| Literature DB >> 32910806 |
Eric Salazar1,2, Suresh V Kuchipudi3,4, Paul A Christensen1, Todd Eagar1,2, Xin Yi1,2, Picheng Zhao1, Zhicheng Jin1, S Wesley Long1,2,5, Randall J Olsen1,2,5, Jian Chen1,2, Brian Castillo1,2, Christopher Leveque1,2, Dalton Towers6, Jason Lavinder6, Jimmy Gollihar7, Jose Cardona7, Gregory Ippolito6,8, Ruth Nissly3, Ian Bird3, Denver Greenawalt3, Randall M Rossi9, Abhinay Gontu3, Sreenidhi Srinivasan9, Indira Poojary9, Isabella M Cattadori4,5,10, Peter J Hudson4,9,10, Nicole M Josleyn11, Laura Prugar11, Kathleen Huie11, Andrew Herbert11, David W Bernard1,2, John M Dye11, Vivek Kapur4,9,12, James M Musser1,2,5.
Abstract
The newly emerged severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) highlights the urgent need for assays that detect protective levels of neutralizing antibodies. We studied the relationship among anti-spike ectodomain (anti-ECD), anti-receptor-binding domain (anti-RBD) IgG titers, and SARS-CoV-2 virus neutralization (VN) titers generated by 2 in vitro assays using convalescent plasma samples from 68 patients with COVID-19. We report a strong positive correlation between both plasma anti-RBD and anti-ECD IgG titers and in vitro VN titers. The probability of a VN titer of ≥160, the FDA-recommended level for convalescent plasma used for COVID-19 treatment, was ≥80% when anti-RBD or anti-ECD titers were ≥1:1350. Of all donors, 37% lacked VN titers of ≥160. Dyspnea, hospitalization, and disease severity were significantly associated with higher VN titer. Frequent donation of convalescent plasma did not significantly decrease VN or IgG titers. Analysis of 2814 asymptomatic adults found 73 individuals with anti-ECD IgG titers of ≥1:50 and strong positive correlation with anti-RBD and VN titers. Fourteen of these individuals had VN titers of ≥1:160, and all of them had anti-RBD titers of ≥1:1350. We conclude that anti-RBD or anti-ECD IgG titers can serve as a surrogate for VN titers to identify suitable plasma donors. Plasma anti-RBD or anti-ECD titers of ≥1:1350 may provide critical information about protection against COVID-19 disease.Entities:
Keywords: Adaptive immunity; Cellular immune response; Immunology; Infectious disease; Molecular pathology
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Year: 2020 PMID: 32910806 PMCID: PMC7685744 DOI: 10.1172/JCI141206
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808