Scientific article
OA Policy
English

Validation of a commercially available SARS-CoV-2 serological immunoassay

Publication date2020
Abstract

Objectives: To validate the diagnostic accuracy of a Euroimmun SARS-CoV-2 IgG and IgA immunoassay for COVID-19. Methods: In this unmatched (1:2) case-control validation study, we used sera of 181 laboratory-confirmed SARS-CoV-2 cases and 326 controls collected before SARS-CoV-2 emergence. Diagnostic accuracy of the immunoassay was assessed against a whole spike protein-based recombinant immunofluorescence assay (rIFA) by receiver operating characteristic (ROC) analyses. Discrepant cases between ELISA and rIFA were further tested by pseudo-neutralization assay.

Keywords
  • COVID-19
  • ELISA
  • Pseudovirus neutralisation assay
  • Recombinant immunofluorescence assay
  • SARS-CoV-2
  • Serological Assays
  • Serological testing strategy
Citation (ISO format)
MEYER, Benjamin et al. Validation of a commercially available SARS-CoV-2 serological immunoassay. In: Clinical Microbiology and Infection, 2020. doi: 10.1016/j.cmi.2020.06.024
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Article (Accepted version)
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Identifiers
Journal ISSN1198-743X
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Technical informations

Creation07/10/2020 12:34:00 PM
First validation07/10/2020 12:34:00 PM
Update time01/13/2025 4:45:00 PM
Status update01/13/2025 4:45:00 PM
Last indexation01/13/2025 4:45:28 PM
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