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MG1141A as a Highly Potent Monoclonal Neutralizing Antibody Against SARS-CoV-2 Variantsopen access

Authors
Lee, S.Jang, S.Kang, J.Park, S.B.Han, Y.W.Nam, H.Kim, M.Lee, J.Cho, K.J.Kim, J.Oh, M.Ryu, J.Seok, J.H.Kim, Y.Lee, J.-B.Park, M.-S.Kim, Y.-S.Park, H.Kim, D.-S.
Issue Date
Nov-2021
Publisher
Frontiers Media S.A.
Keywords
MG1141A; monoclonal antibody; outbreak; SARS-CoV-2; spike protein
Citation
Frontiers in Immunology, v.12
Indexed
SCIE
SCOPUS
Journal Title
Frontiers in Immunology
Volume
12
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/62828
DOI
10.3389/fimmu.2021.778829
ISSN
1664-3224
1664-3224
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. Copyright © 2021 Lee, Jang, Kang, Park, Han, Nam, Kim, Lee, Cho, Kim, Oh, Ryu, Seok, Kim, Lee, Park, Kim, Park and Kim.
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1. Basic Science > Department of Microbiology > 1. Journal Articles
4. Research institute > Institute for Viral Diseases > 1. Journal Articles

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