Wellcome Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, UK; Chinese Academy of Medical Science (CAMS) Oxford Institute (COI), University of Oxford, Oxford, UK.
Diamond Light Source Ltd., Harwell Science & Innovation Campus, Didcot, UK.
Cell. 2021 Aug 5;184(16):4220-4236.e13. doi: 10.1016/j.cell.2021.06.020. Epub 2021 Jun 17.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has undergone progressive change, with variants conferring advantage rapidly becoming dominant lineages, e.g., B.1.617. With apparent increased transmissibility, variant B.1.617.2 has contributed to the current wave of infection ravaging the Indian subcontinent and has been designated a variant of concern in the United Kingdom. Here we study the ability of monoclonal antibodies and convalescent and vaccine sera to neutralize B.1.617.1 and B.1.617.2, complement this with structural analyses of Fab/receptor binding domain (RBD) complexes, and map the antigenic space of current variants. Neutralization of both viruses is reduced compared with ancestral Wuhan-related strains, but there is no evidence of widespread antibody escape as seen with B.1.351. However, B.1.351 and P.1 sera showed markedly more reduction in neutralization of B.1.617.2, suggesting that individuals infected previously by these variants may be more susceptible to reinfection by B.1.617.2. This observation provides important new insights for immunization policy with future variant vaccines in non-immune populations.
严重急性呼吸综合征冠状病毒 2 型(SARS-CoV-2)不断发生进化,具有优势的变异株迅速成为主要谱系,例如 B.1.617。由于明显增加的传染性,变异株 B.1.617.2 导致了目前席卷印度次大陆的感染浪潮,并在英国被指定为关注变异株。在这里,我们研究了单克隆抗体以及恢复期和疫苗血清中和 B.1.617.1 和 B.1.617.2 的能力,并用 Fab/受体结合域(RBD)复合物的结构分析对此进行补充,并绘制了当前变异株的抗原空间。与原始的武汉相关株相比,两种病毒的中和作用均降低,但没有证据表明像 B.1.351 那样存在广泛的抗体逃逸现象。然而,B.1.351 和 P.1 血清对 B.1.617.2 的中和作用明显降低,这表明先前被这些变异株感染的个体可能更容易被 B.1.617.2 再次感染。这一观察结果为未来在非免疫人群中使用变异疫苗的免疫接种政策提供了重要的新见解。