022-02-17 MULTIPLE-DOMAIN FUSION PROTEIN AND ITS USE

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/CN2021/077282 WO2022174451A1 (zh) 2021-02-22 2021-02-22 一种具有抗癌活性的多结构域融合蛋白

Publications (1)

Publication Number Publication Date
WO2022174451A1 true WO2022174451A1 (zh) 2022-08-25

Family

ID=82930269

Family Applications (2)

Application Number Title Priority Date Filing Date
PCT/CN2021/077282 WO2022174451A1 (zh) 2021-02-22 2021-02-22 一种具有抗癌活性的多结构域融合蛋白
PCT/CN2022/076610 WO2022174781A1 (zh) 2021-02-22 2022-02-17 多结构域融合蛋白及其应用

Family Applications After (1)

Application Number Title Priority Date Filing Date
PCT/CN2022/076610 WO2022174781A1 (zh) 2021-02-22 2022-02-17 多结构域融合蛋白及其应用

Country Status (8)

Country Link
US (1) US20240124587A1 (zh)
EP (1) EP4282884A4 (zh)
JP (1) JP2024507856A (zh)
KR (1) KR20230147675A (zh)
CN (2) CN116917334A (zh)
AU (1) AU2022221660A1 (zh)
CA (1) CA3211427A1 (zh)
WO (2) WO2022174451A1 (zh)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116917334A (zh) * 2021-02-22 2023-10-20 浙江道尔生物科技有限公司 一种具有抗癌活性的多结构域融合蛋白

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107428825A (zh) * 2014-10-10 2017-12-01 创祐生技股份有限公司 治疗及/或预防肿瘤生长、侵袭及/或转移的方法
WO2018205985A1 (zh) * 2017-05-12 2018-11-15 江苏恒瑞医药股份有限公司 含有TGF-β受体的融合蛋白及其医药用途
CN109575140A (zh) * 2017-09-29 2019-04-05 北京比洋生物技术有限公司 靶向pd-1或pd-l1且靶向vegf家族的双靶向融合蛋白及其用途
CN109942712A (zh) * 2019-04-01 2019-06-28 华博生物医药技术(上海)有限公司 抗pd-l1/vegf双功能抗体及其用途
WO2020006511A1 (en) * 2018-06-29 2020-01-02 Gensun Biopharma, Inc. Trispecific antagonists
WO2020014285A2 (en) * 2018-07-09 2020-01-16 Intrexon Corporation Fusion constructs and methods of using thereof
CN112552412A (zh) * 2019-12-05 2021-03-26 屈向东 一种包含TGF-β抑制剂、VEGF抑制剂和抗PDL1抗体的三功能融合蛋白

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2013255542C1 (en) * 2012-04-30 2017-06-22 Biocon Limited Targeted/immunomodulatory fusion proteins and methods for making same
CN103965363B (zh) * 2013-02-06 2021-01-15 上海白泽生物科技有限公司 与pd-1和vegf高效结合的融合蛋白、其编码序列及用途
MX2016010067A (es) 2014-02-10 2016-10-07 Merck Patent Gmbh INHIBICION DIRIGIDA DEL FACTOR DE CRECIMIENTO TRANSFORMADOR ß (TGF ß).
CN107022571A (zh) 2017-05-18 2017-08-08 山西大学 一种转染Jurkat细胞的方法
CN111867612A (zh) * 2018-03-26 2020-10-30 阿尔托生物科学有限责任公司 抗PDL1、IL-15和TGF-β受体组合分子
CN111378044B (zh) * 2018-12-28 2022-07-15 长春金赛药业有限责任公司 抗体融合蛋白、制备方法及其应用
EP3996730A2 (en) * 2019-07-09 2022-05-18 The Johns Hopkins University Molecules, compositions and methods for treatment of cancer
CN116917334A (zh) * 2021-02-22 2023-10-20 浙江道尔生物科技有限公司 一种具有抗癌活性的多结构域融合蛋白

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107428825A (zh) * 2014-10-10 2017-12-01 创祐生技股份有限公司 治疗及/或预防肿瘤生长、侵袭及/或转移的方法
WO2018205985A1 (zh) * 2017-05-12 2018-11-15 江苏恒瑞医药股份有限公司 含有TGF-β受体的融合蛋白及其医药用途
CN109575140A (zh) * 2017-09-29 2019-04-05 北京比洋生物技术有限公司 靶向pd-1或pd-l1且靶向vegf家族的双靶向融合蛋白及其用途
WO2020006511A1 (en) * 2018-06-29 2020-01-02 Gensun Biopharma, Inc. Trispecific antagonists
WO2020006509A1 (en) * 2018-06-29 2020-01-02 Gensun Biopharma, Inc. Antitumor antagonists
WO2020014285A2 (en) * 2018-07-09 2020-01-16 Intrexon Corporation Fusion constructs and methods of using thereof
CN109942712A (zh) * 2019-04-01 2019-06-28 华博生物医药技术(上海)有限公司 抗pd-l1/vegf双功能抗体及其用途
CN112552412A (zh) * 2019-12-05 2021-03-26 屈向东 一种包含TGF-β抑制剂、VEGF抑制剂和抗PDL1抗体的三功能融合蛋白

Also Published As

Publication number Publication date
CN116917334A (zh) 2023-10-20
EP4282884A9 (en) 2024-02-14
KR20230147675A (ko) 2023-10-23
WO2022174781A1 (zh) 2022-08-25
EP4282884A4 (en) 2024-07-17
US20240124587A1 (en) 2024-04-18
AU2022221660A1 (en) 2023-09-28
EP4282884A1 (en) 2023-11-29
CA3211427A1 (en) 2022-08-25
CN116761814A (zh) 2023-09-15
JP2024507856A (ja) 2024-02-21
CN116761814B (zh) 2024-08-27

Similar Documents

Publication Publication Date Title
CN105121474B9 (zh) 融合免疫调节蛋白及其制备方法
JP5562257B2 (ja) ヒトc−met受容体のチロシンキナーゼに対し親和性を有する涙液リポカリンの変異タンパク質、及びそれを得るための方法
CN100531796C (zh) Fgfr激动剂
US9676858B2 (en) Human bispecific EGFRvIII antibody and CD3 engaging molecules
CN112409483A (zh) 抗pd-l1纳米抗体
CN109627340B (zh) Cd3和prlr双特异性抗体及其构建与应用
WO2022174451A1 (zh) 一种具有抗癌活性的多结构域融合蛋白
US8703917B2 (en) Epidermal growth factor receptor variants and pharmaceutical compositions thereof
JP7495489B2 (ja) PD-1およびTGFβを標的化する組換えタンパク質
CN115916831A (zh) 包含抗lag-3抗体和il-2的融合蛋白及其用途
WO2020108636A1 (zh) 全人抗gitr抗体及其制备方法
CN115304680B (zh) 基于Pep42构建的双特异性细胞接合器分子的制备及其应用
WO2022174452A1 (zh) 一种具有抗癌活性的双功能融合蛋白
CN113698493B (zh) 一种针对VEGF和TGF-β的双功能蛋白及其应用
EP3082858B1 (en) Adrenomedullin binder for use in therapy of cancer
WO2024041477A1 (zh) 多结构域融合蛋白的用途
CN110627905B (zh) 靶向vegf与egfr的双功能融合蛋白及其应用
Fattah et al. Peptabody‐EGF: A novel apoptosis inducer targeting ErbB1 receptor overexpressing cancer cells
CN113896804B (zh) 嵌合抗原受体(car)及其应用
WO2022141378A1 (zh) 一种抗pd-1的单域抗体
CN117510644A (zh) 重组抗体及其应用
WO2023142109A1 (zh) 一种长效重组人生长激素及其应用
EP4292661A1 (en) Anti-vegf antibody and use thereof
CN117645667A (zh) 双特异性抗体及其应用
CN114456267A (zh) 一种抗cd73人源化单克隆抗体及其应用

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 202180003793.0

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 21926168

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 21926168

Country of ref document: EP

Kind code of ref document: A1