中和抗体
病毒
免疫
抗原
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
效价
免疫学
表位
作者
Wilfredo F. García-Beltrán,Evan C. Lam,Kerri J St Denis,Adam Nitido,Zeidy H. Garcia,Blake M. Hauser,Jared Feldman,Maia Pavlovic,David Gregory,Mark C. Poznansky,Alex Sigal,Aaron Schmidt,A. John Iafrate,Vivek Naranbhai,Alejandro B. Balazs
出处
期刊:Cell
[Elsevier]
日期:2021-04-01
卷期号:184 (9): 2372-2383.e9
被引量:1102
标识
DOI:10.1016/j.cell.2021.03.013
摘要
Vaccination elicits immune responses capable of potently neutralizing SARS-CoV-2. However, ongoing surveillance has revealed the emergence of variants harboring mutations in spike, the main target of neutralizing antibodies. To understand the impact of these variants, we evaluated the neutralization potency of 99 individuals that received one or two doses of either BNT162b2 or mRNA-1273 vaccines against pseudoviruses representing 10 globally circulating strains of SARS-CoV-2. Five of the 10 pseudoviruses, harboring receptor-binding domain mutations, including K417N/T, E484K, and N501Y, were highly resistant to neutralization. Cross-neutralization of B.1.351 variants was comparable to SARS-CoV and bat-derived WIV1-CoV, suggesting that a relatively small number of mutations can mediate potent escape from vaccine responses. While the clinical impact of neutralization resistance remains uncertain, these results highlight the potential for variants to escape from neutralizing humoral immunity and emphasize the need to develop broadly protective interventions against the evolving pandemic.
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