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Evaluation of a peptide‐based enzyme immunoassay for anti‐SARS coronavirus IgG antibody

Identifieur interne : 000990 ( Istex/Curation ); précédent : 000989; suivant : 000991

Evaluation of a peptide‐based enzyme immunoassay for anti‐SARS coronavirus IgG antibody

Auteurs : Paul K. S. Chan [République populaire de Chine, Hong Kong] ; W. K. To [République populaire de Chine] ; Esther Y. M. Liu [République populaire de Chine] ; T. K. Ng [République populaire de Chine] ; John S. Tam [République populaire de Chine] ; Joseph J. Y. Sung [République populaire de Chine] ; Jean-Michel Lacroix [Canada] ; Michel Houde [Canada]

Source :

RBID : ISTEX:0739D6E4A307DF53586757BAC1A3D2894AF8E248

English descriptors

Abstract

High throughput assays for anti‐SARS‐CoV IgG antibody detection are need for large‐scale epidemiologic studies. The performance of a microplate enzyme immunoassay, DETECT‐SARS™, was evaluated for the detection of anti‐SARS‐CoV IgG antibody. This assay is based on synthetic peptides derived from the nucleocapsid and spike proteins. The results showed that the assay provided a high degree of sensitivity (95.9%) for convalescent serum samples. The level of specificity was close to 90%, and did not show significant variation among different control groups. The high degree of sensitivity together with the high‐throughput nature makes it advantageous as a screening assay for studies where handling of a large number of specimens is required. J. Med. Virol. 74:517–520, 2004. © 2004 Wiley‐Liss, Inc.

Url:
DOI: 10.1002/jmv.20207

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ISTEX:0739D6E4A307DF53586757BAC1A3D2894AF8E248

Le document en format XML

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<term>Coronavirus</term>
<term>Disease control</term>
<term>Enzyme immunoassay</term>
<term>Healthy controls</term>
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<div type="abstract" xml:lang="en">High throughput assays for anti‐SARS‐CoV IgG antibody detection are need for large‐scale epidemiologic studies. The performance of a microplate enzyme immunoassay, DETECT‐SARS™, was evaluated for the detection of anti‐SARS‐CoV IgG antibody. This assay is based on synthetic peptides derived from the nucleocapsid and spike proteins. The results showed that the assay provided a high degree of sensitivity (95.9%) for convalescent serum samples. The level of specificity was close to 90%, and did not show significant variation among different control groups. The high degree of sensitivity together with the high‐throughput nature makes it advantageous as a screening assay for studies where handling of a large number of specimens is required. J. Med. Virol. 74:517–520, 2004. © 2004 Wiley‐Liss, Inc.</div>
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