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

Cheolmin KimDong-Kyun RyuJihun LeeYoung-Il KimJi-Min SeoYeon-Gil KimJae-Hee JeongMinsoo KimJong-In KimPankyeom KimJin Soo BaeEun Yeong ShimMin Seob LeeMan Su KimHanmi NohGeun-Soo ParkJae Sang ParkDain SonYongjin AnJeong No LeeKi-Sung KwonJoo-Yeon LeeHansaem LeeJeong-Sun YangKyung-Chang KimSung Soon KimHye-Min WooJun-Won KimMan-Seong ParkKwang-Min YuSe-Mi KimEun-Ha KimSu-Jin ParkSeong Tae JeongChi Ho YuYoungjo SongSe Hun GuHanseul OhBon-Sang KooJung Joo HongChoong-Min RyuWan Beom ParkMyoung-Don OhDavid Hyunjung ChungSoo-Young Lee
Published in: Nature communications (2021)
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.
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