US2017240647A1PendingUtilityA1

Method of modulating the activity of functional immune molecules

Assignee: KYOWA HAKKO KIRIN CO LTDPriority: Apr 9, 1999Filed: Mar 16, 2017Published: Aug 24, 2017
Est. expiryApr 9, 2019(expired)· nominal 20-yr term from priority
A61P 37/06A61P 9/00A61P 37/00A61P 37/08A61P 31/00A61P 29/00A61P 35/00C07K 16/3084G01N 33/53C07K 2317/732C07K 2317/565C12P 21/005C07K 2317/21A61K 2039/505C07K 16/30C07K 2317/52C07K 2317/41C07K 2317/73C07K 2317/24C07K 2319/00C07K 16/2866
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Claims

Abstract

The invention relates to a method for controlling the activity of an immunologically functional molecule, such as an antibody, a protein, a peptide or the like, an agent of promoting the activity of an immunologically functional molecule, and an immunologically functional molecule having the promoted activity.

Claims

exact text as granted — not AI-modified
1 - 4 . (canceled) 
     
     
         5 . A method for producing an antibody composition, said method comprising:
 (1) introducing a vector comprising a nucleotide sequence encoding an antibody into a host cell;   (2) culturing the antibody-producing host cell; and   (3) recovering the antibody from the culture supernatant,   wherein said antibody composition comprises antibody molecules having complex-type and/or hybrid-type N-glycoside-linked sugar chain in a Fc region, wherein all of said antibody molecules have two N-glycoside-linked sugar chains in which fucose is not bound (F0).   
     
     
         6 . The method according to  claim 5 , wherein said antibody molecules comprise N-glycoside-linked sugar chains in which at least one N-acetylglucosamine is bound to a mannose at the non-reducing end of the following structure: 
       
         
           
           
               
               
           
         
       
     
     
         7 . The method according to  claim 5 , wherein said antibody molecules comprise the complex-type N-glycoside-linked sugar chains in which two N-acetylglucosamine are respectively bound to two mannoses at the non-reducing end of the following structure: 
       
         
           
           
               
               
           
         
       
     
     
         8 . The method according to  claim 5 , wherein said antibody molecules have an increased antibody dependent cellular cytotoxicity (ADCC). 
     
     
         9 . The method according to  claim 5 , wherein said antibody molecules are molecules of a human antibody, a humanized antibody, a chimeric antibody or a human CDR-grafted antibody. 
     
     
         10 . The method according to  claim 5 , wherein said antibody molecules are molecules of an IgG class antibody.

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