IP Library Granted Patent US 9,572,837
Granted Patent B2
US 9,572,837 · App. 15/093,643 · Granted Feb 21, 2017

Reducing immune tolerance induced by PD-L1

Inventor: Zhao Wu (Shanghai, CN)
Assignee: Innovative Cellular Therapeutics CO., LTD.
A61K35/17C07K14/70503C07K14/70521C07K16/2803C07K16/30C12N5/0638A61K2039/5158C07K2319/00C07K2319/03C12N2510/02
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Quick Facts
Patent No.
US 9,572,837
App. No.
15/093,643
Granted
Feb 21, 2017
Kind
B2
Abstract

The present disclosure relates to compositions and methods for reducing immune tolerance associated with CAR T cell therapy. Embodiments of the present disclosure include isolated nucleic acid sequence comprising a nucleic acid sequence that encodes modified programmed cell death protein 1 (PD-1) and a nucleic acid sequence that encodes chimeric antigen receptor (CAR).

Claims (19)

1. A pharmaceutical composition comprising a population of human T cells, wherein the population of human T cells include human T cells that comprise a nucleic acid molecule comprising:

a first nucleic acid sequence that encodes modified programmed cell death protein 1 (PD-1), which comprises the amino acid sequence of SEQ ID NO: 13, and

a second nucleic acid sequence that encodes a chimeric antigen receptor (CAR) comprising:

an extracellular domain that recognizes a tumor antigen,

a transmembrane domain, and

an intracellular domain comprising a CD3-zeta signaling domain and one or more signaling domains of one or more costimulatory molecules, wherein the modified PD-1 and the CAR are expressed as gene products that are separate polypeptides.

2. The pharmaceutical composition of claim 1 , wherein an inhibitory effect induced by a target cell on cytokine production of the human T cells is reduced as compared to human T cells that express the CAR and lack the modified PD-1, and the target cell express the tumor antigen and programmed death ligand 1 (PD-L1).

3. The pharmaceutical composition of claim 1 , wherein the tumor antigen is CD19.

4. The pharmaceutical composition of claim 1 , wherein the one or more costimulatory molecules include 4-1 BB.

5. A method of reducing an inhibitory effect induced by a target cell on cytokine production of human T cells that express a chimeric antigen receptor (CAR), the method comprising introducing a nucleic acid molecule into the human T cells, wherein:

the nucleic acid molecule that encodes modified programmed cell death protein 1 (PD-1), which comprises the amino acid sequence of SEQ ID NO: 13,

the CAR comprising:

an extracellular domain that recognizes a tumor antigen,

a transmembrane domain, and

an intracellular domain comprising a CD3-zeta domain and one or more signaling domains of one or more costimulatory molecules,

the target cell express the tumor antigen and programmed death ligand 1 (PD-L1), and

the modified PD-1 and the CAR are expressed as gene products that are separate polypeptides.

6. The method of claim 4 , wherein the tumor antigen is CD19.

7. The method of claim 4 , wherein the one or more costimulatory molecules include 4-1 BB.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 8, 2021
From: INNOVATIVE CELLULAR THERAPEUTICS CO., LTD.
To: INNOVATIVE CELLULAR THERAPEUTICS HOLDINGS, LTD.
Reel/Frame 055181/0119 →
CHANGE OF NAME Recorded Aug 9, 2019
From: SHANGHAI SIDANSAI BIOTECHNOLOGY CO., LTD.
To: INNOVATIVE CELLULAR THERAPEUTICS CO., LTD.
Reel/Frame 050018/0415 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 7, 2016
From: WU, ZHAO
To: SHANGHAI SIDANSAI BIOTECHNOLOGY CO., LTD
Reel/Frame 038387/0579 →
Continuity (3)
Continuation PCTCN2016075061 · Mar 1, 2016
Provisional Application 62126804 · Mar 2, 2015
Related Publication 20160256488A1 · Sep 8, 2016