Comparison of different serological assays for SARS-CoV-2 in real life.


Journal

Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology
ISSN: 1873-5967
Titre abrégé: J Clin Virol
Pays: Netherlands
ID NLM: 9815671

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 17 07 2020
accepted: 29 07 2020
pubmed: 10 8 2020
medline: 6 10 2020
entrez: 10 8 2020
Statut: ppublish

Résumé

The emergence of the global SARS-CoV-2 pandemic required the rapid and large-scale deployment of PCR and serological tests in different formats. Real-life evaluation of these tests is needed. Using 168 samples from patients hospitalized for COVID-19, non-hospitalized patients but infected with SARS-CoV-2, patients participating in screening campaigns, and samples from patients with a history of other seasonal coronavirus infections, we evaluated the clinical performance of 5 serological assays widely used worldwide (WANTAI®, BIORAD®, EUROIMMUN®, ABBOTT® and LIAISON®). For hospitalized patients, all these assays showed a sensitivity of 100 % from day 9 after the symptoms onset. On the other hand, sensitivity was much lower for patients who did not require hospitalization for COVID-19 confirmed by PCR (from 91.6 % for WANTAI® to 69 % for LIAISON®). These differences do not seem to be due to the antigens chosen by the manufacturers but more to the test formats (IgG detection versus total antibodies). In addition, more than 50 days after a positive PCR for CoV-2-SARS the proportion of positive patients seem to decrease. We did not observe any significant cross-reactions for these techniques with the four other seasonal coronaviruses. In conclusion, the evaluation and knowledge of the serological tests used is important and should require an optimized strategy adaptation of the analysis laboratories to best meet patient's expectations in the face of this health crisis.

Sections du résumé

BACKGROUND BACKGROUND
The emergence of the global SARS-CoV-2 pandemic required the rapid and large-scale deployment of PCR and serological tests in different formats.
OBJECTIVES OBJECTIVE
Real-life evaluation of these tests is needed. Using 168 samples from patients hospitalized for COVID-19, non-hospitalized patients but infected with SARS-CoV-2, patients participating in screening campaigns, and samples from patients with a history of other seasonal coronavirus infections, we evaluated the clinical performance of 5 serological assays widely used worldwide (WANTAI®, BIORAD®, EUROIMMUN®, ABBOTT® and LIAISON®).
RESULTS RESULTS
For hospitalized patients, all these assays showed a sensitivity of 100 % from day 9 after the symptoms onset. On the other hand, sensitivity was much lower for patients who did not require hospitalization for COVID-19 confirmed by PCR (from 91.6 % for WANTAI® to 69 % for LIAISON®). These differences do not seem to be due to the antigens chosen by the manufacturers but more to the test formats (IgG detection versus total antibodies). In addition, more than 50 days after a positive PCR for CoV-2-SARS the proportion of positive patients seem to decrease. We did not observe any significant cross-reactions for these techniques with the four other seasonal coronaviruses.
CONCLUSION CONCLUSIONS
In conclusion, the evaluation and knowledge of the serological tests used is important and should require an optimized strategy adaptation of the analysis laboratories to best meet patient's expectations in the face of this health crisis.

Identifiants

pubmed: 32769023
pii: S1386-6532(20)30311-5
doi: 10.1016/j.jcv.2020.104569
pmc: PMC7396207
pii:
doi:

Substances chimiques

Antibodies, Viral 0
Immunoglobulin A 0
Immunoglobulin G 0
Reagent Kits, Diagnostic 0

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104569

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Références

Nature. 2020 Mar;579(7798):270-273
pubmed: 32015507
J Infect. 2020 Aug;81(2):e6-e10
pubmed: 32389784
J Clin Microbiol. 2020 Jul 23;58(8):
pubmed: 32381641
Nat Commun. 2020 Jul 6;11(1):3436
pubmed: 32632160
Science. 2020 May 1;368(6490):489-493
pubmed: 32179701
J Clin Virol. 2020 Aug;129:104544
pubmed: 32663788
Lancet Infect Dis. 2020 Jul;20(7):758-759
pubmed: 32330441
J Infect Dis. 2020 Oct 1;222(9):1435-1438
pubmed: 32651586
Lab Med. 2020 Sep 1;51(5):e59-e65
pubmed: 32657343
Front Microbiol. 2020 Oct 19;11:584251
pubmed: 33193227

Auteurs

Etienne Brochot (E)

Department of Virology, Amiens University Medical Center, Amiens, France; Agents infectieux résistance et chimiothérapie Research Unit, UR4294, Jules Verne University of Picardie, France. Electronic address: etienne.brochot@u-picardie.fr.

Baptiste Demey (B)

Department of Virology, Amiens University Medical Center, Amiens, France; Agents infectieux résistance et chimiothérapie Research Unit, UR4294, Jules Verne University of Picardie, France.

Lynda Handala (L)

Department of Virology, Amiens University Medical Center, Amiens, France; Agents infectieux résistance et chimiothérapie Research Unit, UR4294, Jules Verne University of Picardie, France.

Catherine François (C)

Department of Virology, Amiens University Medical Center, Amiens, France; Agents infectieux résistance et chimiothérapie Research Unit, UR4294, Jules Verne University of Picardie, France.

Gilles Duverlie (G)

Department of Virology, Amiens University Medical Center, Amiens, France; Agents infectieux résistance et chimiothérapie Research Unit, UR4294, Jules Verne University of Picardie, France.

Sandrine Castelain (S)

Department of Virology, Amiens University Medical Center, Amiens, France; Agents infectieux résistance et chimiothérapie Research Unit, UR4294, Jules Verne University of Picardie, France.

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Classifications MeSH