T cell receptors and immune therapy using the same

US11939376B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11939376-B2
Application numberUS-202017000143-A
CountryUS
Kind codeB2
Filing dateAug 21, 2020
Priority dateAug 17, 2016
Publication dateMar 26, 2024
Grant dateMar 26, 2024

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

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.

First claim

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 .

Assignees

Inventors

Classifications

  • Cancer antigens · CPC title

  • T-cell receptors [TCR] · CPC title

  • T-cells, e.g. tumour infiltrating lymphocytes [TIL] or regulatory T [Treg] cells; Lymphokine-activated killer [LAK] cells · CPC title

  • against the immunoglobulin superfamily · CPC title

  • Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US11939376B2 cover?
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 expres…
Who is the assignee on this patent?
Immatics Biotechnologies Gmbh, immatics biotechnology GmbH
What technology area does this patent fall under?
Primary CPC classification C07K16/2803. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Mar 26 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).