US2010278820A1PendingUtilityA1
Reagents that bind ccx-ckr2
Est. expiryApr 21, 2025(expired)· nominal 20-yr term from priority
A61P 35/00A61P 7/00A61P 19/02G01N 33/575C07K 16/2866G01N 2333/715G01N 33/6863G01N 2500/10A61K 39/395
43
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Claims
Abstract
Antibodies that bind to CCX-CKR2 and methods of their use are provided.
Claims
exact text as granted — not AI-modified1 . An antibody that competitively inhibits binding of a competitor antibody to CCX-CKR2, wherein the competitor antibody comprises the complementarity determining region (CDR) of:
SEQ ID NO:12 and SEQ ID NO:14; or SEQ ID NO:16 and SEQ ID NO:18.
2 . The antibody of claim 1 , wherein the antibody is linked to a detectable label.
3 . The antibody of claim 1 , which is a monoclonal antibody.
4 . The antibody of claim 1 , which is a humanized antibody.
5 . A pharmaceutical composition comprising a pharmaceutically acceptable excipient and the antibody of claim 1 .
6 . The pharmaceutical composition of claim 5 , wherein the antibody is a monoclonal antibody.
7 . The pharmaceutical composition of claim 5 , wherein the antibody is a humanized antibody.
8 . The pharmaceutical composition of claim 5 , wherein the antibody comprises the complementarity determining regions (CDRs) of SEQ ID NO:12 and SEQ ID NO:14.
9 . The pharmaceutical composition of claim 5 , wherein the antibody comprises SEQ ID NO:12 and SEQ ID NO:14.
10 . The pharmaceutical composition of claim 5 , wherein the antibody comprises the complementarity determining regions (CDRs) of SEQ ID NO:16 and SEQ ID NO:18.
11 . The pharmaceutical composition of claim 5 , wherein the antibody comprises SEQ ID NO:16 and SEQ ID NO:18.
12 . A method of inhibiting angiogenesis or proliferation of a cancer cell, the method comprising the step of contacting the cell with an antibody of claim 1 .
13 . The method of claim 12 , wherein the cell is in an individual.
14 . The method of claim 13 , wherein the individual has or is pre-disposed to have arthritis.
15 . The method of claim 13 , wherein the individual is not a human.
16 . A method for identifying a modulator of CCX CKR2, comprising:
(a) combining a cell expressing a CCX CKR2 polypeptide or an extract of the cell with a test agent; and (b) conducting an assay to detect whether the test agent competes with a competitor antibody for binding to the CCX CKR2 polypeptide, wherein the competitor antibody comprises the complementarity determining region (CDR) of: SEQ ID NO:12 and SEQ ID NO:14; or SEQ ID NO:16 and SEQ ID NO:18, wherein competition between the competitor antibody and the test agent for binding to the CCX-CKR2 polypeptide is an indication that the test agent is a modulator of CCX CKR2 activity.
17 . A method for testing the efficacy of a test agent that modulates CCX-CKR2 activity, the method comprising,
(a) administering the test reagent to a first animal; (b) administering to a second animal an antibody that competes with a competitor antibody for binding to the CCX CKR2 polypeptide, wherein the competitor antibody comprises the complementarity determining region (CDR) of: SEQ ID NO:12 and SEQ ID NO:14; or SEQ ID NO:16 and SEQ ID NO:18; and (c) comparing the effect of the test reagent on the first animal to the effect of the antibody on the second antibody, thereby determining the efficacy of a test agent.
18 . A polynucleotide encoding SEQ ID NO:12, SEQ ID NO:14, SEQ ID NO:16, or SEQ ID NO:18.
19 . The polynucleotide of claim 18 , wherein the polynucleotide comprises SEQ ID NO:11,SEQ ID NO:13, SEQ ID NO:15, or SEQ ID NO:17.
20 . A method of producing a chimeric antibody, the method comprising operably linking a polynucleotide encoding at least one complementarity determining region (CDR) from SEQ ID NO:12, SEQ ID NO:14, SEQ ID NO:16, or SEQ ID NO:18 to a heterologous polynucleotide encoding at least the framework region of a heavy or light chain of an antibody, to form a fusion polynucleotide encoding a chimeric heavy or light chain of an antibody; and
expressing a chimeric heavy or light chain from the fusion polynucleotide.Join the waitlist — get patent alerts
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