Assessment of viral loads in patients with chronic hepatitis C with AMPLICOR HCV MONITOR version 1.0, COBAS HCV MONITOR version 2.0, and QUANTIPLEX HCV RNA version 2.0 assays

被引:18
作者
Martinot-Peignoux, M [1 ]
Le Breton, V
Fritsch, S
Le Guludec, G
Labouret, N
Keller, F
Marcellin, P
机构
[1] Hop Beaujon, INSERM, U481, Ctr Rech Claude Bernard Hepatites Virales, F-92118 Clichy, France
[2] Hop Beaujon, Serv Hepatol, F-92110 Clichy, France
[3] Fac Med Strasbourg, Inst Virol, F-67000 Strasbourg, France
关键词
D O I
10.1128/JCM.38.7.2722-2725.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The correlation between response to antiviral therapy and pretreatment viral load in patients with chronic hepatitis C has prompted the development of quantitative assays to measure viral load. The aim of our study was to assess the clinical relevance of the newly developed semiautomated PCR system COBAS HCV MONITOR version 2.0 in comparison with (i) the AMPLICOR HCV MONITOR version 1.0 assay, which underestimates RNA concentration of hepatitis C virus (HCV) genotypes 2 to 6, and (ii) the QUANTIPLEX HCV RNA version 2.0 assay, which achieves equivalent quantification for each HCV genotype, with samples from 174 patients diagnosed with chronic hepatitis C before therapy. The level and range of quantification measured with AMPLICOR HCV MONITOR version 1.0 were 1 log lower than when measured with the COBAS HCV MONITOR version 2.0, at 0.261 x 10(6) RNA copies/ml (range, 0.001 x 10(6) to 2.50 x 10(6) RNA copies/ml) and 4.032 x 10(6) RNA copies/ml (range, 0.026 x 10(6) to 72.6 x 10(6) RNA copies/ml), respectively. The two assays showed a poor correlation (r(2) = 0.175). The level and range of quantification were similar when measured with the COBAS HCV MONITOR version 2.0 and QUANTIPLEX HCV RNA version 2.0 assays, at 3.03 x 10(6) RNA copies/ml (range, 0.023 x 10(6) to 72.6 x 10(6) RNA copies/ml) and 4.91 Meq/ml (range, 0.200 to 39.5 Meq/ml), respectively. The two assays showed a strong correlation (r(2) = 0.686) for each HCV genotype. The duration of treatment (6 or 12 months) is modulated according to HCV genotype and viral load. Our results indicate that COBAS HCV MONITOR version 2.0 and QUANTIPLEX HCV RNA version 2.0 assays showing an equal dynamic range for each HCV genotype are suitable tools to assess patients before therapy.
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页码:2722 / 2725
页数:4
相关论文
共 23 条
[1]   Performance of an automated system for quantification of hepatitis C virus RNA [J].
Afonso, AMR ;
Didier, J ;
Plouvier, E ;
Falissard, B ;
Ferey, MP ;
Bogard, M ;
Dussaix, E .
JOURNAL OF VIROLOGICAL METHODS, 2000, 86 (01) :55-60
[2]   Multicenter evaluation of the COBAS AMPLICOR HCV assay, an integrated PCR system for rapid detection of hepatitis C virus RNA in the diagnostic laboratory [J].
Albadalejo, J ;
Alonso, R ;
Antinozzi, R ;
Bogard, M ;
Bourgault, AM ;
Colucci, G ;
Fenner, T ;
Petersen, H ;
Sala, E ;
Vincelette, J ;
Young, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (04) :862-865
[3]  
[Anonymous], 1999, J Hepatol, V30, P956
[4]   Factors predictive of a beneficial response to therapy of hepatitis C [J].
Davis, GL ;
Lau, JYN .
HEPATOLOGY, 1997, 26 (03) :S122-S127
[5]   Interferon alfa-2b alone or in combination with ribavirin for the treatment of relapse of chronic hepatitis C [J].
Davis, GL ;
Esteban-Mur, R ;
Rustgi, V ;
Hoefs, J ;
Gordon, SC ;
Trepo, C ;
Shiffman, ML ;
Zeuzem, S ;
Craxi, A ;
Ling, MH ;
Albrecht, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (21) :1493-1499
[6]   Accurate quantification of hepatitis C virus (HCV) RNA from all HCV genotypes by using branched-DNA technology [J].
Detmer, J ;
Lagier, R ;
Flynn, J ;
Zayati, C ;
Kolberg, J ;
Collins, M ;
Urdea, M ;
SanchezPescador, R .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (04) :901-907
[7]   Second generation of the automated Cobas Amplicor HCV assay improves sensitivity of hepatitis C virus RNA detection and yields results that are more clinically relevant [J].
Doglio, A ;
Laffont, C ;
Caroli-Bosc, FX ;
Rochet, P ;
Lefebvre, JC .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (05) :1567-1569
[8]   ASSESSMENT OF HEPATITIS-C VIREMIA USING MOLECULAR AMPLIFICATION TECHNOLOGIES - CORRELATIONS AND CLINICAL IMPLICATIONS [J].
GRETCH, DR ;
DELAROSA, C ;
CARITHERS, RL ;
WILLSON, RA ;
WILLIAMS, B ;
COREY, L .
ANNALS OF INTERNAL MEDICINE, 1995, 123 (05) :321-329
[9]   Comparison of plasma virus loads among individuals infected with hepatitis C virus (HCV) genotypes 1, 2, and 3 by Quantiplex HCV RNA assay versions 1 and 2, Roche monitor assay, and an in-house limiting dilution method [J].
Hawkins, A ;
Davidson, F ;
Simmonds, P .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (01) :187-192
[10]  
KOLBERG J, 1994, HEPATITIS C VIRUS NE, P57