US2015004170A1PendingUtilityA1

Angiogenic and Immunologic Applications of Anti-CD160 Specific Compounds Obtainable From mAb CL1-R2

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Assignee: INST NAT SANTE RECH MEDPriority: Aug 9, 2004Filed: Jul 8, 2014Published: Jan 1, 2015
Est. expiryAug 9, 2024(expired)· nominal 20-yr term from priority
A61P 37/00A61P 37/08A61P 9/00A61P 43/00A61P 7/00A61P 37/02A61P 9/10A61P 9/12A61P 9/08A61P 3/10A61P 27/02A61P 35/00A61P 29/00A61P 31/04A61P 31/00A61P 19/02A61P 15/00C07K 2317/14A61K 2039/505C07K 16/2836C07K 2317/75C07K 16/2896C07K 16/2803
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Claims

Abstract

The present invention relates to biological and medical applications of an anti-CD160 monoclonal antibody (CL1-R2 CNCM I-3204) and of the conservative equivalents thereof. It more particularly relates to the applications of these anti-CD160 compounds in the fields of EC angiogenesis, and NK and T cytokine production.

Claims

exact text as granted — not AI-modified
1 - 53 . (canceled) 
     
     
         54 . A method for inducing or inhibiting, and/or up- or down-regulating the cytokine production of an individual, comprising administering to said individual an anti-CD160 compound selected from the group consisting of anti-CD160 antibody, anti-CD160 antibody fragment, and anti-CD 160 antibody derivative. 
     
     
         55 . The method according to  claim 54 , wherein said cytokine is selected from the group consisting of IFNγ, TNFα, IL-6, and combinations thereof. 
     
     
         56 . The method according to  claim 54 , wherein administering said anti-CD160 compound is for inducing or inhibiting, and/or up- or down-regulating the adaptive immunity potential of said individual. 
     
     
         57 . The method according to  claim 54 , wherein administering said anti-CD160 compound is for the treatment of an infection. 
     
     
         58 . The method according to  claim 54 , wherein said anti-CD160 compound is comprised in a vaccine composition, or intended as a vaccine adjuvant. 
     
     
         59 . The method according to  claim 54 , wherein administering said anti-CD160 compound is for inducing or inhibiting, and/or up- or down-regulating hematopoiesis in said individual. 
     
     
         60 . The method according to  claim 54 , wherein administering said anti-CD160 compound is for the treatment of irradiated individuals and/or for the treatment or prevention of bone marrow aplasia. 
     
     
         61 . The method according to  claim 54 , wherein administering said anti-CD160 compound is for inducing or inhibiting, and/or up- or down-regulating an inflammatory reaction in said individual. 
     
     
         62 . The method according to  claim 54 , wherein administering said anti-CD160 compound is for the treatment of an allergy in said individual. 
     
     
         63 . The method according to  claim 54 , wherein administering said anti-CD160 compound is for inducing a vasodilatation. 
     
     
         64 . The method according to  claim 54 , wherein said anti-CD160 compound is a soluble compound. 
     
     
         65 . The method according to  claim 54 , wherein said anti-CD160 compound is the anti-CD 160 mAb obtainable from hybridoma CNCM I-3204. 
     
     
         66 . The method according to  claim 64 , wherein said anti-CD160 compound is a conservative fragment of mAb CL1-R2 selected from the group consisting of a Fab, a Fab′, a F(ab)2, a F(ab′)2 or a Fv fragment of said mAb CL1-R2. 
     
     
         67 . The method according to  claim 54 , wherein said anti-CD160 compound is a derivative of mAb CL1-R2 comprising all 6 CDRs of CL1-R2. 
     
     
         68 . The method according to  claim 54 , wherein said anti-CD160 compound is an aggregated compound. 
     
     
         69 . A method for activating natural killer cells, comprising contacting a natural killer cell with an anti-CD160 compound selected from the group consisting of anti-CD160 antibody, anti-CD160 antibody fragment, and anti-CD160 antibody derivative.

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