作者
Rita E Chen, Emma S Winkler, James Brett Case, Ishmael D Aziati, Traci L Bricker, Astha Joshi, Tamarand L Darling, Baoling Ying, John M Errico, Swathi Shrihari, Laura A VanBlargan, Xuping Xie, Pavlo Gilchuk, Seth J Zost, Lindsay Droit, Zhuoming Liu, Spencer Stumpf, David Wang, Scott A Handley, W Blaine Stine Jr, Pei-Yong Shi, Meredith E Davis-Gardner, Mehul S Suthar, Miguel Garcia Knight, Raul Andino, Charles Y Chiu, Ali H Ellebedy, Daved H Fremont, Sean PJ Whelan, James E Crowe Jr, Lisa Purcell, Davide Corti, Adrianus CM Boon, Michael S Diamond
发表日期
2021/8/5
期刊
Nature
卷号
596
期号
7870
页码范围
103-108
出版商
Nature Publishing Group UK
简介
Rapidly emerging SARS-CoV-2 variants jeopardize antibody-based countermeasures. Although cell culture experiments have demonstrated a loss of potency of several anti-spike neutralizing antibodies against variant strains of SARS-CoV-2, –, the in vivo importance of these results remains uncertain. Here we report the in vitro and in vivo activity of a panel of monoclonal antibodies (mAbs), which correspond to many in advanced clinical development by Vir Biotechnology, AbbVie, AstraZeneca, Regeneron and Lilly, against SARS-CoV-2 variant viruses. Although some individual mAbs showed reduced or abrogated neutralizing activity in cell culture against B.1.351, B.1.1.28, B.1.617.1 and B.1.526 viruses with mutations at residue E484 of the spike protein, low prophylactic doses of mAb combinations protected against infection by many variants in K18-hACE2 transgenic mice, 129S2 immunocompetent mice and …
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