Institute of Immunity and Transplantation, Division of Infection and Immunity, University College London, London NW3 2PF, UK.
Advanced Pathogens Diagnostic Unit, Department of Clinical Virology, University College London Hospitals NHS Foundation Trust, London W1T 4EU, UK.
Cell Rep. 2021 Mar 23;34(12):108890. doi: 10.1016/j.celrep.2021.108890. Epub 2021 Mar 6.
Multiple severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines show protective efficacy, which is most likely mediated by neutralizing antibodies recognizing the viral entry protein, spike. Because new SARS-CoV-2 variants are emerging rapidly, as exemplified by the B.1.1.7, B.1.351, and P.1 lineages, it is critical to understand whether antibody responses induced by infection with the original SARS-CoV-2 virus or current vaccines remain effective. In this study, we evaluate neutralization of a series of mutated spike pseudotypes based on divergence from SARS-CoV and then compare neutralization of the B.1.1.7 spike pseudotype and individual mutations. Spike-specific monoclonal antibody neutralization is reduced dramatically; in contrast, polyclonal antibodies from individuals infected in early 2020 remain active against most mutated spike pseudotypes, but potency is reduced in a minority of samples. This work highlights that changes in SARS-CoV-2 spike can alter neutralization sensitivity and underlines the need for effective real-time monitoring of emerging mutations and their effect on vaccine efficacy.
多种严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 疫苗显示出保护效力,这很可能是由识别病毒进入蛋白(刺突)的中和抗体介导的。由于新的 SARS-CoV-2 变体(如 B.1.1.7、B.1.351 和 P.1 谱系)正在迅速出现,因此了解感染原始 SARS-CoV-2 病毒或当前疫苗所诱导的抗体反应是否仍然有效至关重要。在这项研究中,我们评估了一系列基于与 SARS-CoV 差异的突变刺突假型的中和作用,然后比较了 B.1.1.7 刺突假型和单个突变的中和作用。刺突特异性单克隆抗体的中和作用显著降低;相比之下,2020 年初感染的个体的多克隆抗体仍然对大多数突变的刺突假型有效,但在少数样本中效力降低。这项工作强调了 SARS-CoV-2 刺突的变化会改变中和敏感性,并强调需要有效实时监测新出现的突变及其对疫苗效力的影响。