IP Library Granted Patent US 9,220,728
Granted Patent B2
US 9,220,728 · App. 13/595,440 · Granted Dec 29, 2015

Constitutive expression of costimulatory ligands on adoptively transferred T lymphocytes

Inventors: Michel Sadelain (New York, NY); Matthias Stephan (Boston, MA)
Assignee: MEMORIAL SLOAN-KETTERING CANCER CENTER
A61K35/17A61K39/0011A61K45/06C12N5/0636C12N15/85A61K2039/5156A61K2039/5158C12N2501/25C12N2501/51C12N2501/599
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Quick Facts
Patent No.
US 9,220,728
App. No.
13/595,440
Granted
Dec 29, 2015
Kind
B2
Abstract

The present invention provides immunoresponsive cells, including T cells, cytotoxic T cells, regulatory T cells, and Natural Killer (NK) cells, expressing at least one of an antigen-recognizing receptor and a co-stimulatory ligand and methods of use therefore for the treatment of neoplasia and other pathologies where an increase in an antigen-specific immune response is desired.

Claims (30)

1. A method of treating a neoplasia in a subject in need thereof, the method comprising administering to the subject an effective amount of a T cell comprising (1) two exogenous co-stimulatory ligands that are 4-1BBL and CD80, and (2) a receptor that binds an antigen.

2. The method of claim 1 , wherein the method increases an immune response.

3. The method of claim 1 , wherein the neoplasia is selected from the group consisting of prostate cancer, colon cancer, breast cancer, and glioblastoma.

4. The method of claim 1 , wherein the T cell is collected from an autologous or allogeneic donor, or generated in vitro from an engineered progenitor or stem cell.

5. The method of claim 1 , wherein the receptor is constitutively expressed on the surface of the T cell.

6. The method of claim 1 , wherein the two co-stimulatory ligands are constitutively or inducibly expressed on the surface of the T cell.

7. The method of claim 1 , wherein the antigen is a tumor antigen.

8. The method of claim 7 , wherein the antigen is selected from the group consisting of prostate-specific membrane antigen (PSMA), Carcinoembryonic Antigen (CEA), IL13Ralpha, her-2, CD19, NY-ESO-1, Lewis Y, Mart-1, gp100, tyrosinase, WT-1, hTERT, and mesothelin.

9. The method of claim 1 , wherein the receptor that binds the antigen comprises a recombinant antigen receptor.

10. The method of claim 1 , wherein the two co-stimulatory ligands are expressed from a retroviral vector.

11. The method of claim 1 , wherein the T cell is a cytotoxic T lymphocyte (CTL).

12. The method of claim 9 , wherein the recombinant antigen receptor is a chimeric antigen receptor.

13. The method of claim 12 , wherein the chimeric antigen receptor is Pz1.

14. The method of claim 12 , wherein the chimeric antigen receptor is P28z.

15. The method of claim 1 , wherein the receptor that binds the antigen comprises an endogenous antigen receptor.

16. A method of treating a neoplasia in a subject in need thereof, the method comprising administering to the subject an effective amount of a T cell comprising (1) two exogenous co-stimulatory ligands that are 4-1 BBL and CD86, and (2) a receptor that binds an antigen.

17. The method of claim 16 , wherein the method increases an immune response.

18. The method of claim 16 , wherein the neoplasia is selected from the group consisting of prostate cancer, colon cancer, breast cancer, and glioblastoma.

19. The method of claim 16 , wherein the T cell is collected from an autologous or allogeneic donor, or generated in vitro from an engineered progenitor or stem cell.

20. The method of claim 16 , wherein the receptor is constitutively expressed on the surface of the T cell.

21. The method of claim 16 , wherein the two co-stimulatory ligands are constitutively or inducibly expressed on the surface of the T cell.

22. The method of claim 16 , wherein the two co-stimulatory ligands are expressed from a retroviral vector.

23. The method of claim 16 , wherein the antigen is a tumor antigen.

24. The method of claim 23 , wherein the antigen is selected from the group consisting of prostate-specific membrane antigen (PSMA), Carcinoembryonic Antigen (CEA), IL13Ralpha, her-2, CD19, NY-ESO-1, Lewis Y, Mart-1, gp100, tyrosinase, WT-1, hTERT, and mesothelin.

25. The method of claim 16 , wherein the receptor that binds the antigen comprises a recombinant antigen receptor.

26. The method of claim 25 , wherein the recombinant antigen receptor is a chimeric antigen receptor.

27. The method of claim 26 , wherein the chimeric antigen receptor is Pz1.

28. The method of claim 26 , wherein the chimeric antigen receptor is P28z.

29. The method of claim 16 , wherein the receptor that binds the antigen comprises an endogenous antigen receptor.

30. The method of claim 16 , wherein the T cell is a cytotoxic T lymphocyte (CTL).

Assignments (1)
CONFIRMATORY LICENSE Recorded Apr 1, 2013
From: SLOAN-KETTERING INSTITUTE FOR CANCER RES
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 030122/0889 →
Continuity (3)
Division 12593751
Provisional Application 60921144 · Mar 30, 2007
Related Publication 20130121960A1 · May 16, 2013