Performance of SARS-CoV-2 serology tests: Are they good enough?


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 02 10 2020
accepted: 09 01 2021
entrez: 17 2 2021
pubmed: 18 2 2021
medline: 17 3 2021
Statut: epublish

Résumé

In the emergency of the SARS-CoV-2 pandemic, great efforts were made to quickly provide serology testing to the medical community however, these methods have been introduced into clinical practice without the complete validation usually required by the regulatory organizations. SARS-CoV-2 patient samples (n = 43) were analyzed alongside pre-pandemic control specimen (n = 50), confirmed respiratory infections (n = 50), inflammatory polyarthritis (n = 22) and positive for thyroid stimulating immunoglobulin (n = 30). Imprecision, diagnostic sensitivity and specificity and concordance were evaluated on IgG serologic assays from EuroImmun, Epitope Diagnostics (EDI), Abbott Diagnostics and DiaSorin and a rapid IgG/IgM test from Healgen. EDI and EuroImmun imprecision was 0.02-14.0% CV. Abbott and DiaSorin imprecision (CV) ranged from 5.2%-8.1% and 8.2%-9.6% respectively. Diagnostic sensitivity of the assays was 100% (CI: 80-100%) for Abbott, EDI and EuroImmun and 95% (CI: 73-100%) for DiaSorin at ≥14 days post PCR. Only the Abbott assay had a diagnostic specificity of 100% (CI: 91-100%). EuroImmun cross-reacted in 3 non-SARS-CoV-2 respiratory infections and 2 controls. The DiaSorin displayed more false negative results and cross-reacted in six cases across all conditions tested. EDI had one cross-reactive sample. The Healgen rapid test showed excellent sensitivity and specificity. Overall, concordance of the assays ranged from 76.1% to 97.9%. Serological tests for SARS-CoV-2 showed good analytical performance. The head-to-head analysis of samples revealed differences in results that may be linked to the use of nucleocapsid or spike proteins. The point of care device tested demonstrated adequate performance for antibody detection.

Identifiants

pubmed: 33596236
doi: 10.1371/journal.pone.0245914
pii: PONE-D-20-31021
pmc: PMC7888604
doi:

Substances chimiques

Antibodies, Viral 0
Immunoglobulin G 0
Immunoglobulin M 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0245914

Déclaration de conflit d'intérêts

The authors acknowledge the Norfolk, Suffolk, Essex and Bedfordshire Freemasons for their material support in providing funding for some equipment used in this study. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

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Auteurs

Isabelle Piec (I)

BioAnalytical Facility, Faculty of Medicine, University of East Anglia, Norwich, United Kingdom.

Emma English (E)

Faculty of Medicine and Health, University of East Anglia, Norwich, United Kingdom.

Mary Annette Thomas (MA)

WEQAS, Cardiff and Vale University Health Board, Cardiff, United Kingdom.

Samir Dervisevic (S)

Virology Department, Norfolk and Norwich University Hospitals, Norwich, United Kingdom.

William D Fraser (WD)

BioAnalytical Facility, Faculty of Medicine, University of East Anglia, Norwich, United Kingdom.
Clinical Biochemistry Department, Norfolk and Norwich University Hospitals, Norwich, United Kingdom.

William Garry John (WG)

Faculty of Medicine and Health, University of East Anglia, Norwich, United Kingdom.
Clinical Biochemistry Department, Norfolk and Norwich University Hospitals, Norwich, United Kingdom.

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Classifications MeSH