US2003092091A1PendingUtilityA1
Sialoadhesin factor-2 antibodies
Priority: Mar 7, 2000Filed: Aug 29, 2002Published: May 15, 2003
Est. expiryMar 7, 2020(expired)· nominal 20-yr term from priority
Inventors:Julie A. AbrahamsonConnie Erickson-MillerKristine Kay KiklyBruce BochnerRobert SchleimerT. Esra Nutku
A61K 2039/505C07K 16/2803C07K 2317/56C07K 2317/73A61P 35/00
58
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Claims
Abstract
Monoclonal antibodies have been generated that bind to human sialoadhesion factor-2. These antibodies are useful as diagnostic and therapeutic reagents
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . An antibody that binds to human SAF-2.
2 . The antibody of claim 1 wherein the antibody has the identifying characteristics of monoclonal antibody 2C4.
3 . The antibody of claim 2 , wherein the antibody is monoclonal antibody 2C4.
4 . An isolated polypeptide comprising an immunoglobulin complementarity determining region of the antibody of claim 1 .
5 . An isolated polypeptide comprising an immunoglobulin complementarity determining region of the antibody of claim 2 .
6 . An isolated polypeptide comprising an immunoglobulin complementarity determining region of the antibody of claim 3 .
7 . An isolated polynucleotide encoding the polypeptide of claim 4 .
8 . An isolated polynucleotide encoding the polypeptide of claim 5 .
9 . An isolated polynucleotide encoding the polypeptide of claim 6 .
10 . The polypeptide of claim 6 wherein the immunoglobulin complementarity determining region that comprises the polypeptide is set forth in a member of the group consisting of SEQ ID NO:5, 6, 7, 8, 9 and 10.
11 . The polypeptide of claim 10 wherein the immunoglobulin complementarity determining region comprises the polypeptides set forth in SEQ ID NOs:3, 4 and 5.
12 . The polypeptide of claim 10 wherein the immunoglobulin complementarity determining region comprises the polypeptides set forth in SEQ ID NOs:6, 7 and 8.
13 . An isolated polynucleotide encoding the polypeptide of claim 10 .
14 . An isolated polynucleotide encoding the polypeptide of claim 11 .
15 . An isolated polynucleotide encoding thc polypeptide of claim 12 .
16 . The antibody of claim 1 wherein the immunoglobulin complementarity determining region of the antibody comprises the polypeptides set forth in SEQ ID NO:5, 6, 7, 8, 9 and 10.
17 . The antibody of claim 16 comprising a heavy chain variable region polypeptide as set forth in SEQ ID NO:2 and a kappa light chain variable region polypeptide as set forth in SEQ ID NO:4.
18 . An isolated polynucleotide encoding a polypeptide comprising a member selected from the group consisting of SEQ ID NO:2 and SEQ ID NO:4.
19 . A hybridoma cell line that produces a monoclonal antibody having the identifying characteristics the monoclonal antibody 2C4.
20 . A pharmaceutical composition comprising the antibody of claim 1 .
21 . A pharmaceutical composition comprising the antibody of claim 2 .
22 . A pharmaceutical composition comprising the monoclonal antibody of claim 3 .
23 . A method for detecting the presence of a cell in a sample wherein the cell comprises an SAF-2 protein, the method comprising:
a) exposing the sample to an antibody that binds to SAF-2; and b) detecting the antibody that is bound to SAF-2.
24 . The method of claim 23 wherein the sample is treated before exposure to the antibody such that the SAF-2 protein is accessible to binding by the antibody.
25 . The method of claim 23 wherein the cell is a member selected from the group consisting of an eosinophil, a basophil and a mast cell.
26 . The method of claim 23 wherein the antibody has the identifying characteristics of monoclonal antibody 2C4.
27 . The method of claim 26 wherein the antibody is monoclonal antibody 2C4.
28 . A method for altering the function or viability of a cell expressing SAF-2 comprising contacting the cell with a therapeutic agent that binds to SAF-2.
29 . The method of claim 28 wherein the cell is selected from the group consisting of eosinophils, basophils and mast cells.
30 . The method of claim 28 wherein the therapeutic agent is an antibody.
31 . The method of claim 28 wherein contact with the therapeutic agent induces apoptosis of the cell.
32 . A method for preventing or treating a disease or condition mediated by cells expressing SAF-2, the method comprising administering to a subject in need thereof an effective amount of a pharmaceutical composition comprising a therapeutic agent that binds to SAF-2.
33 . The method of claim 32 wherein the disease is an allergic, asthmatic or cancerous disease or a hypereosinophilic syndrome.
34 . The method of claim 33 wherein the disease is a member selected from the group consisting of asthma, allergic rhinitis, atopic dermatitis, chronic urticaria, nasal polyposis, Churg-Strauss Syndrome, allergic bronchopulmonary Aspergillosis or eosinophilic leukemia, eczema, systemic mastocytosis, lymphoma, eosinophilic leukemia and basophilic leukemia.
35 . The method of claim 32 wherein the therapeutic agent is an antibody.
36 . The method of claim 35 wherein the antibody has the identifying characteristics of monoclonal antibody 2C4.
37 . The method of claim 32 wherein the pharmaceutical composition further comprises a cytokine.
38 . The method of claim 37 wherein the cytokine is a member selected from the group consisting of IL-5 and GM-CSF.
39 . A pharmaceutical composition comprising an effective amount of a therapeutic agent that binds to SAF-2.
40 . The pharmaceutical composition of claim 39 wherein the therapeutic agent is an antibody.
41 . The pharmaceutical composition of claim 40 wherein the antibody has the identifying characteristics of monoclonal antibody 2C4.Join the waitlist — get patent alerts
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