IP Library Granted Patent US 10,046,008
Granted Patent B2
US 10,046,008 · App. 14/850,542 · Granted Aug 14, 2018

Methods for treating chronic lymphocytic leukemia (CLL)

Inventors: Carl H. June (Merion Station, PA); Bruce L. Levine (Cherry Hill, NJ); Anne Chew (Cherry Hill, NJ); Stephen J. Schuster (Springfield, PA)
Assignee: The Trustees of the University of Pennsylvania
A61K35/17A61K39/0008C12N5/0636A61K2035/122A61K2039/5158C12N2501/51C12N2501/515
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Quick Facts
Patent No.
US 10,046,008
App. No.
14/850,542
Granted
Aug 14, 2018
Kind
B2
Abstract

The present invention relates generally to the treatment of PML by infusion of activated and expanded autologous lymphocytes.

Claims (19)

1. A method for treating chronic lymphocytic leukemia (CLL) comprising administering to a CLL patient who has underlying progressive multifocal leukoencephalitis (PML):

a) a first population of T cells activated and expanded according to a method comprising,

activating a population of T cells in vitro with an agent which stimulates a TCR/CD3 complex-associated signal in the T cells, wherein the agent is attached on a surface; and

stimulating a CD28 accessory molecule on the surface of the T cells in vitro with a ligand that binds the CD28 accessory molecule on the surface of the T cells, wherein the ligand is attached on the same surface as the agent; the activating and stimulating steps thereby inducing proliferation of the T cells, and

b) a second population of T cells comprising JC virus-specific T cells, wherein when the first and second population of T cells are administered, the CLL patient who has underlying PML is treated.

2. The method of claim 1 , wherein the agent is selected from the group consisting of an anti-CD3 antibody or antigen-binding fragment thereof, an anti-TCR antibody or antigen-binding fragment thereof, a superantigen, an MHC-peptide tetramer, and an antigen in a form suitable to trigger a primary activation signal in the T cell when complexed with the TCR/CD3 complex.

3. The method of claim 1 , wherein the ligand is selected from the group consisting of an anti-CD28 antibody or antigen-binding fragment thereof, CD80 or a CD28-binding fragment thereof, and CD86 or a CD28-binding fragment thereof.

4. The method of claim 1 , wherein the surface is selected from the group consisting of a bead, a lipid bilayer, a cell surface, and a tissue-culture dish.

5. The method of claim 1 , wherein the activated and expanded T cells are administered intravenously.

6. The method of claim 4 , wherein said cell surface is of a human cell line.

7. The method of claim 6 , wherein said human cell line is K562.

8. The method of claim 6 , wherein said human cell line is genetically modified to express a human Fcγ receptor.

9. The method of claim 8 , wherein said human Fcγ receptor comprises CD32 or CD64.

10. The method of claim 6 , wherein said human cell line is further genetically modified to express a co-stimulatory molecule selected from the group consisting of CD80, CD86, 4-1BBL, OX40L, ICOS-L, ICAM, PD-L1 and PD-L2.

11. The method of claim 6 , wherein said human cell line has been modified to express a cytokine.

12. The method of claim 11 , wherein said cytokine is selected from the group consisting of IL-2, GM-CSF, IL-4, TNF-α, and IFN-γ.

13. The method of claim 1 , wherein the JC virus-specific T cells are generated by stimulating a population of T cells in vitro with an antigen selected from the group consisting of a JCV-specific protein or a JCV-specific epitope.

14. The method of claim 13 , wherein the JCV-specific epitopes are selected from the group consisting of VP1 p36 and VP1 p100.

15. The method of claim 1 , wherein the population of T cells are autologous T cells.

Continuity (4)
Continuation 13537330 · Jun 29, 2012
Division 13201829
Provisional Application 61155026 · Feb 24, 2009
Related Publication 20160000829A1 · Jan 7, 2016