| Literature DB >> 20073128 |
Zhiqiang An1, Gail Forrest, Renee Moore, Michael Cukan, Peter Haytko, Lingyi Huang, Salvatore Vitelli, Jing Zhang Zhao, Ping Lu, Jin Hua, Christopher R Gibson, Barrett R Harvey, Donna Montgomery, Dennis Zaller, Fubao Wang, William Strohl.
Abstract
The Fc region of an antibody mediates effector functions such as antibody-dependent cell-mediated cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC), and plays a key role in the in vivo half-life of an antibody. In designing antibody therapeutics, it is sometimes desirable that the antibody has altered Fc-mediated properties. In the case of a "benign blocker" antibody, it is often desirable to diminish or abolish the ADCC and CDC functions while retaining its PK profile. Here, we report a novel engineered IgG isotype, IgG2m4, with reduced Fc functionality. IgG2m4 is based on the IgG2 isotype with four key amino acid residue changes derived from IgG4 (H268Q, V309L, A330S and P331S). An IgG2m4 antibody has an overall reduction in complement and Fc gamma receptor binding in in vitro binding analyses while maintaining the normal in vivo serum half-life in rhesus.Entities:
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Year: 2009 PMID: 20073128 PMCID: PMC2791314 DOI: 10.4161/mabs.1.6.10185
Source DB: PubMed Journal: MAbs ISSN: 1942-0862 Impact factor: 5.857