B7-H5, a costimulatory polypeptide

US11760787B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11760787-B2
Application numberUS-201916707719-A
CountryUS
Kind codeB2
Filing dateDec 9, 2019
Priority dateJun 24, 2004
Publication dateSep 19, 2023
Grant dateSep 19, 2023

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.

B7-H5 costimulatory polypeptides, nucleic acids encoding such polypeptides, and methods for using the polypeptides and nucleic acids to enhance a T cell response are provided herein.

First claim

Opening claim text (preview).

What I claim is: 1. A method of suppressing T cell immunity in a subject, said method comprising administering to the subject a composition comprising a fusion protein and a pharmaceutically acceptable carrier, wherein said fusion protein comprises: a first domain that consists of an amino acid sequence encoded by a nucleic acid sequence that encodes a protein consisting of an extracellular region of a protein, wherein the nucleic acid sequence hybridizes over its full length, after a wash at 50° C. to 60° C. in a buffer containing 0.2× SSC and 0.1% SDS, to the complement of a nucleotide sequence consisting of nucleotide 88 to nucleotide 936 of SEQ ID NO:2; and at least one additional domain comprising an amino acid sequence that is unrelated to SEQ ID NO:1. 2. The method of claim 1 , wherein said at least one additional domain is all or part of an immunoglobulin heavy chain constant region. 3. The method of claim 1 , wherein said fusion protein comprises amino acid 40 to amino acid 190 of SEQ ID NO:1. 4. The method of claim 1 , wherein said fusion protein comprises amino acid 35 to amino acid 190 of SEQ ID NO:1. 5. The method of claim 1 , wherein said fusion protein comprises amino acid 30 to amino acid 190 of SEQ ID NO:1. 6. The method of claim 1 , wherein said nucleic acid sequence hybridizes over its full length, after a wash at 50° C. to 60° C. in a buffer containing 0.2× SSC and 0.1% SDS, to the complement of a nucleotide sequence consisting of nucleotide 88 to nucleotide 570 of SEQ ID NO:2. 7. The method of claim 1 , wherein said pharmaceutically acceptable carrier is physiological saline. 8. A method of suppressing T cell immunity in a subject, said method comprising administering to the subject a composition comprising a fusion protein and a pharmaceutically acceptable carrier, wherein said fusion protein comprises: a first domain consisting of a polypeptide that consists of all or part of amino acid 30 to amino acid 311 of SEQ ID NO:1 and includes at least an V-like Ig domain consisting of amino acid 47 to amino acid 150 of SEQ ID NO:1; and at least one additional domain comprising an amino acid sequence that is unrelated to SEQ ID NO:1. 9. The method of claim 8 , wherein said at least one additional domain is all or part of an immunoglobulin heavy chain constant region. 10. The method of claim 8 , wherein said fusion protein comprises amino acid 40 to amino acid 311 of SEQ ID NO: 1. 11. The method of claim 8 , wherein said fusion protein comprises amino acid 35 to amino acid 311 of SEQ ID NO:1. 12. The method of claim 8 , wherein said fusion protein comprises amino acid 30 to amino acid 311 of SEQ ID NO:1. 13. The method of claim 8 , wherein said pharmaceutically acceptable carrier is physiological saline.

Assignees

Inventors

Classifications

  • B7 molecules, e.g. CD80, CD86 · CPC title

  • against receptors, cell surface antigens or cell surface determinants · CPC title

  • Medicinal preparations containing peptides (peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00) · CPC title

  • Drugs for immunological or allergic disorders · CPC title

  • Hybrid immunoglobulins (hybrids of an immunoglobulin with a peptide not being an immunoglobulin C07K19/00) · 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 US11760787B2 cover?
B7-H5 costimulatory polypeptides, nucleic acids encoding such polypeptides, and methods for using the polypeptides and nucleic acids to enhance a T cell response are provided herein.
Who is the assignee on this patent?
Mayo Found Medical Education & Res
What technology area does this patent fall under?
Primary CPC classification C07K14/70532. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 19 2023 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 5 related publications on this page (citations in our corpus or others sharing the same primary CPC).