IP Library Granted Patent US 9,809,797
Granted Patent B2
US 9,809,797 · App. 12/677,035 · Granted Nov 7, 2017

Enhanced generation of cytotoxic T-lymphocytes by IL-21 mediated FOXP3 suppression

Inventors: Cassian Yee (Seattle, WA); Yongqing Li (Shoreline, WA)
Assignee: NATIONAL INSTITUTES OF HEALTH (NIH) U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS) DIVISION OF EXTRAMURAL INVENTIONS AND TECHNOLOGY
C12N5/0638A61K31/41A61K35/17A61K39/00C12N5/0636A61K35/12A61K2035/124A61K2039/51A61K2039/5154C12N2501/23C12N2501/2321C12N2501/998
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Quick Facts
Patent No.
US 9,809,797
App. No.
12/677,035
Granted
Nov 7, 2017
Kind
B2
Abstract

A method of carrying out adoptive immunotherapy by administering a subject an antigen-specific cytotoxic T lymphocytes (CTL) preparation in a treatment-effective amount is described. In the method, the CTL preparation is preferably administered as a preparation of an in vitro antigen-stimulated and expanded primate CTL population, the CTL population: (i) depleted of FoxP3+ T lymphocytes prior to antigen stimulation; (ii) antigen-stimulated in vitro in the presence of interleukin-21; or (iii) both depleted of FoxP3+ T lymphocytes prior to antigen stimulation and then antigen-stimulated in vitro in the presence of interleukin-21. Methods of preparing such compositions, and compositions useful for carrying out the adoptive immunotherapy, are also described.

Claims (11)

1. A pharmaceutical formulation comprising a single T cell population type, wherein said T cell population consists of CD8 + CD25 − antigen-specific human cytotoxic T lymphocyte (CTL) cells specific for an antigen, said formulation being prepared by a process comprising:

(a) sorting a lymphocyte subpopulation depleted of CD25+ cells from a first lymphocyte population of peripheral blood mononuclear cells (PBMC) to produce a CD8 + CD25 − subpopulation;

(b) promoting the production of antigen-specific CTL cells in said subpopulation by in vitro culturing the sorted CD8 + CD25 − subpopulation with antigen in a medium containing interleukin-21, wherein the number of antigen specific CD8+ CTL are enriched in said CD8 + CD25 − subpopulation by at least 100-fold, as compared to that seen in the same lymphocyte population not subjected to either said separating step (a) or this promoting step (b); and

(c) formulating antigen-specific CTL cells produced therefrom into a pharmaceutical formulation, and

wherein said pharmaceutical formulation comprises at least 10 9 CTL cells.

2. The formulation of claim 1 , wherein said interleukin-21 is included in said culture in an amount of from 1 to 1000 nanograms per milliliter.

3. The formulation of claim 1 , wherein the CTL cells are specific for a tumor antigen.

4. The formulation of claim 1 , wherein (a) the sorting a lymphocyte subpopulation depleted of CD25 + cells from a first lymphocyte population comprises contacting the first lymphocyte population with anti-CD25 antibodies.

5. The formulation of claim 1 , wherein (b) the promoting the production of antigen-specific CTL cells in said subpopulation by in vitro culturing comprises culturing of the CTLs with antigen presenting cells.

6. The formulation of claim 1 , wherein the antigen presenting cells comprise dendritic cells (DCs).

7. The formulation of claim 1 , wherein the antigen-specific CTL cells comprise a transgene.

Assignments (3)
MERGER AND CHANGE OF NAME Recorded Sep 27, 2022
From: FRED HUTCHINSON CANCER RESEARCH CENTER; SEATTLE CANCER CARE ALLIANCE
To: FRED HUTCHINSON CANCER CENTER
Reel/Frame 061613/0897 →
CONFIRMATORY LICENSE Recorded Jan 12, 2017
From: FRED HUTCHINSON CANCER RESEARCH CENTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 041346/0263 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 8, 2010
From: YEE, CASSIAN; LI, YONGQING
To: THE FRED HUTCHINSON CANCER RESEARCH CENTER
Reel/Frame 024206/0698 →
Continuity (2)
Provisional Application 60977150 · Oct 3, 2007
Related Publication 20100330056A1 · Dec 30, 2010