B7-H5, a costimulatory polypeptide
US-10501520-B2 · Dec 10, 2019 · US
US11760787B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11760787-B2 |
| Application number | US-201916707719-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 9, 2019 |
| Priority date | Jun 24, 2004 |
| Publication date | Sep 19, 2023 |
| Grant date | Sep 19, 2023 |
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.
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.
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.
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
Related publications grouped by family.
Answers are generated from the same data shown on this page.