IP Library Granted Patent US 9,763,985
Granted Patent B2
US 9,763,985 · App. 14/125,101 · Granted Sep 19, 2017

Antigen-specific central-memory T cell preparations having high CD4+ fraction

Inventors: Hans-dieter Volk (Berlin, DE); Michael Schmuck (Berlin, DE); Petra Reinke (Berlin, DE)
A61K35/26A61K35/17C12N5/0636C12N2501/2302C12N2501/2307C12N2501/727
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Quick Facts
Patent No.
US 9,763,985
App. No.
14/125,101
Granted
Sep 19, 2017
Kind
B2
Abstract

The invention relates to a method for generation of T cell preparations that are specific for at least one target antigen, comprising the steps of expanding lymphoid cells in vitro in the presence of a target antigen or peptide fragments thereof in an expansion step, isolating cells that secrete interferon gamma and culturing, the cells in the presence of interleukin 2 and interleukin 7 and either an inhibitor of the mTOR Complex 1, or in the presence of an inhibitor of IL-2/IL-2R interaction. The invention further relates to preparations obtained by the method of the invention.

Claims (17)

1. A method for generation of a mixed CD4+ and CD8+ central memory T cell preparation that is specific for at least one target antigen, comprising the steps of:

expanding lymphoid cells in vitro in the presence of a target antigen or peptide fragments thereof in an expansion step, yielding a first T cell preparation, wherein the lymphoid cells are isolated from whole blood peripheral mononuclear cells obtained from a human patient;

isolating responding cells from the first T cell preparation in an isolation step, yielding a second T cell preparation;

culturing, in a culturing step, the cells obtained as second T cell preparation in the presence of a cytokine, preferably interleukin 2 and/or interleukin 7, and

i. an inhibitor of the mTOR Complex 1, preferably rapamycin or a rapamycin analogue, wherein the concentration of the inhibitor of the mTOR complex 1 is between 2 nmol/l and 20 nmol/l, or

ii. an inhibitor of interleukin 2 (IL-2)—interleukin-2-receptor (IL-2R) interaction

thereby generating a mixed CD4+ and CD8+ central memory T cell preparation that is specific for at least one target antigen.

2. The method according to claim 1 , wherein the concentration of inhibitor of IL-2-IL-2R interaction is between 2 to 20 μg/ml.

3. The method according to claim 1 , wherein the inhibitor of IL-2-IL-2R interaction is a monoclonal antibody targeting CD25, particularly Daclizumab or Basiliximab.

4. The method according to claim 1 , wherein the culturing step lasts between 10 and 25 days, between 15 and 21 days, or about 18 days.

5. A method for generation of a mixed CD4+ and CD8+ central memory T cell preparation that is specific for at least one target antigen, comprising the steps of:

expanding lymphoid cells in vitro in the presence of a target antigen or peptide fragments thereof in an expansion step, yielding a first T cell preparation, wherein the lymphoid cells are isolated from whole blood peripheral mononuclear cells obtained from a human patient;

isolating responding cells from the first T cell preparation in an isolation step, yielding a second T cell preparation;

culturing, in a culturing step, the cells obtained as second T cell preparation in the presence of a cytokine, preferably interleukin 2 and/or interleukin 7, and an inhibitor of interleukin 2 (IL-2)—interleukin-2-receptor (IL-2R) interaction thereby generating a mixed CD4+ and CD8+ central memory T cell preparation that is specific for at least one target antigen.

6. The method according to claim 1 , wherein the concentration of the inhibitor of IL-2-IL-2R interaction is between 2 to 20 μg/ml.

7. The method according to claim 1 , wherein the inhibitor of IL-2-IL-2R interaction is a monoclonal antibody targeting CD25, particularly Daclizumab or Basiliximab.

8. The method according to claim 1 , wherein the culturing step lasts between 10 and 25 days, between 15 and 21 days, or about 18 days.

Priority Claims (2)
EP 11169655 · Jun 11, 2011 · regional
EP 11177524 · Aug 12, 2011 · regional
Continuity (1)
Related Publication 20140154228A1 · Jun 5, 2014