Your browser doesn't support javascript.
loading
Antibody reactivity to SARS-CoV-2 in adults from the Vancouver metropolitan area, Canada
Abdelilah Majdoubi; Christina Michalski; Sarah E O'Connell; Sarah Dada; Sandeep Narpala; Jean Gelinas; Disha Mehta; Claire Cheung; Manjula Basappa; Aaron C Liu; Matthias Gorges; Vilte E Barakauskas; Jennifer Mehalko; Dominic Esposito; Inna Sekirov; Agatha N Jassem; David M Goldfarb; Daniel C Douek; Adrian B McDermott; Pascal M Lavoie.
Afiliação
  • Abdelilah Majdoubi; BC Children Hospital Research Institute, Vancouver, British Columbia, Canada
  • Christina Michalski; BC Children Hospital Research Institute, Vancouver, British Columbia, Canada
  • Sarah E O'Connell; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 40 Convent Drive, Bethesda, Maryland 20892, Unite
  • Sarah Dada; BC Children Hospital Research Institute, Vancouver, British Columbia, Canada
  • Sandeep Narpala; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 40 Convent Drive, Bethesda, Maryland 20892, Unite
  • Jean Gelinas; Department of Anesthesiology, Surrey Memorial Hospital, Surrey, British Columbia, Canada
  • Disha Mehta; Department of Anesthesiology, Surrey Memorial Hospital, Surrey, British Columbia, Canada Department of Department of Anesthesiology, Pharmacology and Therapeut
  • Claire Cheung; BC Children Hospital Research Institute, Department of Pediatrics, University of British Columbia, Vancouver, Canada
  • Manjula Basappa; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 40 Convent Drive, Bethesda, Maryland 20892, Unite
  • Aaron C Liu; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada
  • Matthias Gorges; BC Children Hospital Research Institute, Department of Department of Anesthesiology, Pharmacology and Therapeutics, University of British Columbia, Vancouver, B
  • Vilte E Barakauskas; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada
  • Jennifer Mehalko; National Cancer Institute RAS Initiative, Cancer Research Technology Program, Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, Inc
  • Dominic Esposito; National Cancer Institute RAS Initiative, Cancer Research Technology Program, Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, Inc
  • Inna Sekirov; British Columbia Centre for Disease Control Public Health Laboratory, Vancouver, British Columbia, Canada
  • Agatha N Jassem; British Columbia Centre for Disease Control Public Health Laboratory, Vancouver, British Columbia, Canada
  • David M Goldfarb; BC Children Hospital Research Institute, Department of Pediatrics, Division of Medical Microbiology, Department of Pathology and Laboratory Medicine, University
  • Daniel C Douek; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 40 Convent Drive, Bethesda, Maryland 20892, Unite
  • Adrian B McDermott; Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 40 Convent Drive, Bethesda, Maryland 20892, Unite
  • Pascal M Lavoie; BC Children Hospital Research Institute, Vancouver, British Columbia, Canada
Preprint em Inglês | medRxiv | ID: ppmedrxiv-20206664
ABSTRACT
BackgroundQuantifying antibody reactivity against multiple SARS-CoV-2 antigens at the population level may help understand individual differences in COVID-19 severity. Pre-existing low antibody cross-reactivity may be particularly prevalent among childcare providers, including pediatric health care workers (HCW) who may be more exposed to circulating coronaviruses. MethodsCross-sectional study that included adults in the Vancouver area in British Columbia (BC), Canada, between May 17 and June 19, 2020. SARS-CoV-2 seroprevalence was ascertained by measuring total SARS-CoV-2 IgG/M/A antibodies against a recombinant spike (S1) protein and adjusted for bias due to false-positive and false-negative test results. A novel, high sensitivity multiplex assay was also used to profile IgG against four SARS-CoV-2 antigens, SARS-CoV and four circulating coronaviruses. FindingsAmong 276 participants (71% HCW), three showed evidence of direct viral exposure, yielding an adjusted seroprevalence of 0.60% [95%CI 0% - 2.71%], with no difference between HCW and non-HCW, or between paediatric and adult HCW. Among the 273 unexposed individuals, 7.3% [95%CI 4.5% - 11.1%], 48.7 [95%CI 42.7% - 54.8%] and 82.4% [95%CI 77.4% - 86.7%] showed antibody reactivity against SARS-CoV-2 RBD, N or Spike proteins, respectively. SARS-CoV-2 reactivity did not significantly correlate with age, sex, did not significantly differ between HCW and non-HCW (prevalence 1.0% vs 1.0%; P=1.00) and between pediatric and adult HCW (0.7% vs 1.6%; P=0.54), and modestly correlated with reactivity to circulating coronaviruses (Spearman rho range 0.130 to 0.224 for 7 significant (FDR 5%), out of 16 correlations, from 36 correlations tested). InterpretationA substantial proportion of individuals showed low, but detectable antibody reactivity against SARS-CoV-2 antigens in this population despite low evidence of direct SARS-CoV-2 exposure. FundingNIAID/NIH
Licença
cc_no
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Estudo observacional / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2020 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Estudo observacional / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2020 Tipo de documento: Preprint
...