US2011150982A1PendingUtilityA1

Anti-chemokine and associated receptors antibodies for inhibition of growth of neoplasms

Assignee: MOREHOUSE SCHOOL OF MEDICINEPriority: Nov 15, 2002Filed: Jan 26, 2011Published: Jun 23, 2011
Est. expiryNov 15, 2022(expired)· nominal 20-yr term from priority
A61P 35/00A61P 35/02A61P 35/04C07K 16/2866A61K 39/3955C07K 2317/73C07K 16/24
57
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Claims

Abstract

The present invention provides a means of inhibiting the growth and metastasis of cancer cells by administering anti-chemokine antibodies. It is possible to identify the particular chemokines which are over-expressed in the tumor using methods of the invention and administer antibodies against that over-expressed chemokine.

Claims

exact text as granted — not AI-modified
1 - 14 . (canceled) 
     
     
         15 . A method of inhibiting leukemia or myeloma cell growth in a host, comprising:
 administering into said host a leukemia cell growth-inhibiting effective amount or a myeloma cell growth-inhibiting effective amount of a composition comprising:   (1) an anti-CXCL13 antibody, a fragment of an anti-CXCL13 antibody, an anti-CXCR5 antibody, or a fragment of an anti-CXCR5 antibody; and   (2) a pharmaceutically acceptable carrier.   
     
     
         16 . The method of  claim 15 , wherein said anti-CXCL13 antibody or said anti-CXCR5 antibody is a human antibody. 
     
     
         17 . The method of  claim 15 , wherein said anti-CXCL13 antibody or said anti-CXCR5 antibody is a humanized antibody. 
     
     
         18 . The method of  claim 15 , wherein said anti-CXCL13 antibody or said anti-CXCR5 antibody is a chimeric antibody. 
     
     
         19 . The method of  claim 15 , wherein said composition comprises both said anti-CXCL13 antibody and said anti-CXCR5 antibody. 
     
     
         20 . The method of  claim 15 , wherein said pharmaceutically acceptable carrier comprises liposomes. 
     
     
         21 . The method of  claim 15 , wherein said pharmaceutically acceptable carrier comprises microspheres. 
     
     
         22 . The method of  claim 15 , wherein said composition is administered intravenously. 
     
     
         23 . The method of  claim 15 , wherein said composition is administered intramuscularly. 
     
     
         24 . The method of  claim 15 , wherein said anti-CXCL13 antibody, a fragment of an anti-CXCL13 antibody, an anti-CXCR5 antibody, or a fragment of an anti-CXCR5 antibody is administered at a dose range of 0.01-1000 mg/kg/day. 
     
     
         25 . The method of  claim 15 , wherein said anti-CXCL13 antibody or said anti-CXCR5 antibody is administered at a dose range of 0.1-100 mg/kg/day. 
     
     
         26 . The method of  claim 15 , wherein said pharmaceutically acceptable carrier is saline. 
     
     
         27 . The method of  claim 26 , wherein said saline is buffered saline. 
     
     
         28 . The method of  claim 15 , wherein said pharmaceutically acceptable carrier is glucose in saline. 
     
     
         29 . The method of  claim 15 , wherein said composition further comprises an antibody, or a fragment of an antibody, that binds to a chemokine or chemokine receptor selected from the group consisting of CCL1, CCL4, CCL17, CCL19, CCL21, CCL22, CCL25, CXCL12, CCR7, CCR8, CCR9, CXCR4.

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