作者
Alexandra Schäfer, Frauke Muecksch, Julio CC Lorenzi, Sarah R Leist, Melissa Cipolla, Stylianos Bournazos, Fabian Schmidt, Rachel M Maison, Anna Gazumyan, David R Martinez, Ralph S Baric, Davide F Robbiani, Theodora Hatziioannou, Jeffrey V Ravetch, Paul D Bieniasz, Richard A Bowen, Michel C Nussenzweig, Timothy P Sheahan
发表日期
2020/11/19
期刊
Journal of Experimental Medicine
卷号
218
期号
3
页码范围
e20201993
出版商
Rockefeller University Press
简介
SARS-CoV-2, the causative agent of COVID-19, has been responsible for over 42 million infections and 1 million deaths since its emergence in December 2019. There are few therapeutic options and no approved vaccines. Here, we examine the properties of highly potent human monoclonal antibodies (hu-mAbs) in a Syrian hamster model of SARS-CoV-2 and in a mouse-adapted model of SARS-CoV-2 infection (SARS-CoV-2 MA). Antibody combinations were effective for prevention and in therapy when administered early. However, in vitro antibody neutralization potency did not uniformly correlate with in vivo protection, and some hu-mAbs were more protective in combination in vivo. Analysis of antibody Fc regions revealed that binding to activating Fc receptors contributes to optimal protection against SARS-CoV-2 MA. The data indicate that intact effector function can affect hu-mAb …
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