| Literature DB >> 33692386 |
Ling Wang1,2, Juan Zhao1,2, Lam N T Nguyen1,2, James L Adkins1, Madison Schank1,2, Sushant Khanal1,2, Lam N Nguyen1,2, Xindi Dang1,2, Dechao Cao1,2, Bal Krishna Chand Thakuri1,2, Zeyuan Lu1, Jinyu Zhang1,2, Yi Zhang1, Xiao Y Wu1,2, Mohamed El Gazzar1,2, Shunbin Ning1,2, Jonathan P Moorman1,2,3, Zhi Q Yao4,5,6.
Abstract
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.Entities:
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Year: 2021 PMID: 33692386 PMCID: PMC7946952 DOI: 10.1038/s41598-021-84840-3
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379