Genetically-modified cells comprising a modified human t cell receptor alpha constant region gene
US-2017335010-A1 · Nov 23, 2017 · US
US9969975B1 · US · B1
| Field | Value |
|---|---|
| Publication number | US-9969975-B1 |
| Application number | US-201815865089-A |
| Country | US |
| Kind code | B1 |
| Filing date | Jan 8, 2018 |
| Priority date | Oct 5, 2015 |
| Publication date | May 15, 2018 |
| Grant date | May 15, 2018 |
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.
Disclosed herein is a genetically-modified cell comprising in its genome a modified human T cell receptor alpha constant region gene, wherein the cell has reduced cell-surface expression of the endogenous T cell receptor. The present disclosure further relates to methods for producing such a genetically-modified cell, and to methods of using such a cell for treating a disease in a subject.
Opening claim text (preview).
The invention claimed is: 1. A genetically-modified human T cell comprising in its genome a modified human T cell receptor (TCR) alpha constant region gene, wherein said modified human TCR alpha constant region gene comprises from 5′ to 3′: (a) a 5′ region of a human TCR alpha constant region gene which is endogenous to said T cell; (b) an exogenous nucleic acid sequence encoding a chimeric antigen receptor; and (c) a 3′ region of said human TCR alpha constant region gene which is endogenous to said T cell; wherein said chimeric antigen receptor comprises a ligand-binding domain having specificity for an antigen present on a cancer cell, and wherein said genetically-modified human T cell expresses said chimeric antigen receptor and exhibits reduced cell-surface expression of the endogenous T cell receptor when compared to unmodified control cells. 2. The cell of claim 1 , wherein said exogenous nucleic acid sequence comprises a promoter sequence that drives expression of said chimeric antigen receptor. 3. The cell of claim 1 , wherein said chimeric antigen receptor comprises an intracellular cytoplasmic signaling domain. 4. The cell of claim 1 , wherein said chimeric antigen receptor comprises an intracellular co-stimulatory signaling domain. 5. The cell of claim 1 , wherein said chimeric antigen receptor comprises a signal peptide. 6. The cell of claim 1 , wherein said chimeric antigen receptor comprises a hinge domain. 7. The cell of claim 1 , wherein said chimeric antigen receptor comprises a transmembrane domain. 8. The cell of claim 1 , wherein said ligand-binding domain of said chimeric antigen receptor is specific for CD19. 9. The cell of claim 1 , wherein said exogenous nucleic acid sequence is inserted into said TCR alpha constant region gene which is endogenous to said T cell at a position within SEQ ID NO: 3.
Immunoglobulin superfamily · CPC title
containing a localisation/targetting motif · CPC title
containing a signal sequence · CPC title
from tumour cells · CPC title
T-cell receptor (TcR)-CD3 complex · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.