Monospecific and bispecific anti-igf-1r and anti-erbb3 antibodies
US-2017051063-A1 · Feb 23, 2017 · US
US12497462B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12497462-B2 |
| Application number | US-202117922067-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 29, 2021 |
| Priority date | Apr 29, 2020 |
| Publication date | Dec 16, 2025 |
| Grant date | Dec 16, 2025 |
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Provided herein are proteins comprising an anti-CD26 antigen-binding domain. Also provided herein are methods of treating an aging-related disease or an inflammatory disease in a subject that include administering to the subject one of these proteins or a cell expressing one of these proteins.
Opening claim text (preview).
What is claimed is: 1 . A protein comprising an anti-CD26 antigen-binding domain, wherein the anti-CD26 antigen-binding domain comprises: (a) a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 1, a CDR2 comprising SEQ ID NO: 2, and a CDR3 comprising SEQ ID NO: 3, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 4, a CDR2 comprising SEQ ID NO: 5, and a CDR3 comprising SEQ ID NO: 6; (b) a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 7, a CDR2 comprising SEQ ID NO: 8, and a CDR3 comprising SEQ ID NO: 9, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 10, a CDR2 comprising SEQ ID NO: 11, and a CDR3 comprising SEQ ID NO: 12; (c) a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 13, a CDR2 comprising SEQ ID NO: 14, and a CDR3 comprising SEQ ID NO: 15, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 16, a CDR2 comprising SEQ ID NO: 17, and a CDR3 comprising SEQ ID NO: 18; (d) a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 19, a CDR2 comprising SEQ ID NO: 20, and a CDR3 comprising SEQ ID NO: 21, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 22, a CDR2 comprising SEQ ID NO: 23, and a CDR3 comprising SEQ ID NO: 24; (e) a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 25, a CDR2 comprising SEQ ID NO: 26, and a CDR3 comprising SEQ ID NO: 27, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 28, a CDR2 comprising SEQ ID NO: 29, and a CDR3 comprising SEQ ID NO: 30; (f) a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 31, a CDR2 comprising SEQ ID NO: 32, and a CDR3 comprising SEQ ID NO: 33, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 34, a CDR2 comprising SEQ ID NO: 35, and a CDR3 comprising SEQ ID NO: 36; (g) a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 37, a CDR2 comprising SEQ ID NO: 38, and a CDR3 comprising SEQ ID NO: 39, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 40, a CDR2 comprising SEQ ID NO: 41, and a CDR3 comprising SEQ ID NO: 42; (h) a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 43, a CDR2 comprising SEQ ID NO: 44, and a CDR3 comprising SEQ ID NO: 45, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 46, a CDR2 comprising SEQ ID NO: 47, and a CDR3 comprising SEQ ID NO: 48; (i) a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 49, a CDR2 comprising SEQ ID NO: 50, and a CDR3 comprising SEQ ID NO: 51, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 52, a CDR2 comprising SEQ ID NO: 53, and a CDR3 comprising SEQ ID NO: 54; or (j) a heavy chain variable domain comprising a CDR1 comprising SEQ ID NO: 55, a CDR2 comprising SEQ ID NO: 56, and a CDR3 comprising SEQ ID NO: 57, and a light chain variable domain comprising a CDR1 comprising SEQ ID NO: 58, a CDR2 comprising SEQ ID NO: 59, and a CDR3 comprising SEQ ID NO: 60. 2 . The protein of claim 1 , wherein: the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 61 and the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 62; the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 63 and the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 64; the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 65 and the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 66; the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 67 and the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 68; the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 69 and the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 70; the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 71 and the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 72; the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 73 and the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 74; the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 75 and the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 76; the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 77 and the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 78; or the heavy chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 79 and the light chain variable domain comprises a sequence that is at least 80% identical to SEQ ID NO: 80. 3 . The protein of claim 1 , wherein the protein is a multi-chain protein. 4 . The protein of claim 1 , wherein the protein is a single-chain protein. 5 . The protein of claim 1 , wherein the protein is an antibody or an antigen-binding antibody fragment. 6 . The protein of claim 1 , wherein the protein is a chimeric antigen receptor (CAR). 7 . A pharmaceutical composition comprising a protein of claim 1 and a pharmaceutically acceptable carrier. 8 . A kit comprising the pharmaceutical composition of claim 7 . 9 . A nucleic acid encoding a protein of claim 1 . 10 . A vector comprising the nucleic acid of claim 9 . 11 . A cell comprising the nucleic acid of claim 9 . 12 . The cell of claim 11 , wherein the cell is an immune cell. 13 . The cell of claim 12 , wherein the immune cell is a T cell, a B cell, or a natural killer (NK) cell. 14 . A pharmaceutical composition comprising a cell of claim 11 and a pharmaceutically acceptable carrier. 15 . A method of treating an age-related disease or an inflammatory disease in a subject, the method comprising administering to the subject a therapeutically effective amount of the protein of claim 1 . 16 . A method of treating an age-related disease or an inflammatory disease in a subject, the method comprising administering to the subject a therapeutically effective amount of the nucleic acid of claim 9 . 17 . A method of treating an age-related disease or an inflammatory disease in a subject, the method comprising administering to the subject a therapeutically effective amount of the cell of claim 11 . 18 . The method of claim 15 , wherein the subject is further administered: (i) a therapeutically effective amount of an NK cell activating agent and/or an NK cell and/or a monoclonal antibody; and/or (ii) a therapeutically effective amount of a Treg cell activating agent and/or a Treg cell and/or a monoclonal antibody and/or an advanced glycation end product (AGE) inhibitor. 19 . The method of claim 18 , wherein the method comprises administering a therapeutically effective amount of an NK cell to the subject. 20 . A method of treating cancer in a subject, the method comprising administering to the subject a therapeutically effective amount of the protein of claim 1 . 21 . A method of treating an
against enzymes · CPC title
Enzymes · CPC title
Molecules with a "CD" designation not provided for elsewhere · CPC title
Chimeric antigen receptors [CAR] · CPC title
T-cells, e.g. tumour infiltrating lymphocytes [TIL] or regulatory T [Treg] cells; Lymphokine-activated killer [LAK] cells · CPC title
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