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A therapeutic neutralizing antibody targeting receptor binding domain of SARS-CoV-2 spike protein

Authors
Kim, C.Ryu, D.-K.Lee, J.Kim, Y.-I.Seo, J.-M.Kim, Y.-G.Jeong, J.-H.Kim, M.Kim, J.-I.Kim, P.Bae, J.S.Shim, E.Y.Lee, M.S.Kim, M.S.Noh, H.Park, G.-S.Park, J.S.Son, D.An, Y.Lee, J.N.Kwon, K.-S.Lee, J.-Y.Lee, H.Yang, J.-S.Kim, K.-C.Kim, S.S.Woo, H.-M.Kim, J.-W.Park, M.-S.Yu, K.-M.Kim, S.-M.Kim, E.-H.Park, S.-J.Jeong, S.T.Yu, C.H.Song, Y.Gu, S.H.Oh, H.Koo, B.-S.Hong, J.J.Ryu, C.-M.Park, W.B.Oh, M.-D.Choi, Y.K.Lee, S.-Y.
Issue Date
12-1월-2021
Publisher
Nature Research
Citation
Nature Communications, v.12, no.1
Indexed
SCIE
SCOPUS
Journal Title
Nature Communications
Volume
12
Number
1
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/129386
DOI
10.1038/s41467-020-20602-5
ISSN
2041-1723
Abstract
Vaccines and therapeutics are urgently needed for the pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Here, we screen human monoclonal antibodies (mAb) targeting the receptor binding domain (RBD) of the viral spike protein via antibody library constructed from peripheral blood mononuclear cells of a convalescent patient. The CT-P59 mAb potently neutralizes SARS-CoV-2 isolates including the D614G variant without antibody-dependent enhancement effect. Complex crystal structure of CT-P59 Fab/RBD shows that CT-P59 blocks interaction regions of RBD for angiotensin converting enzyme 2 (ACE2) receptor with an orientation that is notably different from previously reported RBD-targeting mAbs. Furthermore, therapeutic effects of CT-P59 are evaluated in three animal models (ferret, hamster, and rhesus monkey), demonstrating a substantial reduction in viral titer along with alleviation of clinical symptoms. Therefore, CT-P59 may be a promising therapeutic candidate for COVID-19. © 2021, The Author(s).
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