Multicenter comparison of three commercial methods for quantification of human immunodeficiency virus type 1 RNA in plasma

被引:96
作者
Schuurman, R
Descamps, D
Weverling, GJ
Kaye, S
Tijnagel, J
Williams, I
vanLeeuwen, R
Tedder, R
Boucher, CAB
BrunVezinet, F
Loveday, C
机构
[1] UNIV UTRECHT, EIJKMAN WINKLER INST MED MICROBIOL, DEPT VIROL, UTRECHT, NETHERLANDS
[2] UNIV AMSTERDAM, ACAD MED CTR, NATL AIDS THERAPY EVALUAT CTR, NL-1105 AZ AMSTERDAM, NETHERLANDS
[3] HOP BICHAT CLAUDE BERNARD, DEPT VIROL, F-75877 PARIS 18, FRANCE
[4] UCL, SCH MED, DEPT VIROL, LONDON, ENGLAND
[5] UCL, SCH MED, DEPT SEXUALLY TRANSMITTED DIS, LONDON, ENGLAND
[6] ROYAL FREE HOSP, DEPT RETROVIROL, LONDON NW3 2QG, ENGLAND
关键词
D O I
10.1128/JCM.34.12.3016-3022.1996
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Three procedures for the quantification of human immunodeficiency virus type 1 (HIV-1) RNA from plasma were compared at three laboratories. The comparison involved the Quantiplex branched DNA assay (version 1.0) by Chiron Diagnostics, the NASBA-QT assay by Organon Teknika, and the Amplicor Monitor assay by Roche Molecular Systems. The laboratories performed each of the three assays with the same sets of reconstructed HIV-1-infected human plasma samples, cross-sectionally collected clinical plasma samples and longitudinally collected plasma samples from patients starting zidovudine therapy. Analysis of the reconstruction panel results for interlaboratory variation demonstrated that no laboratory differences in results were detected for any of the assays, A comparison of the reproducibilities of duplicate samples analyzed by batch and in separate assay runs demonstrated that the reproducibilities of the test results were similar within one assay and appeared to be independent of the HIV-1 concentration. The best reproducibility was obtained with the Quantiplex assay, but all three assays demonstrated equal reliability, which was independent of batched or unbatched analysis of replicate samples. Differences in the absolute concentrations calculated were observed for the assays, in particular in the analysis of reconstructed samples. In all assays, similar changes in plasma HIV-1 RNA concentrations were determined for longitudinally collected clinical samples.
引用
收藏
页码:3016 / 3022
页数:7
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