Enhanced affinity T cell receptors and methods for making the same

Patent metadata

Field	Value
Publication number	US-10875904-B2
Application number	US-201715692846-A
Country	US
Kind code	B2
Filing date	Aug 31, 2017
Priority date	May 3, 2012
Publication date	Dec 29, 2020
Grant date	Dec 29, 2020

Abstract

The present disclosure provides methods for generating enhanced affinity T cell receptors by agonist selection of hematopoietic progenitor cells expressing an antigen specific TCRα cultured with stromal cells expressing Delta-like-1 or Delta-like-4, compositions prepared from such methods, and uses of thereof.

First claim

What is claimed is:

1. A T cell receptor (TCR)-expressing cell, comprising a host cell modified to express on its cell surface a TCR specific for a peptide antigen, wherein the TCR-expressing cell is made by a method comprising:
(a) contacting a cell capable of differentiating into a cell of the T cell lineage with stromal cells and the peptide antigen, under conditions and for a time sufficient to induce differentiation, of the cell capable of differentiating into a cell of the T cell lineage, into a double negative (DN) TCRαβ+ thymocyte,
wherein the cell capable of differentiating into a cell of the T cell lineage comprises a non-endogenous polynucleotide encoding a TCRα chain from a parent αβ TCR that is specific for the peptide antigen, wherein the parent TCR is a wild-type TCR, a human TCR, a mouse TCR, or a rat TCR, and
wherein the stromal cells comprise a non-endogenous polynucleotide encoding Delta-like-1 or Delta-like-4 and a polynucleotide encoding an MHC molecule; and
(b) introducing a polynucleotide encoding a TCRβ chain from the DN TCRαβ+ thymocyte generated in (a) into a cell capable of expressing a TCR on the cell surface and containing the non-endogenous polynucleotide encoding the TCRα chain from step (a), wherein the polynucleotide encoding a TCRβ chain from the DN TCRαβ+ thymocyte comprises the same Vβ gene as the β chain of the parent TCRβ,
wherein the expressed TCRβ chain comprises a variation in a CDR3 as compared to the parent TCRβ chain;
wherein the expressed TCRβ chain and the expressed TCRα chain form a TCR,
and wherein the cell capable of expressing a TCR on the cell surface is derived from TCRα − /β − 58 T cell hybridoma,
thereby generating the TCR-expressing cell.

2. The TCR-expressing cell of claim 1 , wherein the expressed TCR has enhanced affinity to the peptide antigen as compared to the parent TCR.

3. The TCR-expressing cell of claim 1 , wherein the expressed TCRβ chain comprises the same CDR1 and CDR2 domains as the parent TCRβ chain.

4. The TCR-expressing cell of claim 1 , wherein the cell capable of expressing a TCR on the cell surface comprises a CD4+ T cell.

5. The TCR-expressing cell of claim 1 , wherein the cell capable of expressing a TCR on the cell surface comprises a CD8+ T cell.

6. The TCR-expressing cell of claim 1 , wherein the peptide antigen is a viral antigen, a bacterial antigen, a cancer antigen, or an autoimmune antigen.

7. The TCR-expressing cell of claim 6 , wherein the peptide antigen is a WT-1 antigen.

8. The TCR-expressing cell of claim 7 , wherein the peptide antigen is a WT-1 antigen comprising the amino acid sequence of RMFPNAPYL (SEQ ID NO:2).

9. The TCR-expressing cell of claim 6 , peptide antigen is a mesothelin antigen.

10. The TCR-expressing cell of claim 9 , wherein the peptide antigen is a mesothelin antigen comprising the amino acid sequence of GQKMNAQAI (SEQ ID NO:31).

11. The TCR-expressing cell of claim 1 , wherein the polynucleotide encoding the TCRα chain from a parent TCR and the polynucleotide encoding a TCRβ chain from the DN TCRαβ+ thymocyte are each codon optimized.

12. A composition, comprising the TCR-expressing cell of claim 1 and a pharmaceutically acceptable carrier, excipient, or diluent.

13. A method of treating a disease in a subject, comprising administering to the subject the TCR-expressing cell of claim 1 , wherein the disease is associated with the peptide antigen, thereby treating the disease.

14. The method of claim 13 , wherein the TCR-expressing cell comprises a CD4+ T cell.

15. The method of claim 13 , wherein the TCR-expressing cell comprises a CD8+ T cell.

16. The method of claim 13 , wherein the disease is a cancer, an infectious disease, or an autoimmune disease.

17. The method of claim 16 , wherein the cancer is a solid tumor.

18. The method of claim 16 , wherein the cancer is a leukemia.

19. The method of claim 16 , wherein the cancer is selected from breast cancer, ovarian cancer, acute leukemia, vascular neoplasm, melanoma, colon cancer, lung cancer, thyroid cancer, bone and soft tissue sarcoma, or esophageal cancer.

20. The method of claim 18 , wherein the cancer is acute myeloid leukemia, acute lymphocytic leukemia, or chronic myeloid leukemia.

21. The method of claim 16 , wherein the disease is an autoimmune disease.

22. The method of claim 21 , wherein the autoimmune disease is arthritis, inflammatory bowel disease, atherosclerosis, psoriasis, systemic lupus erythematosus, or diabetes.

23. The method of claim 16 , wherein the disease is an infectious disease.

24. The method of claim 23 , wherein the infectious disease is a bacterial infection.

25. The method of claim 23 , wherein the infectious disease is a viral infection.

26. The method of claim 25 , wherein the viral infection is an adenovirus, bunyavirus, herpesvirus, papovavirus, paramyxovirus, picornavirus, rhabdovirus, orthomyxovirus, poxvirus, reovirus, retrovirus, lentivirus, or flavivirus infection.

27. A method of treating a bacterial infection in a subject, comprising administering to the subject a T cell receptor (TCR)-expressing cell, comprising a host cell modified to express on its cell surface a TCR specific for a bacterial peptide antigen,
wherein the TCR-expressing cell is made by a method comprising:
(a) contacting a cell capable of differentiating into a cell of the T cell lineage with stromal cells and the bacterial peptide antigen, under conditions and for a time sufficient to induce differentiation, of the cell capable of differentiating into a cell of the T cell lineage, into a double negative (DN) TCRαβ+ thymocyte,
wherein the cell capable of differentiating into a cell of the T cell lineage comprises a non-endogenous polynucleotide encoding a TCRα chain from a parent αβ TCR that is specific for the bacterial peptide antigen, wherein the parent TCR is a wild-type TCR, a human TCR, a mouse TCR, or a rat TCR, and
wherein the stromal cells comprise a non-endogenous polynucleotide encoding Delta-like-1 or Delta-like-4 and a polynucleotide encoding an MHC molecule; and
(b) introducing a polynucleotide encoding a TCRβ chain from the DN TCRαβ+ thymocyte generated in (a) into a cell capable of expressing a TCR on the cell surface and containing the non-endogenous polynucleotide encoding the TCRα chain from step (a), wherein the polynucleotide encoding a TCRβ chain from the DN TCRαβ+ thymocyte comprises the same Vβ gene as the β chain of the parent TCRβ,
wherein the expressed TCRβ chain comprises a variation in a CDR3 as compared to the parent TCRβ chain;
and wherein the expressed TCRβ chain and the expressed TCRα chain form a TCR.

28. The method of claim 27 , wherein the expressed TCR has enhanced affinity to the bacterial peptide antigen as compared to the parent TCR.

29. The method of claim 27 , wherein the expressed TCRβ chain comprises the same CDR1 and CDR2 domains as the parent TCRβ chain.

30. The method of claim 27 , wherein the cell capable of expressing a TCR on the cell surface comprises a T cell.

31. The method of claim 30 , wherein the cell capable of expressing a TCR on the cell surface comprises a CD4+ T cell.

32. The method of claim 30 , wherein the cell capable of expressing a TCR on the cell surface comprises a CD8+ T cell.

33. The method of claim 30 ,

Assignees

• Hutchinson Fred Cancer Res

Inventors

• Schmitt Thomas M
• Greenberg Philip D

Classifications

• A61K40/4243

  Wilms tumor 1 [WT1] · CPC title

• A61K40/32

  T-cell receptors [TCR] · CPC title

• A61K40/11

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

• C12N5/0636

  T lymphocytes · CPC title

• C12N15/867

  Retroviral vectors · CPC title