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Convalescent plasma anti-SARS-CoV-2 spike protein ectodomain and receptor-binding domain IgG correlate with virus neutralization.
Salazar, Eric; Kuchipudi, Suresh V; Christensen, Paul A; Eagar, Todd; Yi, Xin; Zhao, Picheng; Jin, Zhicheng; Long, S Wesley; Olsen, Randall J; Chen, Jian; Castillo, Brian; Leveque, Christopher; Towers, Dalton; Lavinder, Jason; Gollihar, Jimmy; Cardona, Jose; Ippolito, Gregory; Nissly, Ruth; Bird, Ian; Greenawalt, Denver; Rossi, Randall M; Gontu, Abhinay; Srinivasan, Sreenidhi; Poojary, Indira; Cattadori, Isabella M; Hudson, Peter J; Josleyn, Nicole M; Prugar, Laura; Huie, Kathleen; Herbert, Andrew; Bernard, David W; Dye, John M; Kapur, Vivek; Musser, James M.
  • Salazar E; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas, USA.
  • Kuchipudi SV; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York, USA.
  • Christensen PA; Penn State Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, and.
  • Eagar T; Center for Infectious Disease Dynamics, Pennsylvania State University, University Park, Pennsylvania, USA.
  • Yi X; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas, USA.
  • Zhao P; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas, USA.
  • Jin Z; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York, USA.
  • Long SW; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas, USA.
  • Olsen RJ; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York, USA.
  • Chen J; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas, USA.
  • Castillo B; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas, USA.
  • Leveque C; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas, USA.
  • Towers D; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York, USA.
  • Lavinder J; Center for Molecular and Translational Human Infectious Diseases, Houston Methodist Research Institute, Houston, Texas, USA.
  • Gollihar J; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas, USA.
  • Cardona J; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York, USA.
  • Ippolito G; Center for Molecular and Translational Human Infectious Diseases, Houston Methodist Research Institute, Houston, Texas, USA.
  • Nissly R; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas, USA.
  • Bird I; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York, USA.
  • Greenawalt D; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas, USA.
  • Rossi RM; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York, USA.
  • Gontu A; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas, USA.
  • Srinivasan S; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York, USA.
  • Poojary I; Department of Molecular Biosciences, University of Texas at Austin, Austin, Texas, USA.
  • Cattadori IM; Department of Molecular Biosciences, University of Texas at Austin, Austin, Texas, USA.
  • Hudson PJ; Combat Capabilities Development Command Army Research Laboratory - South, University of Texas, Austin, Texas, USA.
  • Josleyn NM; Combat Capabilities Development Command Army Research Laboratory - South, University of Texas, Austin, Texas, USA.
  • Prugar L; Department of Molecular Biosciences, University of Texas at Austin, Austin, Texas, USA.
  • Huie K; Department of Oncology, Dell Medical School, University of Texas at Austin, Austin, Texas, USA.
  • Herbert A; Penn State Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, and.
  • Bernard DW; Penn State Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, and.
  • Dye JM; Penn State Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, and.
  • Kapur V; Huck Institutes of the Life Sciences and.
  • Musser JM; Penn State Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, and.
J Clin Invest ; 130(12): 6728-6738, 2020 12 01.
Article in English | MEDLINE | ID: covidwho-972513
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 ≥11350. 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 ≥150 and strong positive correlation with anti-RBD and VN titers. Fourteen of these individuals had VN titers of ≥1160, and all of them had anti-RBD titers of ≥11350. 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 ≥11350 may provide critical information about protection against COVID-19 disease.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Immunoglobulin G / Antibodies, Neutralizing / SARS-CoV-2 / COVID-19 / Antibodies, Viral Type of study: Prognostic study Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: English Journal: J Clin Invest Year: 2020 Document Type: Article Affiliation country: JCI141206

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Immunoglobulin G / Antibodies, Neutralizing / SARS-CoV-2 / COVID-19 / Antibodies, Viral Type of study: Prognostic study Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: English Journal: J Clin Invest Year: 2020 Document Type: Article Affiliation country: JCI141206