Serveur d'exploration SRAS

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First external quality assurance of antibody diagnostic for SARS-new coronavirus

Identifieur interne : 001098 ( Ncbi/Checkpoint ); précédent : 001097; suivant : 001099

First external quality assurance of antibody diagnostic for SARS-new coronavirus

Auteurs : Matthias Niedrig [Allemagne] ; Katrin Leitmeyer [Allemagne, Suisse] ; Wilina Lim [République populaire de Chine] ; Malik Peiris [République populaire de Chine] ; John S. Mackenzie [Suisse, Australie] ; Maria Zambon [Royaume-Uni]

Source :

RBID : PMC:7108360

Descripteurs français

English descriptors

Abstract

To confirm an infection with the new coronavirus (SARS-CoV) causing the severe acute respiratory syndrome (SARS) diagnostic assays for detection of SARS-CoV specific antibody are necessary. To evaluate the diagnostic performance of laboratories an external quality assurance (EQA) study was performed in 2004. Participating laboratories (9/20) correctly detected anti-SARS antibodies in serum samples without false positive results in an immunofluorescence assay. In contrast, only 4/13 laboratories detected most of the anti-SARS antibody positive samples without false positive results using enzyme immunoassays (EIA) and/or immunoblot. The overall results clearly demonstrate that serological diagnosis of SARS-CoV remains at an early stage of development, with further technical improvements required, particularly with respect to the use of SARS specific EIAs.


Url:
DOI: 10.1016/j.jcv.2005.01.004
PubMed: 16087120
PubMed Central: 7108360


Affiliations:


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PMC:7108360

Le document en format XML

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<p>To confirm an infection with the new coronavirus (SARS-CoV) causing the severe acute respiratory syndrome (SARS) diagnostic assays for detection of SARS-CoV specific antibody are necessary. To evaluate the diagnostic performance of laboratories an external quality assurance (EQA) study was performed in 2004. Participating laboratories (9/20) correctly detected anti-SARS antibodies in serum samples without false positive results in an immunofluorescence assay. In contrast, only 4/13 laboratories detected most of the anti-SARS antibody positive samples without false positive results using enzyme immunoassays (EIA) and/or immunoblot. The overall results clearly demonstrate that serological diagnosis of SARS-CoV remains at an early stage of development, with further technical improvements required, particularly with respect to the use of SARS specific EIAs.</p>
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<name sortKey="Chang, M S" uniqKey="Chang M">M.S. Chang</name>
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</author>
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