IP Library Granted Patent US 10,865,382
Granted Patent B2
US 10,865,382 · App. 16/404,349 · Granted Dec 15, 2020

Reducing immune tolerance induced by PD-L1

Inventor: Zhao Wu (Shanghai, CN)
Assignee: Innovative Cellular Therapeutics Co., Ltd.
C12N5/0636A61K35/17A61K39/0011A61K39/001112C07K14/7051C07K14/70503C07K14/70521C07K16/2803C07K16/30C12N5/0638A61K2039/5156A61K2039/5158C07K2319/00C07K2319/02C07K2319/03C12N2510/02
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Quick Facts
Patent No.
US 10,865,382
App. No.
16/404,349
Granted
Dec 15, 2020
Kind
B2
Abstract

The present disclosure relates to compositions and methods for reducing immune tolerance associated with CAR T cell therapy. Embodiments of the present disclosure include isolated nucleic acid sequence comprising a nucleic acid sequence that encodes modified programmed cell death protein 1 (PD-1) and a nucleic acid sequence that encodes chimeric antigen receptor (CAR).

Claims (20)

1. A pharmaceutical composition comprising an antitumor effective amount of a population of human T cells, wherein the human T cells of the population include human T cells that comprise an isolated nucleic acid sequence comprising a nucleic acid sequence that encodes modified programmed cell death protein 1 (PD-1) and a nucleic acid sequence that encodes chimeric antigen receptor (CAR), wherein the modified PD-1 comprises amino acid sequence SEQ ID NO: 9, SEQ ID NO: 13, SEQ ID NO: 12, or SEQ ID NO: 14, wherein the modified PD-1 and the CAR are expressed as gene products that are separate polypeptides; and wherein the modified PD-1 is a dominant negative PD-1.

2. The pharmaceutical composition of claim 1 , wherein an inhibitory effect of PD-L1 on cytokine production of the human T cells of the population is less than an inhibitory effect of PD-L1 on cytokine production of human T cells that do not comprise at least a part of the nucleic acid sequence that encodes the modified PD-1.

3. The pharmaceutical composition of claim 1 , wherein the CAR is specific for a tumor antigen that is present on a cancer cell, and wherein the cancer cell or a cell associated with the cancer cell expresses PD-LI.

4. The pharmaceutical composition of claim 3 , wherein the tumor antigen comprises CD19.

5. The pharmaceutical composition of claim 1 , wherein the nucleic acid sequence that encodes the modified PD-1 comprises substitution or deletion of one or more nucleotides as compared to a nucleic acid sequence encoding an intracellular part of wild-type PD-1.

6. The pharmaceutical composition of claim 1 , wherein the nucleic acid sequence that encodes the modified PD-1 comprises deletion of multiple nucleotides as compared to a nucleic acid sequence encoding an intracellular part of wild-type PD-1.

7. The pharmaceutical composition of claim 5 , wherein the nucleic acid sequence that encodes the modified PD-1 comprises a nucleic acid encoding a truncated PD-1 that does not include an intracellular domain.

8. The pharmaceutical composition of claim 1 , wherein the modified PD-1 comprises one or more point mutations as compared to wild-type PD-1.

9. The pharmaceutical composition of claim 8 , wherein the one or more point mutations comprise one or two amino acid point mutations of phosphorylation sites of wild-type PD-1.

10. The pharmaceutical composition of claim 1 , wherein the modified PD-1 comprises a mutation of Tyrosine residue 223 and/or a mutation of Tyrosine residue 248 as compared to wildtype PD-1.

11. The pharmaceutical composition of claim 1 , wherein the modified PD-1 comprises amino acid sequence SEQ ID NO: 13.

12. The pharmaceutical composition of claim 1 for use in the treatment of cancer.

13. The pharmaceutical composition of claim 1 , wherein the nucleic acid sequence encoding modified PD-1 comprises SEQ ID NO: 4.

14. The pharmaceutical composition of claim 10 , wherein the modified PD-1 comprises a mutation of Tyrosine residue 223.

15. The pharmaceutical composition of claim 10 , wherein the modified PD-1 comprises a mutation of Tyrosine residue 248.

16. The pharmaceutical composition of claim 10 , wherein the modified PD-1 comprises a mutation of Tyrosine residue 223 or a mutation of Tyrosine residue 248.

17. A pharmaceutical composition comprising an antitumor effective amount of a population of human T cells, wherein the human T cells of the population include human T cells that comprise an isolated nucleic acid sequence comprising a nucleic acid sequence that encodes modified programmed cell death protein 1 (PD-1) and a nucleic acid sequence that encodes chimeric antigen receptor (CAR), wherein the modified PD-1 comprises amino acid sequence SEQ ID NO: 9, SEQ ID NO: 12, SEQ ID NO: 13, or SEQ ID NO: 14 and inhibits activities of the wild-type PD-1 on the human T cells induced by PD-L1 of a tumor cell.

18. The pharmaceutical composition of claim 1 , wherein the modified PD-1 comprises amino acid sequence SEQ ID NO: 9.

19. The pharmaceutical composition of claim 1 , wherein the modified PD-1 comprising amino acid sequence SEQ ID NO: 12.

20. The pharmaceutical composition of claim 1 , wherein the modified PD-1 comprising amino acid sequence SEQ ID NO: 14.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 8, 2021
From: INNOVATIVE CELLULAR THERAPEUTICS CO., LTD.
To: INNOVATIVE CELLULAR THERAPEUTICS HOLDINGS, LTD.
Reel/Frame 055181/0119 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 8, 2019
From: WU, ZHAO
To: INNOVATIVE CELLULAR THERAPEUTICS CO., LTD.
Reel/Frame 049110/0206 →
Continuity (5)
Continuation 15373012 · Dec 8, 2016
Continuation 15093643 · Apr 7, 2016
Continuation PCTCN2016075061 · Mar 1, 2016
Provisional Application 62126804 · Mar 2, 2015
Related Publication 20190316086A1 · Oct 17, 2019