Clinical performance of three fully automated anti-SARS-CoV-2 immunoassays targeting the nucleocapsid or spike proteins.


Journal

Journal of medical virology
ISSN: 1096-9071
Titre abrégé: J Med Virol
Pays: United States
ID NLM: 7705876

Informations de publication

Date de publication:
04 2021
Historique:
received: 03 08 2020
revised: 26 10 2020
accepted: 10 11 2020
pubmed: 18 11 2020
medline: 20 3 2021
entrez: 17 11 2020
Statut: ppublish

Résumé

This study assesses the clinical performance of three anti-SARS-CoV-2 assays, namely EUROIMMUN anti-SARS-CoV-2 nucleocapsid (IgG) ELISA, Elecsys anti-SARS-CoV-2 nucleocapsid (total antibodies) assay, and LIAISON anti-SARS-CoV-2 spike proteins S1 and S2 (IgG) assay. One hundred and thirty-seven coronavirus disease 2019 (COVID-19) samples from 96 reverse-transcription polymerase chain reaction confirmed patients were chosen to perform the sensitivity analysis. Non-SARS-CoV-2 sera (n = 141) with a potential cross-reaction to SARS-CoV-2 immunoassays were included in the specificity analysis. None of these tests demonstrated a sufficiently high clinical sensitivity to diagnose acute infection. Fourteen days since symptom onset, we did not find any significant difference between the three techniques in terms of sensitivities. However, Elecsys performed better in terms of specificity. All three anti-SARS-CoV-2 assays had equivalent sensitivities 14 days from symptom onset to diagnose past-COVID-19 infection. We also confirmed that anti-SARS-CoV-2 determination before Day 14 is of less clinical interest.

Identifiants

pubmed: 33200836
doi: 10.1002/jmv.26669
pmc: PMC7753716
doi:

Substances chimiques

Antibodies, Viral 0
Coronavirus Nucleocapsid Proteins 0
Immunoglobulin A 0
Immunoglobulin G 0
Phosphoproteins 0
Spike Glycoprotein, Coronavirus 0
nucleocapsid phosphoprotein, SARS-CoV-2 0
spike protein, SARS-CoV-2 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2262-2269

Informations de copyright

© 2020 Wiley Periodicals LLC.

Références

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Auteurs

Julien Favresse (J)

Department of Laboratory Medicine, Clinique St-Luc Bouge, Namur, Belgium.
Department of Pharmacy, Namur Research Institute for Life Sciences, University of Namur, Namur, Belgium.

Julie Cadrobbi (J)

Department of Laboratory Medicine, Clinique St-Luc Bouge, Namur, Belgium.

Christine Eucher (C)

Department of Laboratory Medicine, Clinique St-Luc Bouge, Namur, Belgium.

Marc Elsen (M)

Department of Laboratory Medicine, Clinique St-Luc Bouge, Namur, Belgium.

Kim Laffineur (K)

Department of Laboratory Medicine, Clinique St-Luc Bouge, Namur, Belgium.

Jean-Michel Dogné (JM)

Department of Pharmacy, Namur Research Institute for Life Sciences, University of Namur, Namur, Belgium.

Jonathan Douxfils (J)

Department of Pharmacy, Namur Research Institute for Life Sciences, University of Namur, Namur, Belgium.
Qualiblood sa, Namur, Belgium.

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