WO2023246885A1 - 特异性结合dll3和cd3的抗原结合分子及其医药用途 - Google Patents

特异性结合dll3和cd3的抗原结合分子及其医药用途 Download PDF

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WO2023246885A1
WO2023246885A1 PCT/CN2023/101778 CN2023101778W WO2023246885A1 WO 2023246885 A1 WO2023246885 A1 WO 2023246885A1 CN 2023101778 W CN2023101778 W CN 2023101778W WO 2023246885 A1 WO2023246885 A1 WO 2023246885A1
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dll3
amino acid
seq
acid sequence
strand
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PCT/CN2023/101778
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French (fr)
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叶鑫
姚青青
金薪盛
应华
陶维康
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江苏恒瑞医药股份有限公司
上海恒瑞医药有限公司
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Publication of WO2023246885A1 publication Critical patent/WO2023246885A1/zh

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    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • 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
    • 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
    • C07K16/30Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/46Hybrid immunoglobulins
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K19/00Hybrid peptides, i.e. peptides covalently bound to nucleic acids, or non-covalently bound protein-protein complexes
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    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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    • C12N5/00Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
    • C12N5/10Cells modified by introduction of foreign genetic material

Definitions

  • the present disclosure belongs to the field of biotechnology, and more specifically, the present disclosure relates to DLL3/CD3 antigen-binding molecules and their applications.
  • Small Cell Lung Cancer is a relatively malignant type of lung cancer, accounting for 10%-15% of all lung cancer cases. Small cell lung cancer tumors grow quickly and metastasize easily, and the 5-year survival rate is less than 7%.
  • the therapeutic drugs for small cell lung cancer are relatively limited, mainly chemical drugs, such as platinum/etoposide combination chemotherapy. Patients with small cell lung cancer respond well to chemotherapy in the early stage, but they are prone to drug resistance and recurrence. Immunotherapy in recent years, such as PD-L1 antibodies and PD1 antibodies, has a certain effect on SCLC patients, but the effective rate is about 15%. There are still no specific targeted therapeutic drugs developed.
  • DLL3 is a ligand that inhibits Notch. Under normal conditions, DLL3 is located on the Golgi apparatus. In cancer cells (such as small cell lung cancer cells), DLL3 is expressed on the cell surface. DLL3 binds Notch in a cis-acting manner, preventing Cell-cell binding and Notch endocytosis in target cells inhibit the Notch signaling pathway and promote the growth of tumor cells. DLL3 is mainly expressed in neurological or neuroendocrine tumors, including small cell lung cancer, large cell neuroendocrine cancer, gastrointestinal neuroendocrine tumors, small cell bladder cancer, glioblastoma multiforme, metastatic castrated prostate cancer, melanoma tumors, especially SCLC. More than 80% of SCLC have positive expression of DLL3, but it is not expressed in normal lung cancer tissues and adjacent tissues. This difference in expression makes DLL3 a potential therapeutic target for the treatment of SCLC.
  • CD3 is an isotype or heterodimer antigen expressed on T cells. Functional CD3 is formed by the dimerization of two of four different chains: ⁇ , ⁇ , ⁇ , and ⁇ . CD3 dimer arrangements include ⁇ / ⁇ , ⁇ / ⁇ , and ⁇ / ⁇ . CD3 binds to the T cell receptor complex (TCR) and is required for T cell activation. Therefore, the use of anti-CD3 antibodies that activate T cells has been proposed for the treatment of cancer. However, the administration of anti-CD3 antibodies may trigger T cell activation and related cytokine release. Excessive cytokine release leads to severe cytokine release syndrome (CRS), which is an important challenge in the clinical use of anti-CD3 antibodies.
  • TCRS severe cytokine release syndrome
  • the present disclosure provides an antigen-binding molecule that specifically binds DLL3 and CD3.
  • the present disclosure provides an antigen-binding molecule comprising at least one antigen-binding module that specifically binds DLL3 and at least one antigen-binding module that specifically binds CD3, the antigen-binding module that specifically binds DLL3 comprising a heavy chain variable region DLL3-VH and light chain variable region DLL3-VL, and the antigen-binding module that specifically binds to CD3 includes a heavy chain variable region CD3-VH and a light chain variable region CD3-VL.
  • the antigen-binding molecule as described above, wherein:
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 12, 56 or 57
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in the DLL3-VL respectively comprise the amino acids of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 13, 63, 64, 65, 66 or 67 sequence, or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 14, 79, 80, 81 or 82
  • the amino acid sequence, and DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in the DLL3-VL respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 15, or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 16, 91, 92, 93 or 94.
  • the amino acid sequence, and DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in the DLL3-VL respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 17, or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise DLL3-HCDR1
  • the amino acid sequences of DLL3-HCDR2 and DLL3-HCDR3, and DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in the DLL3-VL respectively comprise DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 19 amino acid sequence.
  • the antigen-binding molecule as described above, wherein:
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 12, and the DLL3- DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in VL respectively contain the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 13; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 54, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 64; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 54, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively include Containing the amino acid sequence of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 63; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 56, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 65; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 56, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 66; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 56, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 67; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 57, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 65; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 57, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 66; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 57, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 67; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 14, and the DLL3- DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 points in VL
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 81, and DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 77; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 79, 80 or 82
  • the DLL3 - DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in VL respectively contain the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 77; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 16
  • the DLL3- DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in VL respectively contain the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 17;
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 91, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 87; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 92, 93 or 94
  • the DLL3 - DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in VL respectively contain the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 87; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 18, and the DLL3- DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in VL respectively contain the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 19; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 109, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively include Containing the amino acid sequence of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 100; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively include DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 107, 108, 110, 112, 113, 114 or 115
  • the amino acid sequence of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in the DLL3-VL respectively includes the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 100.
  • the DLL3-HCDR1, DLL3-HCDR2, DLL3-HCDR3, DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 are defined according to Kabat, IMGT, Chothia, AbM or Contact numbering rules.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and the amino acid sequence comprising SEQ ID NO: 22 DLL3-HCDR3; and said DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, 71, 72 or 73, and comprising SEQ ID NO: 24, 71, 72 or 73.
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 26 or 84, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 27 or 85, and DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 28 or 83 DLL3-HCDR3 having the amino acid sequence; and said DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: DLL3-LCDR3 with an amino acid sequence of 31; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 32, 96, 97, 98 or 99, and DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: : DLL3-HCDR3 with the amino acid sequence of SEQ ID NO: 33; and the DLL3-VL has: DLL3-LCDR1 with the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 with the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR2 with the amino acid sequence of SEQ ID NO: 35 DLL3-LCDR3 of the amino acid sequence NO: 36; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 37, 117, 118, 119 or 120, and comprising SEQ ID NO : DLL3-HCDR3 with the amino acid sequence of SEQ ID NO: 38; and the DLL3-VL has: DLL3-LCDR1 with the amino acid sequence of SEQ ID NO: 39, DLL3-LCDR2 with the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR2 with the amino acid sequence of SEQ ID NO: 35 NO: 40 amino acid sequence of DLL3-LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21 and amino acid sequence comprising SEQ ID NO: 22 DLL3-HCDR3 of the amino acid sequence; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: DLL3-LCDR3 with an amino acid sequence of 25; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 69 or 70 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22 ; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, and DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 25 LCDR3;
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 72, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 73, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 72, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: containing SEQ ID NO: 23 DLL3-LCDR1 which contains the amino acid sequence of SEQ ID NO:73, DLL3-LCDR2 which contains the amino acid sequence of SEQ ID NO:73, and DLL3-LCDR3 which contains the amino acid sequence of SEQ ID NO:74.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 21, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 25 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 21, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 25 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 21, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 72, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 25 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 69, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 74 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 70, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 74 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 69, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 73, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 74 ;or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 70, and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22; and said DLL3-VL having: ammonia containing SEQ ID NO: 23 or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 69, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 25 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 70, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 25 .
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 26, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 85, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 26, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 27, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 84, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 27, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 84, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 85, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 ;or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 26, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 27, and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 28; and said DLL3-VL having: ammonia containing SEQ ID NO: 29 DLL3-LCDR1 containing the amino acid sequence of SEQ ID NO:30, DLL3-LCDR2 containing the amino acid sequence of SEQ ID NO:30, and DLL3-LCDR3 containing the amino acid sequence of SEQ ID NO:31.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 96, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 33; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 36 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 97, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 33; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 36 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 98, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 33; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 36 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 99, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 33; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 36 .
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 119, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 38; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 39, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 40 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 117, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 38; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 39, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 40 ;or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 118, and DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 38 the amino acid sequence of DLL3-HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 39, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 40 The amino acid sequence of DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 120, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 38; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 39, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 40 .
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 21, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 25 .
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22; and
  • the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 25.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 26, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 85, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 .
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 96, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 33; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 36 .
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 119, and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 38; and said DLL3-VL having: ammonia containing SEQ ID NO: 39 DLL3-LCDR1 containing the amino acid sequence of SEQ ID NO: 35, DLL3-LCDR2 containing the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 containing the amino acid sequence of SEQ ID NO: 40.
  • the antigen-binding molecule of any one of the preceding items are defined according to the Kabat numbering rule.
  • the antigen-binding molecule as described in any one of the preceding items is less than 4 ⁇ 10 -9 M, 3 ⁇ 10 -9 M, 2 ⁇ 10 -9 M, 1 ⁇ 10 -9 M, 9 ⁇ 10 -10 M, 8 ⁇ 10 -10 M, 7 ⁇ 10 -10 M, 6 ⁇ 10 -10 M, 5 ⁇ 10 -10 M, 4 ⁇ 10 -10 M, 3 ⁇ 10 -10 M, 2 KD of ⁇ 10 -10 M, 1 ⁇ 10 -10 M, 9 ⁇ 10 -11 M bound to human DLL3 as measured by surface plasmon resonance.
  • the antigen-binding molecule as described in any one of the preceding items wherein the DLL3-VH and DLL3-VL are humanized and comprise the FR region of a human antibody.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and the amino acid comprising SEQ ID NO: 22 DLL3-HCDR3 of the sequence, and the FR region of DLL3-VH includes a group selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A one or more amino acid substitutions in; and
  • the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, 71, 72 or 73, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 or 74
  • the amino acid sequence of DLL3-LCDR3, and the FR region of DLL3-VL includes one or more amino acid substitutions selected from the group consisting of 1N, 36L, 42K, 43S, 44F, 46G, 69A, 71Y, 79Q and 85D ;or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 26 or 84, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 27 or 85, and DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 28 or DLL3-HCDR3 with an amino acid sequence of 83; and
  • the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31, And the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 42G, 44V and 71Y; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 32, 96, 97, 98 or 99, and DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 32, 96, 97, 98 or 99.
  • DLL3-HCDR3 of the amino acid sequence of NO: 33, and the FR region of the DLL3-VH contains one or more amino acid substitutions selected from the group consisting of 1E, 24T, 44S, 71V and 73K; and
  • the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 36 or
  • the antigen-binding molecule as described in any one of the preceding items is less than 4 ⁇ 10 -9 M, 3 ⁇ 10 -9 M, 2 ⁇ 10 -9 M, 1 ⁇ 10 -9 at 25°C .
  • 9 M, 9 ⁇ 10 -10 M, 8 ⁇ 10 -10 M, 7 ⁇ 10 -10 M, 6 ⁇ 10 -10 M, 5 ⁇ 10 -10 M, 4 ⁇ 10 -10 M, 3 ⁇ 10 -10 M, 2 ⁇ 10 ⁇ 10 M, 1 ⁇ 10 ⁇ 10 M, 9 ⁇ 10 ⁇ 11 M bind human DLL3 with KD measured by surface plasmon resonance.
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22, and
  • the FR region of DLL3-VH includes one or more amino acids selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Substitute; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, and DLL3 comprising the amino acid sequence of SEQ ID NO: 25 -LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 1N
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 69 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22, and
  • the FR region of DLL3-VH includes one or more amino acids selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Substitute; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, and DLL3 comprising the amino acid sequence of SEQ ID NO: 25 -LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 1
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 70 and amino acid sequence comprising SEQ ID NO: 22 DLL3-HCDR3 of the amino acid sequence, and the FR region of the DLL3-VH includes a composition selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A one or more amino acid substitutions in the group; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24 DLL3-LCDR3 of the amino acid sequence of ID NO: 25, and the FR region of
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3, and the FR region of DLL3-VH includes one selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A or multiple amino acid substitutions; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and comprising SEQ ID NO: 25 DLL3-LCDR3 of the amino acid sequence, and the FR region of the DLL3-VL contains one or more amino acid substitutions selected from the group consist
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: DLL3-HCDR3 with an amino acid sequence of 22, and the FR region of the DLL3-VH includes a member selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A
  • the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 of the amino acid sequence of SEQ ID NO: 74, and the FR region
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3, and the FR region of DLL3-VH includes one selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A or multiple amino acid substitutions; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 72, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3 of the amino acid sequence, and the FR region of the DLL3-VL contains
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3, and the FR region of DLL3-VH includes one selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A or multiple amino acid substitutions; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 73, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74
  • the amino acid sequence of DLL3-LCDR3, and the FR region of DLL3-VL
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22, And the FR region of DLL3-VH includes one or more selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Amino acid substitution; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 DLL3-LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22, and
  • the FR region of DLL3-VH includes one or more amino acids selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Substitute; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, and DLL3 comprising the amino acid sequence of SEQ ID NO: 25 -LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 1N
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 21, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22, And the FR region of DLL3-VH includes one or more selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Amino acid substitution; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 72, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 DLL3-LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 1
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 69, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22, And the FR region of DLL3-VH includes one or more selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Amino acid substitution; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 70, and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22, And the FR region of DLL3-VH includes one or more selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Amino acid substitution; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 70, and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22, And the FR region of DLL3-VH includes one or more selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Amino acid substitution; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 DLL3-LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 26, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 27, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 , and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 42G, 44V and 71Y; or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 84, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 27, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 , and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 42G, 44V and 71Y; or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 84, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 85, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 , and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 42G, 44V and 71Y; or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 26, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 27, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 28; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 , and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 42G, 44V and 71Y.
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 96, and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 33, And the FR region of the DLL3-VH includes one or more amino acid substitutions selected from the group consisting of 1E, 24T, 44S, 71V and 73K; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 36 and the FR region of the DLL3-VL Comprises one or more amino acid substitutions selected from the group consisting of 1N, 9K, 43S, 68A and 85D.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 119, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 38, And the FR region of DLL3-VH includes a FR region selected from the group consisting of 1E, 3R, 5Q, 7F, 9P, 10V, 12V, 40S, 41H, 44S, 48I, 67A, 69L, 71V, 73K, 75S and 83T.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 52, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of F27Y, S30T, I69L, R71V, D73K and T93A in the FR region of SEQ ID NO: 52.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 62, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 62 selected from the group consisting of F36L, A43S, P44F, S46G, T69A, F71Y, and T85D.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 68, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 68 selected from the group consisting of Y36L, Q42K, L46G, T69A, F71Y, E79Q, and V85D.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 78, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 78.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 75, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of K42G, P44V, and F71Y in the FR region of SEQ ID NO:75.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 95, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of Q1E, A24T, R44S, R71V and T73K in the FR region of SEQ ID NO:95.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 88, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 88 selected from the group consisting of D1N, D9K, P43S, G68A, and V85D.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 116, or a variant thereof.
  • the variant is in the FR region of SEQ ID NO: 116 comprising a member selected from the group consisting of Q1E, Q3R, V5Q, S7F, A9P, E10V, K12V, A40S, P41H, R44S, M48I, V67A, I69L, R71V
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VL contains the amino acid sequence of SEQ ID NO: 100, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of D9K, P43S, G68A, and Y87H in the FR region of SEQ ID NO: 100.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 103, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of A43S, S60D, and Q100S in the FR region of SEQ ID NO: 103.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 56, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 56.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 57, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR-containing region of SEQ ID NO: 57.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 63, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 63; in some embodiments, the amino acid substitution is one selected from the group consisting of A43S and P44F or multiple amino acid substitutions.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 64, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 64; in some embodiments, the amino acid substitution is one selected from the group consisting of A43S and P44F or multiple amino acid substitutions.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 65, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 65; in some embodiments, the amino acid substitution is one selected from the group consisting of A43S and P44F or multiple amino acid substitutions.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 66, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 66; in some embodiments, the amino acid substitution is one selected from the group consisting of A43S and P44F or multiple amino acid substitutions.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 67, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 67.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 79, 80, 81 or 82, or a variant of SEQ ID NO: 79, 80, 81 or 82.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 79, 80, 81 or 82;
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 75, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of K42G, P44V, and F71Y in the FR region of SEQ ID NO:75.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 91, 92, 93 or 94, or a variant of SEQ ID NO: 91, 92, 93 or 94.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 91, 92, 93, or 94;
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 88, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 88 selected from the group consisting of D1N, D9K, P43S, G68A, and V85D.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 107, 108, 109 or 110, or a variant of SEQ ID NO: 107, 108, 109 or 110.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 107, 108, 109 or 110; in some embodiments, the amino acid substitutions are selected from V5Q, S7F One or more amino acid substitutions from the group consisting of , A9P, E10V, K12V, A40S, P41H, M48I, V67A, A75S and R83T.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 112, or a variant of SEQ ID NO: 112.
  • the variant comprises one or more amino acid substitutions in the FR region of SEQ ID NO: 112; in some embodiments, the amino acid substitutions are selected from V5Q, A9P, K12V, A40S, P41H One or more amino acid substitutions from the group consisting of , 4M8I, V67A and R83T.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 113, or a variant of SEQ ID NO: 113.
  • the variant comprises one or more amino acid substitutions in the FR region of SEQ ID NO: 113; in some embodiments, the amino acid substitutions are selected from V5Q, S7F, A9P, E10V, K12V One or more amino acid substitutions from the group consisting of , A40S, P41H, A75S and R83T.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 114, or a variant of SEQ ID NO: 114.
  • the variant comprises one or more amino acid substitutions in the FR region of SEQ ID NO: 114; in some embodiments, the amino acid substitutions are selected from V5Q, S7F, A9P, E10V, K12V One or more amino acid substitutions from the group consisting of , M48I, V67A, A75S and R83T.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 115, or a variant of SEQ ID NO: 115.
  • the variant comprises one or more amino acid substitutions in the FR region of SEQ ID NO: 115; in some embodiments, the amino acid substitutions are selected from V5Q, A9P, K12V, A40S, P41H One or more amino acid substitutions from the group consisting of , M48I and V67A.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VL contains the amino acid sequence of SEQ ID NO: 100, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of D9K, P43S, G68A, and Y87H in the FR region of SEQ ID NO: 100.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 14, 78, 79, 80, 81 or 82
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 15, 75, 76 or 77; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 18, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115 or 116
  • the DLL3-VL comprises SEQ ID NO: 19, 100, 101, 102, 103 or 104 amino acid sequence.
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 43, 44 or 45
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 58, 59 or 60; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 46, 48, 53, 54 or 55
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 61; or
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 78 or 79
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 75, 76 or 77; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 78, 79, 80, 81 or 82, and the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 77.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 89, 90, 91, 92, 93 or 94
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 86 or 87; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 95
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 87.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 105, 106, 107, 108, 109, 110 or 111
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 100, 101 or 102; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 112, 113, 114 or 115, and the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 100, 103 or 104; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 109
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 103.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 54
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 63;
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 54
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 61; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 54
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 64; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 56, and the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 65; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 56
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 66; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 56
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 67; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 57
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 65;
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 57
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 66; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 57
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 67; or
  • said DLL3-VH comprises the amino acid sequence of SEQ ID NO: 81
  • said DLL3-VL comprises the amino acid sequence of SEQ ID NO: 77; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 91
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 87; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 109
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 100.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 12
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 13;
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 14
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 15;
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 16
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 17;
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 18, and the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 19.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 54
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 63.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 54
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 61.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 81
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 77.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 91
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 87.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 109
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 100.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the CD3-VH comprises the amino acid sequence of SEQ ID NO: 136
  • the CD3-VL comprises the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the CD3-VH comprises the amino acid sequence of SEQ ID NO:138
  • the CD3-VL comprises the amino acid sequence of SEQ ID NO:137.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding module that specifically binds DLL3 or the antigen-binding module that specifically binds CD3 comprises a Titin chain and Obscurin capable of forming a dimer chain.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding module that specifically binds DLL3 comprises a Titin chain and an Obscurin chain capable of forming a dimer.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding module that specifically binds CD3 comprises a Titin chain and an Obscurin chain capable of forming a dimer.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the Titin chain comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 192 to SEQ ID NO: 210, and the Obscurin chain comprises an amino acid sequence selected from the group consisting of The amino acid sequence of the group consisting of SEQ ID NO: 211 to SEQ ID NO: 251.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the Obscurin chain comprises the amino acid sequence of SEQ ID NO: 246.
  • the antigen-binding molecule of any one of the preceding items wherein the Titin chain comprises the amino acid sequence of SEQ ID NO: 208, and the Obscurin chain comprises the amino acid sequence of SEQ ID NO: 246.
  • the antigen-binding molecule of any one of the preceding items wherein the antigen-binding molecule comprises a human IgG Fc region.
  • the antigen-binding molecule of any one of the preceding items wherein the antigen-binding molecule comprises a human IgG1 Fc region.
  • the antigen-binding molecule of any one of the preceding items wherein the antigen-binding molecule comprises an Fc region comprising one or more amino acid substitutions capable of reducing the binding of the Fc region to Fc ⁇ receptors.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an Fc region, the Fc region is a human IgG1 Fc region, and the amino acids at positions 234 and 235 are A, and the numbering basis is EU index.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an Fc region, the Fc region comprising a first subunit Fc1 and a second subunit Fc2 capable of associating with each other, so The Fc1 and Fc2 each independently have one or more amino acid substitutions that reduce homodimerization of the Fc region.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an Fc region, the Fc region comprising a first subunit Fc1 and a second subunit Fc2 capable of associating with each other, so
  • the Fc1 has a convex structure according to the pestle and mortar technology
  • the Fc2 has a pore structure according to the pestle and mortar technology.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an Fc region, the Fc region comprising a first subunit Fc1 and a second subunit Fc2 capable of associating with each other, so
  • the Fc1 has a convex structure according to the pestle and mortar technology
  • the Fc2 has a pore structure according to the pestle and mortar technology
  • the amino acid of the Fc1 at position 366 is W
  • the amino acid of Fc2 at position 366 is S
  • the amino acid at position 368 is S.
  • the amino acid is A, and the amino acid at position 407 is V, and the numbering basis is the EU index.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an Fc region, the Fc region comprising a first subunit Fc1 and a second subunit Fc2 capable of associating with each other, so
  • the Fc1 has a convex structure according to the pestle and mortar technology
  • the Fc2 has a pore structure according to the pestle and mortar technology, wherein the amino acid at the 354 position of the Fc1 is C and the amino acid at the 366 position is W; and the Fc2 is at 349
  • the amino acid at position 366 is S
  • the amino acid at position 368 is A
  • the amino acid at position 407 is V.
  • the numbering basis is the EU index.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an Fc region, the Fc region comprising a first subunit Fc1 and a second subunit Fc2 capable of associating with each other, wherein , the Fc1 includes the amino acid sequence of SEQ ID NO: 143; and the Fc2 includes the amino acid sequence of SEQ ID NO: 144.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an Fc region, the Fc region comprising a first subunit Fc1 and a second subunit Fc2 capable of associating with each other, wherein , the amino acid at position 349 of Fc1 is C, the amino acid at position 366 is W, and the amino acid at position 237 is A; and the amino acid at position 354 of Fc2 is C, the amino acid at position 366 is S, and the amino acid at position 368
  • the amino acid at position 407 is V and the amino acid at position 237 is A.
  • the numbering basis is the EU index.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an Fc region, the Fc region comprising a first subunit Fc1 and a second subunit Fc2 capable of associating with each other, wherein , the Fc1 includes the amino acid sequence of SEQ ID NO: 145; and the Fc2 includes the amino acid sequence of SEQ ID NO: 146.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an antigen-binding module that specifically binds DLL3 and an antigen-binding module that specifically binds CD3.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an antigen-binding module that specifically binds DLL3 and an antigen-binding module that specifically binds CD3, wherein:
  • the antigen-binding module that specifically binds DLL3 is Fab; the antigen-binding module that specifically binds CD3 is a replaced Fab, which contains a Titin chain and an Obscurin chain capable of forming dimers.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an antigen-binding module that specifically binds DLL3 and an antigen-binding module that specifically binds CD3, wherein:
  • the antigen-binding module that specifically binds to CD3 is a Fab
  • the antigen-binding module that specifically binds to DLL3 is a replaced Fab that includes a Titin chain and an Obscurin chain capable of forming dimers.
  • the antigen-binding molecule as described in any one of the preceding items includes a first chain having a structure represented by formula (a) and a second chain having a structure represented by formula (b) , a third chain having the structure shown in formula (c) and a fourth chain having the structure shown in formula (d),
  • linker 1 and the linker 2 are the same or different peptide linkers; the structures shown in formulas (a), (b), (c) and (d) are arranged from the N end to the C end. of. "/" means "or”, that is, Fc1 and Fc2 can interchange positions, and Titin chain and Obscurin chain can interchange positions.
  • the antigen-binding molecule as described in any one of the preceding items includes a first chain having a structure represented by formula (a) and a second chain having a structure represented by formula (b) , a third chain having the structure shown in formula (c) and a fourth chain having the structure shown in formula (d),
  • linker 1 and the linker 2 are the same or different peptide linkers; the structures shown in formulas (a), (b), (c) and (d) are arranged from the N end to the C end. ; Fc1 and Fc2 can interchange positions, and Titin chain and Obscurin chain can interchange positions.
  • the antigen-binding molecule as described in any one of the preceding items includes a first chain having a structure represented by formula (a) and a second chain having a structure represented by formula (b) , a third chain having the structure shown in formula (c) and a fourth chain having the structure shown in formula (d),
  • linker 1 and the linker 2 are the same or different peptide linkers; the structures shown in formulas (a), (b), (c) and (d) are arranged from the N end to the C end. of.
  • the antigen-binding molecule as described in any one of the preceding items, includes a first chain having a structure represented by formula (a'), a first chain having a structure represented by formula (b') Two strands, a third strand having the structure shown in formula (c') and a fourth strand having the structure shown in formula (d'),
  • the linker 1 and the linker 2 do not exist, that is, the linker 1 and the linker 2 are both peptide bonds; formulas (a'), (b'), (c') and ( The structure shown in d') is arranged from the N-terminus to the C-terminus.
  • "/" means "or”, that is, Fc1 and Fc2 can interchange positions, and Titin chain and Obscurin chain can interchange positions.
  • the antigen-binding molecule as described in any one of the preceding items, includes a first chain having a structure represented by formula (a'), a first chain having a structure represented by formula (b') Two strands, a third strand having the structure shown in formula (c') and a fourth strand having the structure shown in formula (d'),
  • the linker 1 and the linker 2 do not exist, that is, the linker 1 and the linker 2 are both peptide bonds; formulas (a'), (b'), (c') and ( The structure shown in d') is arranged from the N-terminus to the C-terminus; Fc1 and Fc2 are interchangeable, and the Titin chain and Obscurin chain are interchangeable.
  • the antigen-binding molecule as described in any one of the preceding items includes a first chain having a structure represented by formula (a) and a second chain having a structure represented by formula (b) , a third chain having the structure shown in formula (c) and a fourth chain having the structure shown in formula (d),
  • the linker 1 and the linker 2 do not exist, that is, the linker 1 and the linker 2 are both peptide bonds; the formulas (a), (b), (c) and (d) are The structure shown is arranged from the N-terminus to the C-terminus.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22; and
  • the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 25; and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22; and
  • the DLL3-VL has: DLL3-LCDR1 including the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 including the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 including the amino acid sequence of SEQ ID NO: 25; and
  • the CD3-VH has: CD3-HCDR1 including the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 including the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR3 including the amino acid sequence of SEQ ID NO: 131; and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 134 .
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22; and
  • the DLL3-VL has: DLL3-LCDR1 including the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 including the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 including the amino acid sequence of SEQ ID NO: 25; and
  • the CD3-VH includes the amino acid sequence of SEQ ID NO: 136
  • the CD3-VL includes the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 26, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 85, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 ;and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 96, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 33; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 36 ;and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 96, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 33; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 36 ;and
  • the CD3-VH has: CD3-HCDR1 including the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 including the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR3 including the amino acid sequence of SEQ ID NO: 131; and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 134 .
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 96, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 33; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 36 ;and
  • the CD3-VH has: CD3-HCDR1 including the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 including the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR3 including the amino acid sequence of SEQ ID NO: 135; and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 134 .
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 119, and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 38; and said DLL3-VL having: ammonia containing SEQ ID NO: 39 DLL3-LCDR1 having the amino acid sequence, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 40; and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 96, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 33; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 36 ;and
  • the CD3-VH has: CD3-HCDR1 including the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 including the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR3 including the amino acid sequence of SEQ ID NO: 131; and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 134 .
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 54, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 61; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138 sequence, and the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 54, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 63; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138 sequence, and the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 54, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 63; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136, And the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 81, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 77; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138 sequence, and the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 91, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 87; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138 sequence, and the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 109, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 100; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138 sequence, and the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 91, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 87; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136, And the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the Titin chain and Obscurin chain are any Titin chains in Table 3-1 and Table 3-2 of the present disclosure that can form dimers and Obscurin chain.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the Titin chain comprises the amino acid sequence of SEQ ID NO: 208.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the Obscurin chain comprises an amino acid sequence such as SEQ ID NO: 246.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the linker 1 and the linker 2 are both peptide linkers known in the art, as long as the antigen-binding molecule can exhibit the desired antigen binding active.
  • the peptide linker can be a flexible peptide having 1-50 or 3-20 amino acid residues.
  • the peptide linker is 3-15 amino acid residues in length.
  • the peptide linker 1 and linker 2 each independently have the structure (GGGGS)n, where n is 1, 2, or 3.
  • the sequences of the linker 1 and linker 2 are both GGGGS (SEQ ID NO: 147).
  • the antigen-binding molecule as described in any one of the preceding items, wherein the CH1 is the CH1 sequence of IgG. In some embodiments, the CH1 is CH1 of IgG1. In some embodiments, the CH1 comprises the amino acid sequence of SEQ ID NO: 141.
  • the antigen-binding molecule as described in any one of the preceding items wherein said CL is the light chain constant region of an antibody. In some embodiments, the antigen-binding molecule as described in any one of the preceding items, wherein the CL is the light chain constant region of a kappa chain or a lamada chain. In some embodiments, the CL comprises the amino acid sequence of SEQ ID NO: 142.
  • the antigen-binding molecule as described in any one of the preceding items wherein the antigen-binding molecule comprises an antigen-binding module that specifically binds DLL3 and an antigen-binding module that specifically binds CD3, and the antigen-binding module that specifically binds DLL3
  • the antigen-binding module is Fab; the antigen-binding module that specifically binds CD3 is scFv.
  • the antigen-binding molecule as described in any one of the preceding items, the antigen-binding molecule includes a first chain having a structure represented by formula (e) and a second chain having a structure represented by formula (f) and a third chain having the structure shown in formula (g),
  • linker 3 and the linker 4 are the same or different peptide linkers
  • the antigen-binding molecule as described in any one of the preceding items includes a first chain having a structure represented by formula (e) and a second chain having a structure represented by formula (f) and a third chain having the structure shown in formula (g),
  • linker 3 and the linker 4 are the same or different peptide linkers
  • the antigen-binding molecule as described in any one of the preceding items includes a first chain having a structure represented by formula (e) and a second chain having a structure represented by formula (f) and a third chain having the structure shown in formula (g),
  • linker 3 and the linker 4 are the same or different peptide linkers
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an antigen-binding module that specifically binds DLL3 and an antigen-binding module that specifically binds CD3, and the antigen-binding module that specifically binds DLL3
  • the antigen-binding module is scFv; the antigen-binding module that specifically binds CD3 is Fab.
  • the antigen-binding molecule as described in any one of the preceding items includes a first chain having a structure represented by formula (e'), a first chain having a structure represented by formula (f') Two strands and a third strand having the structure shown in formula (g'),
  • linker 3 and the linker 4 are the same or different peptide linkers
  • the antigen-binding molecule as described in any one of the preceding items includes a first chain having a structure represented by formula (e'), a first chain having a structure represented by formula (f') Two strands and a third strand having the structure shown in formula (g'),
  • linker 3 and the linker 4 are the same or different peptide linkers
  • the antigen-binding molecule as described in any one of the preceding items includes a first chain having a structure represented by formula (e'), a first chain having a structure represented by formula (f') Two strands and a third strand having the structure shown in formula (g'),
  • linker 3 and the linker 4 are the same or different peptide linkers
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22; and
  • the DLL3-VL has: DLL3-LCDR1 including the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 including the amino acid sequence of SEQ ID NO: 24, and DLL3-LCDR3 including the amino acid sequence of SEQ ID NO: 25; and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 26, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 85, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 ;and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 96, and DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 33 the amino acid sequence of DLL3-HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 36 The amino acid sequence of DLL3-LCDR3; and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 119, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 38; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 39, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 40 ;and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 96, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 33; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 36 ;and
  • the CD3-VH has: CD3-HCDR1 including the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 including the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR3 including the amino acid sequence of SEQ ID NO: 135; and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 134 .
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 54, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 61; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138 sequence, and the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 54, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 63; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138 sequence, and the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 91, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 87; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138 sequence, and the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 81, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 77; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138 sequence, and the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 109, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 100; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138 sequence, and the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 91, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 87; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 138, And the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the linker 3 and the linker 4 are both peptide linkers known in the art, as long as the antigen-binding molecule can exhibit the desired antigen binding active.
  • the peptide linker can be a flexible peptide having 1-50 or 3-20 amino acid residues.
  • the peptide linker is 3-15 amino acid residues in length.
  • the peptide linker 3 and linker 4 each independently have the structure of (GGGGS)n, where n is 1-5.
  • n is 1, 2, 3, or 4.
  • the sequence of the linker 3 is GGGGSGGGSGGGGS (SEQ ID NO: 148).
  • the sequence of linker 4 is GGGGS (SEQ ID NO: 147).
  • the antigen-binding molecule as described in any one of the preceding items, wherein the CH1 is the CH1 sequence of IgG. In some embodiments, the CH1 is CH1 of IgG1. In some embodiments, the CH1 comprises the amino acid sequence of SEQ ID NO: 141.
  • the antigen-binding molecule as described in any one of the preceding items wherein said CL is the light chain constant region of an antibody. In some embodiments, the antigen-binding molecule as described in any one of the preceding items, wherein the CL is the light chain constant region of a kappa chain or a lamada chain. In some embodiments, the CL comprises the amino acid sequence of SEQ ID NO: 142.
  • a first strand comprising the amino acid sequence of SEQ ID NO: 173, a second strand comprising the amino acid sequence of SEQ ID NO: 174 and a third strand comprising the amino acid sequence of SEQ ID NO: 160; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 173, a second strand comprising the amino acid sequence of SEQ ID NO: 174 and a third strand comprising the amino acid sequence of SEQ ID NO: 159; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 157, a second strand comprising the amino acid sequence of SEQ ID NO: 158 and a third strand comprising the amino acid sequence of SEQ ID NO: 159; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 157, a second strand comprising the amino acid sequence of SEQ ID NO: 158 and a third strand comprising the amino acid sequence of SEQ ID NO: 160; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 166, a second strand comprising the amino acid sequence of SEQ ID NO: 167 and a third strand comprising the amino acid sequence of SEQ ID NO: 159; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 166, a second strand comprising the amino acid sequence of SEQ ID NO: 167 and a third strand comprising the amino acid sequence of SEQ ID NO: 160; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 180, a second strand comprising the amino acid sequence of SEQ ID NO: 181 and a third strand comprising the amino acid sequence of SEQ ID NO: 159; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 180, a second strand comprising the amino acid sequence of SEQ ID NO: 181 and a third strand comprising the amino acid sequence of SEQ ID NO: 160.
  • a first strand comprising the amino acid sequence of SEQ ID NO: 173, a second strand comprising the amino acid sequence of SEQ ID NO: 174 and a third strand comprising the amino acid sequence of SEQ ID NO: 160.
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an antigen-binding module that specifically binds DLL3 and an antigen-binding module that specifically binds CD3,
  • the antigen-binding molecule includes a first chain having a structure represented by formula (h) and a second chain having a structure represented by formula (i),
  • linker 5, linker 6, linker 7 and linker 8 are the same or different peptide linkers
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an antigen-binding module that specifically binds DLL3 and an antigen-binding module that specifically binds CD3,
  • the antigen-binding molecule includes a first chain having a structure represented by formula (h) and a second chain having a structure represented by formula (i),
  • linker 5, linker 6, linker 7 and linker 8 are the same or different peptide linkers
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an antigen-binding module that specifically binds DLL3 and an antigen-binding module that specifically binds CD3,
  • the antigen-binding molecule includes a first chain having a structure represented by formula (h) and a second chain having a structure represented by formula (i),
  • linker 5, linker 6, linker 7 and linker 8 are the same or different peptide linkers
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an antigen-binding module that specifically binds DLL3 and an antigen-binding module that specifically binds CD3,
  • the antigen-binding molecule includes a first chain having a structure represented by formula (h') and a second chain having a structure represented by formula (i'),
  • linker 5, linker 6, linker 7 and linker 8 are the same or different peptide linkers
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an antigen-binding module that specifically binds DLL3 and an antigen-binding module that specifically binds CD3,
  • the antigen-binding molecule includes a first chain having a structure represented by formula (h') and a second chain having a structure represented by formula (i'),
  • linker 5, linker 6, linker 7 and linker 8 are the same or different peptide linkers
  • the antigen-binding molecule as described in any one of the preceding items, wherein the antigen-binding molecule comprises an antigen-binding module that specifically binds DLL3 and an antigen-binding module that specifically binds CD3,
  • the antigen-binding molecule includes a first chain having a structure represented by formula (h') and a second chain having a structure represented by formula (i'),
  • linker 5, linker 6, linker 7 and linker 8 are the same or different peptide linkers
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22; and
  • the DLL3-VL has: DLL3-LCDR1 including the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 including the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 including the amino acid sequence of SEQ ID NO: 25; and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22; and
  • the DLL3-VL has: DLL3-LCDR1 including the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 including the amino acid sequence of SEQ ID NO: 24, and DLL3-LCDR3 including the amino acid sequence of SEQ ID NO: 25; and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and comprising SEQ ID NO: 131 or 135 CD3-HCDR3 having the amino acid sequence; and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and comprising SEQ ID NO: 134 amino acid sequence of CD3-LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22; and
  • the DLL3-VL has: DLL3-LCDR1 including the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 including the amino acid sequence of SEQ ID NO: 72, and DLL3-LCDR3 including the amino acid sequence of SEQ ID NO: 25; and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 69 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22; and
  • the DLL3-VL has: DLL3-LCDR1 including the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 including the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 including the amino acid sequence of SEQ ID NO: 74; and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 70, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 74 ;and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3; and the CD3-VL has: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 69, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 73, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 74 ;and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 70, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 73, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 74 ;and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 69, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 25 ;and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 70, and DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 22 the amino acid sequence of DLL3-HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 The amino acid sequence of DLL3-LCDR3; and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 26, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 85, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 ;and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 96, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 33; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 36 ;and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 119, and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 38; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 39, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 40 ;and
  • the CD3-VH has: CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 131 or 135.
  • HCDR3 and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3 comprising the amino acid sequence of SEQ ID NO: 134 -LCDR3.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 96, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 33; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 36 ;and
  • the CD3-VH has: CD3-HCDR1 including the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 including the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR3 including the amino acid sequence of SEQ ID NO: 135; and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 134 .
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22; and
  • the DLL3-VL has: DLL3-LCDR1 including the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 including the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 including the amino acid sequence of SEQ ID NO: 25; and
  • the CD3-VH has: CD3-HCDR1 including the amino acid sequence of SEQ ID NO: 129, CD3-HCDR2 including the amino acid sequence of SEQ ID NO: 130, and CD3-HCDR3 including the amino acid sequence of SEQ ID NO: 131; and the CD3-VL having: CD3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 132, CD3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 133, and CD3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 134 .
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 54, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 61; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138 sequence, and the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 54, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 63; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138 sequence, and the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 54, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 64; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138, And the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 56, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 65; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138, And the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 56, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 66; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138, And the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 56, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 67; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138, And the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 57, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 65; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138, And the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 57, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 66; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138, And the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 57, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 67; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138, And the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 91, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 87; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138 sequence, and the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 81, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 77; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138 sequence, and the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 109, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 100; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136 or 138 sequence, and the CD3-VL contains the amino acid sequence of SEQ ID NO: 137.
  • the antigen-binding molecule of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 54, and the DLL3-VL includes the amino acid sequence of SEQ ID NO: 63; and the CD3-VH includes the amino acid sequence of SEQ ID NO: 136, and the CD3-VL contains the amino acid sequence of SEQ ID NO: 137;
  • the peptide linker can be a flexible peptide containing 1-50 or 3-20 amino acid residues.
  • the peptide linker is 1-15 amino acid residues in length.
  • the linker 5 has the structure of (GGGS)nGm, wherein n is 1-5, preferably 1, 2 or 3; m is 1-10, preferably 4, 5, 6, 7 or 8.
  • the sequence of linker 5 is GGGSGGGG (SEQ ID NO: 149).
  • the linker linker 6 and linker 8 have the structure of Gm, where m is 1-5, preferably 1, 2 or 3.
  • the sequence of linker 6 and linker 8 is G (SEQ ID NO: 150).
  • the linker 7 has the structure of (GGGGS)nGm, wherein n is 1-5, preferably 1, 2 or 3; m is 1-10, preferably 4, 5, 6, 7 or 8.
  • the sequence of linker 7 is GGGGSGGGG (SEQ ID NO: 151).
  • a first strand comprising the amino acid sequence of SEQ ID NO: 185 and a second strand comprising the amino acid sequence of SEQ ID NO: 162; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 161 and a second strand comprising the amino acid sequence of SEQ ID NO: 162; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 163 and a second strand comprising the amino acid sequence of SEQ ID NO: 162; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 259 and a second strand comprising the amino acid sequence of SEQ ID NO: 162; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 260 and a second strand comprising the amino acid sequence of SEQ ID NO: 162; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 168 and a second strand comprising the amino acid sequence of SEQ ID NO: 169; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 170 and a second strand comprising the amino acid sequence of SEQ ID NO: 169; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 175 and a second strand comprising the amino acid sequence of SEQ ID NO: 176; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 177 and a second strand comprising the amino acid sequence of SEQ ID NO: 176; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 182 and a second strand comprising the amino acid sequence of SEQ ID NO: 183; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 184 and a second strand comprising the amino acid sequence of SEQ ID NO: 183; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 186 and a second strand comprising the amino acid sequence of SEQ ID NO: 162; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 187 and a second strand comprising the amino acid sequence of SEQ ID NO: 188; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 187 and a second strand comprising the amino acid sequence of SEQ ID NO: 189; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 190 and a second strand comprising the amino acid sequence of SEQ ID NO: 188; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 190 and a second strand comprising the amino acid sequence of SEQ ID NO: 189; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 191 and a second strand comprising the amino acid sequence of SEQ ID NO: 188; or
  • a first strand comprising the amino acid sequence of SEQ ID NO: 191 and a second strand comprising the amino acid sequence of SEQ ID NO: 189.
  • a first strand comprising the amino acid sequence of SEQ ID NO: 185 and a second strand comprising the amino acid sequence of SEQ ID NO: 162.
  • the present disclosure also provides an anti-DLL3 antibody capable of specifically binding to DLL3, the anti-DLL3 antibody comprising a heavy chain variable region DLL3-VH and a light chain variable region DLL3-VL, wherein:
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 12, 56 or 57
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in the DLL3-VL respectively comprise the amino acids of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 13, 63, 64, 65, 66 or 67 sequence, or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 14, 79, 80, 81 or 82 Amino acid sequence
  • DLL3-LCDR1, DLL3-LCDR2 in the DLL3-VL and DLL3-LCDR3 comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively in SEQ ID NO: 15, or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 16, 91, 92, 93 or 94.
  • the amino acid sequence, and DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in the DLL3-VL respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 17, or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise DLL3-HCDR1
  • the amino acid sequences of DLL3-HCDR2 and DLL3-HCDR3, and DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in the DLL3-VL respectively comprise DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 19 amino acid sequence.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 12
  • the DLL3- DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in VL respectively contain the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 13, or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 54, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 64; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 54, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 63; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 56, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 65; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 56, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively include Containing the amino acid sequence of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 66; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 56, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 67; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 57, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 65; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 57, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 66; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 57, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 67; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 14, and the DLL3- DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in VL respectively contain the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 15, or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 81, and DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 77, or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 79, 80 or 82, and the DLL3 -DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in VL Comprising the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively in SEQ ID NO: 77; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 16
  • the DLL3- DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in VL respectively contain the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 17;
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 91, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 87; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 92, 93 or 94
  • the DLL3 - DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in VL respectively contain the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 87; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 18, and the DLL3- DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in VL respectively contain the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 19; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively comprise the amino acid sequences of DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 109, and the DLL3-VL in the DLL3-VL.
  • DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 respectively comprise the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 100; or
  • DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in the DLL3-VH respectively include DLL3-HCDR1, DLL3-HCDR2 and DLL3-HCDR3 in SEQ ID NO: 107, 108, 110, 112, 113, 114 or 115
  • the amino acid sequence of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in the DLL3-VL respectively includes the amino acid sequences of DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 in SEQ ID NO: 100.
  • the DLL3-HCDR1, DLL3-HCDR2, DLL3-HCDR3, DLL3-LCDR1, DLL3-LCDR2 and DLL3-LCDR3 are defined according to Kabat, IMGT, Chothia, AbM or Contact numbering rules.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 69 or 70 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22 ; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, and DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 25 LCDR3;
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 72, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 73, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 72, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 73, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 26 or 84, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 27 or 85, and DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 28 or 83 DLL3-HCDR3 having the amino acid sequence; and said DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: DLL3-LCDR3 with an amino acid sequence of 31; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 32, 96, 97, 98 or 99, and DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: : DLL3-HCDR3 with the amino acid sequence of SEQ ID NO: 33; and the DLL3-VL has: DLL3-LCDR1 with the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 with the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR2 with the amino acid sequence of SEQ ID NO: 35 DLL3-LCDR3 of the amino acid sequence NO: 36; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 37, 117, 118, 119 or 120, and comprising SEQ ID NO : DLL3-HCDR3 with the amino acid sequence of SEQ ID NO: 38; and the DLL3-VL has: DLL3-LCDR1 with the amino acid sequence of SEQ ID NO: 39, DLL3-LCDR2 with the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR2 with the amino acid sequence of SEQ ID NO: 35 NO: 40 amino acid sequence of DLL3-LCDR3.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 69 and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22 ; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, and DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 25 LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 70 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22; and
  • the DLL3-VL has: DLL3-LCDR1 including the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 including the amino acid sequence of SEQ ID NO: 24, and DLL3-LCDR3 including the amino acid sequence of SEQ ID NO: 25; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: containing SEQ ID NO: 23 or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 73, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 73, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 72, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 73, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, and DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 22 HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3 comprising the amino acid sequence of SEQ ID NO: 25 -LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22; and said DLL3-VL having: ammonia containing SEQ ID NO: 23 or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 21, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 72, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 25 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 69, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 74 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 70, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 74 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 69, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 73, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 74 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 70, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 73, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 74 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 69, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 25 ;or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 70, and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22; and said DLL3-VL having: ammonia containing SEQ ID NO: 23 or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 26, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 85, and DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 83 HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3 comprising the amino acid sequence of SEQ ID NO: 31 -LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 26, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 27, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 84, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 27, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 84, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 85, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 ;or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 26, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 27, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 28; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 ;or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 96, and DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 33 HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3 comprising the amino acid sequence of SEQ ID NO: 36 -LCDR3; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 119, and DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 38 HCDR3; and the DLL3-VL having: an ammonia compound containing SEQ ID NO: 39 DLL3-LCDR1 containing the amino acid sequence of SEQ ID NO: 35, DLL3-LCDR2 containing the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 containing the amino acid sequence of SEQ ID NO: 40.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 21, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 25 .
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22; and
  • the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 25.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 26, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 85, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 .
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 96, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 33; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 36 .
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 119, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 38; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 39, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 40 .
  • the anti-DLL3 antibody of any one of the preceding items are defined according to the Kabat numbering rule.
  • the anti-DLL3 antibody as described in any one of the preceding items which is less than 4 ⁇ 10 -9 M, 3 ⁇ 10 -9 M, 2 ⁇ 10 -9 M, 1 ⁇ 10 -9 at 25°C 9 M, 9 ⁇ 10 -10 M, 8 ⁇ 10 -10 M, 7 ⁇ 10 -10 M, 6 ⁇ 10 -10 M, 5 ⁇ 10 -10 M, 4 ⁇ 10 -10 M, 3 ⁇ 10 -10 M, 2 ⁇ 10 ⁇ 10 M, 1 ⁇ 10 ⁇ 10 M, 9 ⁇ 10 ⁇ 11 M bind human DLL3 with KD measured by surface plasmon resonance.
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and the amino acid comprising SEQ ID NO: 22 DLL3-HCDR3 of the sequence, and the FR region of DLL3-VH includes a group selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A one or more amino acid substitutions in; and
  • the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, 71, 72 or 73, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 or 74
  • the amino acid sequence of DLL3-LCDR3, and the FR region of DLL3-VL includes one or more amino acid substitutions selected from the group consisting of 1N, 36L, 42K, 43S, 44F, 46G, 69A, 71Y, 79Q and 85D ;or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 26 or 84, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 27 or 85, and DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 28 or DLL3-HCDR3 with an amino acid sequence of 83; and
  • the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31, And the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 42G, 44V and 71Y; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 32, 96, 97, 98 or 99, and DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 20 DLL3-HCDR3 of the amino acid sequence of NO: 33, and the FR region of the DLL3-VH contains one or more amino acid substitutions selected from the group consisting of 1E, 24T, 44S, 71V and 73K; and
  • the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 36, And the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 1N, 9K, 43S, 68A and 85D; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 37, 117, 118, 119 or 120, and SEQ ID NO. DLL3-HCDR3 of the amino acid sequence of NO: 38, and the FR region of DLL3-VH includes a component selected from the group consisting of 1E, 3R, 5Q, 7F, 9P, 10V, 12V, 40S, 41H, 44S, 48I, 67A, 69L, 71V One or more amino acid substitutions from the group consisting of , 73K, 75S and 83T; and
  • the DLL3-VL has: DLL3-LCDR1 including the amino acid sequence of SEQ ID NO: 39, DLL3-LCDR2 including the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 including the amino acid sequence of SEQ ID NO: 40; And the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 9K, 43S, 60D, 68A, 87H and 100S.
  • the antigen-binding molecule as described in any one of the preceding items is less than 4 ⁇ 10 -9 M, 3 ⁇ 10 -9 M, 2 ⁇ 10 -9 M, 1 ⁇ 10 -9 at 25°C .
  • 9 M, 9 ⁇ 10 -10 M, 8 ⁇ 10 -10 M, 7 ⁇ 10 -10 M, 6 ⁇ 10 -10 M, 5 ⁇ 10 -10 M, 4 ⁇ 10 -10 M, 3 ⁇ 10 -10 M, 2 ⁇ 10 ⁇ 10 M, 1 ⁇ 10 ⁇ 10 M, 9 ⁇ 10 ⁇ 11 M bind human DLL3 with KD measured by surface plasmon resonance.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22, and
  • the FR region of DLL3-VH includes one or more amino acids selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Substitute; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, and DLL3 comprising the amino acid sequence of SEQ ID NO: 25 -LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 1N
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 69 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22, and
  • the FR region of DLL3-VH includes one or more amino acids selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Substitute; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, and DLL3 comprising the amino acid sequence of SEQ ID NO: 25 -LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 1
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 70 and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22, and
  • the FR region of DLL3-VH includes one or more amino acids selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Substitution; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, and DLL3 comprising the amino acid sequence of SEQ ID NO: 25 -LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 1N, 36
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3, and the FR region of DLL3-VH includes one selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A or multiple amino acid substitutions; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and comprising SEQ ID NO: 25 DLL3-LCDR3 of the amino acid sequence, and the FR region of the DLL3-VL contains one or more amino acid substitutions selected from the group consist
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3, and the FR region of DLL3-VH includes one selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A or multiple amino acid substitutions; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 72, and comprising SEQ ID NO: 25 DLL3-LCDR3 of the amino acid sequence, and the FR region of the DLL3-VL contains one or more amino acid substitutions selected from the group consisting
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3, and the FR region of DLL3-VH includes one selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A or multiple amino acid substitutions; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 73, and comprising SEQ ID NO: 25 DLL3-LCDR3 of the amino acid sequence, and the FR region of the DLL3-VL contains one or more amino acid substitutions selected from the group consist
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3, and the FR region of DLL3-VH includes one selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A or multiple amino acid substitutions; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3 of the amino acid sequence, and the FR region of the DLL3-VL
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3, and the FR region of DLL3-VH includes one selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A or multiple amino acid substitutions; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 72, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3 of the amino acid sequence, and the FR region of the DLL3-VL contains
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3, and the FR region of DLL3-VH includes one selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A or multiple amino acid substitutions; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 73, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74
  • the amino acid sequence of DLL3-LCDR3, and the FR region of DLL3-VL
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 21, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22, And the FR region of DLL3-VH includes one or more selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Amino acid substitution; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 DLL3-LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22, And the FR region of DLL3-VH includes one or more selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Amino acid substitution; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 72, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 DLL3-LCDR3, and the DLL3-VL FR
  • the region contains one or more amino acid substitutions selected from the
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 69, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22, And the FR region of DLL3-VH includes one or more selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Amino acid substitution; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 70, and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22, And the FR region of DLL3-VH includes one or more selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Amino acid substitution; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 69, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22, And the FR region of DLL3-VH includes one or more selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Amino acid substitution; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 73, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 70, and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22, And the FR region of DLL3-VH includes one or more selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Amino acid substitution; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 73, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 74 DLL3-LCDR3, and the DLL3-VL FR
  • the region contains one or more amino acid substitutions
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 69, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 22, And the FR region of DLL3-VH includes one or more selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Amino acid substitution; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 DLL3-LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consist
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 70, and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 22, And the FR region of DLL3-VH includes one or more selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A Amino acid substitution; and the DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 71, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 25 DLL3-LCDR3, and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 26, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 85, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 , and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 42G, 44V and 71Y; or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 26, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 27, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 83; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 , and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 42G, 44V and 71Y; or
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 84, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 85, and DLL3-HCDR3 comprising the amino acid sequence of SEQ ID NO: 83; and said DLL3-VL having: ammonia containing SEQ ID NO: 29
  • the DLL3-LCDR1 of the amino acid sequence, the DLL3-LCDR2 of the amino acid sequence of SEQ ID NO:30, and the DLL3-LCDR3 of the amino acid sequence of SEQ ID NO:31, and the FR region of the DLL3-VL includes a polypeptide selected from the group consisting of 42G One or more amino acid substitutions in the group consisting of , 44V and 71Y; or
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 26, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 27, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 28; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 29, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 30, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 31 , and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 42G, 44V and 71Y.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 96, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 33, And the FR region of the DLL3-VH comprises one or more amino acid substitutions selected from the group consisting of 1E, 24T, 44S, 71V and 73K; and the DLL3-VL has: the amino acid sequence comprising SEQ ID NO: 34 DLL3-LCDR1, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR3 comprising the amino acid sequence of SEQ ID NO: 36 and the FR region of the DLL3-VL comprising 1N, 9K, 43S One or more amino acid substitutions in the group consisting of , 68A and 85D.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH has: DLL3-HCDR1 including the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 including the amino acid sequence of SEQ ID NO: 119, and DLL3-HCDR3 including the amino acid sequence of SEQ ID NO: 38, And the FR region of DLL3-VH includes a FR region selected from the group consisting of 1E, 3R, 5Q, 7F, 9P, 10V, 12V, 40S, 41H, 44S, 48I, 67A, 69L, 71V, 73K, 75S and 83T.
  • DLL3-VL has: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 39, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and comprising SEQ ID NO: 40
  • the amino acid sequence of DLL3-LCDR3 and the FR region of DLL3-VL contains one or more amino acid substitutions selected from the group consisting of 9K, 43S, 60D, 68A, 87H and 100S.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 50, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of Q1E, Q43K, M48I, V67A, I69L, R71V, T73K, and S76N in the FR region of SEQ ID NO:50.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 51, or a variant thereof.
  • the variant is in the FR region of SEQ ID NO: 51 comprising one or more amino acids selected from the group consisting of Q1E, 5Q, R38K, V68A, F69L, L71V, T73K, V75S and S76N replace.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 52, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of F27Y, S30T, I69L, R71V, D73K and T93A in the FR region of SEQ ID NO: 52.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 62, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 62 selected from the group consisting of F36L, A43S, P44F, S46G, T69A, F71Y, and T85D.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 68, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 68 selected from the group consisting of Y36L, Q42K, L46G, T69A, F71Y, E79Q, and V85D.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 78, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 78.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 75, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of K42G, P44V, and F71Y in the FR region of SEQ ID NO:75.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 95, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of Q1E, A24T, R44S, R71V and T73K in the FR region of SEQ ID NO:95.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 88, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 88 selected from the group consisting of D1N, D9K, P43S, G68A, and V85D.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 116, or a variant thereof.
  • the variant is in the FR region of SEQ ID NO: 116 comprising a member selected from the group consisting of Q1E, Q3R, V5Q, S7F, A9P, E10V, K12V, A40S, P41H, R44S, M48I, V67A, I69L, R71V
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 100, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 100 selected from the group consisting of D9K, P43S, G68A, and Y87H.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 103, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of A43S, S60D, and Q100S in the FR region of SEQ ID NO: 103.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 56, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 56.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH includes the amino acid sequence of SEQ ID NO: 57, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR-containing region of SEQ ID NO: 57.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 63, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 63; in some embodiments, the amino acid substitution is one selected from the group consisting of A43S and P44F or multiple amino acid substitutions.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 64, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 64; in some embodiments, the amino acid substitution is one selected from the group consisting of A43S and P44F or multiple amino acid substitutions.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 65, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 65; in some embodiments, the amino acid substitution is one selected from the group consisting of A43S and P44F or multiple amino acid substitutions.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 66, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 66; in some embodiments, the amino acid substitution is one selected from the group consisting of A43S and P44F or multiple amino acid substitutions.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 67, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 67.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 79, 80, 81 or 82, or a variant of SEQ ID NO: 79, 80, 81 or 82.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 79, 80, 81 or 82;
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 75, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of K42G, P44V, and F71Y in the FR region of SEQ ID NO:75.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 91, 92, 93 or 94, or a variant of SEQ ID NO: 91, 92, 93 or 94.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 91, 92, 93, or 94;
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 88, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 88 selected from the group consisting of D1N, D9K, P43S, G68A, and V85D.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 107, 108, 109 or 110, or a variant of SEQ ID NO: 107, 108, 109 or 110.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 107, 108, 109 or 110; in some embodiments, the amino acid substitutions are selected from V5Q, S7F One or more amino acid substitutions from the group consisting of , A9P, E10V, K12V, A40S, P41H, M48I, V67A, A75S and R83T.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 112, or a variant of SEQ ID NO: 112.
  • the variant comprises one or more amino acid substitutions in the FR region of SEQ ID NO: 112; in some embodiments, the amino acid substitutions are selected from V5Q, A9P, K12V, A40S, P41H One or more amino acid substitutions from the group consisting of , 4M8I, V67A and R83T.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 113, or a variant of SEQ ID NO: 113.
  • the variant comprises one or more amino acid substitutions in the FR region of SEQ ID NO: 113; in some embodiments, the amino acid substitutions are selected from V5Q, S7F, A9P, E10V, K12V One or more amino acid substitutions from the group consisting of , A40S, P41H, A75S and R83T.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 114, or a variant of SEQ ID NO: 114.
  • the variant comprises one or more amino acid substitutions in the FR region of SEQ ID NO: 114; in some embodiments, the amino acid substitutions are selected from V5Q, S7F, A9P, E10V, K12V One or more amino acid substitutions from the group consisting of , M48I, V67A, A75S and R83T.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 115, or a variant of SEQ ID NO: 115.
  • the variant comprises one or more amino acid substitutions in the FR region of SEQ ID NO: 115; in some embodiments, the amino acid substitutions are selected from V5Q, A9P, K12V, A40S, P41H One or more amino acid substitutions from the group consisting of , M48I and V67A.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VL contains the amino acid sequence of SEQ ID NO: 100, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of D9K, P43S, G68A, and Y87H in the FR region of SEQ ID NO: 100.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VL includes the amino acid sequence of SEQ ID NO: 103, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of A43S, S60D, and Q100S in the FR region of SEQ ID NO: 103.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56 or 57, and the DLL3- VL contains the amino acid sequence of SEQ ID NO: 63, 64, 65, 66 or 67; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 56 or 57
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 58, 59, 60, 61, 62, 63, 64, 65, 66, 67 or 68 amino acid sequence; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 78, 79, 80, 81 or 82
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 75, 76 or 77; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 89, 90, 91, 92, 93, 94 or 95
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 86, 87 or 88; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115 or 116
  • the DLL3-VL comprises SEQ ID NO: The amino acid sequence of 100, 101, 102, 103 or 104.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 43, 44 or 45
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 58, 59 or 60; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 47, 48, 49, 53, 54 or 55
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 59; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 43, 44 or 45
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 60; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 46, 48, 53, 54 or 55
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 61; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 54
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 63 or 64; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 56 or 57
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 65, 66 or 67.
  • an anti-DLL3 antibody as any of the preceding items, wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 78 or 79
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 75, 76 or 77; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 78, 79, 80, 81 or 82, and the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 77.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 89, 90, 91, 92, 93 or 94
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 86 or 87; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 95
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 87.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 105, 106, 107, 108, 109, 110 or 111
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 100, 101 or 102; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 112, 113, 114 or 115, and the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 100, 103 or 104; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 109
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 103.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 54
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 63;
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 54
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 61; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 54
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 64; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 56, and the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 65; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 56
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 66; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 56
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 67; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 57
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 65;
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 57
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 66; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 57
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 67; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 81
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 77; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 91
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 87; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 109
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 100.
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 12
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 13;
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 14
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 15;
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 16
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 17;
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 18, and the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 19.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 54
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 63; or
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 54
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 61.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 81
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 77.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO: 91
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO: 87.
  • the anti-DLL3 antibody of any one of the preceding items wherein:
  • the DLL3-VH comprises the amino acid sequence of SEQ ID NO:109
  • the DLL3-VL comprises the amino acid sequence of SEQ ID NO:100.
  • the anti-DLL3 antibody as described in any one of the preceding items, wherein the antibody fragment is Fab, Fab', F(ab')2, Fd, Fv, scFv, dsFv or dAb.
  • the anti-DLL3 antibody as described in any one of the preceding items, wherein the anti-DLL3 antibody comprises a heavy chain constant region and a light chain constant region.
  • the anti-DLL3 antibody of any one of the preceding items wherein the heavy chain constant region is that of a human IgG.
  • the anti-DLL3 antibody of any one of the preceding items wherein the light chain constant region is that of a human kappa or lambda.
  • the anti-DLL3 antibody of any one of the preceding items wherein the light chain constant region is that of human kappa.
  • the anti-DLL3 antibody as described in any one of the preceding items wherein the heavy chain constant region comprises an amino acid sequence such as SEQ ID NO: 41.
  • the anti-DLL3 antibody as described in any one of the preceding items wherein the light chain constant region comprises an amino acid sequence such as SEQ ID NO: 42.
  • the anti-DLL3 antibody as described in any one of the preceding items, wherein the anti-DLL3 antibody comprises a heavy chain and a light chain, wherein:
  • the heavy chain comprises at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97 %, 98%, 99% sequence identity to an amino acid sequence
  • the light chain comprises an amino acid sequence having at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92% identity with SEQ ID NO: 122 or
  • the heavy chain comprises at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97 %, 98%, 99% sequence identity to an amino acid sequence
  • the light chain comprises an amino acid sequence having at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92% identity with SEQ ID NO: 124 or
  • the heavy chain comprises at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97 %, 98%, 99% sequence identity to an amino acid sequence, and the light chain comprises at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92% to SEQ ID NO: 126 or
  • the heavy chain includes at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97 %, 98%, 99% sequence identity to an amino acid sequence
  • the light chain comprises an amino acid sequence having at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92% identity with SEQ ID NO: 128 %, 93%, 94%, 95%, 96%, 97%, 98%, 99% identical amino acid sequences.
  • the anti-DLL3 antibody as described in any one of the preceding items, wherein the anti-DLL3 antibody comprises a heavy chain and a light chain, wherein:
  • the heavy chain comprises the amino acid sequence of SEQ ID NO: 121, and the light chain comprises the amino acid sequence of SEQ ID NO: 122; or
  • the heavy chain includes the amino acid sequence of SEQ ID NO: 123, and the light chain includes the amino acid sequence of SEQ ID NO: 124;
  • the heavy chain comprises the amino acid sequence of SEQ ID NO: 125, and the light chain comprises the amino acid sequence of SEQ ID NO: 126; or
  • the heavy chain includes the amino acid sequence of SEQ ID NO: 127, and the light chain includes the amino acid sequence of SEQ ID NO: 128.
  • the anti-DLL3 antibody as described in any one of the preceding items, wherein the anti-DLL3 antibody comprises a heavy chain and a light chain, wherein the heavy chain comprises the amino acid sequence of SEQ ID NO: 121, and the The light chain contains the amino acid sequence of SEQ ID NO: 122.
  • the anti-DLL3 antibody as described in any one of the preceding items, wherein the anti-DLL3 antibody comprises a heavy chain and a light chain, wherein the heavy chain comprises the amino acid sequence of SEQ ID NO: 125, and the The light chain contains the amino acid sequence of SEQ ID NO: 126.
  • the anti-DLL3 antibody of any one of the preceding items wherein the anti-DLL3 antibody is a bispecific antibody.
  • the anti-DLL3 antibody as described in any one of the preceding items, wherein the anti-DLL3 antibody is a bispecific antibody, and the bispecific antibody specifically binds DLL3 and CD3.
  • the present disclosure provides a pharmaceutical composition, which contains: a therapeutically effective amount of the antigen-binding molecule of any of the foregoing or the anti-DLL3 antibody of any of the foregoing, and one or more A pharmaceutically acceptable carrier, diluent, buffer or excipient.
  • the pharmaceutical composition further includes at least one second therapeutic agent.
  • the second therapeutic agent is any agent that is advantageously combined with a CD3/DLL3 bispecific antigen binding molecule.
  • the second therapeutic agent is an antibody capable of specifically binding CD28.
  • the second therapeutic agent is a bispecific antibody capable of specifically binding CD28 and a tumor cell surface antigen (TAA).
  • TAA tumor cell surface antigen
  • the second therapeutic agent is a bispecific antibody capable of specifically binding to CD28 and DLL3.
  • the present disclosure also provides an isolated nucleic acid encoding the antigen-binding molecule of any of the foregoing or the anti-DLL3 antibody of any of the foregoing.
  • the present disclosure also provides a vector comprising the aforementioned isolated nucleic acid.
  • the present disclosure also provides a host cell comprising the aforementioned isolated nucleic acid or vector.
  • the present disclosure also provides a method of treating tumors or cancer, the method comprising administering to a subject a therapeutically effective amount of the antigen-binding molecule of any one of the foregoing or the antibody of any of the foregoing.
  • DLL3 antibody or pharmaceutical composition as described in the preceding item.
  • the present disclosure also provides the use of the antigen-binding molecule of any of the foregoing, the antibody of any of the foregoing, or the pharmaceutical composition of any of the foregoing in the preparation of a drug for treating tumors or cancer. .
  • the present disclosure also provides the antigen-binding molecule according to any one of the foregoing items or the anti-DLL3 antibody according to any one of the foregoing items or the pharmaceutical composition according to any one of the foregoing items for use as a medicament.
  • the drug is used to treat tumors or cancer.
  • the tumor or cancer of any one of the preceding items is selected from: head and neck squamous cell carcinoma, head and neck cancer, brain cancer, glioma, glioblastoma multiforme, neuroblastoma Blastoma, central nervous system cancer, neuroendocrine tumors, laryngeal cancer, pharyngeal squamous cell carcinoma, oral squamous cell carcinoma, nasopharyngeal cancer, esophageal cancer, thyroid cancer, malignant pleural mesothelioma, lung cancer, breast cancer, liver cancer, hepatobiliary cancer, Pancreatic cancer, stomach cancer, gastrointestinal cancer, intestinal cancer, colon cancer, colorectal cancer, kidney cancer, clear cell renal cell carcinoma, ovarian cancer, endometrial cancer, cervical cancer, bladder cancer, prostate cancer, testicular cancer, Skin cancer, melanoma, large cell lung cancer, triple negative breast cancer, lymphoma, and small cell lung cancer.
  • the tumor or cancer as described above is a DLL3-expressing cancer.
  • the tumor or cancer as described above is a solid tumor.
  • the tumor or cancer as described above is lung cancer.
  • the tumor or cancer as described above is small cell lung cancer.
  • the method of treating a tumor or cancer is as described above, further comprising using a second therapeutic agent.
  • the second therapeutic agent includes an antineoplastic agent, radiation therapy, an antibody drug conjugate, a bispecific antibody, a bispecific antibody conjugated to an antineoplastic agent, an immune checkpoint inhibitor, or the like. combination.
  • the second therapeutic agent is any agent that is advantageously combined with a CD3/DLL3 bispecific antigen-binding molecule.
  • the second therapeutic agent is an antibody capable of specifically binding CD28.
  • the second therapeutic agent is a bispecific antibody capable of specifically binding CD28 and a tumor cell surface antigen (TAA).
  • TAA tumor cell surface antigen
  • the second therapeutic agent is a bispecific antibody capable of specifically binding to CD28 and DLL3.
  • the second therapeutic agent and the antigen-binding molecule of any one of the present disclosure are administered simultaneously, sequentially, or separately.
  • the antigen-binding molecules provided by the present disclosure have the characteristics of good therapeutic activity, safety, pharmacokinetic properties and druggability (such as stability).
  • Figure 1A shows a schematic structural diagram of Format1 of DLL3-CD3 bispecific antibody, where Ob represents Obscurin.
  • Figure 1B shows a schematic structural diagram of Format2 of DLL3-CD3 bispecific antibody.
  • Figure 1C shows a schematic structural diagram of Format3 of DLL3-CD3 bispecific antibody.
  • Figure 2A shows the experimental results of bispecific antibody binding to DLL1. The results show that the DLL3-CD3 bispecific antibodies of the present disclosure do not bind to DLL1.
  • Figure 2B shows the experimental results of bispecific antibody binding to DLL4. The results show that the DLL3-CD3 bispecific antibodies of the present disclosure do not bind to DLL4.
  • FIG 3 shows the experimental results of the killing effect of bispecific antibodies on cells. The results show that the bispecific antibodies disclosed herein have no killing effect on H460 cells that do not express DLL3.
  • FIG. 4A shows the experimental results of T cell activation by bispecific antibodies. The results show that the bispecific antibodies of the present disclosure have an obvious effect on activating T cells in the presence of DLL3/H82 cells expressing DLL3.
  • Figure 4B shows that bispecific antibodies of the present disclosure do not activate T cells in the presence of H460, a negative cell that does not express DLL3.
  • Figure 5A shows experimental results of cytokine release by bispecific antibodies. The results show that in the presence of H1184 cells, the bispecific antibodies of the present disclosure stimulate PBMC cells to secrete IFN ⁇ at very low levels.
  • Figure 5B shows that in the presence of H1184 cells, the bispecific antibodies of the present disclosure stimulated very low IL-6 secretion by PBMC cells.
  • CD3 and CD3 fragments are used unless specified as being from a non-human species (e.g., “mouse CD3”, “mouse CD3 fragment”, “monkey CD3”, “monkey CD3 fragment”, etc.) Refers to the well-known human CD3 protein or its fragments.
  • amino acid refers to naturally occurring and synthetic amino acids, as well as amino acid analogs and amino acid mimetics that function in a manner similar to naturally occurring amino acids.
  • Naturally occurring amino acids are those encoded by the genetic code, as well as those that are later modified, such as hydroxyproline, gamma-carboxyglutamic acid, and O-phosphoserine.
  • Amino acid analogs refer to compounds that have the same basic chemical structure (i.e., alpha carbon bonded to hydrogen, carboxyl, amino, and R groups) as naturally occurring amino acids, such as homoserine, norleucine, methionine sulfoxide , methionine methyl sulfonium.
  • Such analogs have modified R groups (eg, norleucine) or modified peptide backbones but retain the same basic chemical structure as the naturally occurring amino acid.
  • Amino acid mimetics refer to chemical compounds that have a structure that differs from the general chemical structure of amino acids, but act in a manner similar to naturally occurring amino acids.
  • amino acid mutation includes amino acid substitutions, deletions, insertions and modifications. Any combination of substitutions, deletions, insertions and modifications can be made to achieve the final construct, as long as the final construct possesses the desired properties, such as reduction or binding to Fc receptors.
  • Amino acid sequence deletions and insertions include deletions and insertions at the amino terminus and/or carboxyl terminus of the polypeptide chain.
  • Specific amino acid mutations may be amino acid substitutions.
  • the amino acid mutation is a non-conservative amino acid substitution, ie, one amino acid is replaced by another amino acid with different structural and/or chemical properties.
  • Amino acid substitutions include substitutions by non-naturally occurring amino acids or by derivatives of the 20 natural amino acids (e.g., 4-hydroxyproline, 3-methylhistidine, ornithine, homoserine, 5-hydroxylysine) .
  • Amino acid mutations can be generated using genetic or chemical methods well known in the art. Genetic methods can include site-directed mutagenesis, PCR, gene synthesis, etc. It is expected that methods other than genetic engineering to alter amino acid side chain groups, such as chemical modification, may also be available. Various names may be used herein to refer to the same amino acid mutation.
  • the amino acid residue at a specific position can be represented by position + amino acid residue.
  • 366W means that the amino acid residue at position 366 is W.
  • T366W means that the amino acid residue at position 366 has been mutated from the original T to W.
  • antigen-binding molecule is used in the broadest sense and covers a variety of molecules that specifically bind to antigens, including but not limited to antibodies, other polypeptides with antigen-binding activity, and antibody fusion proteins formed by the fusion of the two, as long as they exhibit the desired Antigen-binding activity.
  • the antigen-binding molecules herein comprise a variable region (VH) and a variable region (VL), which together constitute an antigen-binding domain.
  • VH variable region
  • VL variable region
  • the antigen-binding molecule herein is a bispecific antigen-binding molecule (eg, bispecific antibody).
  • antibody is used in the broadest sense and encompasses a variety of antibody structures including, but not limited to, monoclonal antibodies, polyclonal antibodies; monospecific antibodies, multispecific antibodies (e.g., bispecific antibodies), full-length antibodies, and antibodies Fragments (or antigen-binding fragments, or antibody fragments, or antigen-binding portions) as long as they exhibit the desired antigen-binding activity. Depending on the context, the skilled person will be able to determine what exactly is meant by "antibody”.
  • “Native antibodies” refer to naturally occurring immunoglobulin molecules.
  • natural IgG antibodies are heterotetrameric proteins of approximately 150,000 daltons, composed of two light chains and two heavy chains bonded by disulfide bonds. From N to C-terminus, each heavy chain has a variable region (VH, also known as variable heavy domain, heavy chain variable region), followed by three constant domains (CH1, CH2, and CH3).
  • VH variable heavy domain
  • CH2 variable heavy domain variable region
  • CL constant light domain
  • full-length antibody “intact antibody” and “whole antibody” are used interchangeably herein to refer to an antibody that has a structure substantially similar to that of a native antibody or that has a heavy chain containing an Fc region as defined herein.
  • bispecific antibody refers to an antibody (including antibodies or antigen-binding fragments thereof, such as single-chain antibodies) that can specifically bind to two different antigens or at least two different epitopes of the same antigen.
  • Bispecific antibodies of various structures have been disclosed in the prior art. According to the integrity of the IgG molecule, they can be divided into IgG-like bispecific antibodies and antibody fragment type bispecific antibodies. According to the number of antigen-binding regions, they can be divided into two types. Bispecific antibodies with valent, trivalent, tetravalent or more valence can be divided into symmetric structure bispecific antibodies and asymmetric structure bispecific antibodies according to whether the structure is symmetrical or not.
  • bispecific antibodies based on antibody fragments such as Fab fragments lacking Fc fragments, which form bispecific antibodies by combining 2 or more Fab fragments in one molecule, have lower immunogenicity, and It has small molecular weight and high tumor tissue penetration.
  • Typical antibody structures of this type include bispecific antibodies such as F(ab)2, scFv-Fab, (scFv)2-Fab, etc.; IgG-like bispecific antibodies (such as With Fc fragment), this type of antibody has a relatively large molecular weight.
  • the Fc fragment helps in the later purification of the antibody and improves its solubility and stability.
  • the Fc part may also bind to the receptor FcRn, increasing the serum half-life of the antibody.
  • Bispecific antibody structural models such as KiH, CrossMAb, Triomab quadroma, Fc ⁇ Adp, ART-Ig, BiMAb, Biclonics, BEAT, DuoBody, Azymetric, XmAb, 2:1TCBs, 1Fab-IgG TDB, FynomAb, two-in-one/DAF , scFv-Fab-IgG, DART-Fc, LP-DART, CODV-Fab-TL, HLE-BiTE, F(ab)2-CrossMAb, IgG-(scFv)2, Bs4Ab, DVD-Ig, Tetravalent-DART- Fc, (scFv)4-Fc, CODV-Ig, mAb2, F(ab)4-CrossMAb and other bispecific antibodies (see Aran F. Labrijn et al., Nature Reviews Drug Discovery volume 18, pages 585–608 (2019); Chen S1 et al., J Immunol
  • variable region refers to the domain of an antigen-binding molecule that binds the antigen.
  • the heavy chain variable region in the antigen-binding module that specifically binds to CD3 is labeled CD3-VH
  • the light chain variable region is labeled CD3-VL
  • the heavy chain variable region in the antigen-binding module that specifically binds to CD3 It is labeled CD3-VH
  • the light chain variable region is labeled CD3-VL.
  • VH and VL each contain four conserved framework regions (FR) and three complementarity determining regions (CDR).
  • CD3-VH The three CDR regions in CD3-VH are labeled CD3-HCDR1, CD3-HCDR2 and CD3-HCDR3; the three CDR regions in CD3-VL are labeled CD3-LCDR1, CD3-LCDR2 and CD3-LCDR3 respectively.
  • Each VH and VL from N end to C end are: FR1, CDR1, FR2, CDR2, FR3, CDR3, FR4.
  • a single VH or VL may be sufficient to confer antigen binding specificity.
  • the amino acid sequence boundaries of CDRs can be determined by various well-known schemes, such as: “Kabat” numbering rule (see Kabat et al. (1991), “Sequences of Proteins of Immunological Interest", 5th edition, Public Health Service, National Institutes of Health , Bethesda, MD), "Chothia” numbering rule, “ABM” numbering rule, "contact” numbering rule (see Martin, ACR.Protein Sequence and Structure Analysis of Antibody Variable Domains[J].2001) and ImMunoGenTics (IMGT) numbering Rules (Lefranc, M.P. et al., Dev. Comp. Immunol., 27, 55-77 (2003); Front Immunol. 2018 Oct 16; 9:2278), etc.; the correspondence between various numbering systems is a matter for those skilled in the art Well known.
  • the numbering scheme for this disclosure is set forth in Table 1 below.
  • variable region and CDR sequences in the embodiments of the present disclosure are subject to the "Kabat" numbering rule.
  • antibody fragment refers to a molecule other than an intact antibody that contains portions of an intact antibody that retain the antigen-binding ability of the intact antibody.
  • antibody fragments include, but are not limited to, Fv, Fab, Fab', Fab'-SH, F(ab') 2 , single domain antibodies, single chain Fab (scFab), diabodies, linear antibodies, single chain antibody molecules (e.g. scFv); and multispecific antibodies formed from antibody fragments.
  • Fc region or “fragment crystallizable region” is used to define the C-terminal region of an antibody heavy chain, including native Fc regions and engineered Fc regions.
  • the Fc region contains two subunits that are the same or different.
  • the Fc region of a human IgG heavy chain is defined as extending from the amino acid residue at position Cys226 or from Pro230 to its carboxy terminus.
  • Suitable native sequence Fc regions for use in the antibodies described herein include human IgGl, IgG2 (IgG2A, IgG2B), IgG3 and IgG4. Unless otherwise stated, the numbering convention for the Fc region is the EU index.
  • Titin chain refers to a peptide segment in the Titin protein containing a Titin Ig-like 152 domain or a functional variant thereof with a length of 78-118 amino acids.
  • the Titin chain can interact with Obscurin Ig-like 1 or Obscurin-
  • the Ig-like-like 1 domains combine to form a dimerization complex.
  • Obscurin chain refers to a peptide segment of the Obscurin protein containing the Obscurin Ig-like 1 domain or a functional variant thereof with a length of 87-117 amino acids, or a segment of the Obscurin-like 1 protein with a length of 78-118 amino acids. Peptide fragments of amino acids containing an Obscurin-like Ig-like 1 domain or functional variants thereof.
  • the Obscurin chain can combine with the Titin chain to form a dimerization complex.
  • the Titin chain and Obscurin chain disclosed in the present disclosure can be used to replace CH1 and CL in Fab respectively to form a replaced Fab (Fab-S). This substitution does not affect the binding of the antigen-binding molecule to the antigen.
  • chimeric antibody refers to an antibody in which a portion of the heavy and/or light chain is derived from a specific source or species and the remaining portion of the heavy and/or light chain is derived from a different source or species.
  • affinity refers to the overall strength of non-covalent interactions between a single binding site of a molecule (eg, an antibody) and its binding partner (eg, an antigen).
  • binding affinity refers to the internal binding affinity that reflects a 1:1 interaction between the members of a binding pair (eg, antibody and antigen).
  • KD equilibrium dissociation constant
  • KD refers to the equilibrium dissociation constant, which is obtained from the ratio of kd to ka (i.e., kd/ka) and is expressed as molar concentration (M).
  • M molar concentration
  • the term "monoclonal antibody” refers to a population of antibodies that are substantially homogeneous, ie, the antibody molecules contained in the population are identical in amino acid sequence, except for natural mutations that may be present in minor amounts.
  • polyclonal antibody preparations typically contain multiple different antibodies with different amino acid sequences in their variable domains, often specific for different epitopes.
  • the antibodies provided by the present disclosure are monoclonal antibodies.
  • antigen refers to a molecule or portion of a molecule capable of being bound by a selective binding agent of an antigen-binding molecule, such as an antibody.
  • An antigen may have one or more epitopes capable of interacting with different antigen-binding molecules (eg, antibodies).
  • epitope refers to an area or region on an antigen that is capable of specifically binding to an antibody or antigen-binding fragment thereof.
  • Epitopes may be formed from contiguous amino acids (linear epitopes) or contain non-contiguous amino acids (conformational epitopes), for example due to the folding of the antigen (i.e. the tertiary folding of the antigen by its proteinaceous nature) such that the non-contiguous amino acids are spatially separated. near.
  • the difference between conformational epitopes and linear epitopes is that in the presence of denaturing solvents, the antibody's binding to the conformational epitope is lost.
  • An epitope contains at least 3, at least 4, at least 5, at least 6, at least 7, or 8-10 amino acids in a unique spatial conformation.
  • Screening for antibodies that bind a specific epitope can be performed using methods routine in the art, such as, but not limited to, alanine scanning, peptide blotting (see Meth. Mol. Biol. 248 (2004) 443 -463), peptide cleavage analysis, epitope excision, epitope extraction, chemical modification of antigen (see Prot. Sci. 9 (2000) 487-496), and cross-blocking (see “Antibodies”, Harlow and Lane (Cold Spring Harbor Press, Cold Spring Harb., NY)).
  • does not bind means that the antigen-binding molecule is unable to bind to an antigen or its epitope in the above-mentioned specific binding manner.
  • KD equilibrium dissociation constant
  • antigen-binding module refers to a polypeptide molecule that specifically binds a target antigen.
  • Specific antigen-binding modules include the antigen-binding domain of an antibody, for example, including a heavy chain variable region and a light chain variable region.
  • antigen-binding module that specifically binds CD3 refers to a module that is capable of binding CD3 or an epitope thereof with sufficient affinity such that a molecule containing the module can be used as a diagnostic and/or therapeutic agent targeting CD3.
  • an antigen-binding module that specifically binds CD3 has an equilibrium dissociation constant (KD) of: ⁇ approximately 10 nM, as measured by surface plasmon resonance assay.
  • Antigen binding moieties include antibody fragments as defined herein, such as Fab, substituted Fab or scFv.
  • linker refers to a linking unit that joins two polypeptide fragments.
  • linkers appearing in the same structural formula may be the same or different.
  • the linker can be a peptide linker, which contains one or more amino acids, typically about 1-30, 2-24 or 3-15 amino acids.
  • the linkers used herein may be the same or different.
  • Tm is the solution denaturation temperature (intrinsic fluorescence). When proteins are denatured (heated or denatured), the tertiary structure is opened and the aromatic amino acid microenvironment changes, resulting in a change in the emission fluorescence spectrum.
  • Tm1 refers to the temperature at which the fluorescence changes to half of its maximum value.
  • Tonset is the denaturation starting temperature. It means the temperature at which the protein begins to denature, that is, the temperature at which the fluorescence value begins to change.
  • Tagg is the aggregation onset temperature. By static light scattering, aggregates are detected at two wavelengths, 266 nm and 473 nm, and the temperature at which the sample begins to aggregate is monitored. Tagg 266 refers to the aggregation onset temperature monitored at 266nm.
  • nucleic acid is used interchangeably herein with the term “polynucleotide” and refers to deoxyribonucleotides or ribonucleotides and polymers thereof in single- or double-stranded form.
  • the term encompasses nucleic acids containing known nucleotide analogs or modified backbone residues or linkages that are synthetic, naturally occurring and non-naturally occurring, have similar binding properties to the reference nucleic acid, and are Metabolized in a manner similar to the reference nucleotide.
  • nucleic acid molecules that has been separated from components of its natural environment. Isolated nucleic acids include nucleic acid molecules contained in cells that normally contain the nucleic acid molecule but which are present extrachromosomally or at a chromosomal location that is different from its native chromosomal location.
  • Isolated nucleic acid encoding said antigen-binding molecule refers to one or more nucleic acid molecules encoding antibody heavy and light chains (or fragments thereof), including such one or more nucleic acids in a single vector or separate vectors molecule, and such one or more nucleic acid molecules present at one or more locations in a host cell.
  • a particular nucleic acid sequence also implicitly encompasses conservatively modified variants (eg, degenerate codon substitutions) and complementary sequences thereof as well as sequences explicitly indicated.
  • degenerate codon substitutions can be obtained by generating sequences in which the third position of one or more selected (or all) codons is replaced by a degenerate base and/or Deoxyinosine residue substitution.
  • polypeptide and "protein” are used interchangeably herein to refer to a polymer of amino acid residues.
  • the term applies to amino acid polymers in which one or more amino acid residues are the corresponding artificial chemical mimetics of naturally occurring amino acids, as well as to naturally occurring amino acid polymers and non-naturally occurring amino acid polymers. Unless stated otherwise, a particular polypeptide sequence also implicitly encompasses conservatively modified variants thereof.
  • fusion means that the components (eg, the antigen-binding module and the Fc domain) are covalently linked, either directly or via a linker.
  • vector means a polynucleotide molecule capable of transporting another polynucleotide to which it is linked.
  • plasmid refers to a circular double-stranded DNA circle into which additional DNA segments can be ligated.
  • viral vector such as an adeno-associated viral vector (AAV or AAV2), in which additional DNA segments can be ligated into the viral genome.
  • AAV adeno-associated viral vector
  • Certain vectors are capable of autonomous replication in the host cells into which they are introduced (eg, bacterial vectors with bacterial origins of replication and episomal mammalian vectors).
  • vectors eg, non-episomal mammalian vectors
  • expression vector or "expression construct” refers to a vector suitable for transforming a host cell and containing instructions and/or controls (together with the host cell) with which it is operably A vector ligated to express nucleic acid sequences of one or more heterologous coding regions.
  • Expression constructs may include, but are not limited to, sequences that affect or control transcription, translation, and, in the presence of introns, RNA splicing of the coding region operably linked thereto.
  • host cell refers to cells into which exogenous nucleic acid has been introduced, including the progeny of such cells.
  • Host cells include “transformants” and “transformed cells,” which include the primary transformed cell and progeny derived therefrom, regardless of the number of passages.
  • the progeny may not be identical in nucleic acid content to the parent cells, but may contain mutations.
  • mutant progeny that possess the same functional or biological activity as cells screened or selected in primary transformed cells.
  • Host cells include prokaryotic and eukaryotic host cells, where eukaryotic host cells include, but are not limited to, mammalian cells, insect cell line plant cells, and fungal cells.
  • Mammalian host cells include human, mouse, rat, canine, monkey, porcine, goat, bovine, equine, and hamster cells, including but not limited to Chinese hamster ovary (CHO) cells, NSO, SP2 cells, HeLa cells, baby hamster kidney (BHK) cells, monkey kidney cells (COS), human hepatocellular carcinoma cells (e.g., Hep G2), A549 cells, 3T3 cells, and HEK-293 cells.
  • Fungal cells include yeast and filamentous fungal cells, including, for example, Pichia pastoris, Pichia finlandica, Pichia trehalophila, Pichia koclamae, Pichia membranaefaciens, Pichia minuta (Ogataea minuta, Pichia lindneri), Pichia opuntiae, Pichia thermotolerans, Pichia salictaria), Pichia guercuum, Pichia pijperi, Pichia stiptis, Pichia methanolica, Pichia genus, Saccharomycescerevisiae, Saccharomyces cerevisiae , Hansenula polymorpha, Kluyveromyces lactis, Kluyveromyces lactis, Candida albicans, Aspergillus nidulans, Aspergillus niger, Aspergillus oryzae, Trichoderma reesei, Chrysospor
  • Pichia pastoris any Saccharomyces spp., Hansenula polymorpha, any Kluyveromyces spp., Candida albicans, any Aspergillus spp., Trichoderma reesei, Luck Mold (Chrysosporium lucknowense), any species of Fusarium, Yarrowia lipolytica and Neurospora crassa.
  • the host cells of this patent do not include subjects that are not authorized under the patent law.
  • composition means a mixture containing one or more antigen-binding molecules or antibodies described herein together with other chemical components, such as physiologically/pharmaceutically acceptable carriers and excipients.
  • subject or “individual” includes humans and non-human animals.
  • Non-human animals include all vertebrates (eg, mammals and non-mammals) such as non-human primates (eg, cynomolgus monkeys), sheep, dogs, cattle, chickens, amphibians, and reptiles.
  • patient or “subject” are used interchangeably herein.
  • cyno or “cynomolgus” refers to the crab-eating monkey (Macaca fascicularis).
  • the individual or subject is a human.
  • administering when applied to an animal, human, experimental subject, cell, tissue, organ or biological fluid, means the administration of an exogenous drug, therapeutic, diagnostic or composition to an animal, human , contact with subjects, cells, tissues, organs or biological fluids.
  • sample refers to a collection of similar fluids, cells, or tissues isolated from a subject, as well as fluids, cells, or tissues present in a subject.
  • exemplary samples are biological fluids such as blood, serum and serosal fluids, plasma, lymph fluid, urine, saliva, cyst fluid, tears, excreta, sputum, mucosal secretions of secretory tissues and organs, vaginal secretions, ascites , fluids from the pleura, pericardium, peritoneum, abdominal cavity and other body cavities, fluid collected from bronchial lavage, synovial fluid, fluid solutions in contact with subjects or biological sources, such as cell and organ culture media (including cell or organ conditions culture medium), lavage fluid, etc., tissue biopsy samples, fine needle aspiration, surgically resected tissue, organ culture or cell culture.
  • biological fluids such as blood, serum and serosal fluids, plasma, lymph fluid, urine, saliva, cyst fluid, tears, excreta, sputum, mucosal secretions of secretor
  • Treatment refers to a clinical intervention attempted to be applied to the individual being treated, and may be administered for preventive purposes, or during the course of clinical pathology. Desired effects of treatment include, but are not limited to, prevention of the occurrence or recurrence of the disease, alleviation of symptoms, alleviation/reduction of any direct or indirect pathological consequences of the disease, prevention of metastasis, reduction of the rate of disease progression, amelioration or alleviation of the disease status, and regression or improved prognosis. .
  • the antigen-binding molecules of the present disclosure are used to delay the development of disease or slow the progression of disease.
  • recurrence refers to the return of cancer or disease following clinical assessment of disease resolution.
  • diagnosis of distant cancer metastasis or local recurrence may be considered recurrence.
  • an "effective amount” is generally sufficient to reduce the severity and/or frequency of symptoms, eliminate these symptoms and/or underlying causes, prevent the occurrence of symptoms and/or their underlying causes, and/or ameliorate or ameliorate impairments caused by or associated with a disease state. amount.
  • the effective amount is a therapeutically effective amount or a prophylactically effective amount.
  • a “therapeutically effective amount” is one sufficient to treat a disease state or symptom, particularly a condition or symptom associated with that disease state, or to otherwise prevent, hinder, delay or reverse the disease state or any other adverse effect in any way related to the disease.
  • the ideal amount of symptomatic progression is one sufficient to treat a disease state or symptom, particularly a condition or symptom associated with that disease state, or to otherwise prevent, hinder, delay or reverse the disease state or any other adverse effect in any way related to the disease.
  • a “prophylactically effective amount” is an amount that, when administered to a subject, will have a predetermined prophylactic effect, such as preventing or delaying the onset (or recurrence) of the disease state, or reducing the likelihood of the onset (or recurrence) of the disease state or associated symptoms. . Complete therapeutic or preventive effect does not necessarily occur after a single dose but may occur after a series of Occurs after dose. Thus, a therapeutically or prophylactically effective amount may be administered in one or more administrations.
  • “Therapeutically effective amount” and “prophylactically effective amount” may vary depending on a variety of factors such as the disease state, age, sex, and weight of the individual, as well as the ability of the therapeutic agent or combination of therapeutic agents to elicit the desired response in the individual.
  • Exemplary indicators of an effective therapeutic agent or combination of therapeutic agents include, for example, improved health status of the subject.
  • Antigen binding molecules of the present disclosure are provided.
  • the present disclosure provides antigen-binding molecules with many advantageous properties, such as good in vitro killing activity, therapeutic activity, safety, pharmacokinetic properties and druggability (such as yield, purity and stability, etc.).
  • Antigen-binding molecules of the present disclosure include bispecific antigen-binding molecules (such as bispecific antibodies) that specifically bind DLL3 and CD3 and anti-DLL3 antibodies.
  • the antigen-binding molecules of the present disclosure have any of the following properties:
  • the anti-DLL3 antibody or antigen-binding molecule is present in less than 4 ⁇ 10 -9 M, 3 ⁇ 10 -9 M, 2 ⁇ 10 -9 M, 1 ⁇ 10 -9 M, 9 ⁇ 10 -10 M, 8 ⁇ 10 -10 M, 7 ⁇ 10 -10 M, 6 ⁇ 10 -10 M, 5 ⁇ 10 -10 M, 4 ⁇ 10 -10 M, 3 ⁇ 10 -10 M, 2 ⁇ 10 -10 M , 1 ⁇ 10 -10 M, 9 ⁇ 10 -11 M KD bound to human DLL3, the KD was measured by surface plasmon resonance method.
  • the EC50 of the anti-antigen binding fraction to the DLL3 protein is less than 0.5 nM, 0.4 nM, 0.3 nM, 0.2 nM, 0.1 nM, 0.09 nM, 0.08 nM, 0.07 nM, and the EC50 is detected by ELISA of.
  • the anti-DLL3 antibody binds H1184 cells with an EC50 of less than 0.2 nM, 0.1 nM, 0.09 nM, 0.08 nM, 0.07 nM, 0.06 nM, 0.05 nM, 0.04 nM.
  • the antigen-binding molecule can specifically kill SHP77 cells and H1184 cells expressing DLL3, wherein the killing IC50 of H1184 cells is less than 30pM, 25pM, 20pM, 15pM, 14pM, 13pM, 12pM, 11pM, 10pM, 9pM, 8pM, 7pM.
  • the antigen-binding molecule activates Jurkat Lucia TM NFAT cells with an EC50 of less than 20 pM, 19 pM, 18 pM, 17 pM, 16 pM, 15 pM, 14 pM, 13 pM, 12 pM, 11 pM, 10 pM, 9 pM, 8 pM, 7 pM.
  • the antigen-binding molecule can significantly inhibit the growth of subcutaneously transplanted tumors of mouse SHP77 and H1184 cells.
  • the present disclosure provides an antigen-binding molecule comprising at least one antigen-binding module that specifically binds DLL3 and at least one antigen-binding module that specifically binds CD3, and the antigen-binding module that specifically binds DLL3 includes DLL3-VH and DLL3. -VL, the antigen-binding module that specifically binds CD3 includes CD3-VH and CD3-VL.
  • the present disclosure also provides an anti-DLL3 antibody that can specifically bind DLL3, the antibody comprising DLL3-VH and DLL3-VL.
  • the embodiments herein disclose anti- Body series 6, 98, 110 and 30. The following uses antibodies 6 and 110 as examples to describe the antibodies or antigen-binding molecules herein.
  • Antigen-binding molecules that specifically bind DLL3 and CD3, wherein:
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 21, 69 or 70 and DLL3 comprising the amino acid sequence of SEQ ID NO: 22 -HCDR3; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 23, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 24, 71, 72 or 73, and comprising SEQ ID NO : DLL3-LCDR3 with an amino acid sequence of 25 or 74.
  • the DLL3-VH has: DLL3-HCDR1 comprising the amino acid sequence of SEQ ID NO: 20, DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 32, 96, 97, 98 or 99, and DLL3-HCDR2 comprising the amino acid sequence of SEQ ID NO: 33 DLL3-HCDR3 having the amino acid sequence; and the DLL3-VL having: DLL3-LCDR1 comprising the amino acid sequence of SEQ ID NO: 34, DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 35, and DLL3-LCDR2 comprising the amino acid sequence of SEQ ID NO: 36 amino acid sequence of DLL3-LCDR3.
  • Antigen-binding molecules that specifically bind DLL3 and CD3, wherein:
  • the DLL3-VH includes DLL3-HCDR1 as set forth in SEQ ID NO: 20, DLL3-HCDR2 as set forth in SEQ ID NO: 21, 69 or 70, and DLL3-HCDR3 as set forth in SEQ ID NO: 22, and
  • the DLL3-VL includes DLL3-LCDR1 as shown in SEQ ID NO: 23, DLL3-LCDR2 as shown in SEQ ID NO: 24, 71, 72 or 73 and DLL3 as shown in SEQ ID NO: 25 or 74 -LCDR3.
  • the DLL3-VH includes DLL3-HCDR1 as shown in SEQ ID NO: 20, DLL3-HCDR2 as shown in SEQ ID NO: 32, 96, 97, 98 or 99 and DLL3 as shown in SEQ ID NO: 33 -HCDR3, and the DLL3-VL is DLL3-LCDR1 as set forth in SEQ ID NO:34, DLL3-LCDR2 as set forth in SEQ ID NO:35, and DLL3-LCDR3 as set forth in SEQ ID NO:36.
  • Antigen-binding molecules that specifically bind DLL3 and CD3, wherein:
  • the DLL3-VH includes DLL3-HCDR1 as shown in SEQ ID NO:20, DLL3-HCDR2 as shown in SEQ ID NO:21, and DLL3-HCDR3 as shown in SEQ ID NO:22; and said DLL3 -VL contains DLL3-LCDR1 as shown in SEQ ID NO:23, DLL3-LCDR2 as shown in SEQ ID NO:71, and DLL3-LCDR3 as shown in SEQ ID NO:25.
  • the DLL3-VH includes DLL3-HCDR1 as shown in SEQ ID NO:20, DLL3-HCDR2 as shown in SEQ ID NO:21, and DLL3-HCDR3 as shown in SEQ ID NO:22; and the DLL3 -VL includes DLL3-LCDR1 as set forth in SEQ ID NO:23, DLL3-LCDR2 as set forth in SEQ ID NO:24, and DLL3-LCDR3 as set forth in SEQ ID NO:25; or
  • the DLL3-VH includes DLL3-HCDR1 as shown in SEQ ID NO:20, DLL3-HCDR2 as shown in SEQ ID NO:21, and DLL3-HCDR3 as shown in SEQ ID NO:22; and the DLL3- VL contains DLL3-LCDR1 as set forth in SEQ ID NO: 23, DLL3-LCDR2 as set forth in SEQ ID NO: 72, and DLL3-LCDR3 as set forth in SEQ ID NO: 25; or
  • the DLL3-VH includes DLL3-HCDR1 as shown in SEQ ID NO: 20, DLL3-HCDR2 as shown in SEQ ID NO: 69, and DLL3-HCDR3 as shown in SEQ ID NO: 22; and said DLL3 -VL contains DLL3-LCDR1 as set forth in SEQ ID NO:23, DLL3-LCDR2 as set forth in SEQ ID NO:71, and DLL3-LCDR3 as set forth in SEQ ID NO:74; or
  • the DLL3-VH includes DLL3-HCDR1 as shown in SEQ ID NO: 20, DLL3-HCDR2 as shown in SEQ ID NO: 69, and DLL3-HCDR3 as shown in SEQ ID NO: 22; and said DLL3 -VL contains DLL3-LCDR1 as set forth in SEQ ID NO:23, DLL3-LCDR2 as set forth in SEQ ID NO:24, and DLL3-LCDR3 as set forth in SEQ ID NO:74; or
  • the DLL3-VH includes DLL3-HCDR1 as shown in SEQ ID NO: 20, DLL3-HCDR2 as shown in SEQ ID NO: 69, and DLL3-HCDR3 as shown in SEQ ID NO: 22; and said DLL3 -VL contains DLL3-LCDR1 as set forth in SEQ ID NO:23, DLL3-LCDR2 as set forth in SEQ ID NO:71, and DLL3-LCDR3 as set forth in SEQ ID NO:25; or
  • the DLL3-VH includes DLL3-HCDR1 as shown in SEQ ID NO:20, DLL3-HCDR2 as shown in SEQ ID NO:70, and DLL3-HCDR3 as shown in SEQ ID NO:22; and said DLL3 -VL contains DLL3-LCDR1 as set forth in SEQ ID NO:23, DLL3-LCDR2 as set forth in SEQ ID NO:71, and DLL3-LCDR3 as set forth in SEQ ID NO:25; or
  • the DLL3-VH includes DLL3-HCDR1 as shown in SEQ ID NO:20, DLL3-HCDR2 as shown in SEQ ID NO:70, and DLL3-HCDR3 as shown in SEQ ID NO:22; and said DLL3 -VL contains DLL3-LCDR1 as shown in SEQ ID NO:23, DLL3-LCDR2 as shown in SEQ ID NO:24, and DLL3-LCDR3 as shown in SEQ ID NO:74.
  • the DLL3-VH includes DLL3-HCDR1 as shown in SEQ ID NO: 20, DLL3-HCDR2 as shown in SEQ ID NO: 96, and DLL3-HCDR3 as shown in SEQ ID NO: 33; and said DLL3 -VL contains DLL3-LCDR1 as shown in SEQ ID NO:34, DLL3-LCDR2 as shown in SEQ ID NO:35, and DLL3-LCDR3 as shown in SEQ ID NO:36.
  • the antigen-binding molecule or anti-DLL3 antibody as described above, the DLL3-VH and/or the DLL3-VL is murine or humanized. In some embodiments, the DLL3-VH and/or the DLL3-VL are humanized.
  • the humanized DLL3-VH has FR1, FR2, FR3 derived from IGHV1-3*01, IGHV7-4-1*02, or IGHV3-73*01 and FR3 derived from IGHJ6*01 FR4, and which is unsubstituted or has one or more selected from the group consisting of 1E, 5Q, 27Y, 30T, 38K, 43K, 48I, 67A, 68A, 69L, 71V, 73K, 75S, 76N and 93A amino acid substitution; and/or the humanized DLL3-VL has FR1, FR2, FR3 derived from IGKV1-16*01 or IGKV3-20*02 and FR4 derived from IGKJ4*01, and it is Substituted or having one or more amino acid substitutions selected from the group consisting of 1N, 36L, 42K, 43S, 44F, 46G, 69A, 71Y, 79Q and
  • the humanized DLL3-VH comprises the amino acid sequence of SEQ ID NO: 50, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of 1E, 43K, 48I, 67A, 69L, 71V, 73K and 76N in the FR region of SEQ ID NO: 50.
  • the humanized DLL3-VH comprises the amino acid sequence of SEQ ID NO: 51, or a variant thereof.
  • the variant is in the FR region of SEQ ID NO: 51 comprising one or more amino acids selected from the group consisting of 1E, 5Q, 38K, 68A, 69L, 71V, 73K, 75S and 76N replace.
  • the humanized DLL3-VH comprises the amino acid sequence of SEQ ID NO: 52, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 52 selected from the group consisting of 27Y, 30T69L, 71V, 73K and 93A.
  • the humanized DLL3-VL comprises the amino acid sequence of SEQ ID NO: 62, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of 36L, 43S, 44F, 46G, 69A, 71Y, and 85D in the FR region of SEQ ID NO: 62.
  • the humanized DLL3-VL comprises the amino acid sequence of SEQ ID NO: 68, or a variant thereof.
  • the variant is one or more amino acid substitutions selected from the group consisting of 36L, 42K, 46G, 69A, 71Y, 79Q, and 85D in the FR region of SEQ ID NO: 68.
  • the FR1, FR2, FR3, and FR4 of the humanized DLL3-VH are at least 60%, 70%, 80%, or 90% identical to the FR1, FR2, FR3, and FR4 of SEQ ID NO:95 Sequence identity; FR1, FR2, FR3 and FR4 of the humanized DLL3-VL have at least 60%, 70%, 80% or 90% identity with the FR1, FR2, FR3 and FR4 of SEQ ID NO: 88 Sequence identity.
  • the humanized DLL3-VH has FR1, FR2, FR3 derived from IGHV1-3*01 and FR4 derived from IGHJ6*01, and is unsubstituted or has FR4 derived from IGHJ6*01 , one or more amino acid substitutions in the group consisting of 24T, 44S, 71V and 73K; and/or the humanized DLL3-VL has FR1, FR2, FR3 derived from IGKV4-1*01 and FR4 derived from IGKJ2*01, and is unsubstituted or has a component selected from the group consisting of 1N, 9K, 43S, 68A and 85D One or more amino acid substitutions.
  • the amino acid positions in the variable regions described above are defined according to Kabat numbering rules.
  • the humanized DLL3-VH comprises the amino acid sequence of SEQ ID NO: 95, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 95 selected from the group consisting of 1E, 24T, 44S, 71V, and 73K.
  • the humanized DLL3-VL comprises the amino acid sequence of SEQ ID NO: 88, or a variant thereof.
  • the variant is one or more amino acid substitutions in the FR region of SEQ ID NO: 88 selected from the group consisting of 1N, 9K, 43S, 68A, and 85D.
  • the humanized DLL3-VH comprises the amino acid sequence of SEQ ID NO: 51, or a variant thereof; in some embodiments, the variant is in the FR region of SEQ ID NO: 51 Comprising one or more amino acid substitutions selected from the group consisting of 1E, 38K, 68A, 69L, 71V, 73K, 75S and 76N; and the humanized DLL3-VL comprises the amino acid sequence of SEQ ID NO: 63, Or a variant thereof; in some embodiments, the variant comprises one or more amino acid substitutions in the FR region of SEQ ID NO: 63; in some embodiments, the amino acid substitutions are selected from the group consisting of 43S and 44F One or more amino acids in the group are substituted.
  • the humanized DLL3-VH comprises the amino acid sequence of SEQ ID NO: 91, or a variant of SEQ ID NO: 91; in some embodiments, the variant is in SEQ ID NO:
  • the FR region of 91 contains one or more amino acid substitutions;
  • the humanized DLL3-VL comprises the amino acid sequence of SEQ ID NO: 88, or a variant thereof; in some embodiments, the variant is a FR region of SEQ ID NO: 88 that contains a sequence selected from 1N, 9K One or more amino acid substitutions from the group consisting of , 43S, 68A and 85D.
  • variable regions and CDRs described above are defined according to the Kabat numbering rule.
  • the antigen-binding molecule as described in any one of the preceding items wherein the amino acid sequence of DLL3-VH is consistent with SEQ ID NO: 12, 43, 44, 45, 46, 47, 48, 49, 50, 51 , 52, 53, 54, 55, 56 or 57 have at least 90%, 95%, 96%, 97%, 98% or 99% sequence identity, and the amino acid sequence of DLL3-VL is identical to SEQ ID NO: 13, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67 or 68 have a sequence identity of at least 90%, 95%, 96%, 97%, 98% or 99%.
  • the amino acid sequence of DLL3-VH is SEQ ID NO: 12, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56 or 57 shown
  • the amino acid sequence of the DLL3-VL is shown in SEQ ID NO: 13, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67 or 68.
  • the anti-DLL3 antibody as described in any one of the preceding items wherein the amino acid sequence of DLL3-VH is consistent with SEQ ID NO: 43, 44, 45, 46, 47, 48, 49, 50, 51, 52 , 53, 54, 55, 56 or 57 have at least 90%, 95%, 96%, 97%, 98% or 99% sequence identity, and
  • the amino acid sequence of DLL3-VL has at least 90%, 95%, 96%, 97%, 98% or 99% sequence identity with SEQ ID NO: 63, 64, 65, 66 or 67.
  • the amino acid sequence of DLL3-VH is as shown in SEQ ID NO: 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56 or 57
  • the amino acid sequence of DLL3-VL is shown in SEQ ID NO: 63, 64, 65, 66 or 67.
  • the anti-DLL3 antibody as described in any one of the preceding items, wherein the amino acid sequence of DLL3-VH is at least 90%, 95%, 96%, 97%, 98% identical to SEQ ID NO: 56 or 57 or 99% sequence identity, and the amino acid sequence of DLL3-VL has at least 90%, 95% with SEQ ID NO: 58, 59, 60, 61, 62, 63, 64, 65, 66, 67 or 68 , 96%, 97%, 98% or 99% sequence identity.
  • the amino acid sequence of DLL3-VH is set forth in SEQ ID NO: 56 or 57
  • the amino acid sequence of DLL3-VL is set forth in SEQ ID NO: 58, 59, 60, 61, 62, 63 , 64, 65, 66, 67 or 68.
  • the antigen-binding molecule or anti-DLL3 antibody as described in any one of the preceding items the amino acid sequence of the DLL3-VH is as shown in SEQ ID NO: 54, and the amino acid sequence of the DLL3-VL is as shown in SEQ ID NO: shown in 63; or
  • the amino acid sequence of the DLL3-VH is shown in SEQ ID NO: 54, and the amino acid sequence of the DLL3-VL is shown in SEQ ID NO: 61; or
  • amino acid sequence of DLL3-VH is shown in SEQ ID NO: 54, and the amino acid sequence of DLL3-VL is shown in SEQ ID NO: 64; or
  • the amino acid sequence of DLL3-VH is shown in SEQ ID NO: 56, and the amino acid sequence of DLL3-VL is shown in SEQ ID NO: 67; or
  • amino acid sequence of DLL3-VH is shown in SEQ ID NO: 56, and the amino acid sequence of DLL3-VL is shown in SEQ ID NO: 65; or
  • the amino acid sequence of DLL3-VH is shown in SEQ ID NO: 57, and the amino acid sequence of DLL3-VL is shown in SEQ ID NO: 65; or
  • the amino acid sequence of DLL3-VH is shown in SEQ ID NO: 57, and the amino acid sequence of DLL3-VL is shown in SEQ ID NO: 65.
  • the antigen-binding molecule or anti-DLL3 antibody of any one of the preceding items wherein the amino acid sequence of DLL3-VH is consistent with SEQ ID NO: 16, 89, 90, 91, 92, 93, 94 or 95 Having at least 90%, 95%, 96%, 97%, 98% or 99% sequence identity, and the amino acid sequence of DLL3-VL has at least 90%, 95%, 96%, 97%, 98% or 99% sequence identity.
  • the amino acid sequence of DLL3-VH is as SEQ ID NO: 16, 89, 90, 91, 92, 93, 94 or 95
  • the amino acid sequence of DLL3-VL is shown in SEQ ID NO: 17, 86, 87 or 88.
  • the antigen-binding molecule or anti-DLL3 antibody as described in any one of the preceding items the amino acid sequence of the DLL3-VH is as shown in SEQ ID NO: 91, and the amino acid sequence of the DLL3-VL is as shown in SEQ ID NO:87 shown.
  • amino acid sequence of the heavy chain is shown in SEQ ID NO: 125
  • amino acid sequence of the light chain is shown in SEQ ID NO: 126.
  • the antigen-binding molecule as described above, wherein:
  • variable regions and CDRs described above are defined according to the Kabat numbering rule.
  • the antigen-binding molecule of any one of the preceding items, said CD3-VH and/or said CD3-VL is murine or humanized. In some embodiments, the CD3-VH and/or the CD3-VL are humanized.
  • the antigen-binding molecule as described in any one of the preceding items comprising:
  • the antigen-binding molecule as described in any one of the preceding items comprising:
  • the antigen-binding molecule as described in any one of the preceding items comprising:
  • antigen-binding molecules comprising antibody series 98 and 30 disclosed according to the embodiments herein have the same scope of technical solutions as the above-described antibody series 6 and 110.
  • antigen binding molecules include:

Abstract

本披露涉及特异性结合DLL3和CD3的抗原结合分子及其医药用途,所述抗原结合分子可用于治疗癌症。

Description

特异性结合DLL3和CD3的抗原结合分子及其医药用途 技术领域
本披露属于生物技术领域,更具体地,本披露涉及DLL3/CD3抗原结合分子及其应用。
背景技术
这里的陈述仅提供与本披露有关的背景信息,而不必然地构成现有技术。
小细胞肺癌(Small Cell Lung Cancer,SCLC)属于一种比较恶性的肺癌类型,占所有肺癌病例的10%-15%。小细胞肺癌的肿瘤生长速度快,容易转移,5年生存率低于7%。小细胞肺癌的治疗药物比较局限,主要是化药,如用铂类/依托泊苷联用化疗。小细胞肺癌病人对化疗初期响应良好,但极易产生耐药和复发。近几年的免疫治疗,如PD-L1抗体和PD1抗体,对SCLC患者有一定的效果,但是有效率约为15%。目前仍然还没有开发出特异性的靶向治疗药物。
DLL3是一种抑制Notch的配体,在正常状态下,DLL3处于高尔基体上,在癌细胞中(如小细胞肺癌细胞),DLL3会表达在细胞表面,DLL3以顺式方式结合Notch,阻碍了细胞和细胞结合以及Notch在目标细胞的内吞,从而抑制了Notch信号通路,促进肿瘤细胞的生长。DLL3主要表达于神经或者神经内分泌肿瘤,包括小细胞肺癌、大细胞神经内分泌癌、胃肠道神经内分泌瘤、小细胞膀胱癌、多形性胶质细胞瘤、转移性去势性前列腺癌、黑色素瘤等,尤其是SCLC,超过80%的SCLC有DLL3的阳性表达,而正常肺癌组织及癌旁组织中不表达。这种表达的差异性使得DLL3成为治疗SCLC的一种极具潜力的治疗靶点。
CD3是一种表达于T细胞上的同种型或异型二聚体抗原。功能性CD3由四条不同链:ε、ζ、δ及γ中的两者进行二聚体结合来形成。CD3二聚体排列包括γ/ε、δ/ε及ζ/ζ。CD3与T细胞受体复合物(TCR)结合且为T细胞活化所必需。因此,已提出使用活化T细胞的抗CD3抗体用于治疗癌症。然而,抗CD3抗体的给药可能会触发T细胞活化和相关的细胞因子释放,过度的细胞因子释放导致重度细胞因子释放综合征(CRS),其是抗CD3抗体在临床用药中的重要挑战。
发明内容
本披露提供了一种特异性结合DLL3和CD3抗原结合分子。
在一个方面,本披露提供了一种抗原结合分子,其包含至少一个特异性结合DLL3的抗原结合模块和至少一个特异性结合CD3的抗原结合模块,所述特异性结合DLL3的抗原结合模块包含重链可变区DLL3-VH和轻链可变区DLL3-VL,所述特异性结合CD3的抗原结合模块包含重链可变区CD3-VH和轻链可变区CD3-VL。
在一些实施方式中,如前所述的抗原结合分子,其中:
(i)所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:12、56或57中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:13、63、64、65、66或67中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列,或
(ii)所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:14、79、80、81或82中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:15中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列,或
(iii)所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:16、91、92、93或94中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:17中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列,或
(iv)所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:18、107、108、109、110、112、113、114或115中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:19中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列。
在一些实施方式中,如前所述的抗原结合分子,其中:
(i)所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:12中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:13中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:54中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:64中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:54中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包 含SEQ ID NO:63中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:56中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:65中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:56中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:66中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:56中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:67中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:57中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:65中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:57中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:66中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:57中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:67中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
(ii)所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:14中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分 别包含SEQ ID NO:15中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:81中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:77中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:79、80或82中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:77中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
(iii)所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:16中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:17中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:91中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:87中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:92、93或94中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:87中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
(iv)所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:18中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:19中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:109中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包 含SEQ ID NO:100中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:107、108、110、112、113、114或115中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:100中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列。
在一些实施方案中,所述DLL3-HCDR1、DLL3-HCDR2、DLL3-HCDR3、DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3根据Kabat、IMGT、Chothia、AbM或Contact编号规则定义。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
i)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24、71、72或73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25或74的氨基酸序列的DLL3-LCDR3;或
ii)所述DLL3-VH具有:包含SEQ ID NO:26或84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27或85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:28或83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
iii)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:32、96、97、98或99的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;或
iv)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:37、117、118、119或120的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨 基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23 的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨 基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:28的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨 基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:97的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:98的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:99的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:119的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:117的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:118的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的 氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:120的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:119的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:39的氨 基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,所述DLL3-HCDR1、DLL3-HCDR2、DLL3-HCDR3、DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3是根据Kabat编号规则定义的。
在一些实施方式中,如前任一项所述抗原结合分子在25℃条件下以小于4×10-9M、3×10-9M、2×10-9M、1×10-9M、9×10-10M、8×10-10M、7×10-10M、6×10-10M、5×10-10M、4×10-10M、3×10-10M、2×10-10M、1×10-10M、9×10-11M的KD结合人DLL3,所述KD是通过表面等离子体共振法测量的。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述的DLL3-VH和DLL3-VL是人源化的,其包含人抗体的FR区。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
(i)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和
所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24、71、72或73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25或74的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
(ii)所述DLL3-VH具有:包含SEQ ID NO:26或84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27或85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:28或83的氨基酸序列的DLL3-HCDR3;和
所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自42G、44V和71Y组成的组中的一个或多个氨基酸取代;或
(iii)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:32、96、97、98或99的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、24T、44S、71V和73K组成的组中的一个或多个氨基酸取代;和
所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的 氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、9K、43S、68A和85D组成的组中的一个或多个氨基酸取代;或
(iv)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:37、117、118、119或120的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、3R、5Q、7F、9P、10V、12V、40S、41H、44S、48I、67A、69L、71V、73K、75S和83T组成的组中的一个或多个氨基酸取代;和
所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3;且所述DLL3-VL的FR区包含选自9K、43S、60D、68A、87H和100S组成的组中的一个或多个氨基酸取代。
在一些实施方式中,如前任一项所述的抗原结合分子,其在25℃条件下以小于4×10-9M、3×10-9M、2×10-9M、1×10-9M、9×10-10M、8×10-10M、7×10-10M、6×10-10M、5×10-10M、4×10-10M、3×10-10M、2×10-10M、1×10-10M、9×10-11M的KD结合人DLL3,所述KD是通过表面等离子体共振法测量的。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨 基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO: 22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自42G、44V和71Y组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自42G、44V和71Y组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自42G、44V和71Y组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自42G、44V和71Y组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:28的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自42G、44V和71Y组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、24T、44S、71V和73K组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含 SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3且所述DLL3-VL的FR区包含选自1N、9K、43S、68A和85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:119的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、3R、5Q、7F、9P、10V、12V、40S、41H、44S、48I、67A、69L、71V、73K、75S和83T组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3且所述DLL3-VL的FR区包含选自9K、43S、60D、68A、87H和100S组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:50的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:50的FR区包含选自Q1E、Q43K、M48I、V67A、I69L、R71V、T73K和S76N组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:51的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:51的FR区包含选自Q1E、5Q、R38K、V68A、F69L、L71V、T73K、V75S和S76N组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:52的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:52的FR区包含选自F27Y、S30T、I69L、R71V、D73K和T93A组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VL包含SEQ ID NO:62的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:62的FR区包含选自F36L、A43S、P44F、S46G、T69A、F71Y和T85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VL包含SEQ ID NO:68的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:68的FR区包含选自Y36L、Q42K、L46G、T69A、F71Y、E79Q和V85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:78的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:78的FR区包含一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VL包含SEQ ID NO:75的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:75的FR区包含选自K42G、P44V和F71Y组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:95的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:95的FR区包含选自Q1E、A24T、R44S、R71V和T73K组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VL包含SEQ ID NO:88的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:88的FR区包含选自D1N、D9K、P43S、G68A和V85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:116的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:116的FR区包含选自Q1E、Q3R、V5Q、S7F、A9P、E10V、K12V、A40S、P41H、R44S、M48I、V67A、I69L、R71V、T73K、A75S和R83T组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VL包含SEQ ID NO:100的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:100的FR区包含选自D9K、P43S、G68A、和Y87H组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VL包含SEQ ID NO:103的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:103的FR区包含选自A43S、S60D和Q100S组成的组中的一个或多个氨基酸取代。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:56的FR区包含一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:57的FR包含区一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VL包含SEQ ID NO:63的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:63的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自A43S和P44F组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VL包含SEQ ID NO:64的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:64的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自A43S和P44F组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VL包含SEQ ID NO:65的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:65的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自A43S和P44F组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VL包含SEQ ID NO:66的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:66的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自A43S和P44F组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VL包含SEQ ID NO:67的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:67的FR区包含一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:79、80、81或82的氨基酸序列,或SEQ ID NO:79、80、81或82的变体。在一些实施方案中,所述变体为在SEQ ID NO:79、80、81或82的FR区包含一个或多个氨基酸取代;和
所述DLL3-VL包含SEQ ID NO:75的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:75的FR区包含选自K42G、P44V和F71Y组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:91、92、93或94的氨基酸序列,或SEQ ID NO:91、92、93或94的变体。在一些实施方案中,所述变体为在SEQ ID NO:91、92、93或94的FR区包含一个或多个氨基酸取代;和
所述DLL3-VL包含SEQ ID NO:88的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:88的FR区包含选自D1N、D9K、P43S、G68A和V85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:107、108、109或110的氨基酸序列,或SEQ ID NO:107、108、109或110的变体。在一些实施方案中,所述变体为在SEQ ID NO:107、108、109或110的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自V5Q、S7F、A9P、E10V、K12V、A40S、P41H、M48I、V67A、A75S和R83T组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:112的氨基酸序列,或SEQ ID NO:112的变体。在一些实施方案中,所述变体为在SEQ ID NO:112的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自V5Q、A9P、K12V、A40S、P41H、4M8I、V67A和R83T组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:113的氨基酸序列,或SEQ ID NO:113的变体。在一些实施方案中,所述变体为在SEQ ID NO:113的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自V5Q、S7F、A9P、E10V、K12V、A40S、P41H、A75S和R83T组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:114的氨基酸序列,或SEQ ID NO:114的变体。在一些实施方案中,所述变体为在SEQ ID NO:114的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自V5Q、S7F、A9P、E10V、K12V、M48I、V67A、A75S和R83T组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:115的氨基酸序列,或SEQ ID NO:115的变体。在一些实施方案中,所述变体为在SEQ ID NO:115的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自V5Q、A9P、K12V、A40S、P41H、M48I和V67A组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VL包含SEQ ID NO:100的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:100的FR区包含选自D9K、P43S、G68A、和Y87H组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VL包含SEQ ID NO:103的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:103的FR区包含选自A43S、S60D和Q100S组成的组中的一个或多个氨基酸取代。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
i)所述DLL3-VH包含SEQ ID NO:12、43、44、45、46、47、48、49、50、51、52、53、54、55、56或57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:13、58、59、60、61、62、63、64、65、66、67或68的氨基酸序列;或
ii)所述DLL3-VH包含SEQ ID NO:14、78、79、80、81或82的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:15、75、76或77的氨基酸序列;或
iii)所述DLL3-VH包含SEQ ID NO:16、89、90、91、92、93、94或95的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:17、86、87或88的氨基酸序列;或
iv)所述DLL3-VH包含SEQ ID NO:18、105、106、107、108、109、110、111、112、113、114、115或116的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:19、100、101、102、103或104的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:43、44或45的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:58、59或60的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:47、48、49、53、54或55的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:59的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:43、44或45的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:60的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:46、48、53、54或55的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:61的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:63或64的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:56或57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:65、66或67的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:78或79的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:75、76或77的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:78、79、80、81或82的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:77的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:89、90、91、92、93或94的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:86或87的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:95的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:87的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:105、106、107、108、109、110或111的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:100、101或102的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:112、113、114或115的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:100、103或104的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:109的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:103的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
i)所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:63的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:61的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:64的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:65的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:66的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:67的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:65的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:66的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:67的氨基酸序列;或
ii)所述DLL3-VH包含SEQ ID NO:81的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:77的氨基酸序列;或
iii)所述DLL3-VH包含SEQ ID NO:91的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:87的氨基酸序列;或
iv)所述DLL3-VH包含SEQ ID NO:109的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:100的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
i)所述DLL3-VH包含SEQ ID NO:12的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:13的氨基酸序列;或
ii)所述DLL3-VH包含SEQ ID NO:14的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:15的氨基酸序列;或
iii)所述DLL3-VH包含SEQ ID NO:16的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:17的氨基酸序列;或
iv)所述DLL3-VH包含SEQ ID NO:18的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:19的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:63的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:61的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:81的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:77的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:91的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:87的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:109的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:100的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述CD3-VH包含SEQ ID NO:136的氨基酸序列,和所述CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述CD3-VH包含SEQ ID NO:138的氨基酸序列,和所述CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述特异性结合DLL3的抗原结合模块或所述特异性结合CD3的抗原结合模块包含能够形成二聚体的Titin链和Obscurin链。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述特异性结合DLL3的抗原结合模块包含能够形成二聚体的Titin链和Obscurin链。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述特异性结合CD3的抗原结合模块包含能够形成二聚体的Titin链和Obscurin链。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述Titin链包含选自由SEQ ID NO:192至SEQ ID NO:210组成的组的氨基酸序列,所述Obscurin链包含选自由SEQ ID NO:211至SEQ ID NO:251组成的组的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述Titin链包含SEQ ID NO:208的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述Obscurin链包含SEQ ID NO:246的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述Titin链包含SEQ ID NO:208的氨基酸序列,和所述Obscurin链包含SEQ ID NO:246的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含Fc区。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含人IgG Fc区。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含人IgG1Fc区。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含Fc区,所述Fc区包含一个或多个能够减少Fc区与Fcγ受体结合的氨基酸取代。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含Fc区,所述Fc区是人IgG1Fc区,并且在234和235位置的氨基酸为A,编号依据为EU索引。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含Fc区,所述Fc区包含能够相互缔合的第一亚基Fc1和第二亚基Fc2,所述Fc1和Fc2各自独立地具有一个或多个减少Fc区同源二聚化的氨基酸取代。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含Fc区,所述Fc区包含能够相互缔合的第一亚基Fc1和第二亚基Fc2,所述Fc1具有根据杵臼技术的凸起结构,和所述Fc2具有根据杵臼技术的孔结构。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含Fc区,所述Fc区包含能够相互缔合的第一亚基Fc1和第二亚基Fc2,所述Fc1具有根据杵臼技术的凸起结构,和所述Fc2具有根据杵臼技术的孔结构,所述Fc1在366位置的氨基酸为W;并且所述Fc2在366位置的氨基酸为S、在368位置的氨基酸为A、和在407位置的氨基酸为V,编号依据为EU索引。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含Fc区,所述Fc区包含能够相互缔合的第一亚基Fc1和第二亚基Fc2,所述Fc1具有根据杵臼技术的凸起结构,和所述Fc2具有根据杵臼技术的孔结构,其中,所述Fc1在354位置的氨基酸为C和在366位置的氨基酸为W;并且所述Fc2在349位置的氨基酸为C、在366位置的氨基酸为S、在368位置的氨基酸为A、和在407位置的氨基酸为V,编号依据为EU索引。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含Fc区,所述Fc区包含能够相互缔合的第一亚基Fc1和第二亚基Fc2,其中,所述Fc1包含SEQ ID NO:143的氨基酸序列;和所述Fc2包含SEQ ID NO:144的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含Fc区,所述Fc区包含能够相互缔合的第一亚基Fc1和第二亚基Fc2,其中,所述Fc1在349位置的氨基酸为C、在366位置的氨基酸为W和在237位置的氨基酸为A;并且所述Fc2在354位置的氨基酸为C、在366位置的氨基酸为S、在368位置的氨基酸为A、在407位置的氨基酸为V和和在237位置的氨基酸为A,编号依据为EU索引。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含Fc区,所述Fc区包含能够相互缔合的第一亚基Fc1和第二亚基Fc2,其中,所述Fc1包含SEQ ID NO:145的氨基酸序列;和所述Fc2包含SEQ ID NO:146的氨基酸序列。
应当理解,本公开中的序数词“第一”、“第二”、“式a”、“式b”、“Fc1”、“连接子3”等仅用于区分不同的技术特征、元素、组件、步骤,不意图对水平、顺序、数量构成限制。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含一个特异性结合DLL3的抗原结合模块和一个特异性结合CD3的抗原结合模块。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含一个特异性结合DLL3的抗原结合模块和一个特异性结合CD3的抗原结合模块,其中:
所述特异性结合DLL3的抗原结合模块是Fab;所述特异性结合CD3的抗原结合模块是经替换的Fab,其包含能够形成二聚体的Titin链和Obscurin链。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含一个特异性结合DLL3的抗原结合模块和一个特异性结合CD3的抗原结合模块,其中:
所述特异性结合CD3的抗原结合模块是Fab,所述特异性结合DLL3的抗原结合模块是经替换的Fab,其包含能够形成二聚体的Titin链和Obscurin链。
在一些实施方式中,如前任一项所述的抗原结合分子,所述抗原结合分子包含一条具有式(a)所示结构的第一链、一条具有式(b)所示结构的第二链、一条具有式(c)所示结构的第三链和一条具有式(d)所示结构的第四链,
(a)[DLL3-VH]-[连接子1]-[Titin链]/[Obscurin链]-[Fc2]/[Fc1],
(b)[DLL3-VL]-[连接子2]-[Obscurin链]/[Titin链],
(c)[CD3-VH]-[CH1]-[Fc1]/[Fc2],
(d)[CD3-VL]-[CL],
其中:所述连接子1和所述连接子2是相同或不同的肽连接子;式(a)、(b)、(c)和(d)所示的结构是从N端至C端排列的。“/”表示“或”,即Fc1和Fc2可互换位置,Titin链和Obscurin链可互换位置。
在一些实施方式中,如前任一项所述的抗原结合分子,所述抗原结合分子包含一条具有式(a)所示结构的第一链、一条具有式(b)所示结构的第二链、一条具有式(c)所示结构的第三链和一条具有式(d)所示结构的第四链,
(a)[DLL3-VH]-[连接子1]-[Titin链]-[Fc2],
(b)[DLL3-VL]-[连接子2]-[Obscurin链],
(c)[CD3-VH]-[CH1]-[Fc1],
(d)[CD3-VL]-[CL],
其中:所述连接子1和所述连接子2是相同或不同的肽连接子;式(a)、(b)、(c)和(d)所示的结构是从N端至C端排列的;Fc1和Fc2可互换位置,Titin链和Obscurin链可互换位置。
在一些实施方式中,如前任一项所述的抗原结合分子,所述抗原结合分子包含一条具有式(a)所示结构的第一链、一条具有式(b)所示结构的第二链、一条具有式(c)所示结构的第三链和一条具有式(d)所示结构的第四链,
(a)[DLL3-VH]-[连接子1]-[Titin链]-[Fc2],
(b)[DLL3-VL]-[连接子2]-[Obscurin链],
(c)[CD3-VH]-[CH1]-[Fc1],
(d)[CD3-VL]-[CL],
其中:所述连接子1和所述连接子2是相同或不同的肽连接子;式(a)、(b)、(c)和(d)所示的结构是从N端至C端排列的。
在一些实施方式中,如前任一项所述的抗原结合分子,所述抗原结合分子包含一条具有式(a')所示结构的第一链、一条具有式(b')所示结构的第二链、一条具有式(c')所示结构的第三链和一条具有式(d')所示结构的第四链,
(a')[CD3-VH]-[连接子1]-[Titin链]/Obscurin链]-[Fc2]/[Fc1],
(b')[CD3-VL]-[连接子2]-[Obscurin链]/[Titin链],
(c')[DLL3-VH]-[CH1]-[Fc1]/[Fc2],
(d')[DLL3-VL]-[CL],
其中:所述连接子1和所述连接子2不存在,即所述连接子1和所述连接子2均是肽键;式(a')、(b')、(c')和(d')所示的结构是从N端至C端排列的。“/”表示“或”,即Fc1和Fc2可互换位置,Titin链和Obscurin链可互换位置。
在一些实施方式中,如前任一项所述的抗原结合分子,所述抗原结合分子包含一条具有式(a')所示结构的第一链、一条具有式(b')所示结构的第二链、一条具有式(c')所示结构的第三链和一条具有式(d')所示结构的第四链,
(a')[CD3-VH]-[连接子1]-[Titin链]-[Fc2],
(b')[CD3-VL]-[连接子2]-[Obscurin链],
(c')[DLL3-VH]-[CH1]-[Fc1],
(d')[DLL3-VL]-[CL],
其中:所述连接子1和所述连接子2不存在,即所述连接子1和所述连接子2均是肽键;式(a')、(b')、(c')和(d')所示的结构是从N端至C端排列的;Fc1和Fc2可互换位置,Titin链和Obscurin链可互换位置。
在一些实施方式中,如前任一项所述的抗原结合分子,所述抗原结合分子包含一条具有式(a)所示结构的第一链、一条具有式(b)所示结构的第二链、一条具有式(c)所示结构的第三链和一条具有式(d)所示结构的第四链,
(a')[CD3-VH]-[连接子1]-[Titin链]-[Fc2],
(b')[CD3-VL]-[连接子2]-[Obscurin链],
(c')[DLL3-VH]-[CH1]-[Fc1],
(d')[DLL3-VL]-[CL],
其中:所述连接子1和所述连接子2不存在,即所述连接子1和所述连接子2均是肽键;式(a)、(b)、(c)和(d)所示的结构是从N端至C端排列的。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;和
所述的CD3-VH包含SEQ ID NO:136的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:119的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:39的氨 基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:61的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:63的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:63的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:81的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:77的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:91的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:87的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:109的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:100的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:91的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:87的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述的Titin链和Obscurin链为本披露中表3-1和表3-2中任意可以形成二聚体的Titin链和Obscurin链。在一些实施方式中,如前任一项所述的抗原结合分子,其中所述的Titin链包含如SEQ ID NO:208的氨基酸序列。在一些实施方式中,如前任一项所述的抗原结合分子,其中所述的Obscurin链包含如SEQ ID NO:246的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述的连接子1和连接子2均为本领域已知的肽连接子,只要抗原结合分子能够展现出期望的抗原结合活性。例如,肽连接子可以是具有1-50或3-20个氨基酸残基的柔性肽。在一些实施方案中,所述肽连接子的长度为3-15个氨基酸残基。在一些实施方案中,所述肽连接子1和连接子2各自独立地具有(GGGGS)n的结构,其中n是1、2或3。在一些实施方案中,所述的连接子1和连接子2的序列均为GGGGS(SEQ ID NO:147)。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述的CH1为IgG的CH1序列。在一些实施方案中,所述的CH1为IgG1的CH1。在一些实施方案中,所述的CH1包含SEQ ID NO:141的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述的CL为抗体的轻链恒定区。在一些实施方式中,如前任一项所述的抗原结合分子,其中所述的CL为kappa链或lamada链的轻链恒定区。在一些实施方式中,其中所述的CL包含SEQ ID NO:142的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子具有:
一条包含SEQ ID NO:171的氨基酸序列的第一链、一条包含SEQ ID NO:172的氨基酸序列的第二链、一条包含SEQ ID NO:154的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链;或
一条包含SEQ ID NO:171的氨基酸序列的第一链、一条包含SEQ ID NO:172的氨基酸序列的第二链、一条包含SEQ ID NO:156的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链;或
一条包含SEQ ID NO:152的氨基酸序列的第一链、一条包含SEQ ID NO:153的氨基酸序列的第二链、一条包含SEQ ID NO:154的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链;或
一条包含SEQ ID NO:152的氨基酸序列的第一链、一条包含SEQ ID NO:153的氨基酸序列的第二链、一条包含SEQ ID NO:156的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链;或
一条包含SEQ ID NO:164的氨基酸序列的第一链、一条包含SEQ ID NO:165的氨基酸序列的第二链、一条包含SEQ ID NO:154的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链;或
一条包含SEQ ID NO:164的氨基酸序列的第一链、一条包含SEQ ID NO:165的氨基酸序列的第二链、一条包含SEQ ID NO:156的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链;或
一条包含SEQ ID NO:178的氨基酸序列的第一链、一条包含SEQ ID NO:179的氨基酸序列的第二链、一条包含SEQ ID NO:154的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链;或
一条包含SEQ ID NO:178的氨基酸序列的第一链、一条包含SEQ ID NO:179的氨基酸序列的第二链、一条包含SEQ ID NO:156的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子具有:
一条包含SEQ ID NO:171的氨基酸序列的第一链、一条包含SEQ ID NO:172的氨基酸序列的第二链、一条包含SEQ ID NO:154的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含一个特异性结合DLL3的抗原结合模块和一个特异性结合CD3的抗原结合模块,所述特异性结合DLL3的抗原结合模块是Fab;所述特异性结合CD3的抗原结合模块是scFv。在一些实施方式中,如前任一项所述的抗原结合分子,所述抗原结合分子包含一条具有式(e)所示结构的第一链、一条具有式(f)所示结构的第二链和一条具有式(g)所示结构的第三链,
(e)[DLL3-VL]-[CL],
(f)[DLL3-VH]-[CH1]-[Fc2]/[Fc1],
(g)[CD3-VH]-[连接子3]-[CD3-VL]-[连接子4]-[Fc1]/[Fc2],
其中:所述连接子3和所述连接子4是相同或不同的肽连接子;
式(e)、(f)和(g)所示的结构是从N端至C端排列的。“/”表示“或”,即Fc1和Fc2可互换位置。
在一些实施方式中,如前任一项所述的抗原结合分子,所述抗原结合分子包含一条具有式(e)所示结构的第一链、一条具有式(f)所示结构的第二链和一条具有式(g)所示结构的第三链,
(e)[DLL3-VL]-[CL],
(f)[DLL3-VH]-[CH1]-[Fc2],
(g)[CD3-VH]-[连接子3]-[CD3-VL]-[连接子4]-[Fc1],
其中:所述连接子3和所述连接子4是相同或不同的肽连接子;
式(e)、(f)和(g)所示的结构是从N端至C端排列的;Fc1和Fc2可互换位置。
在一些实施方式中,如前任一项所述的抗原结合分子,所述抗原结合分子包含一条具有式(e)所示结构的第一链、一条具有式(f)所示结构的第二链和一条具有式(g)所示结构的第三链,
(e)[DLL3-VL]-[CL],
(f)[DLL3-VH]-[CH1]-[Fc2],
(g)[CD3-VH]-[连接子3]-[CD3-VL]-[连接子4]-[Fc1],
其中:所述连接子3和所述连接子4是相同或不同的肽连接子;
式(e)、(f)和(g)所示的结构是从N端至C端排列的。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含一个特异性结合DLL3的抗原结合模块和一个特异性结合CD3的抗原结合模块,所述特异性结合DLL3的抗原结合模块是scFv;所述特异性结合CD3的抗原结合模块是Fab。
在一些实施方式中,如前任一项所述的抗原结合分子,所述抗原结合分子包含一条具有式(e')所示结构的第一链、一条具有式(f')所示结构的第二链和一条具有式(g')所示结构的第三链,
(e')[CD3-VL]-[CL],
(f')[CD3-VH]-[CH1]-[Fc2]/[Fc1],
(g')[DLL3-VH]-[连接子3]-[DLL3-VL]-[连接子4]-[Fc1]/[Fc2],
其中:所述连接子3和所述连接子4是相同或不同的肽连接子;
式(e')、(f')和(g')所示的结构是从N端至C端排列的。“/”表示“或”。
在一些实施方式中,如前任一项所述的抗原结合分子,所述抗原结合分子包含一条具有式(e')所示结构的第一链、一条具有式(f')所示结构的第二链和一条具有式(g')所示结构的第三链,
(e')[CD3-VL]-[CL],
(f')[CD3-VH]-[CH1]-[Fc2],
(g')[DLL3-VH]-[连接子3]-[DLL3-VL]-[连接子4]-[Fc1],
其中:所述连接子3和所述连接子4是相同或不同的肽连接子;
式(e')、(f')和(g')所示的结构是从N端至C端排列的;Fc1和Fc2可互换位置。
在一些实施方式中,如前任一项所述的抗原结合分子,所述抗原结合分子包含一条具有式(e')所示结构的第一链、一条具有式(f')所示结构的第二链和一条具有式(g')所示结构的第三链,
(e')[CD3-VL]-[CL],
(f')[CD3-VH]-[CH1]-[Fc2],
(g')[DLL3-VH]-[连接子3]-[DLL3-VL]-[连接子4]-[Fc1],
其中:所述连接子3和所述连接子4是相同或不同的肽连接子;
式(e')、(f')和(g')所示的结构是从N端至C端排列的。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的 氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:119的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:61的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:63的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:91的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:87的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:81的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:77的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:109的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:100的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:91的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:87的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述的连接子3和连接子4均为本领域已知的肽连接子,只要抗原结合分子能够展现出期望的抗原结合活性。例如,肽连接子可以是具有1-50或3-20个氨基酸残基的柔性肽。在一些实施方案中,所述肽连接子的长度为3-15个氨基酸残基。在一些实施方案中,所述肽连接子3和连接子4各自独立地具有(GGGGS)n的结构,其中n是1-5。在一些实施方案中,n为1、2、3或4。在一些实施方案中,所述的连接子3的序列为GGGGSGGGGSGGGGS(SEQ ID NO:148)。在一些实施方案中,所述的连接子4的序列为GGGGS(SEQ ID NO:147)。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述的CH1为IgG的CH1序列。在一些实施方案中,所述的CH1为IgG1的CH1。在一些实施方案中,所述的CH1包含SEQ ID NO:141的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述的CL为抗体的轻链恒定区。在一些实施方式中,如前任一项所述的抗原结合分子,其中所述的CL为kappa链或lamada链的轻链恒定区。在一些实施方式中,其中所述的CL包含SEQ ID NO:142的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子具有:
一条包含SEQ ID NO:173的氨基酸序列的第一链、一条包含SEQ ID NO:174的氨基酸序列的第二链和一条包含SEQ ID NO:160的氨基酸序列的第三链;或
一条包含SEQ ID NO:173的氨基酸序列的第一链、一条包含SEQ ID NO:174的氨基酸序列的第二链和一条包含SEQ ID NO:159的氨基酸序列的第三链;或
一条包含SEQ ID NO:157的氨基酸序列的第一链、一条包含SEQ ID NO:158的氨基酸序列的第二链和一条包含SEQ ID NO:159的氨基酸序列的第三链;或
一条包含SEQ ID NO:157的氨基酸序列的第一链、一条包含SEQ ID NO:158的氨基酸序列的第二链和一条包含SEQ ID NO:160的氨基酸序列的第三链;或
一条包含SEQ ID NO:166的氨基酸序列的第一链、一条包含SEQ ID NO:167的氨基酸序列的第二链和一条包含SEQ ID NO:159的氨基酸序列的第三链;或
一条包含SEQ ID NO:166的氨基酸序列的第一链、一条包含SEQ ID NO:167的氨基酸序列的第二链和一条包含SEQ ID NO:160的氨基酸序列的第三链;或
一条包含SEQ ID NO:180的氨基酸序列的第一链、一条包含SEQ ID NO:181的氨基酸序列的第二链和一条包含SEQ ID NO:159的氨基酸序列的第三链;或
一条包含SEQ ID NO:180的氨基酸序列的第一链、一条包含SEQ ID NO:181的氨基酸序列的第二链和一条包含SEQ ID NO:160的氨基酸序列的第三链。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子具有:
一条包含SEQ ID NO:173的氨基酸序列的第一链、一条包含SEQ ID NO:174的氨基酸序列的第二链和一条包含SEQ ID NO:160的氨基酸序列的第三链。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含一个特异性结合DLL3的抗原结合模块和一个特异性结合CD3的抗原结合模块,
所述抗原结合分子包含一条具有式(h)所示结构的第一链和一条具有式(i)所示结构的第二链,
(h)[DLL3-VL]-[连接子5]-[CD3-VH]-[连接子6]-[Fc1]/[Fc1],
(i)[CD3-VL]-[连接子7]-[DLL3-VH]-[连接子8]-[Fc2]/[Fc2],
其中:所述连接子5、连接子6、连接子7和连接子8是相同或不同的肽连接子;
式(h)和(i)所示的结构是从N端至C端排列的。“/”表示“或”,即Fc1和Fc2可互换位置。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含一个特异性结合DLL3的抗原结合模块和一个特异性结合CD3的抗原结合模块,
所述抗原结合分子包含一条具有式(h)所示结构的第一链和一条具有式(i)所示结构的第二链,
(h)[DLL3-VL]-[连接子5]-[CD3-VH]-[连接子6]-[Fc1],
(i)[CD3-VL]-[连接子7]-[DLL3-VH]-[连接子8]-[Fc2],
其中:所述连接子5、连接子6、连接子7和连接子8是相同或不同的肽连接子;
式(h)和(i)所示的结构是从N端至C端排列的;Fc1和Fc2可互换位置。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含一个特异性结合DLL3的抗原结合模块和一个特异性结合CD3的抗原结合模块,
所述抗原结合分子包含一条具有式(h)所示结构的第一链和一条具有式(i)所示结构的第二链,
(h)[DLL3-VL]-[连接子5]-[CD3-VH]-[连接子6]-[Fc1],
(i)[CD3-VL]-[连接子7]-[DLL3-VH]-[连接子8]-[Fc2],
其中:所述连接子5、连接子6、连接子7和连接子8是相同或不同的肽连接子;
式(h)和(i)所示的结构是从N端至C端排列的。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含一个特异性结合DLL3的抗原结合模块和一个特异性结合CD3的抗原结合模块,
所述抗原结合分子包含一条具有式(h')所示结构的第一链和一条具有式(i')所示结构的第二链,
(h')[CD3-VL]-[连接子5]-[DLL3-VH]-[连接子6]-[Fc1]/[Fc2],
(I')[DLL3-VL]-[连接子7]-[CD3-VH]-[连接子8]-[Fc2]/[Fc1],
其中:所述连接子5、连接子6、连接子7和连接子8是相同或不同的肽连接子;
式(h')和(i')所示的结构是从N端至C端排列的。“/”表示“或”。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含一个特异性结合DLL3的抗原结合模块和一个特异性结合CD3的抗原结合模块,
所述抗原结合分子包含一条具有式(h')所示结构的第一链和一条具有式(i')所示结构的第二链,
(h')[CD3-VL]-[连接子5]-[DLL3-VH]-[连接子6]-[Fc1],
(I')[DLL3-VL]-[连接子7]-[CD3-VH]-[连接子8]-[Fc2],
其中:所述连接子5、连接子6、连接子7和连接子8是相同或不同的肽连接子;
式(h')和(i')所示的结构是从N端至C端排列的;Fc1和Fc2可互换位置。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子包含一个特异性结合DLL3的抗原结合模块和一个特异性结合CD3的抗原结合模块,
所述抗原结合分子包含一条具有式(h')所示结构的第一链和一条具有式(i')所示结构的第二链,
(h')[CD3-VL]-[连接子5]-[DLL3-VH]-[连接子6]-[Fc1],
(I')[DLL3-VL]-[连接子7]-[CD3-VH]-[连接子8]-[Fc2],
其中:所述连接子5、连接子6、连接子7和连接子8是相同或不同的肽连接子;
式(h')和(i')所示的结构是从N端至C端排列的。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135 的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的 氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:119的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131或135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;和
所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:61的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:63的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:64的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:65的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:66的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:67的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:65的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:66的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:67的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:91的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:87的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:81的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:77的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:109的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:100的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列。
在一些实施方式中,如前任一项所述的抗原结合分子,其中:
所述的DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:63的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列;
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述的连接子5、连接子6、连接子7和连接子8均为本领域已知的肽连接子,只要抗原结合分子能够展现出期望的抗原结合活性。例如,肽连接子可以是包含1-50或3-20个氨基酸残基的柔性肽。在一些实施方案中,所述肽连接子的长度为1-15个氨基酸残基。在一些实施方案中,所述连接子5具有(GGGS)nGm的结构,其中n是1-5,优选为1、2或3;m为1-10,优选为4、5、6、7或8。在一些实施方案中,所述连接子5的序列为GGGSGGGG(SEQ ID NO:149)。在一些实施方案中,所述连接子连接子6和连接子8具有Gm的结构,其中m为1-5,优选为1、2或3。在一些实施方案中,连接子6和连接子8的序列为G(SEQ ID NO:150)。在一些实施方案中,所述连接子7具有(GGGGS)nGm的结构,其中n是1-5,优选为1、2或3;m为1-10,优选为4、5、6、7或8。在一些实施方案中,连接子7的序列为GGGGSGGGG(SEQ ID NO:151)。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子具有:
一条包含SEQ ID NO:185的氨基酸序列的第一链和一条包含SEQ ID NO:162的氨基酸序列的第二链;或
一条包含SEQ ID NO:161的氨基酸序列的第一链和一条包含SEQ ID NO:162的氨基酸序列的第二链;或
一条包含SEQ ID NO:163的氨基酸序列的第一链和一条包含SEQ ID NO:162的氨基酸序列的第二链;或
一条包含SEQ ID NO:259的氨基酸序列的第一链和一条包含SEQ ID NO:162的氨基酸序列的第二链;或
一条包含SEQ ID NO:260的氨基酸序列的第一链和一条包含SEQ ID NO:162的氨基酸序列的第二链;或
一条包含SEQ ID NO:168的氨基酸序列的第一链和一条包含SEQ ID NO:169的氨基酸序列的第二链;或
一条包含SEQ ID NO:170的氨基酸序列的第一链和一条包含SEQ ID NO:169的氨基酸序列的第二链;或
一条包含SEQ ID NO:175的氨基酸序列的第一链和一条包含SEQ ID NO:176的氨基酸序列的第二链;或
一条包含SEQ ID NO:177的氨基酸序列的第一链和一条包含SEQ ID NO:176的氨基酸序列的第二链;或
一条包含SEQ ID NO:182的氨基酸序列的第一链和一条包含SEQ ID NO:183的氨基酸序列的第二链;或
一条包含SEQ ID NO:184的氨基酸序列的第一链和一条包含SEQ ID NO:183的氨基酸序列的第二链;或
一条包含SEQ ID NO:186的氨基酸序列的第一链和一条包含SEQ ID NO:162的氨基酸序列的第二链;或
一条包含SEQ ID NO:187的氨基酸序列的第一链和一条包含SEQ ID NO:188的氨基酸序列的第二链;或
一条包含SEQ ID NO:187的氨基酸序列的第一链和一条包含SEQ ID NO:189的氨基酸序列的第二链;或
一条包含SEQ ID NO:190的氨基酸序列的第一链和一条包含SEQ ID NO:188的氨基酸序列的第二链;或
一条包含SEQ ID NO:190的氨基酸序列的第一链和一条包含SEQ ID NO:189的氨基酸序列的第二链;或
一条包含SEQ ID NO:191的氨基酸序列的第一链和一条包含SEQ ID NO:188的氨基酸序列的第二链;或
一条包含SEQ ID NO:191的氨基酸序列的第一链和一条包含SEQ ID NO:189的氨基酸序列的第二链。
在一些实施方式中,如前任一项所述的抗原结合分子,其中所述抗原结合分子具有:
一条包含SEQ ID NO:185的氨基酸序列的第一链和一条包含SEQ ID NO:162的氨基酸序列的第二链。
在另一方面,本披露还提供一种抗DLL3抗体,其能够特异性结合DLL3,所述的抗DLL3抗体包含重链可变区DLL3-VH和轻链可变区DLL3-VL,其中:
(i)所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:12、56或57中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:13、63、64、65、66或67中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列,或
(ii)所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:14、79、80、81或82中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2 和DLL3-LCDR3分别包含SEQ ID NO:15中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列,或
(iii)所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:16、91、92、93或94中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:17中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列,或
(iv)所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:18、107、108、109、110、112、113、114或115中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:19中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
(i)所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:12中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:13中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列,或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:54中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:64中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:54中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:63中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:56中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:65中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:56中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包 含SEQ ID NO:66中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:56中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:67中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:57中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:65中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:57中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:66中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:57中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:67中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
(ii)所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:14中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:15中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列,或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:81中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:77中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列,或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:79、80或82中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3 分别包含SEQ ID NO:77中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
(iii)所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:16中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:17中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:91中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:87中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:92、93或94中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:87中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
(iv)所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:18中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:19中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:109中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:100中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列;或
所述DLL3-VH中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3分别包含SEQ ID NO:107、108、110、112、113、114或115中的DLL3-HCDR1、DLL3-HCDR2和DLL3-HCDR3的氨基酸序列,和所述DLL3-VL中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3分别包含SEQ ID NO:100中的DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3的氨基酸序列。
在一些实施方案中,所述DLL3-HCDR1、DLL3-HCDR2、DLL3-HCDR3、DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3根据Kabat、IMGT、Chothia、AbM或Contact编号规则定义。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
ii)所述DLL3-VH具有:包含SEQ ID NO:26或84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27或85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:28或83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
iii)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:32、96、97、98或99的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;或
iv)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:37、117、118、119或120的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
i)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23 的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
i)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨 基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨 基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
ii)所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:28的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
iii)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;或
iv)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:119的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:39的氨 基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:119的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3。
在一些实施方式中,如前任一项所述的抗DLL3抗体,所述DLL3-HCDR1、DLL3-HCDR2、DLL3-HCDR3、DLL3-LCDR1、DLL3-LCDR2和DLL3-LCDR3是根据Kabat编号规则定义的。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其在25℃条件下以小于4×10-9M、3×10-9M、2×10-9M、1×10-9M、9×10-10M、8×10-10M、7×10-10M、6×10-10M、5×10-10M、4×10-10M、3×10-10M、2×10-10M、1×10-10M、9×10-11M的KD结合人DLL3,所述KD是通过表面等离子体共振法测量的。
在一些实施方式中,如前所述的抗DLL3抗体,其中:
(i)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和
所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24、71、72或73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25或74的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
(ii)所述DLL3-VH具有:包含SEQ ID NO:26或84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27或85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:28或83的氨基酸序列的DLL3-HCDR3;和
所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自42G、44V和71Y组成的组中的一个或多个氨基酸取代;或
(iii)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:32、96、97、98或99的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、24T、44S、71V和73K组成的组中的一个或多个氨基酸取代;和
所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、9K、43S、68A和85D组成的组中的一个或多个氨基酸取代;或
(iv)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:37、117、118、119或120的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、3R、5Q、7F、9P、10V、12V、40S、41H、44S、48I、67A、69L、71V、73K、75S和83T组成的组中的一个或多个氨基酸取代;和
所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3;且所述DLL3-VL的FR区包含选自9K、43S、60D、68A、87H和100S组成的组中的一个或多个氨基酸取代。
在一些实施方式中,如前任一项所述的抗原结合分子,其在25℃条件下以小于4×10-9M、3×10-9M、2×10-9M、1×10-9M、9×10-10M、8×10-10M、7×10-10M、6×10-10M、5×10-10M、4×10-10M、3×10-10M、2×10-10M、1×10-10M、9×10-11M的KD结合人DLL3,所述KD是通过表面等离子体共振法测量的。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR 区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR 区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自42G、44V和71Y组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自42G、44V和71Y组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨 基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自42G、44V和71Y组成的组中的一个或多个氨基酸取代;或
所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:28的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3,且所述DLL3-VL的FR区包含选自42G、44V和71Y组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、24T、44S、71V和73K组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3且所述DLL3-VL的FR区包含选自1N、9K、43S、68A和85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:119的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3,且所述DLL3-VH的FR区包含选自1E、3R、5Q、7F、9P、10V、12V、40S、41H、44S、48I、67A、69L、71V、73K、75S和83T组成的组中的一个或多个氨基酸取代;和所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3且所述DLL3-VL的FR区包含选自9K、43S、60D、68A、87H和100S组成的组中的一个或多个氨基酸取代。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:50的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:50的FR区包含选自Q1E、Q43K、M48I、V67A、I69L、R71V、T73K和S76N组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:51的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:51的FR区包含选自Q1E、5Q、R38K、V68A、F69L、L71V、T73K、V75S和S76N组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:52的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:52的FR区包含选自F27Y、S30T、I69L、R71V、D73K和T93A组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VL包含SEQ ID NO:62的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:62的FR区包含选自F36L、A43S、P44F、S46G、T69A、F71Y和T85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VL包含SEQ ID NO:68的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:68的FR区包含选自Y36L、Q42K、L46G、T69A、F71Y、E79Q和V85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:78的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:78的FR区包含一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VL包含SEQ ID NO:75的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:75的FR区包含选自K42G、P44V和F71Y组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:95的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:95的FR区包含选自Q1E、A24T、R44S、R71V和T73K组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VL包含SEQ ID NO:88的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:88的FR区包含选自D1N、D9K、P43S、G68A和V85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:116的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:116的FR区包含选自Q1E、Q3R、V5Q、S7F、A9P、E10V、K12V、A40S、P41H、R44S、M48I、V67A、I69L、R71V、T73K、A75S和R83T组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VL包含SEQ ID NO:100的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:100的FR区包含选自D9K、P43S、G68A、和Y87H组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VL包含SEQ ID NO:103的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:103的FR区包含选自A43S、S60D和Q100S组成的组中的一个或多个氨基酸取代。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:56的FR区包含一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:57的FR包含区一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VL包含SEQ ID NO:63的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:63的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自A43S和P44F组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VL包含SEQ ID NO:64的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:64的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自A43S和P44F组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VL包含SEQ ID NO:65的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:65的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自A43S和P44F组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VL包含SEQ ID NO:66的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:66的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自A43S和P44F组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VL包含SEQ ID NO:67的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:67的FR区包含一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:79、80、81或82的氨基酸序列,或SEQ ID NO:79、80、81或82的变体。在一些实施方案中,所述变体为在SEQ ID NO:79、80、81或82的FR区包含一个或多个氨基酸取代;和
所述DLL3-VL包含SEQ ID NO:75的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:75的FR区包含选自K42G、P44V和F71Y组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:91、92、93或94的氨基酸序列,或SEQ ID NO:91、92、93或94的变体。在一些实施方案中,所述变体为在SEQ ID NO:91、92、93或94的FR区包含一个或多个氨基酸取代;和
所述DLL3-VL包含SEQ ID NO:88的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:88的FR区包含选自D1N、D9K、P43S、G68A和V85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:107、108、109或110的氨基酸序列,或SEQ ID NO:107、108、109或110的变体。在一些实施方案中,所述变体为在SEQ ID NO:107、108、109或110的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自V5Q、S7F、A9P、E10V、K12V、A40S、P41H、M48I、V67A、A75S和R83T组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:112的氨基酸序列,或SEQ ID NO:112的变体。在一些实施方案中,所述变体为在SEQ ID NO:112的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自V5Q、A9P、K12V、A40S、P41H、4M8I、V67A和R83T组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:113的氨基酸序列,或SEQ ID NO:113的变体。在一些实施方案中,所述变体为在SEQ ID NO:113的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自V5Q、S7F、A9P、E10V、K12V、A40S、P41H、A75S和R83T组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:114的氨基酸序列,或SEQ ID NO:114的变体。在一些实施方案中,所述变体为在SEQ ID NO:114的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自V5Q、S7F、A9P、E10V、K12V、M48I、V67A、A75S和R83T组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:115的氨基酸序列,或SEQ ID NO:115的变体。在一些实施方案中,所述变体为在SEQ ID NO:115的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自V5Q、A9P、K12V、A40S、P41H、M48I和V67A组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VL包含SEQ ID NO:100的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:100的FR区包含选自D9K、P43S、G68A、和Y87H组成的组中的一个或多个氨基酸取代。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VL包含SEQ ID NO:103的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:103的FR区包含选自A43S、S60D和Q100S组成的组中的一个或多个氨基酸取代。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
i)所述DLL3-VH包含SEQ ID NO:43、44、45、46、47、48、49、50、51、52、53、54、55、56或57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:63、64、65、66或67的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:56或57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:58、59、60、61、62、63、64、65、66、67或68的氨基酸序列;或
ii)所述DLL3-VH包含SEQ ID NO:78、79、80、81或82的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:75、76或77的氨基酸序列;或
iii)所述DLL3-VH包含SEQ ID NO:89、90、91、92、93、94或95的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:86、87或88的氨基酸序列;或
iv)所述DLL3-VH包含SEQ ID NO:105、106、107、108、109、110、111、112、113、114、115或116的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:100、101、102、103或104的氨基酸序列。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:43、44或45的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:58、59或60的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:47、48、49、53、54或55的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:59的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:43、44或45的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:60的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:46、48、53、54或55的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:61的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:63或64的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:56或57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:65、66或67的氨基酸序列。
在一些实施方式中,如任一项前所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:78或79的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:75、76或77的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:78、79、80、81或82的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:77的氨基酸序列。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:89、90、91、92、93或94的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:86或87的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:95的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:87的氨基酸序列。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:105、106、107、108、109、110或111的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:100、101或102的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:112、113、114或115的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:100、103或104的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:109的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:103的氨基酸序列。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
i)所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:63的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:61的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:64的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:65的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:66的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:67的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:65的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:66的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:67的氨基酸序列;或
ii)所述DLL3-VH包含SEQ ID NO:81的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:77的氨基酸序列;或
iii)所述DLL3-VH包含SEQ ID NO:91的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:87的氨基酸序列;或
iv)所述DLL3-VH包含SEQ ID NO:109的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:100的氨基酸序列。
在一些实施方式中,如前所述的抗DLL3抗体,其中:
i)所述DLL3-VH包含SEQ ID NO:12的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:13的氨基酸序列;或
ii)所述DLL3-VH包含SEQ ID NO:14的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:15的氨基酸序列;或
iii)所述DLL3-VH包含SEQ ID NO:16的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:17的氨基酸序列;或
iv)所述DLL3-VH包含SEQ ID NO:18的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:19的氨基酸序列。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:63的氨基酸序列;或
所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:61的氨基酸序列。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:81的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:77的氨基酸序列。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:91的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:87的氨基酸序列。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中:
所述DLL3-VH包含SEQ ID NO:109的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:100的氨基酸序列。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中所述的抗DLL3抗体是抗体片段。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中所述的抗体片段为Fab、Fab'、F(ab')2、Fd、Fv、scFv、dsFv或dAb。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中所述的抗DLL3抗体包含重链恒定区和轻链恒定区。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中所述重链恒定区为人IgG的重链恒定区。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中所述轻链恒定区为人κ或λ的轻链恒定区。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中所述重链恒定区为人IgG1的重链恒定区。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中所述轻链恒定区为人κ的轻链恒定区。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中所述重链恒定区包含如SEQ ID NO:41的氨基酸序列。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中所述轻链恒定区包含如SEQ ID NO:42的氨基酸序列。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中所述的抗DLL3抗体包含重链和轻链,其中:
所述重链包含与SEQ ID NO:121具有至少85%、86%、87%、88%、89%、90%、91%、92%、93%、94%、95%、96%、97%、98%、99%序列同一性的氨基酸序列,和所述轻链包含与SEQ ID NO:122具有至少85%、86%、87%、88%、89%、90%、91%、92%、93%、94%、95%、96%、97%、98%、99%序列同一性的氨基酸序列;或
所述重链包含与SEQ ID NO:123具有至少85%、86%、87%、88%、89%、90%、91%、92%、93%、94%、95%、96%、97%、98%、99%序列同一性的氨基酸序列,和所述轻链包含与SEQ ID NO:124具有至少85%、86%、87%、88%、89%、90%、91%、92%、93%、94%、95%、96%、97%、98%、99%序列同一性的氨基酸序列;或
所述重链包含与SEQ ID NO:125具有至少85%、86%、87%、88%、89%、90%、91%、92%、93%、94%、95%、96%、97%、98%、99%序列同一性的氨基酸序列,和所述轻链包含与SEQ ID NO:126具有至少85%、86%、87%、88%、89%、90%、91%、92%、93%、94%、95%、96%、97%、98%、99%序列同一性的氨基酸序列;或
所述重链包含与SEQ ID NO:127具有至少85%、86%、87%、88%、89%、90%、91%、92%、93%、94%、95%、96%、97%、98%、99%序列同一性的氨基酸序列,和所述轻链包含与SEQ ID NO:128具有至少85%、86%、87%、88%、89%、90%、91%、92%、93%、94%、95%、96%、97%、98%、99%同一性的氨基酸序列。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中所述的抗DLL3抗体包含重链和轻链,其中:
所述重链包含SEQ ID NO:121的氨基酸序列,和所述轻链包含SEQ ID NO:122的氨基酸序列;或
所述重链包含SEQ ID NO:123的氨基酸序列,和所述轻链包含SEQ ID NO:124的氨基酸序列;
所述重链包含SEQ ID NO:125的氨基酸序列,和所述轻链包含SEQ ID NO:126的氨基酸序列;或
所述重链包含SEQ ID NO:127的氨基酸序列,和所述轻链包含SEQ ID NO:128的氨基酸序列。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中所述的抗DLL3抗体包含重链和轻链,其中所述重链包含与SEQ ID NO:121的氨基酸序列,和所述轻链包含与SEQ ID NO:122的氨基酸序列。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中所述的抗DLL3抗体包含重链和轻链,其中所述重链包含与SEQ ID NO:125的氨基酸序列,和所述轻链包含与SEQ ID NO:126的氨基酸序列。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中所述的抗DLL3抗体是双特异性抗体。
在一些实施方式中,如前任一项所述的抗DLL3抗体,其中所述的抗DLL3抗体是双特异性抗体,所述双特异性抗体特异性结合DLL3和CD3。
在另一个方面,本披露提供了一种药物组合物,其含有:治疗有效量的前述任一项所述的抗原结合分子或前述任一项所述的抗DLL3抗体,以及一种或更多种药学上可接受的载体、稀释剂、缓冲剂或赋形剂。在一些实施方案中,所述的药物组合物中还包含至少一种第二治疗剂。在一个实施例中,所述第二治疗剂是有利地与CD3/DLL3双特异性抗原结合分子组合的任何药剂。在一些实施方案中,所述第二治疗剂是能够特异性结合CD28的抗体。在一些实施方案中,所述第二治疗剂是能够特异性结合CD28和肿瘤细胞表面抗原(TAA)的双特异性抗体。在一些实施方案中,所述第二治疗剂是能够特异性结合CD28和DLL3的双特异性的抗体。
在另一个方面,本披露还提供分离的核酸,其编码前述任一项所述的抗原结合分子或前述任一项所述的抗DLL3抗体。
在另一个方面,本披露还提供载体,其包含前述的分离的核酸。
在另一个方面,本披露还提供一种宿主细胞,其包含前述的分离的核酸或载体。
在另一个方面,本披露还提供一种治疗肿瘤或癌症的方法,所述方法包括向受试者施用治疗有效量的前述任一项所述的抗原结合分子或前述任一项所述的抗DLL3抗体或如前任一项所述的药物组合物。
在另一个方面,本披露还提供前述任一项所述的抗原结合分子或前述任一项所述的抗体或前述任一项所述的药物组合物在制备治疗肿瘤或癌症的药物中的用途。
在另一个方面,本披露还提供用作药物的前述任一项所述的抗原结合分子或前述任一项所述的抗DLL3抗体或如前任一项所述的药物组合物。在一些实施方案中,所述药物用于治疗肿瘤或癌症。
在一些实施方式中,如前任一项所述的肿瘤或癌症选自:头和颈鳞状细胞癌、头和颈癌、脑癌、神经胶质瘤、多形性成胶质细胞瘤、神经母细胞瘤、中枢神经系统癌、神经内分泌肿瘤、咽喉癌、咽鳞癌、口腔鳞癌、鼻咽癌、食管癌、甲状腺癌、恶性胸膜间皮瘤、肺癌、乳腺癌、肝癌、肝胆癌、胰腺癌、胃癌、胃肠道癌、肠癌、结肠癌、结肠直肠癌、肾癌、透明细胞肾细胞癌、卵巢癌、子宫内膜癌、子宫颈癌、膀胱癌、前列腺癌、睾丸癌、皮肤癌、黑色素瘤、大细胞肺癌、三阴性乳腺癌、淋巴瘤和小细胞肺癌。
在一些实施方式中,如前所述的所述的肿瘤或癌症是表达DLL3的癌症。
在一些实施方式中,如前所述的肿瘤或癌症是实体瘤。
在一些实施方式中,如前所述的肿瘤或癌症是肺癌。
在一些实施方式中,如前所述的肿瘤或癌症是小细胞肺癌。
在一些实施方案中,如前所述治疗肿瘤或癌症的方法,其进一步包括使用第二治疗剂。在一些实施方案中,所述第二治疗剂包括抗肿瘤药剂、放射疗法、抗体药物缀合物、双特异性抗体、与抗肿瘤药剂缀合的双特异性抗体、免疫检查点抑制剂或其组合。
在一些实施方案中,如前所述治疗肿瘤或癌症的方法,所述第二治疗剂是有利地与CD3/DLL3双特异性抗原结合分子组合的任何药剂。在一些实施方案中,所述第二治疗剂是能够特异性结合CD28的抗体。在一些实施方案中,所述第二治疗剂是能够特异性结合CD28和肿瘤细胞表面抗原(TAA)的双特异性抗体。在一些实施方案中,所述第二治疗剂是能够特异性结合CD28和DLL3的双特异性的抗体。
在一些实施方案中,如前所述治疗肿瘤或癌症的方法,所述的第二治疗剂与本披露所任一项所述的抗原结合分子同时施用、序贯施用或分开施用。
本披露提供的抗原结合分子,具有治疗活性、安全性、药物代谢动力学特性和成药性(如稳定性)好的特点。
附图说明
图1A显示DLL3-CD3双特异性抗体的Format1的结构示意图,其中Ob代表Obscurin。
图1B显示DLL3-CD3双特异性抗体的Format2的结构示意图。
图1C显示DLL3-CD3双特异性抗体的Format3的结构示意图。
图2A显示双特异性抗体与DLL1结合的实验结果。结果显示,本披露的DLL3-CD3双特异性抗体不结合DLL1。
图2B显示双特异性抗体与DLL4结合的实验结果。结果显示,本披露的DLL3-CD3双特异性抗体不结合DLL4。
图3显示双特异性抗体对细胞的杀伤作用实验结果。结果显示,本披露的双特异性抗体对不表达DLL3的H460细胞无杀伤作用。
图4A显示双特异性抗体对T细胞的激活的实验结果,结果显示本披露的双特异性抗体在表达DLL3的DLL3/H82细胞存在时,具有明显的激活T细胞的作用。
图4B显示,当存在不表达DLL3的阴性细胞H460时,本披露的双特异性抗体不会激活T细胞。
图5A显示双特异性抗体的细胞因子释放的实验结果,结果显示,在H1184细胞存在的情况下,本披露的双特异性抗体刺激PBMC细胞分泌的IFNγ非常低。
图5B显示,在H1184细胞存在的情况下,本披露的双特异性抗体刺激PBMC细胞分泌的IL-6非常低。
具体实施方式
术语
本文所用的术语只是为了描述实施方案的目的,并非旨在进行限制。除非另外定义,本文所用的全部技术术语和科学术语具有与本披露所属领域的普通技术人员通常所理解的相同意义。
除非上下文另外清楚要求,否则在整个说明书和权利要求书中,应将词语“包含”、“具有”、“包括”等理解为具有包含意义,而不是排他性或穷举性意义;也即,“包括但不仅限于”的意义。除非另有说明,“包含”包括了“由……组成”。例如,对于包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,其明确的涵盖氨基酸序列如SEQ ID NO:20所示的DLL3-HCDR1。
本披露所用氨基酸三字母代码和单字母代码如J.biol.chem,243,p3558(1968)中所述。
术语“和/或”,例如“X和/或Y”应当理解为意指“X和Y”或“X或Y”并且应当被用来提供对两种含义或任一含义的明确支持。
除非被指定为来自非人物种(例如,“小鼠CD3”、“小鼠CD3片段”、“猴CD3”、“猴CD3片段”等),否则如本文使用的“CD3”和“CD3片段”是指众所周知的人CD3蛋白或其片段。
术语“氨基酸”是指天然存在的和合成的氨基酸,以及以与天然存在的氨基酸类似的方式起作用的氨基酸类似物和氨基酸模拟物。天然存在的氨基酸是由遗传密码编码的那些氨基酸,以及后来修饰的那些氨基酸,例如羟脯氨酸、γ-羧基谷氨酸和O-磷酸丝氨酸。氨基酸类似物是指与天然存在的氨基酸具有相同基本化学结构(即与氢、羧基、氨基和R基团结合的α碳)的化合物,例如高丝氨酸、正亮氨酸、甲硫氨酸亚砜、甲硫氨酸甲基锍。此类类似物具有修饰的R基团(例如,正亮氨酸)或修饰的肽骨架,但保留与天然存在的氨基酸相同的基本化学结构。氨基酸模拟物是指具有与氨基酸的一般化学结构不同的结构,但是以与天然存在的氨基酸类似的方式起作用的化学化合物。
术语“氨基酸突变”包括氨基酸取代,缺失,插入和修饰。可以进行取代、缺失、插入和修饰的任意组合来实现最终构建体,只要最终构建体拥有期望的特性,例如降低或对Fc受体的结合。氨基酸序列缺失和插入包括在多肽链的氨基端和/或羧基端的缺失和插入。具体的氨基酸突变可以是氨基酸取代。在一个实施方式中,氨基酸突变是非保守性的氨基酸取代,即将一个氨基酸用具有不同结构和/或化学特性的另一种氨基酸替换。氨基酸取代包括由非天然存在的氨基酸或由20种天然氨基酸的衍生物(例如4-羟脯氨酸、3-甲基组氨酸、鸟氨酸、高丝氨酸、5-羟赖氨酸)替换。可以使用本领域中公知的遗传或化学方法生成氨基酸突变。遗传方法可以包括定点诱变、PCR,基因合成等。预计基因工程以外的改变氨基酸侧链基团的方法,如化学修饰也是可用的。本文中可使用各种名称来指示同一氨基酸突变。本文中,可采用位置+氨基酸残基的方式表示特定位点的氨基酸残基,例如366W,则表示在366位点上的氨基酸残基为W。T366W则表示第366位点上的氨基酸残基由原来的T突变为了W。
术语“抗原结合分子”以最广义使用,涵盖各种特异性结合抗原的分子,包括但不限于抗体、其他具有抗原结合活性的多肽以及两者融合而成的抗体融合蛋白,只要它们展现出期望的抗原结合活性。本文的抗原结合分子包含可变区(VH)和可变区(VL),其共同构成抗原结合域。示例性的,本文中的抗原结合分子是双特异性抗原结合分子(例如:双特异性抗体)。
术语“抗体”以最广义使用,并且涵盖各种抗体结构,包括但不限于单克隆抗体,多克隆抗体;单特异性抗体,多特异性抗体(例如双特异性抗体),全长抗体和抗体片段(或抗原结合片段,或抗体片段,或抗原结合部分),只要它们展现出期望的抗原结合活性。根据上下文,技术人员能够确定“抗体”所指的具体含义。
“天然抗体”指天然存在的免疫球蛋白分子。例如,天然IgG抗体是约150000道尔顿的异四聚糖蛋白,由二硫键结合的两条轻链和两条重链构成。从N至C端,每条重链具有一个可变区(VH,又称作可变重域、重链可变区),接着是三个恒定域(CH1、CH2和CH3)。类似地,从N至C端,每条轻链具有一个可变区(VL,又称作可变轻域,或轻链可变域),接着是一个恒定轻域(轻链恒定区、CL)。术语“全长抗体”、“完整抗体”和“全抗体”在本文可互换使用,指具有与天然抗体结构基本类似的结构或具有含有如本文所限定的Fc区的重链的抗体。
术语“双特异性抗体”指能够对两个不同抗原或同一抗原的至少两个不同抗原表位特异性结合的抗体(包括抗体或其抗原结合片段,如单链抗体)。现有技术已公开了各种结构的双特异性抗体,根据IgG分子的完整性可分为IgG样双特异性抗体和抗体片段型双特异性抗体;根据抗原结合区域的数量,可分为二价、三价、四价或更多价的双特异性抗体,根据结构左右是否对称,可分为对称结构双特异性抗体和不对称结构双特异性抗体。其中,基于抗体片段的双特异性抗体,例如缺乏Fc片段的Fab片段,其通过将2个或多个Fab片段结合在一个分子中形成双特异性抗体,其具有较低的免疫原性,且分子量小,具有较高的肿瘤组织渗透性,该类型的典型的抗体结构如F(ab)2、scFv-Fab、(scFv)2-Fab等双特异性抗体;IgG样双特异性抗体(例如具有Fc片段),这类抗体相对分子量较大,Fc片段有助于抗体后期的纯化,并提高其溶解性、稳定性,Fc部分还可能会与受体FcRn结合,增加抗体血清半衰期,典型的双特异性抗体结构模型如KiH、CrossMAb、Triomab quadroma、FcΔAdp、ART-Ig、BiMAb、Biclonics、BEAT、DuoBody、Azymetric、XmAb、2:1TCBs、1Fab-IgG TDB、FynomAb、two-in-one/DAF、scFv-Fab-IgG、DART-Fc、LP-DART、CODV-Fab-TL、HLE-BiTE、F(ab)2-CrossMAb、IgG-(scFv)2、Bs4Ab、DVD-Ig、Tetravalent-DART-Fc、(scFv)4-Fc、CODV-Ig、mAb2、F(ab)4-CrossMAb等双特异性抗体(参见Aran F.Labrijn等,Nature Reviews Drug Discovery volume 18,pages585–608(2019);Chen S1等,J Immunol Res.2019 Feb 11;2019:4516041)。
术语“可变区”或“可变域”指抗原结合分子中结合抗原的域。本文中,特异性结合CD3的抗原结合模块中的重链可变区标示为CD3-VH,轻链可变区标示为CD3-VL;特异性结合CD3的抗原结合模块中的重链可变区标示为CD3-VH,轻链可变区标示为CD3-VL。VH和VL各包含四个保守的框架区(FR)和三个互补决定区(CDR)。其中,术语“互补决定区”或“CDR”指可变结构域内主要促成与抗原结合的区域;“框架”或“FR”是指除CDR残基之外的可变结构域残基。VH包含3个CDR区:HCDR1、HCDR2和HCDR3;VL包含3个CDR区:LCDR1、LCDR2和LCDR3。本文中,CD3-VH中的3个CDR区分别标示为CD3-HCDR1、CD3-HCDR2和CD3-HCDR3;CD3-VL中的3个CDR区分别标示为CD3-LCDR1、CD3-LCDR2和CD3-LCDR3;CD3-VH中的3个CDR区分别标示为CD3-HCDR1、 CD3-HCDR2和CD3-HCDR3;CD3-VL中的3个CDR区分别标示为CD3-LCDR1、CD3-LCDR2和CD3-LCDR3。每个VH和VL从N端到C端依次为:FR1、CDR1、FR2、CDR2、FR3、CDR3、FR4。单个VH或VL可能足以赋予抗原结合特异性。
可以通过各种公知方案来确定CDR的氨基酸序列边界,例如:“Kabat”编号规则(参见Kabat等(1991),“Sequences of Proteins of Immunological Interest”,第5版,Public Health Service,National Institutes of Health,Bethesda,MD)、“Chothia”编号规则、“ABM”编号规则、“contact”编号规则(参见Martin,ACR.Protein Sequence and Structure Analysis of Antibody Variable Domains[J].2001)和ImMunoGenTics(IMGT)编号规则(Lefranc,M.P.等,Dev.Comp.Immunol.,27,55-77(2003);Front Immunol.2018 Oct 16;9:2278)等;各种编号系统之间的对应关系是本领域技术人员熟知的。本披露的编号规则如下表1中所示。
表1.CDR编号系统之间的关系
除非另有说明,本披露实施方案中的可变区和CDR序列均适用“Kabat”编号规则。
术语“抗体片段”或“抗原结合片段”指不同于完整抗体的分子,其包含完整抗体的部分,所述部分保留了完整抗体的抗原结合能力。抗体片段的实例包括但不限于Fv、Fab、Fab’、Fab’-SH、F(ab′)2、单域抗体、单链Fab(scFab)、双抗体、线性抗体、单链抗体分子(例如scFv);以及由抗体片段形成的多特异性抗体。
术语“Fc区”或“片段可结晶区”用于定义抗体重链的C末端区域,包括天然Fc区和改造的Fc区。在一些实施方式中,Fc区包含了相同或不同的两个亚基。在一些实施方式中,人IgG重链的Fc区定义为从Cys226位置处的氨基酸残基或从Pro230延伸至其羧基末端。用于本文所述抗体的合适天然序列Fc区包括人IgG1、IgG2(IgG2A、IgG2B)、IgG3和IgG4。除非另有说明,Fc区的编号规则为EU索引。
术语“Titin链”是指Titin蛋白中一段长度为78-118个氨基酸的包含Titin Ig-样152结构域的肽段或其功能变体,所述Titin链能够与Obscurin Ig-样1或Obscurin-样Ig-样1结构域结合形成二聚化复合物。
术语“Obscurin链”是指Obscurin蛋白上一段长度为87-117个氨基酸的包含Obscurin Ig-样1结构域的肽段或其功能变体,或Obscurin-样1蛋白上一段长度为78-118个氨基酸的包含Obscurin-样Ig-样1结构域的肽段或其功能变体。
所述Obscurin链能够与Titin链结合形成二聚化复合物。本披露的Titin链与Obscurin链可用于分别替换Fab中的CH1和CL,形成经替换的Fab(Fab-S),该替换不影响抗原结合分子与抗原的结合。
术语“嵌合”抗体指抗体中的重和/或轻链的一部分自特定的来源或物种衍生,而重和/或轻链的剩余部分自不同来源或物种衍生的抗体。
术语“人源化”抗体是保留非人抗体的反应性同时在人中具有较低免疫原性的抗体。例如,可以通过保留非人CDR区并用其人对应物(即,恒定区以及可变区的框架区部分)替换抗体的其余部分来实现。
术语“亲和力”是指分子(例如,抗体)的单个结合部位与其结合配体(例如,抗原)之间非共价相互作用的总体的强度。除非另外指明,如本文所用,“结合亲和力”是指内部结合亲和力,其反映出结合对(例如,抗体与抗原)的成员之间1:1相互作用。分子X对其配体Y的亲和力通常可以由平衡解离常数(KD)表示。亲和力可以通过本领域已知的常规方法(包括本文所述的那些)测量。术语“kassoc”或“ka”指特定抗体-抗原相互作用的缔合(association)速率,而如本文所使用的术语“kdis”或“kd”意在是指特定抗体-抗原相互作用的解离速率。如本文所使用的,术语“KD”指平衡解离常数,其获得自kd与ka的比率(即kd/ka)并且表示为摩尔浓度(M)。可以使用本领域已知的方法测定抗体的KD值,例如表面等离子体共振法、ELISA或溶液平衡滴定法(SET)。
术语“单克隆抗体”指基本上均质的抗体的群,即在该群中包含的抗体分子的氨基酸序列是相同的,除了可能少量存在的天然突变以外。相比之下,多克隆抗体制剂通常包含在其可变结构域具有不同氨基酸序列的多种不同抗体,其通常特异性针对不同表位。在一些实施方式中,本披露提供的抗体是单克隆抗体。
术语“抗原”是指能够由抗原结合分子(例如抗体)的选择性结合剂所结合的分子或分子部分。抗原可具有一个或多个能够与不同的抗原结合分子(例如抗体)相互作用的表位。
术语“表位”指能够与抗体或其抗原结合片段特异性结合的抗原上的区域(area或region)。表位可以由连续氨基酸(线性表位)形成或包含非连续氨基酸(构象表位),例如因抗原的折叠(即通过蛋白质性质的抗原的三级折叠)而使得非连续的氨基酸在空间上得以接近。构象表位和线性表位的差别在于:在变性溶剂的存在下,抗体对构象表位的结合丧失。表位包含处于独特空间构象的至少3,至少4,至少5,至少6,至少7,或8-10个氨基酸。筛选结合特定表位的抗体(即那些结合相同表位的)可以使用本领域例行方法来进行,例如但不限于丙氨酸扫描,肽印迹(见Meth.Mol.Biol.248(2004)443-463),肽切割分析,表位切除,表位提取,抗原的化学修饰(见Prot.Sci.9(2000)487-496),和交叉阻断(见“Antibodies”,Harlow and Lane(Cold Spring Harbor Press,Cold Spring Harb.,NY))。
术语“能够特异性结合”、“特异性结合”或“结合”是指相比其他抗原或表位,抗原结合分子能够以更高的亲和力结合至某个抗原或表位。通常,抗体以约1×10-7M或更小(例如约1×10-8M或更小)的平衡解离常数(KD)结合抗原或表位。在一些实施方式中,抗体与抗原结合的KD为该抗体结合至非特异性抗原(例如BSA、酪蛋白)的KD的10%或更低(例如1%)。可使用已知的方法来测量KD,例如通过FACS或表面等离子体共振测定法所测量的。然而,特异性结合至抗原或其表位的抗体可能对其它相关的抗原具有交叉反应性,例如,对来自其它物种(同源)(诸如人或猴,例如食蟹猕猴(Macaca fascicularis)(cynomolgus,cyno)、黑猩猩(Pan troglodytes)(chimpanzee,chimp))或狨猴(Callithrix jacchus)(commonmarmoset,marmoset)的相应抗原具有交叉反应性。
术语“不结合”是指抗原结合分子不能够以上述特异性结合的方式结合至某个抗原或其表位。例如,当抗体以约1×10-6M或更大的平衡解离常数(KD)结合抗原或其表位。
术语“抗原结合模块”指特异性结合目标抗原的多肽分子。具体的抗原结合模块包括抗体的抗原结合域,例如包含重链可变区和轻链可变区。术语“特异性结合CD3的抗原结合模块”是指能够以足够的亲和力结合CD3或其表位的模块,使得含有该模块的分子可用作靶向CD3的诊断剂和/或治疗剂。例如,特异性结合CD3的抗原结合模块具有以下的平衡解离常数(KD):<约10nM,其是通过表面等离子体共振测定法测量的。抗原结合模块包括如本文定义的抗体片段,例如Fab,经替换的Fab或scFv。
术语“连接子”指连接两个多肽片段的连接单元。在本文中,同一结构式中出现的连接子可以是相同或不同的。连接子可以是肽连接子,其包含一个或多个氨基酸,典型的包含约1-30个、2-24个或3-15个氨基酸。应用于本文的连接子可以是相同或不同的。当“-”出现在结构式中,其表示两侧的单元直接通过共价键连接。
“Tm”是溶解变性温度(内源荧光)。当蛋白质变性(加热或变性剂作用)时,三级结构打开,芳香族氨基酸微环境发生变化,导致发射荧光光谱改变。本披露中,Tm1是指荧光变化到最大值的一半时的温度。
“Tonset”是变性起始温度。意指蛋白质开始变性时的温度,即荧光值开始变化时的温度。
“Tagg”是聚集起始温度。通过静态光散射,在266nm和473nm两个波长下检测聚集体,监测到样品开始聚集时的温度。Tagg 266指的是266nm下监测到聚集起始温度。
术语“核酸”在本文中可与术语“多核苷酸”互换使用,并且是指呈单链或双链形式的脱氧核糖核苷酸或核糖核苷酸及其聚合物。所述术语涵盖含有已知核苷酸类似物或修饰的骨架残基或连接的核酸,所述核酸是合成的、天然存在的和非天然存在的,具有与参考核酸相似的结合特性,并且以类似于参考核苷酸的方式代谢。 此类类似物的实例包括但不限于硫代磷酸酯、氨基磷酸酯、甲基膦酸酯、手性-甲基膦酸酯、2-O-甲基核糖核苷酸、肽-核酸(PNA)。“分离的”核酸指已经与其天然环境的组分分开的核酸分子。分离的核酸包括在下述细胞中含有的核酸分子,所述细胞通常含有该核酸分子,但该核酸分子存在于染色体外或存在于不同于其天然染色体位置的染色体位置处。编码所述抗原结合分子的分离的核酸指编码抗体重链和轻链(或其片段)的一个或更多个核酸分子,包括在单一载体或分开的载体中的这样的一个或更多个核酸分子,和存在于宿主细胞中一个或更多个位置的这样的一个或更多个核酸分子。除非另有说明,否则特定的核酸序列还隐含地涵盖其保守修饰的变体(例如,简并密码子取代)和互补序列以及明确指明的序列。具体地,如下详述,简并密码子取代可以通过产生如下序列而获得,在这些序列中,一个或多个所选的(或全部)密码子的第三位被简并碱基和/或脱氧肌苷残基取代。
应当理解,尽管本公开中没有提供具体的编码核苷酸序列,技术人员根据密码子规则和宿主密码子偏好性,能够在氨基酸序列的基础上确定对应的编码核苷酸序列。
术语“多肽”和“蛋白质”在本文中可互换使用,指氨基酸残基的聚合物。该术语适用于氨基酸聚合物,其中一个或多个氨基酸残基是天然存在的氨基酸相应的人工化学模拟物,以及适用于天然存在的氨基酸聚合物和非天然存在的氨基酸聚合物。除非另外说明,否则特定的多肽序列还隐含地涵盖其保守修饰的变体。
术语序列“同一性”指,当对两条序列进行最佳比对时,两条序列的氨基酸/核酸在等价位置相同的程度(百分比)。在比对过程中,必要时可允许引入间隙以获取最大序列同一性百分比,但任何保守性取代不视为构成序列同一性的一部分。为测定序列同一性百分比,比对可以通过本领域技术已知的技术来实现,例如使用公开可得到的计算机软件,诸如BLAST、BLAST-2、ALIGN、ALIGN-2或Megalign(DNASTAR)软件。本领域技术人员可确定适用于测量比对的参数,包括在所比较的序列全长上达成最大比对所需的任何算法。
术语“融合”或“连接”是指部件(例如抗原结合模块和Fc结构域)直接地或经由连接子共价连接。
术语“载体”意指能够转运与其连接的另一多核苷酸的多核苷酸分子。一种类型的载体是“质粒”,其是指环状双链DNA环,其中可以连接附加的DNA区段。另一种类型的载体是病毒载体,例如腺相关病毒载体(AAV或AAV2),其中另外的DNA区段可以连接到病毒基因组中。某些载体能够在引入它们的宿主细胞中自主复制(例如,具有细菌复制起点的细菌载体和附加型哺乳动物载体)。其他载体(例如,非附加型哺乳动物载体)可以在引入宿主细胞中后整合到宿主细胞的基因组中,从而与宿主基因组一起复制。术语“表达载体”或“表达构建体”是指适用于对宿主细胞进行转化且含有指导及/或控制(连同宿主细胞一起)与其可操作地 连接的一个或多个异源编码区的表达的核酸序列的载体。表达构建体可以包括但不限于影响或控制转录、翻译且在存在内含子时影响与其可操作地连接的编码区的RNA剪接的序列。
术语“宿主细胞”,“宿主细胞系”,和“宿主细胞培养物”可互换使用,并且指已经导入外源核酸的细胞,包括此类细胞的后代。宿主细胞包括“转化体”和“经转化的细胞”,其包括原代的经转化的细胞及自其衍生的后代,而不考虑传代的次数。后代在核酸内容物上可以与亲本细胞不完全相同,而是可以含有突变。本文中,该术语包括突变体后代,其与在原代转化细胞中筛选或选择的细胞具有相同的功能或生物学活性。宿主细胞包括原核和真核宿主细胞,其中真核宿主细胞包括但不限于哺乳动物细胞、昆虫细胞系植物细胞和真菌细胞。哺乳动物宿主细胞包括人、小鼠、大鼠、犬、猴、猪、山羊、牛、马和仓鼠细胞,包括但不限于中国仓鼠卵巢(CHO)细胞、NSO、SP2细胞、HeLa细胞、幼仓鼠肾(BHK)细胞、猴肾细胞(COS)、人肝细胞癌细胞(例如,Hep G2)、A549细胞、3T3细胞和HEK-293细胞。真菌细胞包括酵母和丝状真菌细胞,包括例如巴氏毕赤酵母(Pichiapastoris)、芬兰毕赤酵母(Pichia finlandica)、海藻毕赤酵母(Pichia trehalophila)、科克拉马毕赤酵母(Pichia koclamae)、膜状毕赤酵母(Pichia membranaefaciens)、小毕赤酵母(Pichia minuta)(Ogataea minuta、Pichia lindneri)、仙人掌毕赤酵母(Pichiaopuntiae)、耐热毕赤酵母(Pichia thermotolerans)、柳毕赤酵母(Pichia salictaria)、Pichia guercuum、皮杰普毕赤酵母(Pichia pijperi)、具柄毕赤酵母(Pichia stiptis)、甲醇毕赤酵母(Pichia methanolica)、毕赤酵母属、酿酒酵母(Saccharomycescerevisiae)、酿酒酵母属、多形汉逊酵母(Hansenula polymorpha)、克鲁维酵母属、乳酸克鲁维酵母(Kluyveromyces lactis)、白色念珠菌(Candida albicans)、构巢曲霉(Aspergillus nidulans)、黑曲霉(Aspergillus niger)、米曲霉(Aspergillus oryzae)、里氏木霉(Trichoderma reesei)、勒克氏菌(Chrysosporium lucknowense)、镰刀菌属(Fusarium sp.)、禾谷镰刀菌(Fusarium gramineum)、菜镰刀菌(Fusarium venenatum)、小立碗藓(Physcomitrella patens)和粗糙脉孢菌(Neurospora crassa)。毕赤酵母属、任何酿酒酵母属、多形汉逊酵母(Hansenula polymorpha)、任何克鲁维酵母属、白色念珠菌(Candida albicans)、任何曲霉属、里氏木霉(Trichoderma reesei)、勒克霉菌(Chrysosporium lucknowense)、任何镰刀菌属、解脂耶氏酵母(Yarrowia lipolytica)和粗糙脉孢菌(Neurospora crassa)。本专利的宿主细胞不包括在专利法中不授权的客体。
“任选”或“任选地”意味着随后所描述地事件或环境可以但不必发生,该说明包括该事件或环境发生或不发生的场合。
术语“药物组合物”表示含有一种或多种本文所述的抗原结合分子或抗体与其他化学组分的混合物,所述其他组分例如生理学/可药用的载体和赋形剂。
术语“药学上可接受的载体、稀释剂、缓冲剂或赋形剂”指药物制剂中与活性成分不同的,且对受试者无毒的成分。药学上可接受的载体、稀释剂、缓冲剂或赋形剂包括但不限于缓冲剂、赋形剂、稳定剂或防腐剂。
术语“受试者”或“个体”包括人类和非人类动物。非人动物包括所有脊椎动物(例如哺乳动物和非哺乳动物)例如非人灵长类(例如,食蟹猴)、绵羊、狗、牛、鸡、两栖动物和爬行动物。除非明确指出,否则所述术语“患者”或“受试者”在本文中可互换地使用。如本文所使用的,术语“食蟹猴(cyno)”或“食蟹猴(cynomolgus)”是指食蟹猴(Macaca fascicularis)。在某些实施方案中,个体或受试者是人。
“施用”或“给予”,当其应用于动物、人、实验受试者、细胞、组织、器官或生物流体时,是指外源性药物、治疗剂、诊断剂或组合物与动物、人、受试者、细胞、组织、器官或生物流体的接触。
术语“样本”是指从受试者分离的类似流体、细胞、或组织的采集物,以及存在于受试者体内的流体、细胞或组织。示例性样本为生物流体,诸如血液、血清和浆膜液、血浆、淋巴液、尿液、唾液、囊液、泪液、排泄物、痰、分泌组织和器官的粘膜分泌物、阴道分泌物、腹水、胸膜、心包、腹膜、腹腔和其它体腔的流体、由支气管灌洗液收集的流体、滑液、与受试者或生物来源接触的液体溶液,例如细胞和器官培养基(包括细胞或器官条件培养基)、灌洗液等,组织活检样本、细针穿刺、手术切除的组织、器官培养物或细胞培养物。
“治疗(treatment或treat)”和“处理”(及其语法变型)指试图施加至所治疗个体的临床干预,并且可以为了预防目的、或者在临床病理学的过程期间进行实施。治疗的期望效果包括但不限于预防疾病的发生或复发,减轻症状,减轻/减少疾病的任何直接或间接病理后果,预防转移,降低疾病进展速率,改善或减轻疾病状态,和消退或改善的预后。在一些实施方案中,使用本披露的抗原结合分子来延迟疾病的形成或减缓疾病的进展。
术语“复发(recurrence)”、“复发(relapse)”“复发(relapsed)”是指癌症或疾病在疾病消失的临床评估之后的恢复。远处癌转移或局部复发的诊断可视为复发。
“有效量”一般是足以降低症状的严重程度及/或频率、消除这些症状及/或潜在病因、预防症状及/或其潜在病因出现及/或改良或改善由疾病状态引起或与其相关的损伤的量。在一些实施例中,有效量是治疗有效量或预防有效量。
“治疗有效量”是足以治疗疾病状态或症状、尤其与该疾病状态相关的状态或症状,或者以其他方式预防、阻碍、延迟或逆转该疾病状态或以任何方式与该疾病相关的任何其他不理想症状的进展的量。
“预防有效量”是当给予受试者时将具有预定预防效应,例如预防或延迟该疾病状态的发作(或复发),或者降低该疾病状态或相关症状的发作(或复发)可能性的量。完全治疗或预防效未必在给予一个剂量之后便发生,可能在给予一系列 剂量之后发生。因而,治疗或预防有效量可以一次或多次给予的方式给予。“治疗有效量”和“预防有效量”可取决于多种因素变化:诸如个体的疾病状态、年龄、性别和体重,以及治疗剂或治疗剂组合在个体中引发期望的应答的能力。有效治疗剂或治疗剂组合的示例性指标包括例如受试者改善的健康状况。
本披露的抗原结合分子
本披露提供了抗原结合分子,其具有诸多有利的特性,例如良好的体外杀伤活性、治疗活性、安全性、药物代谢动力学特性和成药性(如产率、纯度和稳定性等)。
示例性的抗原结合分子
本披露的抗原结合分子,包括特异性结合DLL3和CD3的双特异性抗原结合分子(例如双特异性抗体)和抗DLL3抗体。特别的,本披露的抗原结合分子具有如下任一的性质:
a.对DLL3的高亲和力。在一些实施方式中,所述抗DLL3抗体或抗原结合分子以小于4×10-9M、3×10-9M、2×10-9M、1×10-9M、9×10-10M、8×10-10M、7×10-10M、6×10-10M、5×10-10M、4×10-10M、3×10-10M、2×10-10M、1×10-10M、9×10-11M的KD结合人DLL3,所述KD是通过表面等离子体共振法测量的。在一些实施方式中,所述抗抗原结合分与DLL3蛋白的结合EC50小于0.5nM、0.4nM、0.3nM、0.2nM、0.1nM、0.09nM、0.08nM、0.07nM,所述EC50是通过ELISA检测的。
b.对细胞表面表达的DLL3的高亲和力。在一些实施方式中,所述抗DLL3抗体结合H1184细胞的EC50以小于0.2nM、0.1nM、0.09nM、0.08nM、0.07nM、0.06nM、0.05nM、0.04nM。
c.对表达DLL3的细胞的特异性杀伤作用。在一些实施方式中,所述抗原结合分子可特异性杀伤表达DLL3的SHP77细胞和H1184细胞,其中对H1184细胞的杀伤IC50小于30pM、25pM、20pM、15pM、14pM、13pM、12pM、11pM、10pM、9pM、8pM、7pM。
d.对T细胞的体外激活活性。在一些实施方案中,所述的抗原结合分子以小于20pM、19pM、18pM、17pM、16pM、15pM、14pM、13pM、12pM、11pM、10pM、9pM、8pM、7pM的EC50激活Jurkat LuciaTM NFAT细胞。
e.诱导低水平的细胞因子(IL6和IFNγ)释放。
e.更强的体内治疗活性。在一些实施方案中,所述的抗原结合分子可显著抑制小鼠SHP77和H1184细胞皮下移植瘤的生长。
本披露提供了一种抗原结合分子,其包含至少一个特异性结合DLL3的抗原结合模块和至少一个特异性结合CD3的抗原结合模块,所述特异性结合DLL3的抗原结合模块包含DLL3-VH和DLL3-VL,所述特异性结合CD3的抗原结合模块包含CD3-VH和CD3-VL。本披露还提供了一种抗DLL3抗体,其能够特异性结合DLL3,所述的抗体包含DLL3-VH和DLL3-VL。具体地,本文的实施例披露了抗 体系列6、98、110和30。以下以抗体6和110为例描述本文的抗体或抗原结合分子。
特异性结合DLL3和CD3的抗原结合分子,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24、71、72或73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25或74的氨基酸序列的DLL3-LCDR3。
特异性结合DLL3和CD3的抗原结合分子或抗DLL3抗体,其中:
所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:32、96、97、98或99的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3。
特异性结合DLL3和CD3的抗原结合分子,其中:
所述DLL3-VH包含如SEQ ID NO:20所示的DLL3-HCDR1、如SEQ ID NO:21、69或70所示的DLL3-HCDR2和如SEQ ID NO:22所示的DLL3-HCDR3,和所述DLL3-VL包含如SEQ ID NO:23所示的DLL3-LCDR1、如SEQ ID NO:24、71、72或73所示的DLL3-LCDR2和如SEQ ID NO:25或74所示的DLL3-LCDR3。
特异性结合DLL3和CD3的抗原结合分子或抗DLL3抗体,其中:
所述DLL3-VH包含如SEQ ID NO:20所示的DLL3-HCDR1、如SEQ ID NO:32、96、97、98或99所示的DLL3-HCDR2和如SEQ ID NO:33所示的DLL3-HCDR3,和所述DLL3-VL如SEQ ID NO:34所示的DLL3-LCDR1、如SEQ ID NO:35所示的DLL3-LCDR2和如SEQ ID NO:36所示的DLL3-LCDR3。
特异性结合DLL3和CD3的抗原结合分子,其中:
所述DLL3-VH包含如SEQ ID NO:20所示的DLL3-HCDR1,如SEQ ID NO:21所示的DLL3-HCDR2,和如SEQ ID NO:22所示的DLL3-HCDR3;和所述DLL3-VL包含如SEQ ID NO:23所示的DLL3-LCDR1,如SEQ ID NO:71所示的DLL3-LCDR2,和如SEQ ID NO:25所示的DLL3-LCDR3。
特异性结合DLL3和CD3的抗原结合分子或抗DLL3抗体,其中:
所述DLL3-VH包含如SEQ ID NO:20所示的DLL3-HCDR1,如SEQ ID NO:21所示的DLL3-HCDR2,和如SEQ ID NO:22所示的DLL3-HCDR3;和所述DLL3-VL包含如SEQ ID NO:23所示的DLL3-LCDR1,如SEQ ID NO:24所示的DLL3-LCDR2,和如SEQ ID NO:25所示的DLL3-LCDR3;或
所述DLL3-VH包含如SEQ ID NO:20所示DLL3-HCDR1,如SEQ ID NO:21所示的DLL3-HCDR2,和如SEQ ID NO:22所示的DLL3-HCDR3;和所述DLL3-VL包含如SEQ ID NO:23所示的DLL3-LCDR1,如SEQ ID NO:72所示的DLL3-LCDR2,和如SEQ ID NO:25所示的DLL3-LCDR3;或
所述DLL3-VH包含如SEQ ID NO:20所示的DLL3-HCDR1,如SEQ ID NO:69所示的DLL3-HCDR2,和如SEQ ID NO:22所示的DLL3-HCDR3;和所述DLL3-VL包含如SEQ ID NO:23所示的DLL3-LCDR1,如SEQ ID NO:71所示的DLL3-LCDR2,和如SEQ ID NO:74所示的DLL3-LCDR3;或
所述DLL3-VH包含如SEQ ID NO:20所示的DLL3-HCDR1,如SEQ ID NO:69所示的DLL3-HCDR2,和如SEQ ID NO:22所示的DLL3-HCDR3;和所述DLL3-VL包含如SEQ ID NO:23所示的DLL3-LCDR1,如SEQ ID NO:24所示的DLL3-LCDR2,和如SEQ ID NO:74所示的DLL3-LCDR3;或
所述DLL3-VH包含如SEQ ID NO:20所示的DLL3-HCDR1,如SEQ ID NO:69所示的DLL3-HCDR2,和如SEQ ID NO:22所示的DLL3-HCDR3;和所述DLL3-VL包含如SEQ ID NO:23所示的DLL3-LCDR1,如SEQ ID NO:71所示的DLL3-LCDR2,和如SEQ ID NO:25所示的DLL3-LCDR3;或
所述DLL3-VH包含如SEQ ID NO:20所示的DLL3-HCDR1,如SEQ ID NO:70所示的DLL3-HCDR2,和如SEQ ID NO:22所示的DLL3-HCDR3;和所述DLL3-VL包含如SEQ ID NO:23所示的DLL3-LCDR1,如SEQ ID NO:71所示的DLL3-LCDR2,和如SEQ ID NO:25所示的DLL3-LCDR3;或
所述DLL3-VH包含如SEQ ID NO:20所示的DLL3-HCDR1,如SEQ ID NO:70所示的DLL3-HCDR2,和如SEQ ID NO:22所示的DLL3-HCDR3;和所述DLL3-VL包含如SEQ ID NO:23所示的DLL3-LCDR1,如SEQ ID NO:24所示的DLL3-LCDR2,和如SEQ ID NO:74所示的DLL3-LCDR3。
特异性结合DLL3和CD3的抗原结合分子或抗DLL3抗体,其中:
所述DLL3-VH包含如SEQ ID NO:20所示的DLL3-HCDR1,如SEQ ID NO:96所示的DLL3-HCDR2,和如SEQ ID NO:33所示的DLL3-HCDR3;和所述DLL3-VL包含如SEQ ID NO:34所示的DLL3-LCDR1,如SEQ ID NO:35所示的DLL3-LCDR2,和如SEQ ID NO:36所示的DLL3-LCDR3。
在一些实施方案中,如前所述的抗原结合分子或抗DLL3抗体,所述DLL3-VH和/或所述DLL3-VL是鼠源的或人源化的。在一些实施方案中,所述DLL3-VH和/或所述DLL3-VL是人源化的。
在一些实施方案中,所述人源化的DLL3-VH的FR1、FR2、FR3和FR4与SEQ ID NO:50、51或52的FR1、FR2、FR3和FR4具有至少60%、70%、80%或90%的序列同一性;所述人源化的DLL3-VL的FR1、FR2、FR3和FR4与SEQ ID NO: 62或68的FR1、FR2、FR3和FR4具有至少60%、70%、80%或90%的序列同一性。
在一些实施方案中,所述人源化的DLL3-VH具有来源于IGHV1-3*01、IGHV7-4-1*02或IGHV3-73*01的FR1、FR2、FR3和来源于IGHJ6*01的FR4,并且其是未被取代的或具有选自1E、5Q、27Y、30T、38K、43K、48I、67A、68A、69L、71V、73K、75S、76N和93A组成的组中的一个或多个氨基酸取代;和/或所述人源化的DLL3-VL具有来源于IGKV1-16*01或IGKV3-20*02的FR1、FR2、FR3和来源于IGKJ4*01的FR4,并且其是未被取代的或具有选自1N、36L、42K、43S、44F、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代。在一些实施方案中,上述可变区中的氨基酸位置是根据Kabat编号规则定义的。
在一些实施方案中,所述人源化的DLL3-VH包含SEQ ID NO:50的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:50的FR区包含选自1E、43K、48I、67A、69L、71V、73K和76N组成的组中的一个或多个氨基酸取代。
在一些实施方案中,所述人源化的DLL3-VH包含SEQ ID NO:51的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:51的FR区包含选自1E、5Q、38K、68A、69L、71V、73K、75S和76N组成的组中的一个或多个氨基酸取代。
在一些实施方案中,所述人源化的DLL3-VH包含SEQ ID NO:52的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:52的FR区包含选自27Y、30T69L、71V、73K和93A组成的组中的一个或多个氨基酸取代。
在一些实施方案中,所述人源化的DLL3-VL包含SEQ ID NO:62的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:62的FR区包含选自36L、43S、44F、46G、69A、71Y和85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,所述人源化的DLL3-VL包含SEQ ID NO:68的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:68的FR区包含选自36L、42K、46G、69A、71Y、79Q和85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,所述人源化的DLL3-VH的FR1、FR2、FR3和FR4与SEQ ID NO:95的FR1、FR2、FR3和FR4具有至少60%、70%、80%或90%的序列同一性;所述人源化的DLL3-VL的FR1、FR2、FR3和FR4与SEQ ID NO:88的FR1、FR2、FR3和FR4具有至少60%、70%、80%或90%的序列同一性。
在一些实施方案中,所述人源化的DLL3-VH具有来源于IGHV1-3*01的FR1、FR2、FR3和来源于IGHJ6*01的FR4,并且其是未被取代的或具有选自1E、24T、44S、71V和73K组成的组中的一个或多个氨基酸取代;和/或所述人源化的 DLL3-VL具有来源于IGKV4-1*01的FR1、FR2、FR3和来源于IGKJ2*01的FR4,并且其是未被取代的或具有选自1N、9K、43S、68A和85D组成的组中的一个或多个氨基酸取代。在一些实施方案中,上述可变区中的氨基酸位置是根据Kabat编号规则定义的。
在一些实施方案中,所述人源化的DLL3-VH包含SEQ ID NO:95的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:95的FR区包含选自1E、24T、44S、71V和73K组成的组中的一个或多个氨基酸取代。在一些实施方案中,所述人源化的DLL3-VL包含SEQ ID NO:88的氨基酸序列,或其变体。在一些实施方案中,所述变体为在SEQ ID NO:88的FR区包含选自1N、9K、43S、68A和85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,所述人源化的DLL3-VH包含SEQ ID NO:51的氨基酸序列,或其变体;在一些实施方案中,所述变体为在SEQ ID NO:51的FR区包含选自1E、38K、68A、69L、71V、73K、75S和76N组成的组中的一个或多个氨基酸取代;和所述人源化的DLL3-VL包含SEQ ID NO:63的氨基酸序列,或其变体;在一些实施方案中,所述变体为在SEQ ID NO:63的FR区包含一个或多个氨基酸取代;在一些实施方案中,所述的氨基酸取代选自43S和44F组成的组中的一个或多个氨基酸取代。
在一些实施方案中,所述人源化的DLL3-VH包含SEQ ID NO:91的氨基酸序列,或SEQ ID NO:91变体;在一些实施方案中,所述变体为在SEQ ID NO:91的FR区包含一个或多个氨基酸取代;和
所述人源化的DLL3-VL包含SEQ ID NO:88的氨基酸序列,或其变体;在一些实施方案中,所述变体为在SEQ ID NO:88的FR区包含选自1N、9K、43S、68A和85D组成的组中的一个或多个氨基酸取代。
在一些实施方案中,上述可变区和CDR是根据Kabat编号规则定义的。
在一些实施方案中,如前任一项所述的抗原结合分子,其中所述DLL3-VH的氨基酸序列与SEQ ID NO:12、43、44、45、46、47、48、49、50、51、52、53、54、55、56或57具有至少90%、95%、96%、97%、98%或99%的序列同一性,和所述DLL3-VL的氨基酸序列与SEQ ID NO:13、58、59、60、61、62、63、64、65、66、67或68具有至少90%、95%、96%、97%、98%或99%的序列同一性。在一些实施方案中,所述DLL3-VH的氨基酸序列如SEQ ID NO:12、43、44、45、46、47、48、49、50、51、52、53、54、55、56或57所示,和所述DLL3-VL的氨基酸序列如SEQ ID NO:13、58、59、60、61、62、63、64、65、66、67或68所示。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中所述DLL3-VH的氨基酸序列与SEQ ID NO:43、44、45、46、47、48、49、50、51、52、53、54、55、56或57具有至少90%、95%、96%、97%、98%或99%的序列同一性,和所 述DLL3-VL的氨基酸序列与SEQ ID NO:63、64、65、66或67具有至少90%、95%、96%、97%、98%或99%的序列同一性。在一些实施方案中,所述DLL3-VH的氨基酸序列如SEQ ID NO:43、44、45、46、47、48、49、50、51、52、53、54、55、56或57所示,和所述DLL3-VL的氨基酸序列如SEQ ID NO:63、64、65、66或67所示。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其中所述DLL3-VH的氨基酸序列与SEQ ID NO:56或57具有至少90%、95%、96%、97%、98%或99%的序列同一性,和所述DLL3-VL的氨基酸序列与SEQ ID NO:58、59、60、61、62、63、64、65、66、67或68具有至少90%、95%、96%、97%、98%或99%的序列同一性。在一些实施方案中,所述DLL3-VH的氨基酸序列如SEQ ID NO:56或57所示,和所述DLL3-VL的氨基酸序列如SEQ ID NO:58、59、60、61、62、63、64、65、66、67或68所示。
在一些实施方案中,如前任一项所述的抗原结合分子或抗DLL3抗体,所述DLL3-VH的氨基酸序列如SEQ ID NO:54所示,和所述DLL3-VL的氨基酸序列如SEQ ID NO:63所示;或
所述DLL3-VH的氨基酸序列如SEQ ID NO:54所示,和所述DLL3-VL的氨基酸序列如SEQ ID NO:61所示;或
所述DLL3-VH的氨基酸序列如SEQ ID NO:54所示,和所述DLL3-VL的氨基酸序列如SEQ ID NO:64所示;或
所述DLL3-VH的氨基酸序列如SEQ ID NO:56所示,和所述DLL3-VL的氨基酸序列如SEQ ID NO:65所示;或
所述DLL3-VH的氨基酸序列如SEQ ID NO:56所示,和所述DLL3-VL的氨基酸序列如SEQ ID NO:67所示;或
所述DLL3-VH的氨基酸序列如SEQ ID NO:56所示,和所述DLL3-VL的氨基酸序列如SEQ ID NO:65所示;或
所述DLL3-VH的氨基酸序列如SEQ ID NO:57所示,和所述DLL3-VL的氨基酸序列如SEQ ID NO:65所示;或
所述DLL3-VH的氨基酸序列如SEQ ID NO:57所示,和所述DLL3-VL的氨基酸序列如SEQ ID NO:67所示;或
所述DLL3-VH的氨基酸序列如SEQ ID NO:57所示,和所述DLL3-VL的氨基酸序列如SEQ ID NO:65所示。
在一些实施方案中,如前任一项所述的抗原结合分子或抗DLL3抗体,其中所述DLL3-VH的氨基酸序列与SEQ ID NO:16、89、90、91、92、93、94或95具有至少90%、95%、96%、97%、98%或99%的序列同一性,和所述DLL3-VL的氨基酸序列与SEQ ID NO:17、86、87或88具有至少90%、95%、96%、97%、98%或99%的序列同一性。在一些实施方案中,所述DLL3-VH的氨基酸序列如 SEQ ID NO:16、89、90、91、92、93、94或95所示,和所述DLL3-VL的氨基酸序列如SEQ ID NO:17、86、87或88所示。
在一些实施方案中,如前任一项所述的抗原结合分子或抗DLL3抗体,所述DLL3-VH的氨基酸序列如SEQ ID NO:91所示,和所述DLL3-VL的氨基酸序列如SEQ ID NO:87所示。
在一些实施方案中,如前任一项所述的抗DLL3抗体,其包含重链和轻链,其中:
所述重链的氨基酸序列如SEQ ID NO:121所示,和所述轻链的氨基酸序列如SEQ ID NO:122所示;或
所述重链的氨基酸序列如SEQ ID NO:125所示,和所述轻链的氨基酸序列如SEQ ID NO:126所示。
在一些实施方案中,如前所述的抗原结合分子,其中:
i)所述CD3-VH包含如SEQ ID NO:129所示的CD3-HCDR1,如SEQ ID NO:130所示的CD3-HCDR2,和如SEQ ID NO:131所示的CD3-HCDR3;和所述CD3-VL包含如SEQ ID NO:132所示的CD3-LCDR1,如SEQ ID NO:133所示的CD3-LCDR2,和如SEQ ID NO:134所示的CD3-LCDR3;或
ii)所述CD3-VH包含如SEQ ID NO:129所示的CD3-HCDR1,如SEQ ID NO:130所示的CD3-HCDR2,和如SEQ ID NO:135所示的CD3-HCDR3;和所述CD3-VL包含如SEQ ID NO:132所示的CD3-LCDR1,如SEQ ID NO:133所示的CD3-LCDR2,和如SEQ ID NO:134所示的CD3-LCDR3。
在一些实施方案中,上述可变区和CDR是根据Kabat编号规则定义的。
在一些实施方案中,如前任一项所述的抗原结合分子,所述CD3-VH和/或所述CD3-VL是鼠源的或人源化的。在一些实施方案中,所述CD3-VH和/或所述CD3-VL是人源化的。
在一些实施方案中,如前任一项所述的抗原结合分子,其中所述CD3-VH的氨基酸序列如SEQ ID NO:136或138所示,和所述CD3-VL的氨基酸序列SEQ ID NO:137所示。
在一些实施方案中,如前任一项所述的抗原结合分子,其包含:
如SEQ ID NO:152所示的第一链、如SEQ ID NO:153所示的第二链、如SEQ ID NO:154所示的第三链和如SEQ ID NO:155所示的第四链;或
如SEQ ID NO:152所示的第一链、如SEQ ID NO:153所示的第二链、如SEQ ID NO:156所示的第三链和如SEQ ID NO:155所示的第四链。
在一些实施方案中,如前任一项所述的抗原结合分子,其包含:
如SEQ ID NO:157所示的第一链、如SEQ ID NO:158所示的第二链和如SEQ ID NO:159所示的第三链;或
如SEQ ID NO:157所示的第一链、如SEQ ID NO:158所示的第二链和如SEQ ID NO:160所示的第三链。
在一些实施方案中,如前任一项所述的抗原结合分子,其包含:
如SEQ ID NO:161所示的第一链和如SEQ ID NO:162所示的第二链;或
如SEQ ID NO:163所示的第一链和如SEQ ID NO:162所示的第二链;或
如SEQ ID NO:185所示的第一链和如SEQ ID NO:162所示的第二链;或
如SEQ ID NO:186所示的第一链和如SEQ ID NO:162所示的第二链;或
如SEQ ID NO:259所示的第一链和如SEQ ID NO:162所示的第二链;或
如SEQ ID NO:260所示的第一链和如SEQ ID NO:162所示的第二链;或
如SEQ ID NO:187所示的第一链和如SEQ ID NO:188所示的第二链;或
如SEQ ID NO:187所示的第一链和如SEQ ID NO:189所示的第二链;或
如SEQ ID NO:190所示的第一链和如SEQ ID NO:188所示的第二链;或
如SEQ ID NO:190所示的第一链和如SEQ ID NO:189所示的第二链;或
如SEQ ID NO:191所示的第一链和如SEQ ID NO:188所示的第二链;或
如SEQ ID NO:191所示的第一链和如SEQ ID NO:189所示的第二链。
在一些实施方案中,如前任一项所述的抗原结合分子,其包含:
如SEQ ID NO:171所示的第一链、如SEQ ID NO:172所示的第二链、如SEQ ID NO:154所示的第三链和如SEQ ID NO:155所示的第四链;或
如SEQ ID NO:171所示的第一链、如SEQ ID NO:172所示的第二链、如SEQ ID NO:156所示的第三链和如SEQ ID NO:155所示的第四链。
在一些实施方案中,如前任一项所述的抗原结合分子,其包含:
如SEQ ID NO:173所示的第一链、如SEQ ID NO:174所示的第二链和如SEQ ID NO:159所示的第三链;或
如SEQ ID NO:173所示的第一链、如SEQ ID NO:174所示的第二链和如SEQ ID NO:160所示的第三链。
在一些实施方案中,如前任一项所述的抗原结合分子,其包含:
如SEQ ID NO:175所示的第一链和如SEQ ID NO:176所示的第二链;或
如SEQ ID NO:177所示的第一链和如SEQ ID NO:176所示的第二链。
根据本文实施例所披露的包含抗体系列98和30的抗原结合分子与以上所描述的抗体系列6和110具有同等的技术方案范围。
抗原结合分子的结构
本披露的双特异性抗原结合分子并不受限于特定的分子结构,只要其具有所期望的抗原结合功能。例如,本文的双特异性抗原结合分子可以是双价(1+1)的、三价(2+1)的或4价(2+2)的。抗原结合分子中的抗原结合模块可以是任意的具有抗原结合活性的抗体片段,其通过肽连接子融合。本披露的肽连接子(例如连接子1至8)可以是任意适宜的肽链,只要抗原结合分子能够展现出期望的抗原 结合活性。例如,肽连接子可以是包含1-50或3-20个氨基酸残基的柔性肽。在一些实施方案中,所述肽连接子各自独立地具有(GGGGS)n的结构,其中n是1、2或3。在一些实施方案中,所述的连接子1和连接子2的序列均为GGGGS(SEQ ID NO:147)。在一些实施方案中,所述的连接子3的序列为GGGGSGGGGSGGGGS(SEQ ID NO:148)。在一些实施方案中,所述的连接子4的序列为GGGGS(SEQ ID NO:147)。在一些实施方案中,所述连接子5的序列为GGGSGGGG(SEQ ID NO:149)。在一些实施方案中,连接子6和连接子8的序列为G(SEQ ID NO:150)。在一些实施方案中,连接子7的序列为GGGGSGGGG(SEQ ID NO:151)。
示例性的,本披露的所述抗原结合分子具有式(a-1)所示结构的第一链、一条具有式(b-1)所示结构的第二链、一条具有式(c)所示结构的第三链和一条具有式(d)所示结构的第四链,
(a-1)[DLL3-VH]-[GGGGS]-[Titin链]-[Fc2],
(b-1)[DLL3-VL]-[GGGGS]-[Obscurin链],
(c)[CD3-VH]-[CH1]-[Fc1],
(d)[CD3-VL]-[CL],
式(a-1)、(b-1)、(c)和(d)所示的结构是从N端至C端排列的。
示例性的抗原结合分子包含:
一条如SEQ ID NO:171所示的第一链、一条如SEQ ID NO:172所示第二链、一条如SEQ ID NO:154所示的第三链和一条如SEQ ID NO:155所示的第四链;或
一条如SEQ ID NO:171所示的第一链、一条如SEQ ID NO:172所示的第二链、一条如SEQ ID NO:156所示的第三链和一条如SEQ ID NO:155所示的第四链;或
一条如SEQ ID NO:152所示的第一链、一条如SEQ ID NO:153所示的第二链、一条如SEQ ID NO:154所示的第三链和一条如SEQ ID NO:155所示的第四链;或
一条如SEQ ID NO:152所示的第一链、一条如SEQ ID NO:153所示的第二链、一条如SEQ ID NO:156所示的第三链和一条如SEQ ID NO:155所示的第四链;或
一条如SEQ ID NO:164所示的第一链、一条如SEQ ID NO:165所示的第二链、一条如SEQ ID NO:154所示的第三链和一条如SEQ ID NO:155所示的第四链;或
一条如SEQ ID NO:164所示的第一链、一条如SEQ ID NO:165所示的第二链、一条如SEQ ID NO:156所示的第三链和一条如SEQ ID NO:155所示的第四链;或
一条如SEQ ID NO:178所示的第一链、一条如SEQ ID NO:179所示的第二链、一条如SEQ ID NO:154所示的第三链和一条如SEQ ID NO:155所示的第四链;或
一条如SEQ ID NO:178所示的第一链、一条如SEQ ID NO:179所示的第二链、一条如SEQ ID NO:156所示的第三链和一条如SEQ ID NO:155所示的第四链。
示例性的,所述抗原结合分子包含一条具有式(e)所示结构的第一链、一条具有式(f)所示结构的第二链和一条具有式(g-1)所示结构的第三链,
(e)[DLL3-VL]-[CL],
(f)[DLL3-VL]-[CH1]-[Fc2],
(g-1)[CD3-VH]-[GGGGSGGGGSGGGGS]-[CD3-VL]-[GGGGS]-[Fc1],
式(e)、(f)和(g-1)所示的结构是从N端至C端排列的。
示例性的抗原结合分子具有:
一条如SEQ ID NO:173所示的第一链、一条如SEQ ID NO:174所示的第二链和一条如SEQ ID NO:160所示的第三链;或
一条如SEQ ID NO:173所示的第一链、一条如SEQ ID NO:174所示的第二链和一条如SEQ ID NO:159所示的第三链;或
一条如SEQ ID NO:157所示的第一链、一条如SEQ ID NO:158所示的第二链和一条如SEQ ID NO:159所示的第三链;或
一条如SEQ ID NO:157所示的第一链、一条如SEQ ID NO:158所示的第二链和一条如SEQ ID NO:160所示的第三链;或
一条如SEQ ID NO:166所示的第一链、一条如SEQ ID NO:167所示的第二链和一条如SEQ ID NO:159所示的第三链;或
一条如SEQ ID NO:166所示的第一链、一条如SEQ ID NO:167所示的第二链和一条如SEQ ID NO:160所示的第三链;或
一条如SEQ ID NO:180所示的第一链、一条如SEQ ID NO:181所示的第二链和一条如SEQ ID NO:159所示的第三链;或
一条如SEQ ID NO:180所示的第一链、一条如SEQ ID NO:181所示的第二链和一条如SEQ ID NO:160所示的第三链。
示例性的,所述抗原结合分子包含一条具有式(i-1)所示结构的第一链和一条具有式(h-1)所示结构的第二链,
(h-1)[DLL3-VL]-[GGGSGGGG]-[CD3-VH]-[G]-[Fc1],
(i-1)[CD3-VL]-[GGGGSGGGG]-[DLL3-VH]-[G]-[Fc2],
式(h-1)和(i-1)所示的结构是从N端至C端排列的。
示例性的抗原结合分子具有:
一条如SEQ ID NO:185所示的第一链和一条如SEQ ID NO:162所示的第二链;或
一条如SEQ ID NO:161所示的第一链和一条如SEQ ID NO:162所示的第二链;或
一条如SEQ ID NO:163所示的第一链和一条如SEQ ID NO:162所示的第二链;或
一条如SEQ ID NO:259所示的第一链和一条如SEQ ID NO:162所示的第二链;或
一条如SEQ ID NO:260所示的第一链和一条如SEQ ID NO:162所示的第二链;或
一条如SEQ ID NO:168所示的第一链和一条如SEQ ID NO:169所示的第二链;或
一条如SEQ ID NO:170所示的第一链和一条如SEQ ID NO:169所示的第二链;或
一条如SEQ ID NO:175所示的第一链和一条如SEQ ID NO:176所示的第二链;或
一条如SEQ ID NO:177所示的第一链和一条如SEQ ID NO:176所示的第二链;或
一条如SEQ ID NO:182所示的第一链和一条如SEQ ID NO:183所示的第二链;或
一条如SEQ ID NO:184所示的第一链和一条如SEQ ID NO:183所示的第二链;或
一条如SEQ ID NO:186所示的第一链和一条如SEQ ID NO:162所示的第二链;或
一条如SEQ ID NO:187所示的第一链和一条如SEQ ID NO:188所示的第二链;或
一条如SEQ ID NO:187所示的第一链和一条如SEQ ID NO:189所示的第二链;或
一条如SEQ ID NO:190所示的第一链和一条如SEQ ID NO:188所示的第二链;或
一条如SEQ ID NO:190所示的第一链和一条如SEQ ID NO:189所示的第二链;或
一条如SEQ ID NO:191所示的第一链和一条如SEQ ID NO:188所示的第二链;或
一条如SEQ ID NO:191所示的第一链和一条如SEQ ID NO:189所示的第二链。
抗原结合分子的变体
在某些实施方案中,涵盖本文中提供的抗原结合分子的氨基酸序列变体。例如,可以期望改善抗体的结合亲和力和/或其它生物学特性。可以通过将合适的修饰引入编码抗体的核苷酸序列中,或者通过肽合成来制备抗体的氨基酸序列变体。此类修饰包括例如对抗原结合分子的氨基酸序列内的残基的删除、和/或插入、和/或取代。可以进行删除、插入、和取代的任何组合以得到最终的构建体,只要最终的构建体拥有期望的特征,例如抗原结合特性。
取代、插入、和删除变体
在某些实施方案中,提供了具有一处或多处氨基酸取代的抗原结合分子变体。可以在CDR和FR进行取代。保守取代在表2中在“优选的取代”的标题下显示。更实质的变化在表2中在“示例性取代”的标题下提供,并且如下文参照氨基酸侧链类别进一步描述的。可以将氨基酸取代引入感兴趣的抗体中,并且对产物筛选期望的活性,例如保留/改善的抗原结合,降低的免疫原性,或改善的ADCC或CDC。
表2.氨基酸的取代
依照常见的侧链特性,氨基酸可以如下分组:
(1)疏水性的:正亮氨酸,Met,Ala,Val,Leu,Ile;
(2)中性,亲水性的:Cys,Ser,Thr,Asn,Gln;
(3)酸性的:Asp,Glu;
(4)碱性的:His,Lys,Arg;
(5)影响链取向的残基:Gly,Pro;
(6)芳香族的:Trp,Tyr,Phe。
非保守取代会是指用一个类别的成员替换另一个类别的成员。
一类取代变体涉及取代亲本抗体(例如人源化或人抗体)的一个或多个CDR残基。一般地,经选择用于进一步研究的所得变体相对于亲本抗体会具有某些生物学特性(例如升高的亲和力,降低的免疫原性)的改变(例如改善),和/或会基本上保留亲本抗体的某些生物学特性。一种示例性的取代变体是亲和力成熟的抗体,可以例如使用基于噬菌体展示的亲和力成熟技术(如本文所述的那些技术),便利地产生所述抗体。简言之,将一个或多个CDR残基突变,并将变体抗体在噬菌体上展示,并对其筛选特定的生物学活性(例如结合亲和力)。可以对CDR做出改变(例如取代),例如以改善抗体亲和力。可以对CDR“热点”,即在体细胞成熟过程期间以高频率经历突变的密码子所编码的残基,和/或接触抗原的残基做出此类改变,同时对所得的变体VH或VL测试结合亲和力。在亲和力成熟的一些实施方案中,通过多种方法(例如易错PCR、链改组、或寡核苷酸指导的诱变)的任一种,将多样性引入所选择用于成熟的可变基因中。然后,创建次级文库。然后,筛选文库以鉴定具有期望的亲和力的任何抗体变体。另一种引入多样性的方法涉及CDR定向的方法,其中将几个CDR残基(例如一次4-6个残基)随机化。可以例如使用丙氨酸扫描诱变或建模来特异性鉴定涉及抗原结合的CDR残基。
在某些实施方案中,取代、插入或缺失可以在一个或多个CDR内发生,只要此类变化不实质性降低抗体结合抗原的能力。例如,可以对CDR做出保守变化(例如保守取代,如本文中提供的),其不实质性降低结合亲和力。在上文提供的变体VH和VL序列的某些实施方案中,每个CDR是未改变的,或者含有不超过1、2或3处氨基酸取代。
一种可用于鉴定抗体中可以作为诱变靶位的残基或区域的方法称作“丙氨酸扫描诱变”。在这种方法中,鉴定一个残基或残基组(例如带电荷的残基,诸如Arg、Asp、His、Lys和Glu),并且替换为中性或带负电荷的氨基酸(例如,Ala或聚丙氨酸),以确定该抗体与抗原的相互作用是否受影响。可以在对初始取代显示功能敏感性的氨基酸位置引入进一步的取代。此外,可通过研究抗原-抗体复合物的晶体结构来鉴定抗体与抗原间的接触点。这些接触残基及邻近残基可以作为取代候选物被打靶或消除。可以筛选变体以确定它们是否含有期望的特性。
氨基酸序列插入包括:在氨基和/或羧基端融合1个残基或长度为100或更多个残基的多肽;和单个或多个氨基酸残基的序列内插入。在末端插入的例子包括具有N端甲硫氨酰基残基的抗体。抗体分子的其它插入变体包括,在抗体的N或C端融合有酶(或延长抗体的血清半衰期的多肽)的融合物。
Fab的改造
在一个方面,本披露的抗原结合分子中,所述特异性结合CD3的抗原结合模块和所述特异性结合DLL3的抗原结合模块两者之一是经替换的Fab,所述经替换的Fab包含重链可变区、轻链可变区、Titin链和Obscurin链。在经替换的Fab中,Fab原有的CH1和CL被Titin链和Obscurin链所替换。示例性的,Titin链和Obscurin链的序列如表3-1和表3-2所示。本披露中,Titin链和Obscurin链与重轻可变区与轻链可变区的组合都是可以互换的。
表3-1.Titin链的氨基酸序列

表3-2.Obscurin链的氨基酸序列


Fc区的改造
在一个方面,本披露的抗原结合分子的Fc区包含一个或多个氨基酸取代,所述一个或多个氨基酸取代减少其与Fc受体的结合,例如其与Fcγ受体的结合,并且降低或消除效应子功能。天然IgG Fc区,具体地是IgG1Fc区或IgG4Fc区,可能导致本披露的抗原结合分子靶向表达Fc受体的细胞,而不是表达抗原的细胞。本披露改造的Fc区表现出降低的对Fc受体的结合亲和力和/或降低的效应子功能。在一些实施方案中,改造的Fc区与天然Fc区相比,对Fc受体的结合亲和力下降50%、80%、90%或95%以上。在一些实施方案中,所述的Fc受体是Fcγ受体。在一些实施方案中,所述Fc受体是人Fcγ受体,例如FcγRI、FcγRIIa、FcγRIIB、FcγRIIIa。在一些实施方案中,改造的Fc区与天然Fc区相比,对补体,如C1q的结合亲和力也降低。在一些实施方案中,改造的Fc区与天然Fc区相比,对新生儿Fc受体(FcRn)的结合亲和力不降低。在一些实施例中,改造的Fc区具有降低的效应子功能,所述降低的效应子功能可以包括但不限于以下中的一个或多个: 降低的补体依赖性细胞毒性(CDC)、降低的抗体依赖性细胞介导的细胞毒性(ADCC)、降低的抗体依赖性细胞吞噬(ADCP)、减少的细胞因子分泌、减少的免疫复合物介导的抗原呈递细胞的抗原摄取、减少的与NK细胞的结合、减少的与巨噬细胞的结合、减少的与单核细胞的结合、减少的与多形核细胞的结合、减少的直接信号传导诱导性细胞凋亡、降低的树突细胞成熟或减少的T细胞引发。对于IgG1Fc区,在238、265、269、270、297、327和329等位置的氨基酸残基取代可降低的效应子功能。在一些实施方案中,所述Fc区是人IgG1Fc区,并且在234和235位置的氨基酸残基为A,编号依据为EU索引。对于IgG4Fc区,在228等位置的氨基酸残基取代可降低的效应子功能。
抗原结合分子还可包含二硫键改造,例如第一亚基的354C和第二亚基的349C。为增加抗原结合分子的血清半衰期,可以引入252Y、254T和256E的突变。
当抗原结合分子包含与Fc区的两个亚基融合的不同结合模块,可能导致不期望的同源二聚化。为了提高产率和纯度,因此在本披露的抗原结合分子的Fc区中引入促进异源二聚化的修饰将是有利的。在一些实施方式中,本披露的Fc区包含根据杵臼(knob-into-hole,KIH)技术的改造,该方法涉及在第一亚基的界面处引入凸起结构(knob)以及在第二亚基的界面处引入孔结构(hole)。使得所述凸起结构可以定位在孔结构中,促进异源二聚体的形成并抑制同源二聚体的产生。凸起结构是通过用较大侧链(例如酪氨酸或色氨酸)取代来自第一亚基的界面的小氨基酸侧链而构建的。而孔结构是通过用较小的氨基酸侧链(例如丙氨酸或苏氨酸)取代大氨基酸侧链而在第二亚基的界面中创建的。凸起结构和孔结构通过改变编码多肽的核酸来制备,可选的氨基酸取代如下表所示:
表4.KIH突变组合
除了杵臼技术外,用于修饰重链的CH3结构域以实现异源二聚化的其他技术也是本领域中已知的,例如WO1996027011A1、WO1998050431、EP1870459、WO2007110205、WO2009089004、WO2010129304、WO201190754、WO2011143545、WO2012058768、WO2013157954和WO2013096291。
Fc区的C末端可以是以氨基酸残基PGK结束的完整C末端;也可以是截短的C末端,例如在所述截短的C末端中去除了一个或两个C末端氨基酸残基。在一个优选的方面中,重链的C末端是以PG结束的缩短的C末端。因此,在一些实施方式中,完整抗体的组合物可以包括去除了所有K447残基和/或G446+K447残基的抗体群体。在一些实施方式中,完整抗体的组合物可以包括没有去除K447 残基和/或G446+K447残基的抗体群体。在一些实施方式中,完整抗体的组合物具有带有和不带有K447残基和/或G446+K447残基的抗体混合物的抗体群体。
重组方法
抗原结合分子可以使用重组方法来产生。对于这些方法,提供编码抗原结合分子的一个或更多个分离的核酸。
在天然抗体、天然抗体片段或具有同源二聚体重链的双特异性抗体的情况下,需要两个核酸,一个用于轻链或其片段,一个用于重链或其片段。此类核酸编码包含抗体VL的氨基酸序列和/或包含抗体VH的氨基酸序列(例如抗体的轻链和/或重链)。这些核酸可以在相同的表达载体上或在不同的表达载体上。
在具有异二聚体重链的双特异性抗体的情况下,需要例如四个核酸,一个用于第一轻链,一个用于包含第一异源单体Fc区多肽的第一重链,一个用于第二轻链,并且一个用于包含第二异源单体Fc区多肽的第二重链。这四个核酸可包含在一个或更多个核酸分子或表达载体中,通常这些核酸位于两个或三个表达载体上,即一个载体可包含这些核酸中的多于一个。
在一个实施方案中,本披露提供了编码如前所述的抗体的分离的核酸。此类核酸可以独立地编码前述的任一多肽链。在另一方面中,本披露提供了包含此类核酸的一种或多种载体(例如表达载体)。在另一方面中,本披露提供了包含此类核酸的宿主细胞。在一个实施方案中,提供制备抗原结合分子的方法,其中所述方法包括,在适合抗体表达的条件下,培养包含编码所述抗体的核酸的宿主细胞,如上文所提供的,和任选地从宿主细胞(或宿主细胞培养基)回收所述抗体。
为了重组产生抗原结合分子,将编码蛋白的核酸分离并插入一个或更多个载体中,用于在宿主细胞中进一步克隆和/或表达。此类核酸可以使用常规程序容易地分离和测序(例如通过使用能够与编码抗体重链和轻链的基因特异性结合的寡核苷酸探针),或者通过重组方法产生或通过化学合成获得。
用于克隆或表达编码抗体的载体的适当宿主细胞包括本文描述的原核或真核细胞。例如,抗体可在细菌中产生,特别是当抗体不需要糖基化和Fc效应子功能时。在表达后,抗体可以在可溶级分中从细菌细胞糊状物分离,并且可进一步纯化。
除了原核生物以外,真核微生物诸如丝状真菌或酵母也是用于编码抗体的载体的合适的克隆或表达宿主,包括真菌和酵母菌株,其糖基化途径已经“人源化”,导致产生具有部分或完全人糖基化模式的抗体。适于表达(糖基化)抗体的合适的宿主细胞也可源自多细胞生物体(无脊椎动物和脊椎动物);无脊椎动物细胞的例子包括植物和昆虫细胞。已经鉴定了许多杆状病毒株,其可与昆虫细胞联合使用,特别是用于草地贪夜蛾(Spodoptera frugiperda)细胞的转染;还可利用植物细胞培养物作为宿主,例如US5959177、US 6040498、US6420548、US 7125978和US6417429;也可将脊椎动物细胞用作宿主,例如适应于在悬浮液中生长的哺 乳动物细胞系。适宜的哺乳动物宿主细胞系的其它例子是经SV40转化的猴肾CVl系(COS-7);人胚肾系(293或293T细胞);幼仓鼠肾细胞(BHK);小鼠塞托利(sertoli)细胞(TM4细胞);猴肾细胞(CV1);非洲绿猴肾细胞(VERO-76);人宫颈癌细胞(HELA);犬肾细胞(MDCK);水牛鼠(buffalo rat)肝细胞(BRL3A);人肺细胞(W138);人肝细胞(Hep G2);小鼠乳房肿瘤(MMT 060562);TRI细胞;MRC 5细胞;和FS4细胞。其它适宜的哺乳动物宿主细胞系包括中国仓鼠卵巢(CHO)细胞,包括DHFR-CHO细胞;以及骨髓瘤细胞系,如Y0、NS0和Sp2/0。关于适合产生抗体的某些哺乳动物宿主细胞系的综述参见例如Yazaki,P.和Wu,A.M.,Methods in Molecular Biology,Vol.248,Lo,B.K.C.(编),Humana Press,Totowa,NJ(2004),第255-268页。
诊断与治疗组合物
在某些实施方案中,本披露提供的抗原结合分子可用于检测生物学样品中DLL3和/或DLL3的存在。在用于本文时,术语“检测”涵盖定量或定性检测。在某些实施方案中,生物学样品包含细胞或组织,诸如肿瘤组织。
在一个实施方案中,提供了在诊断或检测方法中使用的抗原结合分子。在又一方面,提供了检测生物学样品中DLL3和/或DLL3的存在的方法。在某些实施方案中,该方法包括在适宜条件下使生物学样品与抗原结合分子接触,并检测是否在检测试剂与抗原之间形成复合物。此类方法可以是体外或体内方法。在一个实施方案中,使用抗原结合分子来选择适合治疗的受试者,例如DLL3和/或DLL3是用于选择患者的生物标志物。
可使用本披露的抗原结合分子来诊断的示例性病症,例如肿瘤或癌症。
在某些实施方案中,提供了经标记的抗原结合分子。标记物包括但不限于直接检测的标记物或模块(诸如荧光、发色、电子致密、化学发光、和放射性标记物),和间接检测的模块(例如,经由酶反应或分子相互作用间接检测的模块,诸如酶或配体)。
在另外的方面,提供包含所述抗原结合分子的药物组合物,例如,用于以下任何治疗方法。在一个方面,药物组合物包含本文提供的任何抗原结合分子和药学上可接受的载体。在另一个方面,药物组合物包含本文提供的任何抗原结合分子和至少一种另外的治疗剂。
本披露所述的抗原结合分子的药物组合物通过以下制备:将具有所需纯度的此类抗原结合分子与一种或更多种任选的药学上可接受的载体混合,所述药物组合物为冻干组合物或水溶液的形式。用于体内施用的制剂一般是无菌的。无菌性可容易地实现,例如通过穿过无菌滤膜过滤。
治疗方法与施用途径
本文提供的任何抗原结合分子可用于治疗方法。
在又一个方面,本披露提供抗原结合分子在药物的制造或制备中的用途。在一个实施方案中,所述药物用于治疗增殖性疾病或肿瘤。并且所述药物是以对上述疾病的有效量的形式存在的。在一些实施方式中,所述有效量是单位日剂量或单位周剂量。在一个此类实施方案中,所述用途进一步包括向受试者施用有效量的至少一种另外的治疗剂(例如一种、两种、三种、四种、五种或六种另外的治疗剂)。根据任意以上实施方案的“受试者”可以是人。
在又一个方面,提供包含所述抗原结合分子的药物组合物,例如,其用于以上任何制药用途或治疗方法。在另一个实施方案中,药物组合物还包含至少一种另外的治疗剂。
本披露的抗原结合分子可单独使用或与其他试剂联合用于治疗。例如,本披露的抗原结合分子可与至少一种另外的治疗剂共同施用。在一些实施方案中,所述的另外的治疗剂是特异性结合DLL3和CD28的双特异性抗体。
本披露的抗原结合分子(和任何另外的治疗剂)可通过任何合适的手段施用,包括肠胃外、肺内和鼻内,并且如果需要局部治疗,则病灶内施用。肠胃外输注包括肌肉内、静脉内、动脉内、腹膜内或皮下施用。给药可以通过任何适当的途径,例如,通过注射,诸如静脉内或皮下注射,这部分取决于施用是短期的还是长期的。本文考虑多种给药时间方案,包括但不限于,单次或在多个时间点多次施用,推注施用和脉冲输注。
本披露的抗原结合分子将以符合良好医疗实践的方式配制、给药和施用。在此背景下考虑的因素包括所治疗的具体病症、所治疗的具体哺乳动物、个体患者的临床状况、病症的起因、试剂的递送部位、施用方法、施用时间安排以及医学从业者已知的其他因素。抗原结合分子无需但任选地与目前用于预防或治疗所述病症的一种或更多种试剂一起配制。此类其它试剂的有效量取决于药物组合物中存在的抗原结合分子的量、病症或治疗的类型以及上文讨论的其它因素。这些通常以与本文所述相同的剂量和施用路径使用,或以本文所述剂量的约1至99%使用,或以任何剂量使用,并通过经验/临床确定为合适的任何途径使用。
为了预防或治疗疾病,本披露的抗原结合分子(当单独使用或与一种或更多种其他另外的治疗剂组合使用时)的适当的剂量将取决于待治疗的疾病的类型,治疗分子的类型,疾病的严重性和病程,是为预防还是治疗目的施用,之前的治疗,患者的临床病史和对治疗分子的响应,和主治医师的判断。治疗分子恰当地以一次或经过一系列治疗施用于患者。取决于疾病的类型和严重性,约1μg/kg至15mg/kg的抗原结合分子可以是用于施用至患者的初始候选剂量,不管例如是通过一次或更多次分开的施用还是通过连续输注。一种典型的每日剂量可能在约1μg/kg至100mg/kg或更多的范围内,这取决于上文提及的因素。相应的,以50kg体重为例,示例性的单位日剂量为50μg-5g。
制品(药盒)
在本披露的另一方面中,提供一种制品,所述制品包含可用于治疗、预防和/或诊断上述病症的材料。该制品包含容器和在容器上或与容器联合的标签或包装插页(package insert)。合适的容器包括,例如,瓶子、管形瓶、注射器、IV溶液袋等。容器可以自各种材料诸如玻璃或塑料形成。容器装有单独或与另一种组合物组合有效治疗,预防和/或诊断疾患的组合物,并且可具有无菌的存取口(例如,容器可以是具有由皮下注射针可刺穿的塞子的静脉内溶液袋或管形瓶)。组合物中的至少一种活性试剂是本披露的抗原结合分子。标签或包装插页指示使用该组合物是来治疗选择的病况。此外,制品可以包含:(a)其中装有组合物的第一容器,其中所述组合物包含本披露的抗原结合分子;和(b)其中装有组合物的第二容器,其中所述组合物包含另外的细胞毒性剂或其他方面的治疗剂。本披露的该实施方案中的制品可进一步包含包装插页,所述包装插页指示所述组合物可以用于治疗特定病况。备选地,或另外地,制品可进一步包含第二(或第三)容器,所述第二(或第三)容器包含药学上可接受的缓冲液。从商业和用户立场,它可进一步包括所需的其他材料,包括其他缓冲剂、稀释剂、滤器、针头和注射器。
实施例与测试例
以下结合实施例和测试例进一步描述本披露,但这些实施例和测试例并非限制着本披露的范围。本披露实施例和测试例中未注明具体条件的实验方法,通常按照常规条件,如冷泉港的抗体技术实验手册,分子克隆手册;或按照原料或商品制造厂商所建议的条件。未注明具体来源的试剂,为市场购买的常规试剂。
实施例1.含有Titin链/Obscurin链的抗原结合分子
本披露的Titin链/Obscurin链可以来源于任意适宜的多肽,包括来源于WO2021139758(通过援引完整收入本文)和CN202110527339.7及将其作为优先权文件的专利(通过援引完整收入本文)中的多肽。构建双特异性抗体,其中CL为WO2021139758中的kappa轻链恒定区,Titin链和Obscurin链的氨基酸序列见表3-1和表3-2,连接子序列包括GGGGS(SEQ ID NO:147)、ASTKG(SEQ ID NO:255)或RTVAS(SEQ ID NO:256),本实施例中的Fc1、Fc2、CH1的氨基酸序列如下所示。
>实施例1-Fc1(knob,SEQ ID NO:143)
>实施例1-Fc2(hole,SEQ ID NO:144)
>实施例1-CH1(SEQ ID NO:141)。
1.1 DI双特异性抗体
参照WO2021139758的实施例5,构建抗hNGF和hRANKL的DI双特异性抗体:DI-2至DI-20,其包含如下所述的第一重链、第二重链、第一轻链和第二轻链:
第一重链:从N端到C端依次为:[VH1-I]-[连接子1]-[Obscurin链]-[Fc2],
第一轻链:从N端到C端依次为:[VL1-I]-[连接子2]-[Titin链],
第二重链:从N端到C端依次为:[VH2-D]-[CH1]-[Fc1],和
第二轻链:从N端到C端依次为:[VL2-D]-[CL];
其中,VH1-I和VL1-I分别为WO2021139758中I0的重链可变区和轻链可变区,VH2-D和VL2-D分别为WO2021139758中D0的重链可变区和轻链可变区。本实施例中DI双特异性抗体中Obscurin链、Titin链、连接子1、连接子2结构见下表5。
表5.DI双特异性抗体中Obscurin链/Titin链和连接子对应表
注:表格中Titin链和Obscurin链的编号见表3-1和表3-2。
采用WO2021139758的测试例4中的方法检测DI-2至DI-20双特异性抗体与其抗原的结合活性。对抗体进行热稳定性研究。研究方法:用PBS将抗体的浓度稀释至5mg/mL,采用高通量微分扫描荧光仪(UNCHAINED,规格型号:Unit)测定其热稳定性。实验结果表明,改造后的双特异性抗体对抗原的结合活性没有显著变化;并且,与DI-2相比,DI-4至DI-8、DI-10至DI-16、DI-20的Tm1(℃)、Tonset(℃)有明显的提升,双特异性抗体的热稳定性更优。
表6.DI双特异性抗体的结合活性检测
表7.DI双特异性抗体的热稳定性实验结果
采用10mM乙酸,pH5.5,9%蔗糖的缓冲液配制含DI双特异性抗体的溶液,将溶液置于40℃恒温箱中孵育四周,结束后将抗体浓度浓缩至孵育开始时浓度,观察溶液沉淀情况。实验结果表明,DI-2双特异性抗体组溶液出现沉淀,DI-3至DI-7相比DI-2具有更好的稳定性。
表8.DI双特异性抗体的沉淀

1.2 PL双特异性抗体
构建抗hPDL1和hCTLA4的PL双特异性抗体:PL-1至PL-19,其包含如下所述的第一重链、第二重链、第一轻链和第二轻链:
第一重链:从N端到C端依次为:[VH1-P]-[连接子1]-[Obscurin链]-[Fc1],
第一轻链:从N端到C端依次为:[VL1-P]-[连接子2]-[Titin链],
第二重链:从N端到C端依次为:[VH2-L]-[CH1]-[Fc2],和
第二轻链:从N端到C端依次为:[VL2-L]-[CL];
其中,VH1-P和VL1-P分别为WO2020177733A1中h1831K抗体的重链可变区和轻链可变区,VH2-L和VL2-L的氨基酸序列如下所示。
>VH2-L(SEQ ID NO:257)
>VL2-L(SEQ ID NO:258)
本实施例中PL双特异性抗体中Obscurin链、Titin链、连接子1、连接子2结构见下表。
表9.PL双特异性抗体中Obscurin链/Titin链和连接子对应表

注:表格中Titin链和Obscurin链的编号见表3-1和表3-2。
参照WO2021139758中测试例4中的ELISA方法检测PL双特异性抗体的结合活性,其中hPDL1、hCTLA4抗原购自:Sino biology。对抗体进行热稳定性研究。方法:用PBS将抗体的浓度稀释至1.4-3mg/mL,采用高通量微分扫描荧光仪(UNCHAINED,规格型号:Unit)测定其热稳定性。实验结果表明,PL双特异性抗体对抗原仍具有良好的结合活性;并且,与PL-1相比,PL-2至PL-19的Tm1(℃)、Tagg 266(℃)、Tonset(℃)有明显的提升,双特异性抗体的热稳定性更优。
表10.PL双特异性抗体的结合活性检测
表11.PL双特异性抗体的热稳定性实验结果
1.3 HJ双特异性抗体
构建抗hIL5和hTSLP的HJ双特异性抗体:HJ-3至HJ11,其包含如下所述的第一重链、第二重链、第一轻链和第二轻链:
第一重链:从N端到C端依次为:[VH1-H]-[连接子1]-[Titin链]-[Fc1],
第一轻链:从N端到C端依次为:[VL1-H]-[连接子2]-[Obscurin链],
第二重链:从N端到C端依次为:[VH2-J]-[CH1]-[Fc2],和
第二轻链:从N端到C端依次为:[VL2-J]-[CL];
其中,VH1-H和VL1-H分别为WO2021139758中H0的重链可变区和轻链可变区,VH2-J和VL2-J分别为WO2021139758中J1的重链可变区和轻链可变区。本实施例中HJ双特异性抗体中Obscurin链、Titin链、连接子1、连接子2结构见下表。
表12.HJ双特异性抗体中Obscurin链/Titin链和连接子对应表
参照WO2021139758中测试例4中的方法检测HJ双特异性抗体的抗原结合活性。对抗体的热稳定性进行研究,方法:用10mM乙酸pH5.5、9%蔗糖的缓冲液配制HJ双特异性抗体稀释溶液,然后通过超滤浓缩的方法将双特异性抗体浓缩,获得不同浓度的HJ双特异性抗体溶液(HJ双特异性抗体的浓度见表13-2),然后将浓缩溶液置于40℃恒温箱中孵育,第0天(也即40℃孵育开始前,D0),第7天(40℃孵育第7天,D7),第14天(40℃孵育第14天,D14),第21天(40℃孵育第21天,D21)和第28天(40℃孵育第28天,D28)检测样品的SEC纯度,40℃孵育28天后,马上取样检测样品CE-SDS纯度。实验结果表明,本披露构建的HJ双特异性抗体对抗原的结合活性没有显著变化;并且,与HJ-3相比,HJ-5至HJ-11双特异性抗体的热稳定性更优。
表13-1.HJ双特异性抗体的结合活性检测

表13-2.HJ双特异性抗体加速稳定性实验结果
实施例2.DLL3抗原及检测用蛋白和稳转细胞株的制备
2.1高表达DLL3的细胞株构建
包含SEQ ID NO:1-2的pCDH慢病毒表达载体质粒(由GENEWIZ公司合成),pCDH质粒分别与pVSVG,pCMV慢病毒包装载体用Lipofectamine 3000(Invitrogen,L3000015)转染试剂转染至293T细胞(中科院细胞库,GNHu17)中,收集含有病毒的培养基上清,过滤并进行超高速离心,弃去上清后,用0.2mL无菌PBS重悬。使用浓缩后的病毒分别感染中国仓鼠卵巢细胞CHO-s(Invitrogen,R80007),DMS53(ATCC,CRL-2062)和H82(ATCC,HTB-175),经嘌呤霉素(puromycin)筛选两至三周,再进行FACS单细胞分选。将挑选出的单克隆细胞株扩大培养,冻存,以便后续实验。
包含表达LUC和GFP基因的pCDH-CMV-MCS-EF1-puro慢病毒表达载体质粒(由GENEWIZ公司合成),pCDH质粒分别与pVSVG,pCMV慢病毒包装载体用Lipofectamine 3000(Invitrogen,L3000015)转染试剂转染至293T细胞(中科院细胞库,GNHu17)中,收集含有病毒的培养基上清,过滤并进行超高速离心,弃去上清后,用0.2mL无菌PBS重悬。使用浓缩后的病毒分别感染SHP77(ATCC,CRL-2195),H1184(ATCC,CRL-5858),H460(中国科学院细胞库,TCHu205)经嘌呤霉素(puromycin)筛选两至三周,再进行FACS单细胞分选。将挑选出的单克隆细胞株扩大培养,冻存,以便后续实验。
使用的相关蛋白序列如下:
1.人DLL3全长蛋白(SEQ ID NO:1):

2.食蟹猴DLL3全长蛋白(SEQ ID NO:2):
3.大鼠DLL3全长蛋白(SEQ ID NO:3):
4.小鼠DLL3全长蛋白(SEQ ID NO:4):
5.人DLL1全长蛋白(SEQ ID NO:5):
6.人DLL4全长蛋白(SEQ ID NO:6):

2.2抗原的制备
以人DLL3(Uniprot,Q9NYJ7)、食蟹猴DLL3(Uniprot,A0A2K5WSR4)和小鼠DLL3(Uniprot,O88516)序列为模板,设计含有不同标签的人DLL3ECD融合蛋白,分别克隆到pTT5载体上,经293E细胞表达后,获得抗原。相关蛋白氨基酸序列如下:
1.His-hDLL3(ECD)(SEQ ID NO:7):
注:点划线为信号肽序列,单划线为his标签和连接子,双划线为DLL3胞外区。
2.Fc-hDLL3(ECD)(SEQ ID NO:8):

注:点划线为信号肽序列,单划线为Fc标签和连接子,双划线为DLL3胞外区。
3.hDLL3(ECD)-strep twin(SEQ ID NO:9):
注:点划线为信号肽序列,双划线为DLL3胞外区,单划线为strep twin标签。
4.cynoDLL3(ECD)-strep twin(SEQ ID NO:10):
注:点划线为信号肽序列,双划线为DLL3胞外区,单划线为strep twin标签。
5.mouDLL3(ECD)-strep twin(SEQ ID NO:11):

注:点划线为信号肽序列,双划线为DLL3胞外区,单划线为strep twin标签。
实施例3.抗人DLL3抗体的制备
3.1抗人DLL3杂交瘤抗体的筛选和鉴定
通过杂交瘤技术制备针对人DLL3的单克隆抗体,免疫方式如下:
第一组,以His-hDLL3(ECD)(SEQ ID NO:7)为免疫原,用Gold Adjuvant(Sigma Cat No.T2684)与ThermoAlum(Thermo Cat No.77161)佐剂交叉免疫。抗原与佐剂(Gold Adjuvant)比例为1:1,抗原与佐剂(ThermoAlum)比例为3:1,50μg/只/次(首次免疫),25μg/只/次(加强免疫)。用ELISA方法确定小鼠血清中的抗体滴度。
第二组小鼠的免疫抗原为DLL3-CHO-s细胞和Fc-hDLL3(ECD)(SEQ ID NO:8),免疫方式为细胞和蛋白抗原交替免疫。细胞免疫按照每只小鼠腹膜内注射0.1mL生理盐水稀释至108/mL浓度的细胞液。Fc-hDLL3(ECD)抗原用Gold Adjuvant(Sigma Cat No.T2684)与ThermoAlum(Thermo Cat No.77161)佐剂交叉免疫。抗原与佐剂(Gold Adjuvant)比例为1:1,抗原与佐剂(ThermoAlum)比例为3:1,50μg/只/次(首次免疫),25μg/只/次(加强免疫)。用ELISA方法确定小鼠血清中的抗体滴度。
采用优化的电融合方法将脾淋巴细胞与骨髓瘤细胞Sp2/0细胞(CRL-8287TM)进行融合得到杂交瘤细胞。根据杂交瘤细胞生长密度,用结合DLL3蛋白的ELISA方法和结合DLL3CHO-s细胞FACS方法进行杂交瘤培养上清检测。选择结合人DLL3蛋白,猴DLL3蛋白以及DLL3CHO-s细胞,同时不结合野生型CHO-s细胞的克隆及时进行冻存扩增保种和一到二次亚克隆直至获得单细胞克隆。通过以上实验筛选得到杂交瘤克隆mAb6,mAb98和mAb110。
将杂交瘤克隆扩培养,提取RNA,利用mouse-Ig的简并引物进行反转录扩增(RT-PCR),最后得到抗体的可变区序列。
mAb6重链可变区(SEQ ID NO:12):
mAb6轻链可变区(SEQ ID NO:13):
mAb98重链可变区(SEQ ID NO:14):
mAb98轻链可变区(SEQ ID NO:15):
mAb110重链可变区(SEQ ID NO:16):
mAb110轻链可变区(SEQ ID NO:17):
3.2免疫库筛选抗体的方案及抗体序列
将经免疫获得的小鼠脾细胞采用Trizol试剂提取总RNA,并反转录合成cDNA。以cDNA为模板采用简并引物扩增抗体的重轻链可变区序列,并将扩增的片段构建于优化的噬菌体展示载体,随后将构建完成的载体电击转化大肠杆菌TG1菌株,即获得DLL3免疫文库。将获得DLL3免疫文库包装噬菌体,采用生物素标记的人DLL3蛋白进行两轮文库筛选。将筛选获得的单克隆,接种于96孔板中包装噬菌体。采用ELISA检测可结合人DLL3蛋白和猴DLL3蛋白的噬菌体,并将对应的单克隆进行测序分析,最终获得抗DLL3的抗体的可变区序列。
mAb30重链可变区(SEQ ID NO:18):
mAb30轻链可变区(SEQ ID NO:19):
表14.抗体的CDR

注:VH/VL的CDR的氨基酸残基由Kabat编号系统确定并注释。
将鼠抗体的重链可变区和轻链可变区分别克隆到包含SEQ ID NO:41所示的人IgG1重链恒定区和SEQ ID NO:42所示的κ轻链恒定区的pTT5载体质粒,然后转染HEK293细胞,得到了抗DLL3的嵌合抗体M6CHI,M98CHI,M110CHI和P30CHI。
人IgG1重链恒定区(SEQ ID NO:41):
人κ轻链恒定区(hκ)(SEQ ID NO:42):
实施例4.抗DLL3单克隆抗体的人源化
通过比对Kabat人类抗体重轻链可变区种系基因数据库,分别挑选同源性高的重、轻链可变区种系基因作为模板,将鼠源抗体的CDR分别嫁接(graft)到相应 的人源模板中,形成次序为FR1-CDR1-FR2-CDR2-FR3-CDR3-FR4的可变区序列。并对可变区的某些氨基酸进行氨基酸取代,再与恒定区重组(示例性的,与SEQ ID NO:41所示的人IgG1重链恒定区和SEQ ID NO:42所示的人κ轻链恒定区),获得全长的人源化抗体。
4-1.mAb6抗体的人源化
mAb6抗体的人种系轻链模版为IGKV1-16*01或IGKV3-20*02和IGKJ4*01,人种系重链模版为IGHV1-3*01、IGHV7-4-1*02或IGHV3-73*01和IGHJ6*01。任选地,对人源化抗体的轻链可变区上第1、36、42、43、44、46、52、56、69、71、79、85和/或94位的氨基酸残基进行取代;和/或对人源化抗体的重链可变区上第1、27、30、38、43、48、67、68、69、71、73、75、76、93、56、58和/或5位的氨基酸残基进行取代。
表15.mAb6鼠源抗体的人源化模板及相应点突变

注:表中的氨基酸位置按照为kabat编号,F36L表示依照Kabat编号系统,将36位F突变为L下同。
获得的hu6人源化抗体可变区的序列如下:
hu6 VH1(SEQ ID NO:43)
hu6 VH2(SEQ ID NO:44)
hu6 VH3(SEQ ID NO:45)
hu6 VH4(SEQ ID NO:46)
hu6 VH5(SEQ ID NO:47)
hu6 VH6(SEQ ID NO:48)
hu6 VH7(SEQ ID NO:49)
hu6VH8(SEQ ID NO:50)(Graft IGHV1-3*01)
hu6VH9(SEQ ID NO:51)(Graft IGHV7-4-1*02)
hu6VH10(SEQ ID NO:52)(Graft IGHV3-73*01)
hu6VH11(SEQ ID NO:53)
hu6VH12(SEQ ID NO:54)
hu6VH13(SEQ ID NO:55)
hu6VH14(SEQ ID NO:56)
hu6VH15(SEQ ID NO:57)
hu6 VL1(SEQ ID NO:58)
hu6 VL2(SEQ ID NO:59)
hu6 VL3(SEQ ID NO:60)
hu6 VL4(SEQ ID NO:61)
hu6VL5(SEQ ID NO:62)(Graft IGKV1-16*01)
hu6VL6(SEQ ID NO:63)
hu6VL7(SEQ ID NO:64)
hu6VL8(SEQ ID NO:65)
hu6VL9(SEQ ID NO:66)
hu6VL10(SEQ ID NO:67)
Graft(IGKV3-20*02)+Y36L,Q42K,L46G,T69A,F71Y,E79Q,V85D+D56E
hu6VL11(SEQ ID NO:68)Graft(IGKV3-20*02)+D56E
注:单下划线部分为CDR,双下划线处为氨基酸取代位点,其余部分为FR区,下同。
mAb6的人源化抗体的CDR如下:
表16.mAb6人源化抗体的CDR
3-2.mAb98的人源化
mAb98抗体的人种系轻链模版为IGKV1-39*01和IGKJ4*01,人种系重链模版为IGHV3-7*01和IGHJ6*01。任选地,对人源化抗体的轻链可变区上第42、44和/或71位的氨基酸残基进行取代;和/或对人源化抗体的重链可变区上第34、57和/或98位的氨基酸残基进行取代。
表17.mAb98鼠源抗体的人源化模板及相应点突变
获得的hu98人源化抗体可变区的序列如下:
hu98VL1 Graft(IGKV1-39*01)(SEQ ID NO:75)
hu98VL2 Graft(IGKV1-39*01)+P44V,F71Y(SEQ ID NO:76)
hu98VL3 Graft(IGKV1-39*01)+K42G,P44V,F71Y(SEQ ID NO:77)
hu98VH1 Graft(IGHV3-7*01)(SEQ ID NO:78)
hu98VH2 Graft(IGHV3-7*01)+D98E(SEQ ID NO:79)
hu98VH3(SEQ ID NO:80)
hu98VH4(SEQ ID NO:81)
hu98VH5(SEQ ID NO:82)
表18.hu98的CDR
3-3.mAb110的人源化
mAb110抗体的人种系轻链模版为IGKV4-1*01和IGKJ2*01,人种系重链模版为IGHV1-3*01和IGHJ6*01。任选地,对人源化抗体的轻链可变区上第1、9、43、68和/或85位的氨基酸残基进行取代;和/或对人源化抗体的重链可变区上第1、24、44、71、73、54和/或55位的氨基酸残基进行取代。
表19.mAb110鼠源抗体的人源化模板及相应点突变
获得的hu110人源化抗体可变区的序列如下:
hu110VL1 Graft(IGKV4-1*01)+P43S,G68A(SEQ ID NO:86)
hu110VL2 Graft(IGKV4-1*01)+D1N,D9K,P43S,G68A,V85D(SEQ ID NO:87)
hu110VL3 Graft(IGKV4-1*01):(SEQ ID NO:88)
hu110VH1 Graft(IGHV1-3*01)+R71V,T73K+Q1E(SEQ ID NO:89)
hu110VH2 Graft(IGHV1-3*01)+A24T,R44S,R71V,T73K+Q1E(SEQ ID NO:90)
hu110VH3 Graft(IGHV1-3*01)+A24T,R44S,R71V,T73K+Q1E,N54Q(SEQ ID NO:91)
hu110VH4 Graft(IGHV1-3*01)+A24T,R44S,R71V,T73K+Q1E,N54S(SEQ ID NO:92)
hu110VH5 Graft(IGHV1-3*01)+A24T,R44S,R71V,T73K+Q1E,N54T(SEQ ID NO:93)
hu110VH6 Graft(IGHV1-3*01)+A24T,R44S,R71V,T73K+Q1E,G55V(SEQ ID NO:94)
hu110VH7 Graft(IGHV1-3*01)(SEQ ID NO:95)
表20.hu110的CDR
3-4.mAb30的人源化
mAb30抗体的人种系轻链模版为IGKV4-1*01或IGKV1-39*01和IGKJ2*01,人种系重链模版为IGHV1-3*01和IGHJ6*01。任选地,对人源化抗体的轻链可变区上第9、43、60、68、87和/或100位的氨基酸残基进行取代;和/或对人源化抗体的重链可变区上第1、3、5、7、9、10、12、40、44、41、48、67、69、71、73、75、83、54和/或55位的氨基酸残基进行取代。
表21.mAb30鼠源抗体的人源化模板及相应点突变
获得的hu30人源化抗体可变区的序列如下:
hu30VL1 Graft(IGKV4-1*01)(SEQ ID NO:100)
hu30VL2 Graft(IGKV4-1*01)+G68A,Y87H(SEQ ID NO:101)
hu30VL3 Graft(IGKV4-1*01)+D9K,P43S,G68A,Y87H(SEQ ID NO:102)
hu30VL4 Graft(IGKV1-39*01)(SEQ ID NO:103)
hu30VL5 Graft(IGKV1-39*01)+A43S,S60D,Q100S(SEQ ID NO:104)
hu30VH1 Graft(IGHV1-3*01)+R44S,R71V,T73K+Q1E(SEQ ID NO:105)
hu30VH2 Graft(IGHV1-3*01)+Q3R,R44S,I69L,R71V,T73K+Q1E(SEQ ID NO:106)
hu30VH3 Graft(IGHV1-3*01)+Q3R,R44S,I69L,R71V,T73K+Q1E,N54Q(SEQ ID NO:107)
hu30VH4 Graft(IGHV1-3*01)+Q3R,R44S,I69L,R71V,T73K+Q1E,N54S(SEQ ID NO:108)
hu30VH5 Graft(IGHV1-3*01)+Q3R,R44S,I69L,R71V,T73K+Q1E,N54T(SEQ ID NO:109)
hu30VH6 Graft(IGHV1-3*01)+Q3R,R44S,I69L,R71V,T73K+Q1E,G55V(SEQ ID NO:110)
hu30VH7 Graft(IGHV1-3*01)+Q3R,V5Q,A9P,E10V,K12V,R44S,I69L,R71V,T73K+Q1E(SEQ ID NO:111)
hu30VH8 Graft(IGHV1-3*01)+Q3R,S7F,E10V,R44S,I69L,R71V,T73K,A75S+Q1E,N54T(SEQ ID NO:112)
hu30VH9 Graft(IGHV1-3*01)+Q3R,R44S,M48I,V67A,I69L,R71V,T73K+Q1E,N54T(SEQ ID NO:113)
hu30VH10 Graft(IGHV1-3*01)+Q3R,A40S,P41H,R44S,I69L,R71V,T73K+Q1E,N54T(SEQ ID NO:114)
hu30VH11 Graft(IGHV1-3*01)+Q3R,S7F,E10V,R44S,I69L,R71V,T73K,A75S,R83T+Q1E,N54T(SEQ ID NO:115)
hu30VH12 Graft(IGHV1-3*01)(SEQ ID NO:116)
表22.hu30的CDR
将人源化抗体的重链可变区和轻链可变区分别与重链恒定区和轻链恒定区重组,示例性的重链恒定区的序列为SEQ ID NO:41,轻链恒定区的序列为SEQ ID NO:42,获得全长的人源化抗体。具体的人源化抗体的可变区组合见下表。
表23-1.mAb6的人源化抗体
注:hu6L1H1表示该抗体包含重链可变区hu6VH1和轻链可变区hu6VL1,且其重链恒定区的序列为SEQ ID NO:41,轻链恒定区的序列为SEQ ID NO:42,其他类推。
表23-2.mAb6的人源化抗体
表23-3.mAb98的人源化抗体
注:hu98L1H1表示该抗体包含重链可变区hu98VH1和轻链可变区hu98VL1,且其重链恒定区的序列为SEQ ID NO:41,轻链恒定区的序列为SEQ ID NO:42,其他类推。
表23-4.mAb110的人源化抗体
注:hu110L1H1表示该抗体包含重链可变区hu110VH1和轻链可变区hu110VL1,且其重链恒定区的序列为SEQ ID NO:41,轻链恒定区的序列为SEQ ID NO:42,其他类推。
表23-5.mAb30的人源化抗体
注:hu30L1H1表示该抗体包含重链可变区hu30VH1和轻链可变区hu30VL1,且其重链恒定区的序列为SEQ ID NO:41,轻链恒定区的序列为SEQ ID NO:42,其他类推。
分别克隆、表达、纯化上述抗体,经蛋白结合实验(测试例3)、细胞结合实验(测试例2)、Biacore(测试例1),最终选出活性较好的人源化抗体。示例性的人源化抗体的重、轻链氨基酸序列如下:
Hu6(也称hu6L4H12)重链(SEQ ID NO:121):
Hu6(也称hu6L4H12)轻链(SEQ ID NO:122):
Hu98(也称hu98L3H4)重链(SEQ ID NO:123):
Hu98(也称hu98L3H4)轻链(SEQ ID NO:124):
Hu110(也称hu110L2H3)重链(SEQ ID NO:125):

Hu110(也称hu110L2H3)轻链(SEQ ID NO:126):
Hu30(也称hu30L1H5)重链(SEQ ID NO:127):
Hu30(也称hu30L1H5)轻链(SEQ ID NO:128):
注:序列中下划线部分为可变区,斜体部分为恒定区。
实施例5.抗DLL3-CD3双特异性抗体的制备
5.1本披露使用的CD3抗体
本披露的CD3结合部分可以来源于任意适宜的抗体。具体的,本披露的实施例采用的是S107E和I2C,其可变区及CDR序列如下:
表24.S107E的CDR

S107E可变区序列如下:
>S107E-VH(SEQ ID NO:136)
>S107E-VL(SEQ ID NO:137)
I2C可变区序列如下:
>I2C-VH(SEQ ID NO:138)
>I2C-VL(SEQ ID NO:137)
注:下划线部分为CDR。
>S107E-scFv(SEQ ID NO:139):
>I2C-scFv(SEQ ID NO:140):
注:双下划线部分为连接子。
5.2本披露的DLL3-CD3双特异性抗体的结构
本披露的DLL3-CD3双特异性抗体分子的结构为Format1、Format2和Format3,具体结构如下:
1.Format1为非对称结构Hot-Ig,完整分子共四条链,四条链均不相同,具体如下:
链1:VL(anti-DLL3)-连接子1-Obscurin
链2:VH(anti-DLL3)-连接子1-Titin-IgG1Fc(Hole,L234A,L235A,Y349C,T366S,L368A,Y407V);
链3:VH(anti-CD3)-IgG1(CH1)-IgG1Fc(Knob,L234A/L235A/S354C/T366W);
链4:VL(anti-CD3)-hλ;
其示意图如图1A所示,其中Ob代表Obscurin。
2.Format2为非对称结构分子Y body,完整分子包含3条链,具体如下:
链1:VL(anti-DLL3)-hκ
链2:VH(anti-DLL3-IgG1(CH1)-IgG1Fc(Hole,L234A/L235A/Y349C/T366S/L368A/Y407V);
链3:VH(anti-CD3)-连接子2-VL(anti-CD3)-连接子1-IgG1Fc(Knob,L234A/L235A/S354C/T366W);
其示意图如图1B所示。
3.Format3为diabody,完整分子包含两条链,具体如下:
链1:VL(anti-DLL3)-连接子3-VH(anti-CD3)-连接子4-Fc(Knob,L234A,L235A,G237A,Y349C,T366W)
链2:VL(anti-CD3)-连接子5-VH(anti-DLL3)-连接子4-Fc(hole,L234A,L235A,G237A,S354C,T366S,L368A,Y407A);
其示意图如图1C所示。
相关序列如下:
>IgG1(CH1)(SEQ ID NO:141)
>hλ(SEQ ID NO:142)
>IgG1Fc(Knob,L234A/L235A/S354C/T366W)(SEQ ID NO:143)

>IgG1Fc(Hole,L234A,L235A,Y349C,T366S,L368A,Y407V)(SEQ ID NO:144)
>Obscurin(SEQ ID NO:246)
>Titin(SEQ ID NO:208)
>Fc(Knob,L234A,L235A,G237A,Y349C,T366W)(SEQ ID NO:145)
>Fc(hole,L234A,L235A,G237A,S354C,T366S,L368A,Y407V)(SEQ ID NO:146)
>连接子1(SEQ ID NO:147)
>连接子2(SEQ ID NO:148)
>连接子3(SEQ ID NO:149)
>连接子4(SEQ ID NO:150)
G
>连接子5(SEQ ID NO:151)
基于mAb6、mAb98、mAb110、mAb30人源化抗体氨基酸序列,分别构建了如下所示的双特异性抗体。
表25.本披露的双特异性抗体


注:hu6-S107E-hot Ig表示该分子采用mAb6及其人源化抗体的可变区作为DLL3结合域,S107E的可变区作为CD3结合域,采用hot Ig作为分子结构。其余类推。
本披露DLL3-CD3双特异性抗体的氨基酸序列如下:
>hu6VL-G4S-Obscurin(SEQ ID NO:152)
>hu6VH-G4S-Titin-hole(SEQ ID NO:153)
>S107EVH-CH1-knob(SEQ ID NO:154)
>CD3VL-hλ(SEQ ID NO:155)
>I2CVH-CH1-knob(SEQ ID NO:156)
>hu6VL-hκ(SEQ ID NO:157)
>hu6VH-CH1-hole(SEQ ID NO:158)

>S107E_scFv-knob(SEQ ID NO:159)
>I2C_scFv-knob(SEQ ID NO:160)
>hu6VL-S107EVH-knob(SEQ ID NO:161)

>CD3VL-hu6VH-hole(SEQ ID NO:162)
>hu6VL-I2CVH-knob(SEQ ID NO:163)
>hu98VL-G4S-Obscurin(SEQ ID NO:164)
>hu98VH-G4S-Titin-hole(SEQ ID NO:165)

>hu98VL-hκ(SEQ ID NO:166)
>hu98VH-CH1-hole(SEQ ID NO:167)
>hu98VL-S107EVH-knob(SEQ ID NO:168)
>CD3VL-hu98VH-hole(SEQ ID NO:169)

>hu98VL-I2CVH-knob(SEQ ID NO:170)
>hu110VL-G4S-Obscurin(SEQ ID NO:171)
>hu110VH-G4S-Titin-hole(SEQ ID NO:172)
>hu110VL-hκ(SEQ ID NO:173)
>hu110VH-CH1-hole(SEQ ID NO:174)

>hu110VL-S107EVH-knob(SEQ ID NO:175)
>CD3VL-hu110VH-hole(SEQ ID NO:176)
>hu110VL-I2CVH-knob(SEQ ID NO:177)

>hu30VL-G4S-Obscurin(SEQ ID NO:178)
>hu30VH-G4S-Titin-hole(SEQ ID NO:179)
>hu30VL-hκ(SEQ ID NO:180)
>hu30VH-CH1-hole(SEQ ID NO:181)
>hu30VL-S107EVH-knob(SEQ ID NO:182)

>CD3VL-hu30VH-hole(SEQ ID NO:183)
>hu30VL-I2CVH-knob(SEQ ID NO:184)
>hu6VL(D56E)-S107EVH-knob(hu6(D56E)-S107E-diabody-C1(SEQ ID NO:185)

>hu6VL(D56E)-I2CVH-knob(SEQ ID NO:259)
>hu6VL(D56S)-I2CVH-knob(SEQ ID NO:260)
>hu6VL(D56S)-S107EVH-knob(SEQ ID NO:186)
>hu6VL8-S107EVH-knob(SEQ ID NO:187)

>CD3VL-hu6VH14-hole(SEQ ID NO:188)
>CD3VL-hu6VH15-hole(SEQ ID NO:189)
>hu6VL9-S107EVH-knob(SEQ ID NO:190)
>hu6VL10-S107EVH-knob(SEQ ID NO:191)
本披露中使用的对照分子AMG-75,其参考WO2017021349制备;BI-764532其参考WO2019234220制备。对照分子的序列如下:
AMG-757(SEQ ID NO:252):
BI-764532:
>BI-764532链1(SEQ ID NO:253):
>BI-764532链2(SEQ ID NO:254):
测试例
测试例1:Biacore抗体亲和力测定
用Protein A生物传感芯片(Cat.#29127556,Cytiva)亲和捕获待测抗体18秒,然后于芯片表面流经抗原人DLL3(ACRO,DLL3-H52H4),食蟹猴DLL3(KACTUS,DLL-RM103),小鼠DLL3(KACTUS,DLL-MM103),人CD3D&3E(ACRO,CDD-H52W1)和猴CD3D&3E(ACRO,CDD-C52W4)180秒,然后解离600秒。 用Biacore 8K(Cytiva)仪器实时检测反应信号获得结合和解离曲线。在每个实验循环解离完成后,用10mM甘氨酸-盐酸溶液(pH 1.5,Cat.#BR-1003-54,Cytiva)将芯片洗净再生。数据拟合模型采用1:1Model。结果见表26-1至表26-9。
表26-1.抗体与人DLL3的亲和力(基于克隆6)
表26-2.抗体与人DLL3的亲和力(基于克隆98)
表26-3.抗体与人DLL3的亲和力(基于克隆110)

表26-4.抗体与人DLL3的亲和力(基于克隆30)

表26-5.双特异性抗体与人DLL3的亲和力
表26-6.双特异性抗体与食蟹猴DLL3的亲和力
表26-7.双特异性抗体与小鼠DLL3的亲和力
表26-8.双特异性抗体与人CD3的亲和力
表26-9.双特异性抗体与食蟹猴CD3的亲和力

结果显示,本披露的特异性结合DLL3的人源化抗体,嵌合抗体与人DLL3均具有良好亲和力;双特异性抗体与人和食蟹猴的DLL3和CD3均具有良好的亲和力。
测试例2:DLL3细胞水平的FACS结合实验
将表达DLL3的小细胞肺癌细胞系H1184(ATCC,货号CRL-5858),DLL3/H82,DLL3/SHP77,hDLL3/CHO-s,cynoDLL3/CHO-s细胞,表达CD3的细胞Jurkat(ATCC,TIB-152)用FACS缓冲液(1%BSA+pH 7.4 PBS)制备成1×106/mL的细胞悬液,100μL/孔加入96孔圆底板中。300g离心5分钟,去除上清。加入不同浓度待测抗体,100μL/孔。放于4℃冰箱中避光孵育1小时。300g离心洗涤3次后,加入工作浓度的APC anti-human IgG Fc(BioLegend,410712)或者PE F(ab')2-羊抗人IgG(invitrogen,H10104),放于4℃冰箱中避光孵育40分钟。300g离心洗涤3次后,在Invitrogen流式细胞仪上检测几何平均数荧光强度,计算抗体对表达DLL3的细胞的结合EC50值。结果见表27-1至27-6。
表27-1.抗体与表达人DLL3的H1184细胞的结合活性
表27-2.抗体与表达人DLL3的H1184细胞的结合活性

表27-3.抗体与过表达人DLL3的H82细胞的结合活性
表27-4.抗体与过表达人DLL3的H82细胞的结合活性
表27-5.抗体与表达人DLL3的SHP77细胞的结合活性
表27-6.双特异性抗体与细胞的结合活性
结果显示,本披露的抗DLL3人源化抗体与表达人DLL3的细胞具有良好结合能力;双特异性抗体对表达人和食蟹猴的DLL3细胞以及CD3的细胞有良好的结合能力。
测试例3:DLL3蛋白水平的ELISA结合实验
将streptavidin(abcam,ab136200,1μg/ml)包板,100μL/孔,4℃过夜。用PBST溶液(PBS含0.1%吐温20)250μL/孔,洗板3次。5%牛奶封闭,250μL/孔,37℃封闭2小时。用PBST溶液250μL/孔,洗板3次。加入生物素化的DLL3抗原(1μg/mL)(SEQ ID NO:9),37℃孵育1小时。使用PBST溶液250μL/孔,洗板3次。配制抗体(最高浓度400nM,4倍梯度稀释),37℃孵育1小时。使用PBST溶液250μL/孔,洗板6次。加入工作浓度的human IgG(H+L)-HRP(Jackson,109-035-003,1:4000稀释)抗体,100μL/孔,37℃孵育1小时。使用PBST溶液250μL/孔,洗板6次。加入TMB(KPL,5120-0077)显色液100μL/孔,室温显色5-10分钟。加入1M H2SO4,100μL/孔,中止显色,酶标仪(Molecular Devices,VERSA max)450nm读数。
表28.双特异性抗体与人DLL3蛋白的结合活性

结果显示,本披露的双特异性抗体对人DLL3蛋白有良好的亲和力。
测试例4:DLL1和DLL4蛋白的ELISA结合实验
将DLL1(ACRO,DL1-H52H8,1μg/mL)和DLL4(ACRO,DL4-H5227,1μg/mL)包板,100μL/孔,4℃过夜。用PBST溶液(PBS含0.1%吐温20)250μL/孔,洗板3次。5%牛奶封闭,250μL/孔,37℃封闭2小时。用PBST溶液250μL/孔,洗板3次。加入待检测抗体(最高浓度100nM,4倍梯度稀释),37℃孵育1小时。使用PBST溶液250μL/孔,洗板6次。加入工作浓度的human IgG(H+L)-HRP(Jackson,109-035-003,1:4000稀释)抗体,100μL/孔,37℃孵育1小时。使用PBST溶液250μL/孔,洗板6次。加入TMB(KPL,5120-0077)显色液100μL/孔,室温显色5-10分钟。加入1M H2SO4,100μL/孔,中止显色,酶标仪(Molecular Devices,VERSA max)450nm读数,结果见图2A-图2B。
结果显示,本披露的双特异性抗体未检测到结合人DLL1和DLL4蛋白。
测试例5.本披露的双特异性抗体对细胞的杀伤活性
本测试例研究了双特异性抗体作为T细胞衔接分子对肿瘤细胞的杀伤活性。用表达LUC-GFP的SHP77、H1184和H460稳转细胞系作为靶细胞来检测本披露的双特异性抗体的靶点特异性细胞毒活性。
SHP77/lucG细胞培养在1640+10%FBS+10μg/mL嘌呤霉素(puromycin)完全培养基中,一周传代2-3次。H1184/lucG细胞培养在1640+5%FBS+10μg/mL嘌呤霉素(puromycin)完全培养基中,一周传代1次。H460/lucG细胞培养在1640+10%FBS完全培养基中,一周传代2-3次。冻存PBMC(妙顺生物)复苏后用1640+10%FBS完全培养基重悬,置于T75培养瓶培养4小时(密度为2E6cells/mL)。PBMC收集离心后用1640+10%FBS重悬、计数,调整细胞数为1.5E6cells/mL。将上述PBMC悬液和靶细胞悬液按照等体积混合,每孔加入100μL确保E:T Ratio为10:1。另外设置PBMC ONLY组,将上述PBMC悬液和1640+10%FBS完全培养基按照等体积混合。抗体用1640+10%FBS培养基稀释,起始浓度为600nM(6x终浓度),5倍稀释,9个剂量点,每孔加入20μL。处理好的细胞放在37℃,5%CO2的培养箱培养48小时。取出培养板,1000rpm离心3分钟,吸取50μL上清于新的3788板中用于检测细胞因子检测,-20℃保存。在培养板中加入50μL ONE-GloTMLuciferase(Promega,E6120),室温孵育5分钟后,用Vendor检测Luminescence,计算抗体在不同浓度下的杀伤作用。使用Graphpad Prism8.0软件 根据抗体的对数浓度和信号值做出量效曲线图,得出抗体介导杀伤的IC50。将只有靶细胞、PBMC不加抗体的孔设为0%抑制,计算抗体的最大抑制率Imax。结果见表29-1至表29-4,表30及图3。
表29-1.抗体对SHP77的细胞毒活性
表29-2.抗体对SHP77的细胞毒活性
表29-3.抗体对SHP77的细胞毒活性
表29-4.抗体对SHP77的细胞毒活性
表30.双特异性抗体对H1184细胞的杀伤
结果显示,本披露的双特异性抗体对表达DLL3的细胞SHP77和H1184有较强的杀伤作用;而对不表达DLL3的H460细胞无杀伤作用(图3)。
测试例6.本披露的双特异性抗体的体外T细胞激活活性
H82/DLL3细胞培养在1640+10%FBS完全培养基中,一周传代2-3次,传代比例1:3左右。H460细胞培养在1640+10%FBS完全培养基中,一周传代2-3次,传代比例1:10左右。Jurkat LuciaTM NFAT细胞(InvivoGen)培养在1640+10%FBS+100μg/ml zeocin(InvivoGen,ant-zn-1)完全培养基中,一周传代2-3次,传代比例1:10左右。收集Jurkat LuciaTM NFAT细胞,1000rpm离心3分钟,重悬、计数,调整细胞数为1E6cells/mL。收集靶细胞H82/DLL3细胞,1000rpm离心3分钟,重悬、计数,调整细胞数为2E5cells/mL。收集H82/DLL3和H460细胞,1000rpm离心3分钟,重悬、计数,调整细胞数为4E5cells/mL。将上述Jurkat LuciaTM NFAT和靶细胞按照等体积混合,每孔加入100μL,确保H82/DLL3细胞E:T Ratio为5:1,H82/DLL3和H460细胞E:T Ratio为2.5:1。抗体用1640+10%FBS培养基稀释,起始浓度为600nM(6×终浓度),5倍稀释,9个剂量点,每孔加入20μL。处理好的细胞放在37℃,5%CO2的培养箱培养5小时。用25mL的ddH2O溶解QUANTI-LucTM Gold试剂(Invivogen,rep-qlcg5)。加入50μL QUANTI-LucTM Gold,室温孵育5分钟后,用Vendor检测Luminescence,计算抗体在不同浓度下对Jurkat LuciaTM NFAT细胞的激活作用。使用Graphpad Prism8.0软件做图,结果见图4A至图4B和表31。
激活倍数的公式N=待测抗体的荧光读值/阴性孔的荧光读值
表31.双特异性抗体对T细胞的激活结果
结果显示,本披露的双特异性抗体只有在存在表达DLL3的DLL3/H82细胞时,才会激活T细胞;当存在不表达DLL3的阴性细胞H460时,不会激活T细胞。
测试例7.本披露的双特异性抗体的细胞因子释放水平
1.本披露的双特异性抗体的细胞因子IFNγ释放水平
使用HTRF法检测在DLL3/CD3双抗在H1184细胞存在的情况下,分别刺激PBMC中细胞因子IFNγ分泌情况。
取出细胞杀伤实验中(测试例5)收集的冻存于-20℃冰箱的上清,常温解冻,震荡混匀。使用无菌水溶解IFNγ标准品粉末,使用1640+10%FBS培养基稀释标准品至需要的浓度。取出要检测IFNγ的试剂盒(CISBIO,62HIFNGPEG),平衡试剂盒至常温,使用detection buffer稀释试剂盒中的两个检测抗体(20倍稀释)。取16μL细胞上清(10倍稀释用于IFNγ检测)及IFNγ标准品于96孔板中,加入4μL稀释好的对应的检测抗体;震荡混匀,1000rpm离心1分钟,常温孵育过夜。 取出孵育过夜的样品,1000rpm离心1分钟,使用PHERAstar多功能酶标仪读取665nm和620nm的吸收值。用Graphpad Prism 8分析数据,结果见图5A。
结果显示,本披露的双特异性抗体释放IFNγ的水平非常低。
2.本披露的双特异性抗体的细胞因子IL-6释放水平
使用ELISA法检测在DLL3/CD3双抗在H1184细胞存在的况下,刺激PBMC中细胞因子IL-6分泌的情况。
取出细胞杀伤实验中(测试例5)收集的冻存于-20℃冰箱的上清,常温解冻,震荡混匀,样品使用样品稀释液稀释5倍备用。细胞因子检测前,取出IL-6ELISA试剂盒(欣博盛生物科技有限公司,EHC007.96)常温平衡,根据说明书分别稀释IL-6标准品和进行检测测量OD450值,用Graphpad Prism 8分析数据。结果见图5B。
结果显示,本披露的双特异性抗体释放IL6的水平非常低,说明本披露的双特异性抗体具有更好的安全性。
体内活性评价
测试例8.本披露的双特异性抗体在SHP77皮下移植瘤模型中的药效
本披露采用重度联合免疫缺陷NOG小鼠接种SHP-77细胞,接种后腹腔注射人PBMC,成瘤后分组给药。
NOG小鼠,雌性,体重15-17g左右,购自维通利华。SHP-77细胞来自ATCC。人PBMCs购自于妙顺(上海)生物科技有限公司,货号:ID#A10S115034。
将SHP-77细胞(4×106个/只小鼠)100μL接种于NOG小鼠右肋部皮下。接种当天,复苏冻存的hPBMC。接种第2天,每只小鼠腹腔注射hPBMC 5×106/100μL的细胞悬液。接种8天后,待肿瘤体积在~120mm3后去除体重、肿瘤过大和过小的,按肿瘤体积将小鼠随机分为5组,每组8只,当天开始给等摩尔量的抗体,给药量如表32所示。通过腹腔注射相应等摩尔量的抗体,每5天给药1次,共给药3次,给药到第15天。每周测2次瘤体积,称体重,记录数据。
肿瘤体积(V)计算公式为:V=1/2×L×L 2
相对肿瘤增殖率T/C(%)=(T-T0)/(C-C0)×100%,其中T、C为实验结束时治疗组和对照组的肿瘤体积;T0、C0为实验开始时的肿瘤体积。
抑瘤率TGI(%)=100-T/C(%)。
表32.抗体在SHP77皮下移植瘤模型中的药效(给药后第15天)

结果显示,本披露的双特异性抗体可以显著抑制SHP-77移植瘤的生长。
测试例9.本披露的双特异性抗体在H1184皮下移植瘤模型中的药效
本披露采用重度联合免疫缺陷NOG小鼠接种H1184细胞,接种后腹腔注射人PBMC,成瘤后分组给药。
NOG小鼠,雌性,体重15-17g左右,购自维通利华。H1184细胞来自ATCC。人PBMCs购自于妙顺(上海)生物科技有限公司,货号:ID#A10S115034。
将H1184细胞(3.5×106个,含50%MatriGel)200μL/只接种于NOG小鼠右肋部皮下。接种第11天,复苏8支冻存hPBMC(ID#A10S115034)。接种第12天,每只小鼠腹腔注射人PBMC 5×106/100μL的细胞悬液。接种18天后,待肿瘤体积在~140mm3后去除体重、肿瘤过大和过小的,按肿瘤体积将小鼠随机分为组,每组8只,当天开始给等摩尔量的抗体,给药量如表33所示。通过腹腔注射抗体,共给药4次,每周2次。每周测2次瘤体积,称体重,记录数据。
使用Excel统计软件记录数据:平均值以avg计算;SD值以STDEV计算;SEM值以STDEV/SQRT(每组动物数)计算;采用GraphPad Prism软件作图,采用Two-way ANOVA、One-way ANOVA、t-test对数据进行统计学分析。
肿瘤体积(V)计算公式为:V=1/2×L×L 2
相对肿瘤增殖率T/C(%)=(T-T0)/(C-C0)×100%,其中T、C为实验结束时治疗组和对照组的肿瘤体积;T0、C0为实验开始时的肿瘤体积。
抑瘤率TGI(%)=100-T/C(%)。
表33.抗体在H1184皮下移植瘤模型中的药效(给药后第15天)
结果显示,本披露的双特异性抗体可以显著抑制H1184移植瘤的生长。
虽然为了清楚的理解,已经借助于附图和实例详细描述了上述发明,但是描述和实例不应当解释为限制本披露的范围。本文中引用的所有专利和科学文献的公开内容通过引用完整地清楚结合。

Claims (19)

  1. 一种特异性结合DLL3和CD3的抗原结合分子,其包含至少一个特异性结合DLL3的抗原结合模块和至少一个特异性结合CD3的抗原结合模块,
    所述特异性结合DLL3的抗原结合模块包含重链可变区DLL3-VH和轻链可变区DLL3-VL,
    所述特异性结合CD3的抗原结合模块包含重链可变区CD3-VH和轻链可变区CD3-VL;其中:
    i)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71、24、72或73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25或74的氨基酸序列的DLL3-LCDR3;或
    ii)所述DLL3-VH具有:包含SEQ ID NO:26或84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85或27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83或28的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
    iii)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96、32、97、98或99的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;或
    iv)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:119、37、117、118或120的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3;
    优选地,
    i)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
    ii)所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:28的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
    iii)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;或
    iv)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:119的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3;
    更优选地,
    所述抗原结合分子在25℃条件下以小于4×10-9M的KD结合人DLL3,所述KD是通过表面等离子体共振法测量的。
  2. 根据权利要求1所述的特异性结合DLL3和CD3的抗原结合分子,其中:
    i)所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:131的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3;或
    ii)所述CD3-VH具有:包含SEQ ID NO:129的氨基酸序列的CD3-HCDR1,包含SEQ ID NO:130的氨基酸序列的CD3-HCDR2,和包含SEQ ID NO:135的氨基酸序列的CD3-HCDR3;和所述CD3-VL具有:包含SEQ ID NO:132的氨基酸序列的CD3-LCDR1,包含SEQ ID NO:133的氨基酸序列的CD3-LCDR2,和包含SEQ ID NO:134的氨基酸序列的CD3-LCDR3。
  3. 根据权利要求1或2所述的特异性结合DLL3和CD3的抗原结合分子,其中:
    i)所述DLL3-VH包含SEQ ID NO:54、12、43、44、45、46、47、48、49、50、51、52、53、55、56或57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:63、13、58、59、60、61、62、64、65、66、67或68的氨基酸序列;或
    ii)所述DLL3-VH包含SEQ ID NO:81、14、78、79、80或82的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:77、15、75或76的氨基酸序列;或
    iii)所述DLL3-VH包含SEQ ID NO:91、16、89、90、92、93、94或95的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:87、17、86或88的氨基酸序列;或
    iv)所述DLL3-VH包含SEQ ID NO:109、18、105、106、107、108、110、111、112、113、114、115或116的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:100、19、101、102、103或104的氨基酸序列;
    优选地,
    i)所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:63的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:61的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:64的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:65的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:66的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:67的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:65的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:66的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:67的氨基酸序列;或
    ii)所述DLL3-VH包含SEQ ID NO:81的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:77的氨基酸序列;或
    iii)所述DLL3-VH包含SEQ ID NO:91的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:87的氨基酸序列;或
    iv)所述DLL3-VH包含SEQ ID NO:109的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:100的氨基酸序列。
  4. 根据权利要求1至3中任一项所述的特异性结合DLL3和CD3的抗原结合分子,其中:
    i)所述CD3-VH包含SEQ ID NO:136的氨基酸序列,和所述CD3-VL包含SEQ ID NO:137的氨基酸序列;或
    ii)所述CD3-VH包含SEQ ID NO:138的氨基酸序列,和所述CD3-VL包含SEQ ID NO:137的氨基酸序列。
  5. 根据权利要求1至4中任一项所述的特异性结合DLL3和CD3的抗原结合分子,其中:
    所述特异性结合DLL3的抗原结合模块包含能够形成二聚体的Titin链和Obscurin链;或
    所述特异性结合CD3的抗原结合模块包含能够形成二聚体的Titin链和Obscurin链;
    优选地,
    所述Titin链包含选自由SEQ ID NO:192至SEQ ID NO:210组成的组的氨基酸序列,
    所述Obscurin链包含选自由SEQ ID NO:211至SEQ ID NO:251组成的组的氨基酸序列;
    更优选地,
    所述Titin链包含SEQ ID NO:208的氨基酸序列,和所述Obscurin链包含SEQ ID NO:246的氨基酸序列。
  6. 根据权利要求1至5中任一项所述的特异性结合DLL3和CD3的抗原结合分子,其包含Fc区,所述Fc区优选为人IgG Fc区,进一步优选为人IgG1 Fc区;
    更优选地,所述Fc区包含一个或多个能够减少Fc区与Fcγ受体结合的氨基酸取代;
    最优选地,所述Fc区是人IgG1 Fc区,并且在234和235位置的氨基酸为A,编号依据为EU索引。
  7. 根据权利要求1至6中任一项所述的特异性结合DLL3和CD3的抗原结合分子,其包含Fc区,所述Fc区包含能够相互缔合的第一亚基Fc1和第二亚基Fc2,所述Fc1和Fc2各自独立地具有一个或多个减少Fc区同源二聚化的氨基酸取代;
    优选地,所述Fc1具有根据杵臼技术的凸起结构,和所述Fc2具有根据杵臼技术的孔结构;
    更优选地,所述Fc1在366位置的氨基酸为W;并且所述Fc2在366位置的氨基酸为S,在368位置的氨基酸为A,和在407位置的氨基酸为V,编号依据为EU索引;
    最优选地,所述Fc1包含SEQ ID NO:143的氨基酸序列;和所述Fc2包含SEQ ID NO:144的氨基酸序列;或所述Fc1包含SEQ ID NO:145的氨基酸序列;和所述Fc2包含SEQ ID NO:146的氨基酸序列。
  8. 根据权利要求7所述的特异性结合DLL3和CD3的抗原结合分子,其中所述抗原结合分子包含一个特异性结合DLL3的抗原结合模块和一个特异性结合CD3的抗原结合模块,所述特异性结合DLL3的抗原结合模块是经替换的Fab,其包含能够形成二聚体的Titin链和Obscurin链;和所述特异性结合CD3的抗原结合模块是Fab;或
    所述特异性结合DLL3的抗原结合模块是Fab,和所述特异性结合CD3的抗原结合模块是经替换的Fab,其包含能够形成二聚体的Titin链和Obscurin链;
    优选地,
    所述特异性结合DLL3和CD3的抗原结合分子包含一条具有式(a)所示结构的第一链、一条具有式(b)所示结构的第二链、一条具有式(c)所示结构的第三链和一条具有式(d)所示结构的第四链,
    式(a)[DLL3-VH]-[连接子1]-[Titin链]-[Fc2],
    式(b)[DLL3-VL]-[连接子2]-[Obscurin链],
    式(c)[CD3-VH]-[CH1]-[Fc1],
    式(d)[CD3-VL]-[CL],
    其中:所述连接子1和连接子2是相同或不同的肽连接子;或所述连接子1和/或连接子2不存在;
    式(a)、(b)、(c)和(d)所示的结构是从N端至C端排列的;
    所述Titin链和所述Obscurin链是可互换的;
    所述Fc1和所述Fc2是可互换的;
    更优选地,所述特异性结合DLL3和CD3的抗原结合分子具有:
    一条包含SEQ ID NO:171的氨基酸序列的第一链、一条包含SEQ ID NO:172的氨基酸序列的第二链、一条包含SEQ ID NO:154的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链;或
    一条包含SEQ ID NO:171的氨基酸序列的第一链、一条包含SEQ ID NO:172的氨基酸序列的第二链、一条包含SEQ ID NO:156的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链;或
    一条包含SEQ ID NO:152的氨基酸序列的第一链、一条包含SEQ ID NO:153的氨基酸序列的第二链、一条包含SEQ ID NO:154的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链;或
    一条包含SEQ ID NO:152的氨基酸序列的第一链、一条包含SEQ ID NO:153的氨基酸序列的第二链、一条包含SEQ ID NO:156的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链;或
    一条包含SEQ ID NO:164的氨基酸序列的第一链、一条包含SEQ ID NO:165的氨基酸序列的第二链、一条包含SEQ ID NO:154的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链;或
    一条包含SEQ ID NO:164的氨基酸序列的第一链、一条包含SEQ ID NO:165的氨基酸序列的第二链、一条包含SEQ ID NO:156的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链;或
    一条包含SEQ ID NO:178的氨基酸序列的第一链、一条包含SEQ ID NO:179的氨基酸序列的第二链、一条包含SEQ ID NO:154的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链;或
    一条包含SEQ ID NO:178的氨基酸序列的第一链、一条包含SEQ ID NO:179的氨基酸序列的第二链、一条包含SEQ ID NO:156的氨基酸序列的第三链和一条包含SEQ ID NO:155的氨基酸序列的第四链。
  9. 根据权利要求7所述的特异性结合DLL3和CD3的抗原结合分子,其中所述抗原结合分子包含一个特异性结合DLL3的抗原结合模块和一个特异性结合CD3的抗原结合模块,所述特异性结合DLL3的抗原结合模块是Fab;所述特异性结合CD3的抗原结合模块是scFv;
    优选地,
    所述特异性结合DLL3和CD3的抗原结合分子包含一条具有式(e)所示结构的第一链、一条具有式(f)所示结构的第二链和一条具有式(g)所示结构的第三链,
    式(e)[DLL3-VL]-[CL],
    式(f)[DLL3-VH]-[CH1]-[Fc2],
    式(g)[CD3-VH]-[连接子3]-[CD3-VL]-[连接子4]-[Fc1],
    其中:所述连接子3和连接子4是相同或不同的肽连接子;
    式(e)、(f)和(g)所示的结构是从N端至C端排列的;
    所述Fc1和所述Fc2是可互换的;
    更优选地,所述特异性结合DLL3和CD3的抗原结合分子具有:
    一条包含SEQ ID NO:173的氨基酸序列的第一链、一条包含SEQ ID NO:174的氨基酸序列的第二链和一条包含SEQ ID NO:160的氨基酸序列的第三链;或
    一条包含SEQ ID NO:173的氨基酸序列的第一链、一条包含SEQ ID NO:174的氨基酸序列的第二链和一条包含SEQ ID NO:159的氨基酸序列的第三链;或
    一条包含SEQ ID NO:157的氨基酸序列的第一链、一条包含SEQ ID NO:158的氨基酸序列的第二链和一条包含SEQ ID NO:159的氨基酸序列的第三链;或
    一条包含SEQ ID NO:157的氨基酸序列的第一链、一条包含SEQ ID NO:158的氨基酸序列的第二链和一条包含SEQ ID NO:160的氨基酸序列的第三链;或
    一条包含SEQ ID NO:166的氨基酸序列的第一链、一条包含SEQ ID NO:167的氨基酸序列的第二链和一条包含SEQ ID NO:159的氨基酸序列的第三链;或
    一条包含SEQ ID NO:166的氨基酸序列的第一链、一条包含SEQ ID NO:167的氨基酸序列的第二链和一条包含SEQ ID NO:160的氨基酸序列的第三链;或
    一条包含SEQ ID NO:180的氨基酸序列的第一链、一条包含SEQ ID NO:181的氨基酸序列的第二链和一条包含SEQ ID NO:159的氨基酸序列的第三链;或
    一条包含SEQ ID NO:180的氨基酸序列的第一链、一条包含SEQ ID NO:181的氨基酸序列的第二链和一条包含SEQ ID NO:160的氨基酸序列的第三链。
  10. 根据权利要求7所述的特异性结合DLL3和CD3的抗原结合分子,其中所述抗原结合分子包含一个特异性结合DLL3的抗原结合模块和一个特异性结合CD3的抗原结合模块,
    所述特异性结合DLL3和CD3的抗原结合分子包含一条具有式(h)所示结构的第一链和一条具有式(i)所示结构的第二链,
    式(h)[DLL3-VL]-[连接子5]-[CD3-VH]-[连接子6]-[Fc1],
    式(i)[CD3-VL]-[连接子7]-[DLL3-VH]-[连接子8]-[Fc2],
    其中:所述连接子5、连接子6、连接子7和连接子8是相同或不同的肽连接子;
    式(h)和(i)所示的结构是从N端至C端排列的;
    所述Fc1和所述Fc2是可互换的;
    优选地,其中:
    i)所述的DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:63的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列;或
    所述的DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:61的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列;或
    所述的DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:64的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列;或
    所述的DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:65的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列;或
    所述的DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:66的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列;或
    所述的DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:67的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列;或
    所述的DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:65的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列;或
    所述的DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:66的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列;或
    所述的DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:67的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列;或
    ii)所述的DLL3-VH包含SEQ ID NO:91的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:87的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列;或
    iii)所述的DLL3-VH包含SEQ ID NO:81的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:77的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列;或
    iv)所述的DLL3-VH包含SEQ ID NO:109的氨基酸序列,和所述的DLL3-VL包含SEQ ID NO:100的氨基酸序列;并且所述的CD3-VH包含SEQ ID NO:136或138的氨基酸序列,和所述的CD3-VL包含SEQ ID NO:137的氨基酸序列;
    更优选地,所述特异性结合DLL3和CD3的抗原结合分子具有:
    一条包含SEQ ID NO:185的氨基酸序列的第一链和一条包含SEQ ID NO:162的氨基酸序列的第二链;或
    一条包含SEQ ID NO:161的氨基酸序列的第一链和一条包含SEQ ID NO:162的氨基酸序列的第二链;或
    一条包含SEQ ID NO:163的氨基酸序列的第一链和一条包含SEQ ID NO:162的氨基酸序列的第二链;或
    一条包含SEQ ID NO:259的氨基酸序列的第一链和一条包含SEQ ID NO:162的氨基酸序列的第二链;或
    一条包含SEQ ID NO:260的氨基酸序列的第一链和一条包含SEQ ID NO:162的氨基酸序列的第二链;或
    一条包含SEQ ID NO:168的氨基酸序列的第一链和一条包含SEQ ID NO:169的氨基酸序列的第二链;或
    一条包含SEQ ID NO:170的氨基酸序列的第一链和一条包含SEQ ID NO:169的氨基酸序列的第二链;或
    一条包含SEQ ID NO:175的氨基酸序列的第一链和一条包含SEQ ID NO:176的氨基酸序列的第二链;或
    一条包含SEQ ID NO:177的氨基酸序列的第一链和一条包含SEQ ID NO:176的氨基酸序列的第二链;或
    一条包含SEQ ID NO:182的氨基酸序列的第一链和一条包含SEQ ID NO:183的氨基酸序列的第二链;或
    一条包含SEQ ID NO:184的氨基酸序列的第一链和一条包含SEQ ID NO:183的氨基酸序列的第二链;或
    一条包含SEQ ID NO:186的氨基酸序列的第一链和一条包含SEQ ID NO:162的氨基酸序列的第二链;或
    一条包含SEQ ID NO:187的氨基酸序列的第一链和一条包含SEQ ID NO:188的氨基酸序列的第二链;或
    一条包含SEQ ID NO:187的氨基酸序列的第一链和一条包含SEQ ID NO:189的氨基酸序列的第二链;或
    一条包含SEQ ID NO:190的氨基酸序列的第一链和一条包含SEQ ID NO:188的氨基酸序列的第二链;或
    一条包含SEQ ID NO:190的氨基酸序列的第一链和一条包含SEQ ID NO:189的氨基酸序列的第二链;或
    一条包含SEQ ID NO:191的氨基酸序列的第一链和一条包含SEQ ID NO:188的氨基酸序列的第二链;或
    一条包含SEQ ID NO:191的氨基酸序列的第一链和一条包含SEQ ID NO:189的氨基酸序列的第二链。
  11. 一种抗DLL3抗体,其能够特异性结合DLL3,所述的抗DLL3抗体包含重链可变区DLL3-VH和轻链可变区DLL3-VL,其中:
    i)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:24的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21、69或70的氨基酸序列的DLL3-HCDR2和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
    ii)所述DLL3-VH具有:包含SEQ ID NO:26或84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85或27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83或28的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
    iii)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96、32、97、98或99的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;或
    iv)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:119、37、117、118或120的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3;
    优选地,
    i)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:21的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:72的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:73的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:74的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:69的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:70的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:22的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:23的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:71的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:25的氨基酸序列的DLL3-LCDR3;或
    ii)所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:84的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:85的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:83的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
    所述DLL3-VH具有:包含SEQ ID NO:26的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:27的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:28的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:29的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:30的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:31的氨基酸序列的DLL3-LCDR3;或
    iii)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:96的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:33的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:34的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:36的氨基酸序列的DLL3-LCDR3;或
    iv)所述DLL3-VH具有:包含SEQ ID NO:20的氨基酸序列的DLL3-HCDR1,包含SEQ ID NO:119的氨基酸序列的DLL3-HCDR2,和包含SEQ ID NO:38的氨基酸序列的DLL3-HCDR3;和所述DLL3-VL具有:包含SEQ ID NO:39的氨基酸序列的DLL3-LCDR1,包含SEQ ID NO:35的氨基酸序列的DLL3-LCDR2,和包含SEQ ID NO:40的氨基酸序列的DLL3-LCDR3;
    更优选地,
    所述抗DLL3抗体在25℃条件下以小于4×10-9M的KD结合人DLL3,所述KD是通过表面等离子体共振法测量的。
  12. 根据权利要求11所述的抗DLL3抗体,所述的抗DLL3抗体包含重链可变区DLL3-VH和轻链可变区DLL3-VL,其中:
    i)所述DLL3-VH包含SEQ ID NO:54、43、44、45、46、47、48、49、50、51、52、53、55、56或57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:63、64、65、66或67的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:56或57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:58、59、60、61、62、63、64、65、66、67或68的氨基酸序列;或
    ii)所述DLL3-VH包含SEQ ID NO:81、78、79、80或82的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:77、75或76的氨基酸序列;或
    iii)所述DLL3-VH包含SEQ ID NO:91、89、90、92、93、94或95的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:87、86或88的氨基酸序列;或
    iv)所述DLL3-VH包含SEQ ID NO:109、105、106、107、108、110、111、112、113、114、115或116的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:100、101、102、103或104的氨基酸序列;
    优选地,
    i)所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:63的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:61的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:54的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:64的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:65的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:66的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:56的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:67的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:65的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:66的氨基酸序列;或
    所述DLL3-VH包含SEQ ID NO:57的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:67的氨基酸序列;或
    ii)所述DLL3-VH包含SEQ ID NO:81的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:77的氨基酸序列;或
    iii)所述DLL3-VH包含SEQ ID NO:91的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:87的氨基酸序列;或
    iv)所述DLL3-VH包含SEQ ID NO:109的氨基酸序列,和所述DLL3-VL包含SEQ ID NO:100的氨基酸序列。
  13. 根据权利要求11或12所述的抗DLL3抗体,其中所述的抗DLL3抗体是抗体片段;优选地,所述的抗体片段为Fab、Fab'、F(ab')2、Fd、Fv、scFv、dsFv或dAb。
  14. 根据权利要求11至13中任一项所述的抗DLL3抗体,其包含重链恒定区和轻链恒定区;优选地,所述重链恒定区包含SEQ ID NO:41的氨基酸序列,和/或所述轻链恒定区包含SEQ ID NO:42的氨基酸序列。
  15. 根据权利要求14所述的抗DLL3抗体,其包含重链和轻链,其中:
    所述重链包含与SEQ ID NO:121具有至少85%序列同一性的氨基酸序列,和所述轻链包含与SEQ ID NO:122具有至少85%序列同一性的氨基酸序列;或
    所述重链包含与SEQ ID NO:123具有至少85%序列同一性的氨基酸序列,和所述轻链包含与SEQ ID NO:124具有至少85%序列同一性的氨基酸序列;或
    所述重链包含与SEQ ID NO:125具有至少85%序列同一性的氨基酸序列,和所述轻链包含与SEQ ID NO:126具有至少85%序列同一性的氨基酸序列;或
    所述重链包含与SEQ ID NO:127具有至少85%序列同一性的氨基酸序列,和所述轻链包含与SEQ ID NO:128具有至少85%序列同一性的氨基酸序列;
    优选地,
    所述重链包含SEQ ID NO:121的氨基酸序列,和所述轻链包含SEQ ID NO:122的氨基酸序列;或
    所述重链包含SEQ ID NO:123的氨基酸序列,和所述轻链包含SEQ ID NO:124的氨基酸序列;或
    所述重链包含SEQ ID NO:125的氨基酸序列,和所述轻链包含SEQ ID NO:126的氨基酸序列;或
    所述重链包含SEQ ID NO:127的氨基酸序列,和所述轻链包含SEQ ID NO:128的氨基酸序列。
  16. 一种药物组合物,其含有:
    治疗有效量的权利要求1至10中任一项所述的特异性结合DLL3和CD3的抗原结合分子,或权利要求11至15中任一项所述的抗DLL3抗体,以及一种或更多种药学上可接受的载体、稀释剂、缓冲剂或赋形剂。
  17. 分离的核酸,其编码权利要求1至10中任一项所述的特异性结合DLL3和CD3的抗原结合分子,或权利要求11至15中任一项所述的抗DLL3抗体。
  18. 一种宿主细胞,其包含如权利要求17所述的分离的核酸。
  19. 根据权利要求1至10中任一项所述的特异性结合DLL3和CD3的抗原结合分子,或权利要求11至15中任一项所述的抗DLL3抗体,或根据权利要求16所述的药物组合物在制备用于治疗肿瘤或癌症的药物中的用途;优选地,其中所述肿瘤或癌症选自:
    头和颈鳞状细胞癌、头和颈癌、脑癌、神经胶质瘤、多形性成胶质细胞瘤、神经母细胞瘤、中枢神经系统癌、神经内分泌肿瘤、咽喉癌、咽鳞癌、口腔鳞癌、鼻咽癌、食管癌、甲状腺癌、恶性胸膜间皮瘤、肺癌、乳腺癌、肝癌、肝胆癌、胰腺癌、胃癌、胃肠道癌、肠癌、结肠癌、结肠直肠癌、肾癌、透明细胞肾细胞癌、卵巢癌、子宫内膜癌、子宫颈癌、膀胱癌、前列腺癌、睾丸癌、皮肤癌、黑色素瘤、大细胞肺癌、三阴性乳腺癌、淋巴瘤和小细胞肺癌;
    更优选地,其中所述的肿瘤或癌症是表达DLL3的肿瘤或癌症。
PCT/CN2023/101778 2022-06-23 2023-06-21 特异性结合dll3和cd3的抗原结合分子及其医药用途 WO2023246885A1 (zh)

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Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108271376A (zh) * 2015-07-31 2018-07-10 安进研发(慕尼黑)股份有限公司 结合dll3和cd3的双特异性抗体构建体
CN112513092A (zh) * 2018-06-09 2021-03-16 勃林格殷格翰国际有限公司 Dll3-cd3双特异性抗体

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108271376A (zh) * 2015-07-31 2018-07-10 安进研发(慕尼黑)股份有限公司 结合dll3和cd3的双特异性抗体构建体
CN112513092A (zh) * 2018-06-09 2021-03-16 勃林格殷格翰国际有限公司 Dll3-cd3双特异性抗体

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