Anti-hla-A2 antibodies and methods of using the same

US12049504B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12049504-B2
Application numberUS-201816648967-A
CountryUS
Kind codeB2
Filing dateSep 19, 2018
Priority dateSep 19, 2017
Publication dateJul 30, 2024
Grant dateJul 30, 2024

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Provided are humanized anti-HLA-A2 antibodies. In certain aspects, the humanized anti-HLA-A2 antibodies are capable of constituting an antigen binding domain of a chimeric antigen receptor (CAR), where the CAR is capable of being expressed in a human cell such that the CAR specifically binds to HLA-A2. Also provided are CARs that include the humanized anti-HLA-A2 antibodies. Modified cells including the antibodies and CARs, as well as methods of using such modified cells are also provided.

First claim

Opening claim text (preview).

The invention claimed is: 1. A chimeric antigen receptor (CAR) comprising: a) an extracellular domain comprising a humanized anti-HLA-A2 antibody or an antigen-binding fragment thereof that exhibits reduced binding to one or more HLA-A subtypes selected from the group consisting of HLA-A*25, HLA-A*29, and HLA-A*30 as compared to antibody BB7.2 (ATCC Deposit No. HB-82), wherein said humanized anti-HLA-A2 antibody or antigen-binding fragment comprises i) a heavy chain variable domain (VH) comprising the amino acid sequence of SEQ ID NO: 61 and a light chain variable domain (VL) comprising the amino acid sequence of SEQ ID NO: 68; ii) a VH comprising the amino acid sequence of SEQ ID NO: 64 and a VL comprising the amino acid sequence of SEQ ID NO: 68; iii) a VH comprising the amino acid sequence of SEQ ID NO: 65 and a VL comprising the amino acid sequence of SEQ ID NO: 68; iv) a VH comprising the amino acid sequence of SEQ ID NO: 66 and a VL comprising the amino acid sequence of SEQ ID NO: 68; v) a VH comprising the amino acid sequence of SEQ ID NO: 64 and a VL comprising the amino acid sequence of SEQ ID NO: 69; vi) a VH comprising the amino acid sequence of SEQ ID NO: 65 and a VL comprising the amino acid sequence of SEQ ID NO: 69; or vii) a VH comprising the amino acid sequence of SEQ ID NO: 63 and a VL comprising the amino acid sequence of SEQ ID NO: 70; b) a transmembrane domain; and c) a cytoplasmic domain comprising an intracellular signaling domain; wherein said CAR is capable of being expressed in an immune cell such that said CAR specifically binds to HLA-A2. 2. The CAR of claim 1 , wherein the humanized anti-HLA-A2 antibody or antigen-binding fragment is an scFv comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 73, 81, 83, 84, 87, 88 and 91. 3. The CAR of claim 1 , wherein the humanized anti-HLA-A2 antibody or antigen-binding fragment is an scFv comprising the amino acid sequence of SEQ ID NO: 73. 4. The CAR of claim 1 , further comprising a hinge region that comprises a stalk region of CD8α. 5. The CAR of claim 1 , wherein the transmembrane domain is a CD8 transmembrane domain and the intracellular signaling domain comprises a CD28 costimulatory domain and a CD3 zeta primary signaling domain. 6. The CAR of claim 1 , comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 120, 128, 130, 131, 134, 135, 138 and 213. 7. A chimeric antigen receptor (CAR) comprising the amino acid sequence of SEQ ID NO: 213. 8. A nucleic acid molecule encoding the CAR of claim 1 . 9. An immune cell comprising the CAR of claim 1 . 10. The immune cell of claim 9 , wherein the immune cell is a regulatory T cell. 11. A pharmaceutical composition comprising the immune cell of claim 9 and a pharmaceutically acceptable excipient. 12. A method for: a) preventing or treating organ or tissue transplant rejection in a subject; b) preventing or treating graft versus host disease (GVHD) in a subject; c) promoting immune tolerance in a subject in need thereof; d) inducing tolerance to a transplanted organ or tissue in a subject; or e) any combination of a)-d); wherein said method comprises administering an immune cell of claim 9 to the subject. 13. The method of claim 12 , wherein the subject is undergoing or has undergone a hematopoietic stem cell transplant. 14. The CAR of claim 1 , wherein said transmembrane domain comprises a transmembrane domain of a protein selected from the group consisting of: CD3 gamma, CD3 delta, CD3 epsilon, CD3 zeta, the alpha chain of the T cell receptor, the beta chain of the T cell receptor, the gamma chain of the T cell receptor, the delta chain of the T cell receptor, CD28, CD45, CD4, CD5, CD8, CD9, CD16, CD22, CD33, CD37, CD64, CD80, CD86, CD134, CD137, CD154, and any combination thereof. 15. The CAR of claim 1 , wherein said intracellular signaling domain comprises a functional signaling domain of a protein selected from the group consisting of: CD3 gamma, CD3 delta, CD3 epsilon, CD3 zeta, FcR gamma, FcR alpha, FcR epsilon, CD5, CD22, CD79a, CD79b, and CD66d, and any combination thereof. 16. The CAR of claim 1 , wherein said intracellular signaling domain comprises a functional signaling domain of CD3 zeta. 17. The CAR of claim 1 , wherein said intracellular signaling domain comprises a functional signaling domain and a costimulatory domain, wherein the costimulatory domain comprises a functional signaling domain of a protein selected from the group consisting of OX40, CD27, CD28, lymphocyte function-associated antigen-1 (LFA-1) (CD11a/CD18), TNFR1 (CD120a/TNFRSF1A), TNFR2 (CD120b/TNFRSF1B), CTLA-4 (CD152), CD95, ICOS (CD278), 4-1BB (CD137), CD2, CD30, CD40, PD-1, CD7, LIGHT, NKG2C, B7-H3, ICAM-1, a ligand that specifically binds to CD83, IL2Ra (CD25), IL6Ra (CD126), IL-7Ra (CD127), IL-13RA1, IL-13RA2, IL-33R(IL1RL1), IL-10RA, IL-10RB, IL-4R, IL-5R (CSF2RB), ARHR, BAFF receptor, IL-21R, TGFbR1, TGFbR2, TGFbR3, common gamma chain, and any combination thereof. 18. The CAR of claim 1 , wherein said intracellular signaling domain comprises a costimulatory domain, wherein said costimulatory domain comprises a functional signaling domain of a protein selected from CD28 and 4-1BB.

Assignees

Inventors

Classifications

  • T-cells, e.g. tumour infiltrating lymphocytes [TIL] or regulatory T [Treg] cells; Lymphokine-activated killer [LAK] cells · CPC title

  • Chimeric antigen receptors [CAR] · CPC title

  • Her-2/neu/ErbB2, Her-3/ErbB3 or Her 4/ ErbB4 · CPC title

  • Antigens related to induction of tolerance to non-self · CPC title

  • Viral antigens · CPC title

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What does patent US12049504B2 cover?
Provided are humanized anti-HLA-A2 antibodies. In certain aspects, the humanized anti-HLA-A2 antibodies are capable of constituting an antigen binding domain of a chimeric antigen receptor (CAR), where the CAR is capable of being expressed in a human cell such that the CAR specifically binds to HLA-A2. Also provided are CARs that include the humanized anti-HLA-A2 antibodies. Modified cells incl…
Who is the assignee on this patent?
Univ British Columbia, Cdrd Ventures Inc
What technology area does this patent fall under?
Primary CPC classification C07K14/705. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jul 30 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).