Singapore Immunology Network, Agency of Science, Technology and Research, Immunos, Biopolis, Singapore, 138648, Singapore.
Department of Biological Science, National University of Singapore, Singapore, Singapore.
Nat Commun. 2020 Jun 1;11(1):2806. doi: 10.1038/s41467-020-16638-2.
Given the ongoing SARS-CoV-2 pandemic, identification of immunogenic targets against the coronavirus spike glycoprotein will provide crucial advances towards the development of sensitive diagnostic tools and potential vaccine candidate targets. In this study, using pools of overlapping linear B-cell peptides, we report two IgG immunodominant regions on SARS-CoV-2 spike glycoprotein that are recognised by sera from COVID-19 convalescent patients. Notably, one is specific to SARS-CoV-2, which is located in close proximity to the receptor binding domain. The other region, which is localised at the fusion peptide, could potentially function as a pan-SARS target. Functionally, antibody depletion assays demonstrate that antibodies targeting these immunodominant regions significantly alter virus neutralisation capacities. Taken together, identification and validation of these neutralising B-cell epitopes will provide insights towards the design of diagnostics and vaccine candidates against this high priority coronavirus.
鉴于当前 SARS-CoV-2 大流行,鉴定针对冠状病毒刺突糖蛋白的免疫原性靶标将为开发敏感诊断工具和潜在疫苗候选靶标提供重要进展。在这项研究中,我们使用重叠线性 B 细胞肽池,报告了 SARS-CoV-2 刺突糖蛋白上两个 IgG 免疫优势区域,这些区域可被 COVID-19 康复患者的血清识别。值得注意的是,其中一个区域特异性地位于受体结合域附近,是 SARS-CoV-2 所特有的。另一个区域位于融合肽附近,可能作为泛 SARS 靶标发挥作用。功能上,抗体耗竭实验表明,针对这些免疫优势区域的抗体显著改变了病毒中和能力。总之,这些中和 B 细胞表位的鉴定和验证将为针对这种高优先级冠状病毒的诊断和疫苗候选物的设计提供深入了解。