Systems and methods for assessing modulators of immune checkpoints
US-2016169869-A1 · Jun 16, 2016 · US
US10501520B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10501520-B2 |
| Application number | US-201715845158-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 18, 2017 |
| Priority date | Jun 24, 2004 |
| Publication date | Dec 10, 2019 |
| Grant date | Dec 10, 2019 |
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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.
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I claim: 1. A composition comprising a fusion protein and a pharmaceutically acceptable carrier, wherein the 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 composition of claim 1 , wherein the at least one additional domain is all or part of an immunoglobulin heavy chain constant region. 3. The composition of claim 1 , wherein said fusion protein comprises amino acid 40 to amino acid 190 of SEQ ID NO:1. 4. The composition of claim 1 , wherein said fusion protein comprises amino acid 35 to amino acid 190 of SEQ ID NO:1. 5. The composition of claim 1 , wherein said fusion protein comprises amino acid 30 to amino acid 190 of SEQ ID NO:1. 6. The composition 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 composition of claim 1 , wherein said pharmaceutically acceptable carrier is physiological saline. 8. 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 composition of claim 8 , wherein said at least one additional domain is all or part of an immunoglobulin heavy chain constant region. 10. The composition of claim 8 , wherein said fusion protein comprises amino acid 40 to amino acid 311 of SEQ ID NO: 1. 11. The composition of claim 8 , wherein said fusion protein comprises amino acid 35 to amino acid 311 of SEQ ID NO:1. 12. The composition of claim 8 , wherein said fusion protein comprises amino acid 30 to amino acid 311 of SEQ ID NO:1. 13. The composition of claim 8 , wherein said pharmaceutically acceptable carrier is physiological saline.
Drugs for immunological or allergic disorders · CPC title
B7 molecules, e.g. CD80, CD86 · CPC title
against material from animals or humans · CPC title
Hybrid immunoglobulins (hybrids of an immunoglobulin with a peptide not being an immunoglobulin C07K19/00) · CPC title
containing domain for protein-protein interaction · CPC title
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