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MG1141A as a Highly Potent Monoclonal Neutralizing Antibody Against SARS-CoV-2 Variants.
Lee, Sua; Jang, Shina; Kang, Jihoon; Park, Soo Bin; Han, Young Woo; Nam, Hyemi; Kim, Munkyung; Lee, Jeewon; Cho, Ki Joon; Kim, Jeonghun; Oh, Miyoung; Ryu, Jihye; Seok, Jong Hyeon; Kim, Yunhwa; Lee, Jee-Boong; Park, Man-Seong; Kim, Yong-Sung; Park, Hosun; Kim, Dong-Sik.
Afiliación
  • Lee S; Department of Protein Engineering, Mogam Institute for Biomedical Research, Yongin, South Korea.
  • Jang S; Department of Protein Engineering, Mogam Institute for Biomedical Research, Yongin, South Korea.
  • Kang J; Department of Protein Engineering, Mogam Institute for Biomedical Research, Yongin, South Korea.
  • Park SB; Department of Protein Engineering, Mogam Institute for Biomedical Research, Yongin, South Korea.
  • Han YW; Department of Infectious Disease Research, Mogam Institute for Biomedical Research, Yongin, South Korea.
  • Nam H; Department of Target ID & Assay Development, Mogam Institute for Biomedical Research, Yongin, South Korea.
  • Kim M; Department of Target ID & Assay Development, Mogam Institute for Biomedical Research, Yongin, South Korea.
  • Lee J; Department of Target ID & Assay Development, Mogam Institute for Biomedical Research, Yongin, South Korea.
  • Cho KJ; Department of Protein Engineering, Mogam Institute for Biomedical Research, Yongin, South Korea.
  • Kim J; Department of Microbiology, Institute for Viral Diseases, Korea University College of Medicine, Seoul, South Korea.
  • Oh M; Department of Protein Engineering, Mogam Institute for Biomedical Research, Yongin, South Korea.
  • Ryu J; Department of Translational Research, Mogam Institute for Biomedical Research, Yongin, South Korea.
  • Seok JH; Department of Microbiology, Institute for Viral Diseases, Korea University College of Medicine, Seoul, South Korea.
  • Kim Y; Department of Microbiology, College of Medicine, Yeungnam University, Daegu, South Korea.
  • Lee JB; Department of Target ID & Assay Development, Mogam Institute for Biomedical Research, Yongin, South Korea.
  • Park MS; Department of Microbiology, Institute for Viral Diseases, Korea University College of Medicine, Seoul, South Korea.
  • Kim YS; Department of Molecular Science and Technology, Ajou University, Suwon, South Korea.
  • Park H; Department of Microbiology, College of Medicine, Yeungnam University, Daegu, South Korea.
  • Kim DS; Department of Protein Engineering, Mogam Institute for Biomedical Research, Yongin, South Korea.
Front Immunol ; 12: 778829, 2021.
Article en En | MEDLINE | ID: mdl-34868052
ABSTRACT
Since the coronavirus disease outbreak in 2019, several antibody therapeutics have been developed to treat severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections. Antibody therapeutics are effective in neutralizing the virus and reducing hospitalization in patients with mild and moderate infections. These therapeutics target the spike protein of SARS-CoV-2; however, emerging mutations in this protein reduce their efficiency. In this study, we developed a universal SARS-CoV-2 neutralizing antibody. We generated a humanized monoclonal antibody, MG1141A, against the receptor-binding domain of the spike protein through traditional mouse immunization. We confirmed that MG1141A could effectively neutralize live viruses, with an EC50 of 92 pM, and that it exhibited effective Fc-mediated functions. Additionally, it retained its neutralizing activity against the alpha (UK), beta (South Africa), and gamma (Brazil) variants of SARS-CoV-2. Taken together, our study contributes to the development of a novel antibody therapeutic approach, which can effectively combat emerging SARS-CoV-2 mutations.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anticuerpos Neutralizantes / SARS-CoV-2 / COVID-19 / Anticuerpos Monoclonales / Anticuerpos Antivirales Límite: Animals / Humans Idioma: En Revista: Front Immunol Año: 2021 Tipo del documento: Article País de afiliación: Corea del Sur

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anticuerpos Neutralizantes / SARS-CoV-2 / COVID-19 / Anticuerpos Monoclonales / Anticuerpos Antivirales Límite: Animals / Humans Idioma: En Revista: Front Immunol Año: 2021 Tipo del documento: Article País de afiliación: Corea del Sur