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Structure-guided antibody cocktail for prevention and treatment of COVID-19
Authors:Shih-Chieh Su  Tzu-Jing Yang  Pei-Yu Yu  Kang-Hao Liang  Wan-Yu Chen  Chun-Wei Yang  Hsiu-Ting Lin  Mei-Jung Wang  Ruei-Min Lu  Hsien-Cheng Tso  Meng-Jhe Chung  Tzung-Yang Hsieh  Yu-Ling Chang  Shin-Chang Lin  Fang-Yu Hsu  Feng-Yi Ke  Yi-Hsuan Wu  Yu-Chyi Hwang  I-Ju Liu  Jian-Jong Liang  Chun-Che Liao  Hui-Ying Ko  Cheng-Pu Sun  Ping-Yi Wu  Jia-Tsrong Jan  Yuan-Chih Chang  Yi-Ling Lin  Mi-Hua Tao  Shang-Te Danny Hsu  Han-Chung Wu
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.
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