Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Department of Epidemiology, UNC Chapel Hill School of Public Health, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA.
Science. 2021 Aug 13;373(6556). doi: 10.1126/science.abh1766. Epub 2021 Jul 1.
The emergence of highly transmissible SARS-CoV-2 variants of concern (VOCs) that are resistant to therapeutic antibodies highlights the need for continuing discovery of broadly reactive antibodies. We identified four receptor binding domain-targeting antibodies from three early-outbreak convalescent donors with potent neutralizing activity against 23 variants, including the B.1.1.7, B.1.351, P.1, B.1.429, B.1.526, and B.1.617 VOCs. Two antibodies are ultrapotent, with subnanomolar neutralization titers [half-maximal inhibitory concentration (IC) 0.3 to 11.1 nanograms per milliliter; IC 1.5 to 34.5 nanograms per milliliter). We define the structural and functional determinants of binding for all four VOC-targeting antibodies and show that combinations of two antibodies decrease the in vitro generation of escape mutants, suggesting their potential in mitigating resistance development.
高传染性的 SARS-CoV-2 变异株(VOCs)的出现对治疗性抗体具有耐药性,这凸显了继续发现广谱反应性抗体的必要性。我们从三名早期爆发的恢复期供体中鉴定出四种靶向受体结合域的抗体,这些抗体对 23 种变体具有强大的中和活性,包括 B.1.1.7、B.1.351、P.1、B.1.429、B.1.526 和 B.1.617 VOCs。两种抗体具有超强的效力,其纳米级中和效价(半最大抑制浓度(IC)为 0.3 至 11.1 纳克/毫升;IC 为 1.5 至 34.5 纳克/毫升)。我们定义了所有四种 VOC 靶向抗体的结合结构和功能决定因素,并表明两种抗体的组合可降低体外逃逸突变体的产生,这表明它们在减轻耐药性发展方面具有潜在作用。