IP Library Granted Patent US 10,808,225
Granted Patent B2
US 10,808,225 · App. 15/476,476 · Granted Oct 20, 2020

Use of PDL1 expressing cells to convert T cells into regulatory T cells

Inventors: James L. Riley (Downingtown, PA); Daniel H. Fowler (Bethesda, MD); Shoba Amarnath (Washington, DC)
Assignees: The Trustees of the University of Pennsylvania; Government of The United States of America, as represented by the Secretary, Department of Health and Human Services
C12N5/0637A61K35/17C12N2501/998C12N2502/99C12N2506/11C12N2506/115
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Quick Facts
Patent No.
US 10,808,225
App. No.
15/476,476
Granted
Oct 20, 2020
Kind
B2
Abstract

The present invention provides methods and compositions for converting a T cell into a cell that exhibits at least one regulatory T cell phenotype. The converted T cell is generated by contacting a T cell with a cell that is modified to comprise an agent capable of activating PD1 signaling in a T cell. The converted T cell is useful for preventing, suppressing, blocking or inhibiting an immune response. For example the converted T cell is useful for preventing rejection of a transplanted tissue in a human or other animal host, or protecting against graft versus host disease. The converted T cell can also be used to treat autoimmune diseases.

Claims (17)

1. A method for generating an immunosuppressive effect in a mammal having an alloresponse or autoimmune response, the method comprising administering to said mammal an effective amount of a cell population, wherein said cell population comprises a K562 cell modified to express an agent capable of activating PD1 signaling in a T cell thereby generating an immunosuppressive effect in said mammal, wherein the agent is selected from the group consisting of PDL1, PDL2, and an anti-PD1 antibody.

2. A method for preventing an alloresponse in a mammal, the method comprising administering to said mammal, an effective amount of a cell population, wherein said cell population comprises a K562 cell modified to express an agent capable of activating PD1 signaling in a T cell thereby preventing said response in said mammal, wherein the agent is selected from the group consisting of PDL1, PDL2, and an anti-PD1 antibody.

3. A method of treating a transplant recipient to reduce in said recipient an immune response by a transplant against the transplant recipient, the method comprising administering to a transplant recipient, an effective amount of a cell population, wherein said cell population comprises a K562 cell modified to express an agent capable of activating PD1 signaling in a T cell thereby reducing an immune response against an antigen, wherein the agent is selected from the group consisting of PDL1, PDL2, and an anti-PD1 antibody.

4. The method of claim 3 , wherein the immune response against the transplant is graft-versus-host disease (GvHD).

5. The method of claim 3 , wherein the cell population further comprises a T cell.

6. The method of claim 5 , wherein the T cell is selected from the group consisting of a Th1 cell, a Th2 cell, a Th17 cell, and any combination thereof.

7. The method of claim 3 , wherein the cell population further comprises a cell that exhibits at least one regulatory T cell phenotype, wherein the at least one regulatory phenotype is selected from the group consisting of the expression of Foxp3, suppression of effector T cell activation, and a combination thereof.

8. The method of claim 1 , wherein the cell population further comprises a T cell.

9. The method of claim 8 , wherein the T cell is selected from the group consisting of a Th1 cell, a Th2 cell, a Th17 cell, and any combination thereof.

10. The method of claim 1 , wherein the cell population further comprises a cell that exhibits at least one regulatory T cell phenotype, wherein the at least one regulatory T cell phenotype is selected from the group consisting of expression of Foxp3, suppression of effector T cell activation, and a combination thereof.

11. The method of claim 2 , wherein the cell population further comprises a T cell.

12. The method of claim 11 , wherein the T cell is selected from the group consisting of a Th1 cell, a Th2 cell, a Th17 cell, and any combination thereof.

13. The method of claim 2 , wherein the cell population further comprises a cell that exhibits at least one regulatory T cell phenotype, wherein the regulatory T cell phenotype is selected from the group consisting of expression of Foxp3, suppression of effector T cell activation, and a combination thereof.

14. A method of treating a transplant recipient to reduce in said recipient an immune response against the transplant, the method comprising administering to a transplant recipient, an effective amount of a cell population, wherein said cell population comprises a K562 cell modified to express an agent capable of activating PD1 signaling in a T cell thereby reducing an immune response against an antigen, wherein the agent is selected from the group consisting of PDL1, PDL2, and an anti-PD1 antibody.

15. The method of claim 14 , wherein the cell population further comprises a T cell.

16. The method of claim 15 , wherein the T cell is selected from the group consisting of a Th1 cell, a Th2 cell, a Th17 cell, and any combination thereof.

17. The method of claim 14 , wherein the cell population further comprises a cell that exhibits at least one regulatory T cell phenotype, wherein the at least one regulatory T cell phenotype is selected from the group consisting of expression of Foxp3, suppression of effector T cell activation, and a combination thereof.

Assignments (1)
CONFIRMATORY LICENSE Recorded Jan 30, 2019
From: UNIVERSITY OF PENNSYLVANIA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 048196/0356 →
Continuity (4)
Division 14359764
Provisional Application 61563273 · Nov 23, 2011
Provisional Application 61564174 · Nov 28, 2011
Related Publication 20170211042A1 · Jul 27, 2017