Use of icos-based cars to enhance antitumor activity and car persistence
US-2015017141-A1 · Jan 15, 2015 · US
US10040846B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10040846-B2 |
| Application number | US-201314375015-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 22, 2013 |
| Priority date | Feb 22, 2012 |
| Publication date | Aug 7, 2018 |
| Grant date | Aug 7, 2018 |
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Official abstract text for this publication.
The present invention provides compositions and methods for generating a genetically modified T cells comprising a chimeric antigen receptor (CAR) having an antigen binding domain, a transmembrane domain, a costimulatory signaling region, and a CD3 zeta signaling domain, wherein the T cell exhibits prolonged exponential expansion in culture that is ligand independent and independent of the addition of exogenous cytokines or feeder cells.
Opening claim text (preview).
What is claimed is: 1. An isolated nucleic acid sequence encoding a chimeric antigen receptor (CAR), wherein the CAR comprises an anti-c-Met antibody or fragment thereof, an IgG4 hinge domain, a CD28 transmembrane domain, a CD28 costimulatory signaling region, and a CD3 zeta signaling domain, and further wherein the CAR comprises the amino acid sequence of SEQ ID NO: 1. 2. A T cell comprising a nucleic acid sequence that expresses a chimeric antigen receptor (CAR), the CAR comprising an anti-c-Met antibody or fragment thereof, an IgG4 hinge domain, a CD28 transmembrane domain, a CD28 costimulatory signaling region, and a CD3 zeta signaling domain, and further wherein the CAR comprises the amino acid sequence of SEQ ID NO: 1. 3. A vector comprising a nucleic acid sequence encoding a chimeric antigen receptor (CAR), the CAR comprising an anti-c-Met antibody or fragment thereof, an IgG4 hinge domain, a CD28 transmembrane domain, a CD28 costimulatory signaling region, and a CD3 zeta signaling domain, and further wherein the CAR comprises the amino acid sequence of SEQ ID NO: 1.
CD28, CD152 · CPC title
Genetically modified cells · CPC title
fusions for targeting to specific cell types, e.g. tissue specific targeting, targeting of a bacterial subspecies · CPC title
T-cell receptor (TcR)-CD3 complex · CPC title
T lymphocytes · CPC title
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