Evaluation of a recombinant nucleocapsid protein-based assay for anti-SARS-CoV IgG detection

被引:14
|
作者
Chan, PKS [1 ]
Liu, EYM
Leung, DTM
Cheung, JLK
Ma, CH
Tam, FCH
Hui, MM
Tam, JS
Lim, PL
机构
[1] Chinese Univ Hong Kong, Dept Microbiol, Prince Wales Hosp, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Prince Wales Hosp, Ctr Emerging Infect Dis, Shatin, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Prince Wales Hosp, Clin Immunol Unit, Shatin, Hong Kong, Peoples R China
关键词
coronavirus; diagnosis; enzyme; immunoassay; SARS; serology;
D O I
10.1002/jmv.20254
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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(TM) 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. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:181 / 184
页数:4
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