Evaluation of hepatitis C virus RNA RT/PCR qualitative and quantitative second generation assays

被引:10
作者
Castro, FJ
Sauleda, S
Esteban, JI
Viladomiu, L
Martell, M
Dragon, E
Esteban, R
Guardia, J
机构
[1] Hosp Univ Vall Dhebron, Dept Med, Liver Unit, Serv Med Interna Hepatol, Barcelona, Spain
[2] Roche Mol Syst, Banchburg, NJ USA
关键词
HCV RNA; hepatitis C; RT/PCR;
D O I
10.1016/S0166-0934(00)00243-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Hepatitis C virus (HCV) RNA qualitative and quantitative second generation assays (Amplicor HCV v2.0 and Amplicor HCV Monitor v2.0, respectively) were evaluated by testing serum samples from 132 blood donors anti-HCV positive HCV RNA negative by first generation qualitative assay and 326 viremic patients. An HCV RNA transcript was synthesized and ten-fold dilutions were used to assess sensitivity. Second generation assays were one log more sensitive than their respective first generation tests (10(2) copies per mi vs. 10(3) for the qualitative tests; 103 copies per mi vs. 10(4) for the quantitative tests). From the 132 anti-HCV positive RNA negative subjects, 6 (5%) were positive by Amplicor v2.0. Quantification figures by Monitor v2.0 were similar in genotypes 1, 2 and 3, whereas Monitor 1.0 values were higher in genotype 1 than in genotype 2 or 3. In 114 patients, branched-DNA v2.0 obtained higher values than Monitor v2.0 and Monitor v1.0 (6.6 +/- 0.6 log RNA copies per mi, 6.4 +/- 0.6, and 5.3 +/- 0.7, respectively, P < 0.001). HCV RNA qualitative and quantitative second generation assays are more sensitive and genotype independent than first generation assays. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:51 / 58
页数:8
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