Starr Tyler N, Greaney Allison J, Addetia Amin, Hannon William W, Choudhary Manish C, Dingens Adam S, Li Jonathan Z, Bloom Jesse D
Basic Sciences and Computational Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98109.
Department of Genome Sciences, University of Washington, Seattle, WA 98109.
bioRxiv. 2020 Dec 1:2020.11.30.405472. doi: 10.1101/2020.11.30.405472.
Antibodies are becoming a frontline therapy for SARS-CoV-2, but the risk of viral evolutionary escape remains unclear. Here we map how all mutations to SARS-CoV-2's receptor-binding domain (RBD) affect binding by the antibodies in Regeneron's REGN-COV2 cocktail and Eli Lilly's LY-CoV016. These complete maps uncover a single amino-acid mutation that fully escapes the REGN-COV2 cocktail, which consists of two antibodies targeting distinct structural epitopes. The maps also identify viral mutations that are selected in a persistently infected patient treated with REGN-COV2, as well as in lab viral escape selections. Finally, the maps reveal that mutations escaping each individual antibody are already present in circulating SARS-CoV-2 strains. Overall, these complete escape maps enable immediate interpretation of the consequences of mutations observed during viral surveillance.
抗体正成为治疗新冠病毒(SARS-CoV-2)的一线疗法,但病毒发生进化逃逸的风险仍不明确。在此,我们绘制了新冠病毒受体结合域(RBD)的所有突变如何影响再生元公司的REGN-COV2鸡尾酒疗法中的抗体以及礼来公司的LY-CoV016的结合情况。这些完整图谱揭示了一个能完全逃逸REGN-COV2鸡尾酒疗法的单氨基酸突变,该疗法由两种靶向不同结构表位的抗体组成。这些图谱还识别出在用REGN-COV2治疗的持续感染患者以及实验室病毒逃逸筛选中所选择的病毒突变。最后,这些图谱显示,逃逸每种单独抗体的突变已存在于正在传播的新冠病毒毒株中。总体而言,这些完整的逃逸图谱能够立即解读病毒监测期间观察到的突变所产生的后果。