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Comprehensive engineering of a therapeutic neutralizing antibody targeting SARS-CoV-2 spike protein to neutralize escape variants.
Kuramochi, Taichi; Gan, Siok Wan; Ho, Adrian W S; Wang, Bei; Kageji, Nagisa; Nambu, Takeru; Iida, Sayaka; Okuda-Miura, Momoko; Chia, Wei Shan; Yeo, Chiew Ying; Chen, Dan; Lee, Wen-Hsin; Ngoh, Eve Zi Xian; Mohd Salleh, Siti Nazihah; Wang, Cheng-I; Igawa, Tomoyuki; Shimada, Hideaki.
Afiliación
  • Kuramochi T; Discovery Biologics Department, Research Division, Chugai Pharmaceutical Co., Ltd., Kamakura, Kanagawa, Japan.
  • Gan SW; Protein Analysis Unit, Research Division, Chugai Pharmabody Research Pte. Ltd, Singapore.
  • Ho AWS; Protein Analysis Unit, Research Division, Chugai Pharmabody Research Pte. Ltd, Singapore.
  • Wang B; Pharmacology Unit, Research Division, Chugai Pharmabody Research Pte. Ltd, Singapore.
  • Nambu T; Protein Analysis Unit, Research Division, Chugai Pharmabody Research Pte. Ltd, Singapore.
  • Iida S; Pharmacokinetics Unit, Research Division, Chugai Pharmabody Research Pte. Ltd, Singapore.
  • Okuda-Miura M; Protein Analysis Unit, Research Division, Chugai Pharmabody Research Pte. Ltd, Singapore.
  • Chia WS; Pharmacokinetics Unit, Research Division, Chugai Pharmabody Research Pte. Ltd, Singapore.
  • Yeo CY; Protein Analysis Unit, Research Division, Chugai Pharmabody Research Pte. Ltd, Singapore.
  • Chen D; Protein Analysis Unit, Research Division, Chugai Pharmabody Research Pte. Ltd, Singapore.
  • Lee WH; Protein Production Unit, Research Division, Chugai Pharmabody Research Pte. Ltd, Singapore.
  • Ngoh EZX; Protein Analysis Unit, Research Division, Chugai Pharmabody Research Pte. Ltd, Singapore.
  • Mohd Salleh SN; Lead Optimization Unit, Research Division, Chugai Pharmabody Research Pte. Ltd, Singapore.
  • Wang CI; Protein Analysis Unit, Research Division, Chugai Pharmabody Research Pte. Ltd, Singapore.
  • Igawa T; Lead Optimization Unit, Research Division, Chugai Pharmabody Research Pte. Ltd, Singapore.
  • Shimada H; Pharmacology Unit, Research Division, Chugai Pharmabody Research Pte. Ltd, Singapore.
MAbs ; 14(1): 2040350, 2022.
Article en En | MEDLINE | ID: mdl-35293276
ABSTRACT
The emergence of escape variants of SARS-CoV-2 carrying mutations in the spike protein poses a challenge for therapeutic antibodies. Here, we show that through the comprehensive engineering of the variable region of the neutralizing monoclonal antibody 5A6, the engineered antibody, 5A6CCS1, is able to neutralize SARS-CoV-2 variants that escaped neutralization by the original 5A6 antibody. In addition to the improved affinity against variants, 5A6CCS1 was also optimized to achieve high solubility and low viscosity, enabling a high concentration formulation for subcutaneous injection. In cynomolgus monkeys, 5A6CCS1 showed a long plasma half-life and good subcutaneous bioavailability through engineering of the variable and constant region. These data demonstrate that 5A6CCS1 is a promising antibody for development against SARS-CoV-2 and highlight the importance of antibody engineering as a potential method to counteract escape variants.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Glicoproteína de la Espiga del Coronavirus / COVID-19 Límite: Humans Idioma: En Revista: MAbs Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Glicoproteína de la Espiga del Coronavirus / COVID-19 Límite: Humans Idioma: En Revista: MAbs Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Japón