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Engineering a bispecific antibody with a common light chain: Identification and optimization of an anti-CD3 epsilon and anti-GPC3 bispecific antibody, ERY974.
Shiraiwa, Hirotake; Narita, Atsushi; Kamata-Sakurai, Mika; Ishiguro, Takahiro; Sano, Yuji; Hironiwa, Naoka; Tsushima, Takashi; Segawa, Hiroaki; Tsunenari, Toshiaki; Ikeda, Yosuke; Kayukawa, Yoko; Noguchi, Mizuho; Wakabayashi, Tetsuya; Sakamoto, Akihisa; Konishi, Hiroko; Kuramochi, Taichi; Endo, Mika; Hattori, Kunihiro; Nezu, Junichi; Igawa, Tomoyuki.
Afiliación
  • Shiraiwa H; Research Division, Chugai Pharmaceutical Co., Ltd., Gotemba, Shizuoka, Japan. Electronic address: shiraiwahrt@chugai-pharm.co.jp.
  • Narita A; Research Division, Chugai Pharmaceutical Co., Ltd., Gotemba, Shizuoka, Japan.
  • Kamata-Sakurai M; Research Division, Chugai Pharmaceutical Co., Ltd., Gotemba, Shizuoka, Japan.
  • Ishiguro T; Translational Clinical Research Division, Chugai Pharmaceutical Co., Ltd., Chuo-ku, Tokyo, Japan.
  • Sano Y; Research Division, Chugai Pharmaceutical Co., Ltd., Kamakura, Kanagawa, Japan.
  • Hironiwa N; Research Division, Chugai Pharmaceutical Co., Ltd., Gotemba, Shizuoka, Japan.
  • Tsushima T; Chugai Pharmabody Research Pte. Ltd., Biopolis Drive, Singapore.
  • Segawa H; Research Division, Chugai Pharmaceutical Co., Ltd., Gotemba, Shizuoka, Japan.
  • Tsunenari T; Research Division, Chugai Pharmaceutical Co., Ltd., Kamakura, Kanagawa, Japan.
  • Ikeda Y; Chugai Pharma Manufacturing Co., Ltd., Kita-ku, Tokyo, Japan.
  • Kayukawa Y; Research Division, Chugai Pharmaceutical Co., Ltd., Kamakura, Kanagawa, Japan.
  • Noguchi M; Research Division, Chugai Pharmaceutical Co., Ltd., Kamakura, Kanagawa, Japan.
  • Wakabayashi T; Research Division, Chugai Pharmaceutical Co., Ltd., Gotemba, Shizuoka, Japan.
  • Sakamoto A; Research Division, Chugai Pharmaceutical Co., Ltd., Gotemba, Shizuoka, Japan.
  • Konishi H; Research Division, Chugai Pharmaceutical Co., Ltd., Gotemba, Shizuoka, Japan.
  • Kuramochi T; Chugai Pharmabody Research Pte. Ltd., Biopolis Drive, Singapore.
  • Endo M; Research Division, Chugai Pharmaceutical Co., Ltd., Kamakura, Kanagawa, Japan.
  • Hattori K; Research Division, Chugai Pharmaceutical Co., Ltd., Kamakura, Kanagawa, Japan.
  • Nezu J; Research Division, Chugai Pharmaceutical Co., Ltd., Gotemba, Shizuoka, Japan.
  • Igawa T; Chugai Pharmabody Research Pte. Ltd., Biopolis Drive, Singapore.
Methods ; 154: 10-20, 2019 02 01.
Article en En | MEDLINE | ID: mdl-30326272
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Inmunoglobulina G / Ingeniería de Proteínas / Cadenas Ligeras de Inmunoglobulina / Anticuerpos Biespecíficos Tipo de estudio: Diagnostic_studies Límite: Animals / Humans Idioma: En Revista: Methods Asunto de la revista: BIOQUIMICA Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Inmunoglobulina G / Ingeniería de Proteínas / Cadenas Ligeras de Inmunoglobulina / Anticuerpos Biespecíficos Tipo de estudio: Diagnostic_studies Límite: Animals / Humans Idioma: En Revista: Methods Asunto de la revista: BIOQUIMICA Año: 2019 Tipo del documento: Article