Engineering a bispecific antibody with a common light chain: Identification and optimization of an anti-CD3 epsilon and anti-GPC3 bispecific antibody, ERY974

双特异性抗体 免疫球蛋白轻链 抗体 计算生物学 蛋白质工程 计算机科学 化学 单克隆抗体 免疫学 生物 生物化学
作者
Hirotake Shiraiwa,Atsushi Narita,Mika Kamata‐Sakurai,Takahiro Ishiguro,Yuji Sano,Naoka Hironiwa,Takashi Tsushima,Hiroaki Segawa,Toshiaki Tsunenari,Yosuke Ikeda,Yoko Kayukawa,Mizuho Noguchi,Tetsuya Wakabayashi,Akihisa Sakamoto,Hiroko Konishi,Taichi Kuramochi,Mika Endo,Kunihiro Hattori,Jun‐ichi Nezu,Tomoyuki Igawa
出处
期刊:Methods [Elsevier BV]
卷期号:154: 10-20 被引量:52
标识
DOI:10.1016/j.ymeth.2018.10.005
摘要

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.
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