T cell-antigen coupler with various construct optimizations

US10640562B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10640562-B2
Application numberUS-201916442274-A
CountryUS
Kind codeB2
Filing dateJun 14, 2019
Priority dateJul 17, 2018
Publication dateMay 5, 2020
Grant dateMay 5, 2020

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.

A trifunctional molecule is provided, comprising (i) a target-specific ligand, (ii) a ligand that binds a protein associated with a TCR complex, and (iii) a T cell receptor signaling domain polypeptide. Variants of the molecule are provided, including variants that exhibit optimized surface expression, transduction efficiency, and effector functionality. Variations include, for example, different ligands that bind CD3 epsilon (e.g., OKT3, L2K, F6A, UCHT1 and humanized UCHT1), different signaling domains, and different linkers between domains.

First claim

Opening claim text (preview).

What is claimed is: 1. A nucleic acid sequence encoding a CD19 Trifunctional T cell-antigen coupler (CD19-TAC) comprising: (a) a first polynucleotide encoding a ligand that selectively binds a CD 19 antigen; (b) a second polynucleotide encoding a humanized variant of a UCHT1 (huUCHT1) that binds a CD3 protein associated with a TCR complex on a T cell expressing said CD-19-TAC, wherein the huUCHT1 comprises an amino acid sequence having at least 80% sequence identity with SEQ ID NO: 46 and having an Y to T substitution at position 177 of SEQ ID NO:46 (Y177T); and (c) a third polynucleotide encoding a T cell anchoring co-receptor domain polypeptide comprising a CD4 cytosolic domain and a CD4 transmembrane domain; wherein the ligand encoded by (a), the huUCHT1 encoded by (b), and the polypeptide encoded by (c) are fused directly to each other, or joined by at least one linker. 2. The nucleic acid sequence of claim 1 , wherein the nucleic acid sequence does not encode a co-stimulatory domain, an activation domain, or both a co-stimulatory domain and an activation domain. 3. The nucleic acid sequence of claim 1 , wherein the ligand that selectively binds the CD19 antigen is a single chain variable fragment (scFv). 4. The nucleic acid sequence of claim 1 , wherein the ligand that selectively binds the CD19 antigen comprises an amino acid sequence having at least 80% sequence identity with SEQ ID NO: 36. 5. The nucleic acid sequence of claim 1 , wherein the ligand that selectively binds the CD19 antigen comprises an amino acid sequence of SEQ ID NO: 36. 6. The nucleic acid sequence of claim 1 , wherein the huUCHT1 comprising the Y177T mutation as defined in SEQ ID NO:46 is a single chain antibody. 7. The nucleic acid sequence of claim 1 , wherein the huUCHT1 comprising the Y177T mutation comprises an amino acid sequence of SEQ ID NO: 46. 8. The nucleic acid sequence of claim 1 , wherein the third polynucleotide encodes a polypeptide comprising an amino acid sequence having at least 80% sequence identity with SEQ ID NO: 18. 9. The nucleic acid sequence of claim 1 , wherein the third polynucleotide encodes a polypeptide comprising an amino acid sequence of SEQ ID NO: 18. 10. The nucleic acid sequence of claim 1 , wherein the at least one linker is a G4S flexible linker, a large protein domain, a long helix structure, or a short helix structure. 11. The nucleic acid sequence of claim 1 , wherein the at least one linker comprises an amino acid sequence having at least 80% sequence identity with SEQ ID NO: 12, SEQ ID NO: 32, SEQ ID NO: 30, or SEQ ID NO: 28. 12. The nucleic acid sequence of claim 1 , wherein the at least one linker comprises an amino acid sequence of SEQ ID NO: 12, SEQ ID NO: 32, SEQ ID NO: 30, or SEQ ID NO: 28. 13. The nucleic acid sequence of claim 1 , wherein the CD19-TAC comprises a nucleic acid sequence having at least 80% sequence identity with SEQ ID NO: 63. 14. The nucleic acid sequence of claim 1 , wherein the CD19-TAC comprises an amino acid sequence having at least 80% sequence identity with SEQ ID NO: 64. 15. The nucleic acid sequence of claim 1 , wherein the CD19-TAC comprises a sequence of SEQ ID NO: 63 or SEQ ID NO: 64. 16. A vector construct comprising: (a) a nucleic acid sequence of claim 1 ; and (b) a promoter functional in a mammalian cell. 17. A composition comprising the vector of claim 16 , and an excipient. 18. A polypeptide encoded by the nucleic acid sequence of claim 1 .

Assignees

Inventors

Classifications

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 US10640562B2 cover?
A trifunctional molecule is provided, comprising (i) a target-specific ligand, (ii) a ligand that binds a protein associated with a TCR complex, and (iii) a T cell receptor signaling domain polypeptide. Variants of the molecule are provided, including variants that exhibit optimized surface expression, transduction efficiency, and effector functionality. Variations include, for example, differe…
Who is the assignee on this patent?
Univ Mcmaster
What technology area does this patent fall under?
Primary CPC classification C07K16/2809. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 05 2020 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 3 related publications on this page (citations in our corpus or others sharing the same primary CPC).