US2019360015A1PendingUtilityA1

Antibody composition-producing cell

Assignee: KYOWA HAKKO KIRIN CO LTDPriority: Oct 6, 2000Filed: Jan 29, 2019Published: Nov 28, 2019
Est. expiryOct 6, 2020(expired)· nominal 20-yr term from priority
A61P 37/08A61P 37/02A61P 37/00A61P 29/00A61P 31/04A61P 31/12A61P 35/00C07K 16/1145C07K 16/2896C07K 2317/565C07K 2317/732C12N 15/8258C07K 16/44C07K 16/2812C12N 9/1051C12P 21/005C12Y 204/01068C07K 16/3084C07K 16/2866C07K 16/32C07K 16/2863C12N 15/8257C12N 15/8245C07K 2317/41C12N 9/90C07K 2319/30C07K 16/2887C07K 16/18C12N 9/0006C07K 2317/24C07K 16/241C12P 21/00C07K 16/1063
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Claims

Abstract

The present invention relates to a cell for the production of an antibody molecule such as an antibody useful for various diseases having high antibody-dependent cell-mediated cytotoxic activity, a fragment of the antibody and a fusion protein having the Fc region of the antibody or the like, a method for producing an antibody composition using the cell, the antibody composition and use thereof.

Claims

exact text as granted — not AI-modified
1 . A method of producing an antibody composition which comprises antibody molecules, wherein said method comprises culturing a mammalian cell that produces an antibody molecule, said mammalian cell having a decrease in, or an absence of, α1,6-fucosyltransferase activity,
 wherein said decrease in, or absence of, α1,6-fucosyltransferase activity results from deleting a gene encoding α1,6-fucosyltransferase, or from mutating said gene to reduce or eliminate the α1,6-fucosyltransferase activity. 
 
     
     
         2 . The method of  claim 1 , wherein said antibody molecule has an Fc region comprising two complex-type and/or hybrid-type N-glycoside-linked sugar chains bound to the Fc region, wherein said sugar chains comprise a reducing terminal which contains an N-acetylglucosamine, and wherein at least one of said sugar chains does not contain fucose bound to the 6-position of the N-acetylglucosamine in the reducing terminal of the sugar chain. 
     
     
         3 . The method of  claim 1 , wherein at least 80% of the antibody molecules produced by said cell are non-fucosylated antibody molecules. 
     
     
         4 . The method of  claim 3 , wherein the antibody molecules in said composition consist essentially of the non-fucosylated antibody molecules. 
     
     
         5 . The method of  claim 3 , wherein the antibody molecules in said composition consist of the non-fucosylated antibody molecules. 
     
     
         6 - 22 . (canceled) 
     
     
         23 . An antibody composition which comprises an antibody molecule, wherein said antibody molecule has an Fc region comprising two complex-type and/or hybrid-type N-glycoside-linked sugar chains bound to the Fc region, wherein said sugar chains comprise a reducing terminal which contains an N-acetylglucosamine, and wherein at least one of said sugar chains does not contain fucose bound to the 6-position of the N-acetylglucosamine in the reducing terminal of the sugar chain. 
     
     
         24 . A mammalian cell that has a decrease in, or an absence of, α1,6-fucosyltransferase activity, wherein said decrease in, or absence of, α1,6-fucosyltransferase activity is caused by deletion of a gene encoding α1,6-fucosyltransferase, or a mutation of said gene that reduces or eliminates the α1,6-fucosyltransferase activity. 
     
     
         25 . A method of treating a cancer, comprising administering the composition of  claim 23  to a subject in need thereof.

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