| Literature DB >> 30326272 |
Hirotake Shiraiwa1, Atsushi Narita2, Mika Kamata-Sakurai2, Takahiro Ishiguro3, Yuji Sano4, Naoka Hironiwa2, Takashi Tsushima5, Hiroaki Segawa2, Toshiaki Tsunenari4, Yosuke Ikeda6, Yoko Kayukawa4, Mizuho Noguchi4, Tetsuya Wakabayashi2, Akihisa Sakamoto2, Hiroko Konishi2, Taichi Kuramochi5, Mika Endo4, Kunihiro Hattori4, Junichi Nezu2, Tomoyuki Igawa5.
Abstract
The antibody drug market is rapidly expanding, and various antibody engineering technologies are being developed to create antibodies that can provide better benefit to patients. Although bispecific antibody drugs have been researched for more than 30 years, currently only a limited number of bispecific antibodies have achieved regulatory approval. Of the few successful examples of industrially manufacturing a bispecific antibody, the "common light chain format" is an elegant technology that simplifies the purification of a whole IgG-type bispecific antibody. Using this IgG format, the bispecific function can be introduced while maintaining the natural molecular shape of the antibody. In this article, we will first introduce the outline, prospects, and limitations of the common light chain format. Then, we will describe the identification and optimization process for ERY974, an anti-glypican-3 × anti-CD3ε T cell-redirecting bispecific antibody with a common light chain. This format includes one of Chugai's proprietary technologies, termed ART-Ig technology, which consists of a method to identify a common light chain, isoelectric point (pI) engineering to purify the desired bispecific IgG antibody from byproducts, and Fc heterodimerization by an electrostatic steering effect. Furthermore, we describe some tips for de-risking the antibody when engineering a T cell redirecting antibody.Entities:
Keywords: Bispecific antibody engineering; Common light chain; ERY974; T cell redirecting
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Year: 2018 PMID: 30326272 DOI: 10.1016/j.ymeth.2018.10.005
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608