US2010266499A1PendingUtilityA1
Cytokine receptor zcytor17 multimers
Est. expiryJan 18, 2022(expired)· nominal 20-yr term from priority
Inventors:Cindy A. SprecherZeren GaoJoseph L. KuijperMaria M. DasovichFrancis J. GrantScott R. PresnellTheodore E. WhitmoreAngela K. HammondJulia E. NovakJane A. GrossStacey R. Dillon
A61P 37/06A61P 39/02A61P 43/00A61P 37/08A61P 37/00A61P 31/04A61P 29/00A61P 31/00A61P 35/00A61P 13/08A61P 11/06A61P 11/00A61P 17/06A61P 1/02A61P 19/02A61P 1/18A61P 1/04A61P 17/04A61P 15/00A61P 1/16A61P 17/00C07K 14/715C07K 16/2866A01K 2217/05A61K 38/00C07K 2317/76C07K 2317/24C07K 14/52
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Abstract
Novel polypeptide combinations, polynucleotides encoding the polypeptides, and related compositions and methods are disclosed for zcytor17-containing multimeric or heterodimer cytokine receptors that may be used as novel cytokine antagonists, and within methods for detecting ligands that stimulate the proliferation and/or development of hematopoietic, lymphoid and myeloid cells in vitro and in vivo. The present invention also includes methods for producing the multimeric or heterodimeric cytokine receptor, uses therefor and antibodies thereto.
Claims
exact text as granted — not AI-modified1 . A method of reducing zcytor17lig-induced inflammation in a mammal suffering from an inflammatory disease comprising administering to the mammal an effective amount of a composition comprising a soluble receptor polypeptide comprising amino acid residues 20-519 of SEQ ID NO:111, wherein the soluble receptor polypeptide forms a heterodimeric or multimeric soluble receptor polypeptide with a second soluble receptor polypeptide comprising amino acid residues 28-739 of SEQ ID NO:7; and a pharmaceutically acceptable vehicle, wherein after administration the inflammation is reduced.
2 . The method of claim 1 wherein the heterodimeric or multimeric soluble receptor polypeptide is fused to an immunoglobulin heavy chain constant region.
3 . The method of claim 2 wherein the immunoglobulin heavy chain constant region is an F c fragment.
4 . The method of claim 1 wherein the inflammatory disease is a chronic inflammatory disease.
5 . The method of claim 4 wherein the chronic inflammatory disease is selected from the group consisting of inflammatory bowel disease, ulcerative colitis, Crohn's disease, atopic dermatitis, and eczema.
6 . The method of claim 1 wherein the inflammatory disease is an acute inflammatory disease.
7 . The method of claim 6 wherein the acute inflammatory disease is selected from the group consisting of endotoxemia, septicemia, and toxic shock syndrome.
8 . The method of claim 1 wherein the heterodimeric or multimeric soluble receptor polypeptide further comprises a radionuclide, enzyme, substrate, cofactor, fluorescent marker, chemiluminescent marker, peptide tag, magnetic particle, drug, or toxin.Cited by (0)
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