Chimeric antigen receptor and methods of use thereof
US-10632152-B2 · Apr 28, 2020 · US
US12371466B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12371466-B2 |
| Application number | US-202017115565-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 8, 2020 |
| Priority date | Feb 15, 2013 |
| Publication date | Jul 29, 2025 |
| Grant date | Jul 29, 2025 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present disclosure provides a heterodimeric, conditionally active chimeric antigen receptor (CAR), and a nucleic acid comprising a nucleotide sequence encoding the CAR. The present disclosure provides cells genetically modified to produce the CAR. A CAR of the present disclosure can be used in various methods, which are also provided.
Opening claim text (preview).
What is claimed is: 1. One or more nucleic acids comprising a nucleotide sequence(s) encoding a heterodimeric chimeric antigen receptor (CAR) comprising: a first polypeptide comprising a first member of a dimerization pair, a first transmembrane domain, and an intracellular signaling domain; and a second polypeptide comprising a scFv or VHH domain that specifically binds to mesothelin, a second member of the dimerization pair, and a second transmembrane domain; wherein: the first and second members of the dimerization pair are intracellular, a dimerizing agent dimerizes the heterodimeric CAR when the first and second polypeptides are expressed by a cell with the dimerizing agent bound between the dimerization pair members of the first and second polypeptides, the first polypeptide does not comprise an antigen-binding domain and the second polypeptide does not comprise an intracellular signaling domain capable of inducing cell activation, and activation of the cell by the formed heterodimeric CAR binding mesothelin or said antigen is increased as compared to activation of the cell in the absence of the dimerizing agent. 2. The one or more nucleic acids according to claim 1 , wherein the intracellular signaling domain is a CD3-zeta intracellular signaling domain or a ZAP-70 intracellular signaling domain. 3. The one or more nucleic acids according to claim 1 , wherein the intracellular signaling domain comprises an immunoreceptor tyrosine-based activation motif (ITAM). 4. The one or more nucleic acids according to claim 1 , wherein the first polypeptide, the second polypeptide or both comprise an intracellular costimulatory polypeptide. 5. The one or more nucleic acids according to claim 1 , wherein the intracellular costimulatory polypeptides are selected from the group consisting of: 4-1BB, CD28, ICOS, OX-40, BTLA, CD27, CD30, GITR, and HVEM. 6. The one or more nucleic acids according to claim 1 , wherein the first polypeptide comprises a first costimulatory polypeptide comprising an amino acid sequence and the second polypeptide comprises a second costimulatory polypeptide comprising an amino acid sequence that has at least 95% amino acid identity to the amino acid sequence of the first costimulatory polypeptide in the first polypeptide. 7. The one or more nucleic acids according to claim 1 , wherein the dimerizer agent is selected from the group consisting of: rapamycin, coumermycin, methotrexate, AP20187, abscisic acid, gibberellin and analogs thereof. 8. The one or more nucleic acids according to claim 1 , wherein the first and second members of the dimerization pair are selected from the group consisting of: a) FK506 binding protein (FKBP) and FKBP-rapamycin associated protein (FRB); b) a Gibberellic Acid Insensitive (GAI) protein and a gibberellin receptor (GID1) protein; c) FKBP and calcineurin catalytic subunit A (CnA); d) an abscisic acid receptor (PYL) protein and an abscissic acid insensitive (ABI) protein; and e) FKBP and cyclophilin. 9. The one or more nucleic acids according to claim 1 , wherein the first and second members of the dimerization pair are selected from the group consisting of: a) FK506 binding protein (FKBP) and FKBP; b) gyrase B (GyrB) and GyrB; c) dihydrofolate reductase (DHFR) and DHFR; and d) DmrB and DmrB. 10. An isolated cell comprising the one or more nucleic acids according to claim 1 . 11. The isolated cell according to claim 10 , wherein the isolated cell is an immune cell. 12. The isolated cell according to claim 11 , wherein the immune cell is a lymphocyte or a NK cell. 13. The isolated cell according to claim 10 , wherein the cell is a human cell.
Genetically modified cells · CPC title
T lymphocytes · CPC title
Hydrolases (3) · CPC title
containing a fusion for binding to a cell surface receptor · CPC title
NGF/TNF-superfamily, e.g. CD70, CD95L, CD153, CD154 (NGF C07K14/48, TNF C07K14/525) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.