Immunotherapy against several tumors including gastrointestinal and gastric cancer
US-10064913-B2 · Sep 4, 2018 · US
US11939376B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11939376-B2 |
| Application number | US-202017000143-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 21, 2020 |
| Priority date | Aug 17, 2016 |
| Publication date | Mar 26, 2024 |
| Grant date | Mar 26, 2024 |
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The present invention pertains to antigen recognizing constructs against COL6A3 antigens. The invention in particular provides novel T cell receptor (TCR) based molecules which are selective and specific for the tumor expressed antigen COL6A3. The TCR of the invention, and COL6A3 antigen binding fragments derived therefrom, are of use for the diagnosis, treatment and prevention of COL6A3 expressing cancerous diseases. Further provided are nucleic acids encoding the antigen recognizing constructs of the invention, vectors comprising these nucleic acids, recombinant cells expressing the antigen recognizing constructs and pharmaceutical compositions comprising the compounds of the invention.
Opening claim text (preview).
The invention claimed is: 1. A T cell transduced with a nucleic acid encoding an antigen recognizing construct comprising an alpha chain and a beta chain, wherein the alpha chain comprises SEQ ID NO: 13, SEQ ID NO: 14, SEQ ID NO: 15, and the beta chain comprises SEQ ID NO: 19, SEQ ID NO: 20, and SEQ ID NO: 21. 2. The T cell of claim 1 , wherein the alpha chain further comprises an alpha constant domain comprising at least 95% sequence identity to SEQ ID NO: 17 and the beta chain further comprises a beta constant domain comprising at least 95% sequence identity to SEQ ID NO: 23. 3. The T cell of claim 1 , wherein the alpha chain further comprises an alpha constant domain comprising SEQ ID NO: 17 and the beta chain further comprises a beta constant domain comprising SEQ ID NO: 23. 4. The T cell of claim 1 , wherein the alpha chain comprises an alpha variable domain comprising at least 95% sequence identity to SEQ ID NO: 16 and the beta chain comprises a beta variable domain comprising at least 95% sequence identity to SEQ ID NO: 22. 5. The T cell of claim 1 , wherein the alpha chain comprises an alpha variable domain comprising SEQ ID NO: 16 and the beta chain comprises a beta variable domain comprising SEQ ID NO: 22. 6. The T cell of claim 1 , wherein the alpha chain comprises at least 95% sequence identity to SEQ ID NO: 18 and the beta chain comprises at least 95% sequence identity to SEQ ID NO: 24. 7. The T cell of claim 1 , wherein the alpha chain comprises SEQ ID NO: 18 and the beta chain comprises SEQ ID NO: 24. 8. The T cell of claim 1 , wherein the antigen recognizing construct binds to the peptide sequence consisting of SEQ ID NO: 58 in a complex with an MHC class I molecule. 9. The T cell of claim 1 , wherein the antigen recognizing construct comprises the CDR1α chain comprising SEQ ID NO: 13, the CDR2α chain comprising SEQ ID NO: 14, the CDR3α chain comprising SEQ ID NO: 15, the CDR1β chain comprising SEQ ID NO: 19, the CDR2β chain comprising SEQ ID NO: 20, and the CDR3β chain comprising SEQ ID NO: 21. 10. The T cell of claim 9 , wherein the antigen recognizing construct binds to the peptide sequence consisting of SEQ ID NO: 58 in a complex with an MHC class I molecule. 11. The T cell of claim 1 , wherein the antigen recognizing construct comprises the CDR1α chain consisting of SEQ ID NO: 13, the CDR2α chain consisting of SEQ ID NO: 14, the CDR3α chain comprising SEQ ID NO: 15, the CDR1β chain consisting of SEQ ID NO: 19, the CDR2β chain consisting of SEQ ID NO: 20, and the CDR3β chain comprising SEQ ID NO: 21. 12. The T cell of claim 1 , wherein the antigen recognizing construct comprises the CDR1α chain comprising SEQ ID NO: 13, the CDR2α chain consisting of SEQ ID NO: 14, the CDR3α chain comprising SEQ ID NO: 15, the CDR1β chain comprising SEQ ID NO: 19, the CDR2β chain consisting of SEQ ID NO: 20, and the CDR3β chain comprising SEQ ID NO: 21. 13. The T cell of claim 1 , wherein the antigen recognizing construct comprises the CDR1α chain consisting of SEQ ID NO: 13, the CDR2α chain comprising SEQ ID NO: 14, the CDR3α chain consisting of SEQ ID NO: 15, the CDR1β chain consisting of SEQ ID NO: 19, the CDR2β chain comprising SEQ ID NO: 20, and the CDR3β chain consisting of SEQ ID NO: 21. 14. The T cell of claim 1 , wherein the antigen recognizing construct comprises the CDR1α chain consisting of SEQ ID NO: 13, the CDR2α chain consisting of SEQ ID NO: 14, the CDR3α chain consisting of SEQ ID NO: 15, the CDR1β chain consisting of SEQ ID NO: 19, the CDR2β chain consisting of SEQ ID NO: 20, and the CDR3β chain consisting of SEQ ID NO: 21. 15. The T cell of claim 1 , wherein the alpha chain comprises an alpha variable domain comprising at least 90% sequence identity to SEQ ID NO: 16 and wherein the alpha chain comprises the CDR1, CDR2 and CDR3 of SEQ ID NO: 16; and the beta chain comprises a beta variable domain comprising at least 95% sequence identity to SEQ ID NO: 22 and wherein the beta chain comprises the CDR1, CDR2 and CDR3 of SEQ ID NO: 22. 16. The T cell of claim 1 , wherein the antigen recognizing construct specifically binds to a COL6A3-002 peptide-MHC molecule complex, wherein the COL6A3-002 peptide consists of SEQ ID NO:58, and the MHC molecule is an HLA class I molecule. 17. An expression vector comprising the nucleic acid of claim 1 operably linked to at least one promoter sequence. 18. The T cell of claim 1 comprises CD8+ cells. 19. The T cell of claim 1 comprises CD4+ cells. 20. A pharmaceutical composition comprising the T cell of claim 1 .
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