US2017240647A1PendingUtilityA1
Method of modulating the activity of functional immune molecules
Est. expiryApr 9, 2019(expired)· nominal 20-yr term from priority
Inventors:Nobuo HanaiKazuyasu NakamuraEmi HosakaMotoo YamasakiKazuhisa UchidaToyohide ShinkawaSusumu ImabeppuYutaka KandaNaoko YamaneHideharu Anazawa
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-modified1 - 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.Join the waitlist — get patent alerts
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