US2011262390A1PendingUtilityA1
Composition and method for treating inflammatory disorders
Est. expiryApr 28, 2019(expired)· nominal 20-yr term from priority
A61P 37/00C07K 16/244C07K 14/5428A61K 2039/505C12N 2799/022A61P 29/00C07K 14/54C07K 2317/76A61K 38/20
58
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Claims
Abstract
Inhibitors of IL-22 are disclosed as well as pharmaceutical compositions and methods of using same. The inhibitors include IL-22 antibodies and are useful for treating inflammatory disorders.
Claims
exact text as granted — not AI-modified1 - 33 . (canceled)
34 . A method of treating an IL-22 related disorder comprising administering an IL-22 agonist in an amount effective to
(1) modulate an IL-22 signal transduction pathway; (2) modulate proinflammatory cytokine production; (3) modulate lymphokine production and/or secretion; (4) modulate production of adhesion molecules and/or cellular adhesion; (5) modulate expression or activity of nuclear transcription factors; (6) modulate secretion of IL-1; (7) compete with receptors for other cytokines; (8) compete with another IL-22 family member protein for binding to a IL-22 receptor; (9) modulate nuclear translocation of internalized IL-22 receptor; (10) modulate cellular immune responses; (11) modulate acute phase protein synthesis by hepatocytes, fever, or prostaglandin synthesis; and/or (12) promote and/or potentiate wound healing.
35 . A method of protecting gut tissue in a patient comprising administering an effective amount IL-22 agonist to the patient.
36 . The method of claim 34 or 35 , wherein the IL-22 agonist is selected from the group consisting of human IL-22 protein; fragments, deletion mutants and addition mutants of human IL-22 protein; and peptide and small molecule compounds that interact with the receptor or other target to which human IL-22 is directed.
37 . The method of claim 34 or 35 , wherein the IL-22 agonist is human IL-22 protein.
38 . The method of claim 37 , wherein the human IL-22 protein comprises amino acids 1-179 of SEQ ID NO:2.Join the waitlist — get patent alerts
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