Center of Excellence for Inflammation, Infectious Disease and Immunity, James H. Quillen College of Medicine, East Tennessee State University, Johnson City, TN, 37614, USA.
Division of Infectious, Inflammatory and Immunologic Diseases, Department of Internal Medicine, Quillen College of Medicine, ETSU, Johnson City, TN, 37614, USA.
Sci Rep. 2021 Mar 10;11(1):5558. doi: 10.1038/s41598-021-84840-3.
The recent COVID-19 pandemic poses a serious threat to global public health, thus there is an urgent need to define the molecular mechanisms involved in SARS-CoV-2 spike (S) protein-mediated virus entry that is essential for preventing and/or treating this emerging infectious disease. In this study, we examined the blocking activity of human COVID-19 convalescent plasma by cell-cell fusion assays using SARS-CoV-2-S-transfected 293 T as effector cells and ACE2-expressing 293 T as target cells. We demonstrate that the SARS-CoV-2 S protein exhibits a very high capacity for membrane fusion and is efficient in mediating virus fusion and entry into target cells. Importantly, we find that COVID-19 convalescent plasma with high titers of IgG neutralizing antibodies can block cell-cell fusion and virus entry by interfering with the SARS-CoV-2-S/ACE2 or SARS-CoV-S/ACE2 interactions. These findings suggest that COVID-19 convalescent plasma may not only inhibit SARS-CoV-2-S but also cross-neutralize SARS-CoV-S-mediated membrane fusion and virus entry, supporting its potential as a preventive and/or therapeutic agent against SARS-CoV-2 as well as other SARS-CoV infections.
最近的 COVID-19 大流行对全球公共卫生构成了严重威胁,因此迫切需要定义 SARS-CoV-2 刺突(S)蛋白介导的病毒进入所涉及的分子机制,这对于预防和/或治疗这种新发传染病至关重要。在这项研究中,我们使用 SARS-CoV-2-S 转染的 293T 作为效应细胞和 ACE2 表达的 293T 作为靶细胞,通过细胞融合试验来检查人 COVID-19 恢复期血浆的阻断活性。我们证明 SARS-CoV-2 S 蛋白具有非常高的膜融合能力,能够有效地介导病毒融合和进入靶细胞。重要的是,我们发现高滴度 IgG 中和抗体的 COVID-19 恢复期血浆可以通过干扰 SARS-CoV-2-S/ACE2 或 SARS-CoV-S/ACE2 相互作用来阻断细胞融合和病毒进入。这些发现表明 COVID-19 恢复期血浆不仅可以抑制 SARS-CoV-2-S,还可以中和 SARS-CoV-S 介导的膜融合和病毒进入,支持其作为预防和/或治疗 SARS-CoV-2 以及其他 SARS-CoV 感染的潜在药物。