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Relationship between Anti-Spike Protein Antibody Titers and SARS-CoV-2 In Vitro Virus Neutralization in Convalescent Plasma.
Salazar, Eric; Kuchipudi, Suresh V; Christensen, Paul A; Eagar, Todd N; Yi, Xin; Zhao, Picheng; Jin, Zhicheng; Long, S Wesley; Olsen, Randall J; Chen, Jian; Castillo, Brian; Leveque, Christopher; Towers, Dalton M; Lavinder, Jason; Gollihar, Jimmy D; Cardona, Jose; Ippolito, Gregory C; Nissly, Ruth H; Bird, Ian M; Greenawalt, Denver; Rossi, Randall M; Gontu, Abinhay; Srinivasan, Sreenidhi; Poojary, Indira B; Cattadori, Isabella M; Hudson, Peter J; Joselyn, Nicole; Prugar, Laura; Huie, Kathleen; Herbert, Andrew; Bernard, David W; Dye, John; Kapur, Vivek; Musser, James M.
Afiliación
  • Salazar E; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.
  • Kuchipudi SV; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York.
  • Christensen PA; Penn State Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, Pennsylvania State University, University Park, Pennsylvania.
  • Eagar TN; Center for Infectious Disease Dynamics, The Pennsylvania State University, University Park, Pennsylvania.
  • Yi X; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.
  • Zhao P; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.
  • Jin Z; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York.
  • Long SW; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.
  • Olsen RJ; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York.
  • Chen J; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.
  • Castillo B; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.
  • Leveque C; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.
  • Towers DM; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York.
  • Lavinder J; Center for Molecular and Translational Human Infectious Diseases, Houston Methodist Research Institute, Houston, Texas.
  • Gollihar JD; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.
  • Cardona J; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York.
  • Ippolito GC; Center for Molecular and Translational Human Infectious Diseases, Houston Methodist Research Institute, Houston, Texas.
  • Nissly RH; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.
  • Bird IM; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York.
  • Greenawalt D; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.
  • Rossi RM; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York.
  • Gontu A; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.
  • Srinivasan S; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York.
  • Poojary IB; Department of Molecular Biosciences, University of Texas at Austin.
  • Cattadori IM; Department of Molecular Biosciences, University of Texas at Austin.
  • Hudson PJ; CCDC Army Research Laboratory-South, University of Texas, Austin, Texas.
  • Joselyn N; CCDC Army Research Laboratory-South, University of Texas, Austin, Texas.
  • Prugar L; Department of Molecular Biosciences, University of Texas at Austin.
  • Huie K; Department of Oncology, Dell Medical School, University of Texas at Austin, Austin, Texas.
  • Herbert A; Penn State Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, Pennsylvania State University, University Park, Pennsylvania.
  • Bernard DW; Penn State Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, Pennsylvania State University, University Park, Pennsylvania.
  • Dye J; Penn State Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, Pennsylvania State University, University Park, Pennsylvania.
  • Kapur V; Huck Institutes of the Life Sciences, Pennsylvania State University, University Park, Pennsylvania.
  • Musser JM; Penn State Animal Diagnostic Laboratory, Department of Veterinary and Biomedical Sciences, Pennsylvania State University, University Park, Pennsylvania.
bioRxiv ; 2020 Jun 09.
Article en En | MEDLINE | ID: mdl-32577662
ABSTRACT
Newly emerged pathogens such as SARS-CoV-2 highlight the urgent need for assays that detect levels of neutralizing antibodies that may be protective. We studied the relationship between anti-spike ectodomain (ECD) and anti-receptor binding domain (RBD) IgG titers, and SARS-CoV-2 virus neutralization (VN) titers generated by two different in vitro assays using convalescent plasma samples obtained from 68 COVID-19 patients, including 13 who donated plasma multiple times. Only 23% (16/68) of donors had been hospitalized. We also studied 16 samples from subjects found to have anti-spike protein IgG during surveillance screening of asymptomatic individuals. We report a strong positive correlation between both plasma anti-RBD and anti-ECD IgG titers, and in vitro VN titer. Anti-RBD plasma IgG correlated slightly better than anti-ECD IgG titer with VN titer. The probability of a VN titer ≥160 was 80% or greater with anti-RBD or anti-ECD titers of ≥11350. Thirty-seven percent (25/68) of convalescent plasma donors lacked VN titers ≥160, the FDA-recommended level for convalescent plasma used for COVID-19 treatment. Dyspnea, hospitalization, and disease severity were significantly associated with higher VN titer. Frequent donation of convalescent plasma did not significantly decrease either VN or IgG titers. Analysis of 2,814 asymptomatic adults found 27 individuals with anti-RBD or anti-ECD IgG titers of ≥11350, and evidence of VN ≥1160. Taken together, 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 titer of ≥11350 may provide critical information about protection against COVID-19 disease.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2020 Tipo del documento: Article