IP Library Granted Patent US 12,037,606
Granted Patent B2
US 12,037,606 · App. 16/736,389 · Granted Jul 16, 2024

Methods of T cell expansion and activation

Inventors: Peiman Hematti (Middleton, WI); Debra Bloom (Sun Prairie, WI)
Assignee: Wisconsin Alumni Research Foundation
C12N5/0638A61K9/0019A61K35/17C12N5/0636A61K2039/5158C12N2501/25C12N2501/50C12N2501/51C12N2501/515C12N2501/599C12N2510/00
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Quick Facts
Patent No.
US 12,037,606
App. No.
16/736,389
Granted
Jul 16, 2024
Kind
B2
Abstract

The present disclosure relates to methods, cells, and compositions for preparing T cell populations and compositions for adoptive cell therapy. In particular, provided herein are methods for efficiently expanding and activating T cell populations for genetic engineering and adoptive T cell immunotherapies. Also provided are cells and compositions produced by the methods and methods of their use.

Claims (23)

1. A method of killing a melanoma or myeloma cancer cell comprising administering to the melanoma or myeloma cancer cell a therapeutically effective amount of an ex vivo cultured T cell population,

wherein the T cell population has reduced BAFF-R receptor activity; and

wherein the T cell population was cultured for about 3 to about 14 days in the presence of an anti-CD3 antibody, or a CD3-binding fragment thereof, and an anti-CD28 antibody, or a CD28-binding fragment thereof, under conditions appropriate for activating cytotoxic T cells.

2. The method of claim 1 , wherein the T cell population is administered in a pharmaceutical composition.

3. The method of claim 1 , wherein the T cell population is administered by intravenous injection, intratumoral injection, intrathecal injection, intradermal injection, intramuscular injection, intratracheal, intraluminal, or intracerebral injection.

4. The method of claim 1 , wherein the T cell population prior to BAFF-R receptor reduction is selected from the group consisting of a leukocyte-containing cell mixture and a purified T cell population.

5. The method of claim 4 , wherein the leukocyte-containing cell mixture or purified T cell population was obtained from apheresis of peripheral blood of a human subject.

6. The method of claim 4 , wherein the leukocyte-containing cell mixture or purified T cell population was obtained from peripheral blood mononuclear cells of a human subject.

7. The method of claim 1 , wherein the ex vivo cultured T cell population comprises at least one of activated CD4 + T cells and CD8 + T cells.

8. The method of claim 1 , wherein the T cell population was cultured in the presence of a BAFF-R antagonist; and/or a BAFF-R specific shRNA to reduce BAFF-R receptor activity.

9. The method of claim 8 , wherein the BAFF-R antagonist is a neutralizing BAFF-R antibody.

10. The method of claim 1 , wherein

the T cell population was additionally provided a chimeric antigen receptor to generate an ex vivo cultured, activated T cell population comprising the chimeric antigen receptor for administration to the cancer cell.

11. The method of claim 10 , wherein the T cell population was provided a chimeric antigen receptor by

(i) introducing the chimeric antigen receptor into the T cell population; or

(ii) transfecting a nucleic acid vector encoding the chimeric antigen receptor into the T cell population whereby the T cell population expresses the chimeric antigen receptor.

12. The method of claim 10 , wherein the T cell population was cultured in the presence of a BAFF-R antagonist; and/or a BAFF-R specific shRNA to reduce BAFF-R receptor activity.

13. The method of claim 12 , wherein the BAFF-R antagonist is a neutralizing BAFF-R antibody.

14. The method of claim 1 , wherein the anti-CD3 antibody is an anti-CD3c antibody.

15. The method of claim 14 , wherein the anti-CD3E antibody is selected from the group consisting of clone UCHT1 and clone OKT3.

16. The method of claim 1 , wherein the anti-CD28 antibody is selected from the group consisting of clone 37407 and clone 9.3.

17. The method of claim 1 , wherein the T cell population has enhanced T cell cytotoxicity compared to a T cell population without reduced BAFF-R receptor activity.

18. The method of claim 1 , wherein the T cell population has increased IFNγ production and/or granzyme B production.

Assignments (2)
CONFIRMATORY LICENSE Recorded Aug 2, 2022
From: UNIVERSITY OF WISCONSIN MADISON
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 061054/0649 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2020
From: HEMATTI, PEIMAN; BLOOM, DEBRA
To: WISCONSIN ALUMNI RESEARCH FOUNDATION
Reel/Frame 051460/0058 →
Continuity (3)
Division 15458339 · Mar 14, 2017
Provisional Application 62307989 · Mar 14, 2016
Related Publication 20200149010A1 · May 14, 2020