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Sex, age, and hospitalization drive antibody responses in a COVID-19 convalescent plasma donor population.
Klein, Sabra L; Pekosz, Andrew; Park, Han-Sol; Ursin, Rebecca L; Shapiro, Janna R; Benner, Sarah E; Littlefield, Kirsten; Kumar, Swetha; Naik, Harnish Mukesh; Betenbaugh, Michael J; Shrestha, Ruchee; Wu, Annie A; Hughes, Robert M; Burgess, Imani; Caturegli, Patricio; Laeyendecker, Oliver; Quinn, Thomas C; Sullivan, David; Shoham, Shmuel; Redd, Andrew D; Bloch, Evan M; Casadevall, Arturo; Tobian, Aaron Ar.
  • Klein SL; W. Harry Feinstone Department of Molecular Microbiology and Immunology.
  • Pekosz A; Department of Biochemistry and Molecular Biology.
  • Park HS; Department of International Health, and.
  • Ursin RL; W. Harry Feinstone Department of Molecular Microbiology and Immunology.
  • Shapiro JR; Department of Environmental Health and Engineering, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
  • Benner SE; W. Harry Feinstone Department of Molecular Microbiology and Immunology.
  • Littlefield K; Department of Biochemistry and Molecular Biology.
  • Kumar S; Department of International Health, and.
  • Naik HM; Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Betenbaugh MJ; W. Harry Feinstone Department of Molecular Microbiology and Immunology.
  • Shrestha R; Advanced Mammalian Biomanufacturing Innovation Center, Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, Maryland, USA.
  • Wu AA; Advanced Mammalian Biomanufacturing Innovation Center, Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, Maryland, USA.
  • Hughes RM; Advanced Mammalian Biomanufacturing Innovation Center, Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, Maryland, USA.
  • Burgess I; Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Caturegli P; Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Laeyendecker O; Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Quinn TC; Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Sullivan D; Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Shoham S; Department of Medicine, Division of Infectious Diseases, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Redd AD; Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda, Maryland, USA.
  • Bloch EM; Department of Medicine, Division of Infectious Diseases, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
  • Casadevall A; Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda, Maryland, USA.
  • Tobian AA; W. Harry Feinstone Department of Molecular Microbiology and Immunology.
J Clin Invest ; 130(11): 6141-6150, 2020 11 02.
Article in English | MEDLINE | ID: covidwho-696006
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ABSTRACT
Convalescent plasma is a leading treatment for coronavirus disease 2019 (COVID-19), but there is a paucity of data identifying its therapeutic efficacy. Among 126 potential convalescent plasma donors, the humoral immune response was evaluated using a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus neutralization assay with Vero-E6-TMPRSS2 cells; a commercial IgG and IgA ELISA to detect the spike (S) protein S1 domain (EUROIMMUN); IgA, IgG, and IgM indirect ELISAs to detect the full-length S protein or S receptor-binding domain (S-RBD); and an IgG avidity assay. We used multiple linear regression and predictive models to assess the correlations between antibody responses and demographic and clinical characteristics. IgG titers were greater than either IgM or IgA titers for S1, full-length S, and S-RBD in the overall population. Of the 126 plasma samples, 101 (80%) had detectable neutralizing antibody (nAb) titers. Using nAb titers as the reference, the IgG ELISAs confirmed 95%-98% of the nAb-positive samples, but 20%-32% of the nAb-negative samples were still IgG ELISA positive. Male sex, older age, and hospitalization for COVID-19 were associated with increased antibody responses across the serological assays. There was substantial heterogeneity in the antibody response among potential convalescent plasma donors, but sex, age, and hospitalization emerged as factors that can be used to identify individuals with a high likelihood of having strong antiviral antibody responses.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Blood Donors / Convalescence / Coronavirus Infections / Pandemics / Betacoronavirus / Hospitalization / Antibodies, Viral Type of study: Experimental Studies / Prognostic study Limits: Adult / Aged / Animals / Female / Humans / Male / Middle aged Language: English Journal: J Clin Invest Year: 2020 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Blood Donors / Convalescence / Coronavirus Infections / Pandemics / Betacoronavirus / Hospitalization / Antibodies, Viral Type of study: Experimental Studies / Prognostic study Limits: Adult / Aged / Animals / Female / Humans / Male / Middle aged Language: English Journal: J Clin Invest Year: 2020 Document Type: Article