IP Library Granted Patent US 8,840,899
Granted Patent B2
US 8,840,899 · App. 13/057,057 · Granted Sep 23, 2014

Use of mTOR inhibitors to enhance T cell immune responses

Inventors: Rafi Ahmed (Atlanta, GA); Christian P. Larsen (Atlanta, GA); Koichi Araki (Atlanta, GA)
Assignee: Emory University
A61K31/4745C07K14/005A61K39/12C12N2740/13013A61K45/06A61K2039/55561A61K2039/53C12N2730/10134A61K2039/55516C12N2760/10034A61K39/39C12N2770/10022A61K2039/5258C12N2710/10343C12N2710/24122
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Quick Facts
Patent No.
US 8,840,899
App. No.
13/057,057
Filed
Feb 1, 2011
Granted
Sep 23, 2014
Kind
B2
Art Unit
1648
USPC
424/184.1
Abstract

It is disclosed herein that treatment of a subject with an mTOR inhibitor enhances antigen-specific T cell immune responses. Thus, provided herein is a method of enhancing an antigen-specific T cell response in a subject by administering to the subject a therapeutically effective amount of an mTOR inhibitor. The antigen can be any antigen, such as an antigen from a pathogen or a vaccine, or a tumor antigen. In some embodiments, the method further comprises administering to the subject a vaccine, such as a virus vaccine or a cancer vaccine. The mTOR inhibitor can be administered either before or after vaccination to enhance the quantity and quality of the T cell immune response and immunological memory. In some examples, the mTOR inhibitor is rapamycin or a rapamycin analog.

Claims (13)

1. A method of enhancing an antigen-specific T cell response in a subject, comprising: (1) administering to the subject a therapeutically effective amount of an antigen; and (2) administering to the subject a therapeutically effective amount of a mammalian target of rapamycin (mTOR) inhibitor during the T cell contraction phase.

2. The method of claim 1 , wherein the T cells are CD8+ T cells.

3. The method of claim 2 , wherein the CD8+ T cells are CD8+ memory T cells.

4. The method of claim 1 , wherein the T cells are CD4+ T cells.

5. The method of claim 4 , wherein the CD4+ T cells are CD4+ memory T cells.

6. The method of claim 1 , wherein the antigen is from a pathogen.

7. The method of claim 6 , wherein the pathogen is a virus, bacterium, fungus or parasite.

8. The method of claim 1 , wherein the antigen comprises a tumor antigen.

9. The method of claim 8 , wherein the tumor is a hematologic cancer or a solid tumor.

10. The method of claim 9 , wherein the hematologic cancer is a leukemia or a lymphoma.

11. The method of claim 9 , wherein the solid tumor is a carcinoma, melanoma, sarcoma or central nervous system tumor.

12. The method of claim 1 , wherein the mTOR inhibitor is rapamycin or a rapamycin analog.

13. A method of determining the increase in the proportion of antigen-specific CD127 High KLRG-1 Low CD8+ T cells in the subject, comprising: (1) administering to the subject a therapeutically effective amount of an antigen; and (2) administering to the subject a therapeutically effective amount of a mammalian target of rapamycin (mTOR) inhibitor during the T cell contraction phase; and (3) measuring the proportion of antigen-specific CD127 High KLRG-1 Low CD8+ T cells in the subject relative to the proportion of CD127 High KLRG-1 Low CD8+ T cells in the absence of treatment.

Assignments (1)
CONFIRMATORY LICENSE Recorded Apr 26, 2011
From: EMORY UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 026178/0974 →
Continuity (2)
Provisional Application 61086350 · Aug 5, 2008
Related Publication 20110129496A1 · Jun 2, 2011