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Evaluation of a recombinant nucleocapsid protein‐based assay for Anti‐SARS‐CoV IgG detection

Identifieur interne : 004C14 ( Main/Exploration ); précédent : 004C13; suivant : 004C15

Evaluation of a recombinant nucleocapsid protein‐based assay for Anti‐SARS‐CoV IgG detection

Auteurs : Paul K. S. Chan [République populaire de Chine, Hong Kong] ; Esther Y. M. Liu [République populaire de Chine] ; Danny T. M. Leung [République populaire de Chine] ; Jo L. K. Cheung [République populaire de Chine] ; C. H. Ma [République populaire de Chine] ; Frankie C. H. Tam [République populaire de Chine] ; Mamie Hui [République populaire de Chine] ; John S. Tam [République populaire de Chine] ; Pak Leong Lim [République populaire de Chine]

Source :

RBID : ISTEX:24A6F87DD48E97A7192641B87F192C01D9752EA4

Descripteurs français

English descriptors

Abstract

A high throughput accurate assay for anti‐SARS‐CoV IgG detection is needed for large‐scale epidemiological studies. The evaluation of a commercial recombinant nucleocapsid protein‐based microtitre plate enzyme immunoassay, ELISARS™ is described. The results on 150 sera from SARS patients and 450 sera from non‐SARS controls showed that this assay had a high level of sensitivity (96.2% for late serum samples) and specificity (97.8%). The performance and setup of this assay fulfills the requirement as a screening test for large‐scale studies. A vast majority of SARS patients developed antibodies against the nucleocapsid protein. In some patients (10/45), a high level of anti‐nucleocapsid antibody appeared very early in the course of the illness. In contrast, a minority (4 of 105 patients) never developed these antibodies. The implication of differences in antibody response to the nucleocapsid protein deserves further investigation. J. Med. Virol. 75:181–184, 2005. © 2004 Wiley‐Liss, Inc.

Url:
DOI: 10.1002/jmv.20254


Affiliations:


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Le document en format XML

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<front>
<div type="abstract" xml:lang="en">A high throughput accurate assay for anti‐SARS‐CoV IgG detection is needed for large‐scale epidemiological studies. The evaluation of a commercial recombinant nucleocapsid protein‐based microtitre plate enzyme immunoassay, ELISARS™ is described. The results on 150 sera from SARS patients and 450 sera from non‐SARS controls showed that this assay had a high level of sensitivity (96.2% for late serum samples) and specificity (97.8%). The performance and setup of this assay fulfills the requirement as a screening test for large‐scale studies. A vast majority of SARS patients developed antibodies against the nucleocapsid protein. In some patients (10/45), a high level of anti‐nucleocapsid antibody appeared very early in the course of the illness. In contrast, a minority (4 of 105 patients) never developed these antibodies. The implication of differences in antibody response to the nucleocapsid protein deserves further investigation. J. Med. Virol. 75:181–184, 2005. © 2004 Wiley‐Liss, Inc.</div>
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