Structure-guided antibody cocktail for prevention and treatment of COVID-19

Author:

Su Shih-Chieh,Yang Tzu-Jing,Yu Pei-Yu,Liang Kang-Hao,Chen Wan-Yu,Yang Chun-Wei,Lin Hsiu-Ting,Wang Mei-Jung,Lu Ruei-Min,Tso Hsien-Cheng,Chung Meng-Jhe,Hsieh Tzung-Yang,Chang Yu-Ling,Lin Shin-Chang,Hsu Fang-Yu,Ke Feng-Yi,Wu Yi-Hsuan,Hwang Yu-Chyi,Liu I-Ju,Liang Jian-Jong,Liao Chun-Che,Ko Hui-Ying,Sun Cheng-Pu,Wu Ping-Yi,Jan Jia-Tsrong,Chang Yuan-ChihORCID,Lin Yi-Ling,Tao Mi-Hua,Hsu Shang-Te Danny,Wu Han-ChungORCID

Abstract

Development of effective therapeutics for mitigating the COVID-19 pandemic is a pressing global need. Neutralizing antibodies are known to be effective antivirals, as they can be rapidly deployed to prevent disease progression and can accelerate patient recovery without the need for fully developed host immunity. Here, we report the generation and characterization of a series of chimeric antibodies against the receptor-binding domain (RBD) of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein. Some of these antibodies exhibit exceptionally potent neutralization activities in vitro and in vivo, and the most potent of our antibodies target three distinct non-overlapping epitopes within the RBD. Cryo-electron microscopy analyses of two highly potent antibodies in complex with the SARS-CoV-2 spike protein suggested they may be particularly useful when combined in a cocktail therapy. The efficacy of this antibody cocktail was confirmed in SARS-CoV-2-infected mouse and hamster models as prophylactic and post-infection treatments. With the emergence of more contagious variants of SARS-CoV-2, cocktail antibody therapies hold great promise to control disease and prevent drug resistance.

Funder

Academia Sinica

Ministry of Science and Technology, Taiwan

Publisher

Public Library of Science (PLoS)

Subject

Virology,Genetics,Molecular Biology,Immunology,Microbiology,Parasitology

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