US2012034219A1PendingUtilityA1
Uses of il-23 agonists and antagonists; related reagents
Est. expiryMar 10, 2023(expired)· nominal 20-yr term from priority
A61P 35/02A61P 9/14A61P 37/02A61P 35/00A61P 43/00A61P 29/00A61P 1/14A61K 2039/505C07K 14/7155C07K 16/244C07K 14/54A61K 38/00A61K 39/00
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Claims
Abstract
Provided are methods of treatment for tumors. In particular, methods are provided for modulating activity of a cytokine molecule and its receptor.
Claims
exact text as granted — not AI-modified1 . A method of modulating tumor growth comprising contacting a tumor cell with an effective amount of an agonist or antagonist of IL-23.
2 . The method of claim 1 , wherein the antagonist of IL-23 inhibits or prevents tumor growth.
3 . The method of claim 1 , wherein the tumor cell expresses IL-23.
4 . The method of claim 1 , wherein the agonist or antagonist of IL-23 comprises a binding composition that specifically binds a polypeptide or nucleic acid of:
a) p19 (SEQ ID NOs:1, 2, 3, or 4); or b) IL-23R (SEQ ID NOs:5 or 6).
5 . The method of claim 4 , wherein the binding composition comprises:
a) an antigen-binding site of an antibody; b) an extracellular region of IL-23R (SEQ ID NOs:5 or 6); c) a small molecule; d) an anti-sense nucleic acid or small interference RNA (siRNA); or e) a detectable label.
6 . The method of claim 4 , wherein the binding composition comprises:
a) a polyclonal antibody; b) a monoclonal antibody; c) a humanized antibody, or a fragment thereof; d) an Fab, Fv, or F(ab′) 2 fragment; or e) a peptide mimetic of an antibody.
7 . The method of claim 1 , wherein the tumor cell is:
a) a colon cancer cell; b) an ovarian cancer cell; c) a breast cancer cell; or d) a melanoma cell.
8 . A method of treating a subject suffering from a cancer or tumor comprising administering to the subject an effective amount of an agonist or antagonist of IL-23.
9 . The method of claim 8 , wherein the antagonist of IL-23 inhibits:
a) growth of the cancer or tumor; b) cachexia; c) anorexia; or d) angiogenesis.
10 . The method of claim 8 , wherein the antagonist of IL-23 comprises a binding composition that specifically binds a polypeptide or nucleic acid of:
a) p19 (SEQ ID NOs:1, 2, 3, or 4); or b) IL-23R (SEQ ID NOs:5 or 6).
11 . The method of claim 10 , wherein the binding composition comprises:
a) an antigen-binding site of an antibody; b) an extracellular region of IL-23R (SEQ ID NOs:5 or 6); c) an anti-sense nucleic acid or small interference RNA (siRNA); d) a small molecule; or e) a detectable label.
12 . The method of claim 10 , wherein the binding composition comprises:
a) a polyclonal antibody; b) a monoclonal antibody; c) a humanized antibody, or a fragment thereof; d) an Fab, Fv, or F(ab′) 2 fragment; or e) a peptide mimetic of an antibody.
13 . The method of claim 8 , wherein the cancer or tumor is of the:
a) gastrointestinal tract; b) respiratory tract; c) reproductive system; or d) endocrine system.
14 . The method of claim 8 , wherein the cancer or tumor is:
a) colon cancer; b) ovarian cancer; c) a melanoma; or d) breast cancer.
15 . A method of diagnosis of a cancer or tumor comprising contacting a sample from a subject with the binding composition of the method of claim 10 .
16 . The method of claim 15 , wherein the binding composition comprises a nucleic acid probe or primer that specifically binds or hybridizes to the polynucleotide of SEQ ID NOs:1, 2, or 5.
17 . A kit for the diagnosis of a cancer or tumor comprising the binding composition of the method of claim 10 and:
a) a compartment; or
b) instructions for use or disposal.
18 . The kit of claim 17 , wherein the binding composition comprises an antibody that specifically binds to:
a) p19 (SEQ ID NOs:1, 2, 3, or 4); or b) IL-23R (SEQ ID NOs:5 or 6).Cited by (0)
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