Performance of a time-resolved fluorescence immunoassay for measuring varicella-zoster virus immunoglobulin G levels in adults and comparison with commercial enzyme immunoassays and Merck glycoprotein enzyme immunoassay

被引:38
作者
Maple, PAC
Gray, J
Breuer, J
Kafatos, G
Parker, S
Brown, D
机构
[1] Hlth Protect Agcy, Ctr Infect, Virus Reference Dept, London NW9 5HT, England
[2] Hlth Protect Agcy, Ctr Infect, Stat Unit, London NW9 5EQ, England
[3] Queen Mary Univ London, Inst Cell & Mol Sci, Ctr Infect Dis, London E1 1BB, England
关键词
D O I
10.1128/CVI.13.2.214-218.2006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Highly sensitive and specific, quantitative assays are needed to detect varicella-zoster virus (VZV) immunoglobulin G in human sera, particularly for determining immune status and response following vaccination. A time-resolved fluorescence immunoassay (TRFIA) has been developed, and its performance was compared to that of two commercial enzyme immunoassays (EIAs) and Merck glycoprotein EIA (gpEIA). The TRFIA had equivalent sensitivity (97.8%) and high specificity (93.5%) in relation to gpEIA. A commercial (Behring) EIA compared favorably with TRFIA in terms of sensitivity (98.4%) but had lower specificity (80.7%). Another commercial EIA (Diamedix) had high specificity (97.1%) but low sensitivity (76.4%) compared to TRFIA if equivocal test results were treated as negative for VZV antibody. A novel feature of the TRFIA was that the cutoff was generated using population mixture modeling and was expressed in mIU/ml, as the assay was calibrated using the British standard VZV antibody.
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页码:214 / 218
页数:5
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