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

Author:

Kim Cheolmin,Ryu Dong-KyunORCID,Lee JihunORCID,Kim Young-Il,Seo Ji-Min,Kim Yeon-Gil,Jeong Jae-Hee,Kim Minsoo,Kim Jong-In,Kim Pankyeom,Bae Jin SooORCID,Shim Eun Yeong,Lee Min SeobORCID,Kim Man Su,Noh Hanmi,Park Geun-Soo,Park Jae Sang,Son Dain,An Yongjin,Lee Jeong No,Kwon Ki-Sung,Lee Joo-Yeon,Lee Hansaem,Yang Jeong-Sun,Kim Kyung-Chang,Kim Sung Soon,Woo Hye-Min,Kim Jun-Won,Park Man-Seong,Yu Kwang-Min,Kim Se-Mi,Kim Eun-Ha,Park Su-Jin,Jeong Seong Tae,Yu Chi Ho,Song Youngjo,Gu Se Hun,Oh Hanseul,Koo Bon-Sang,Hong Jung Joo,Ryu Choong-Min,Park Wan Beom,Oh Myoung-don,Choi Young KiORCID,Lee Soo-YoungORCID

Abstract

AbstractVaccines 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.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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