Quantitative and cost comparison of ultrasensitive human immunodeficiency virus type 1 RNA viral load assays: Bayer bDNA Quantiplex versions 3.0 and 2.0 and Roche PCR Amplicor Monitor version 1.5

被引:56
作者
Elbeik, T
Charlebois, E
Nassos, P
Kahn, J
Hecht, FM
Yajko, D
Ng, V
Hadley, K
机构
[1] San Francisco Gen Hosp, Dept Lab Med, Clin Labs, San Francisco, CA 94110 USA
[2] San Francisco Gen Hosp, Posit Hlth Program, San Francisco, CA 94110 USA
[3] Univ Calif San Francisco, Dept Lab Med, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
关键词
D O I
10.1128/JCM.38.3.1113-1120.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Quantification of human immunodeficiency virus type 1 (HIV-1) RNA as a measure of viral load has greatly improved the monitoring of therapies for infected individuals. With the significant reductions in viral load now observed in individuals treated with highly active anti-retroviral therapy (HAART), viral load assays have been adapted to achieve greater sensitivity. Two commercially available ultrasensitive assays, the Bayer Quantiplex HIV-1 bDNA version 3.0 (bDNA 3.0) assay and the Roche Amplicor HIV-1 Monitor Ultrasensitive version 1.5 (Amplicor 1.5) assay, are now being used to monitor HIV-1-infected individuals. Both of these ultrasensitive assays have a reported lower limit of 50 HIV-1 RNA copies/ml and were developed from corresponding older generation assays with lower limits of 400 to 500 copies/ml. However, the comparability of viral load data generated by these ultrasensitive assays and the relative costs of labor, disposables, and biohazardous wastes were not determined in most cases. In this study, we used matched clinical plasma samples to compare the quantification of the newer bDNA 3.0 assay with that of the older bDNA 2.0 assay and to compare the quantification and costs of the bDNA 3.0 assay and the Amplicor 1.5 assay. We found that quantification by the bDNA 3.0 assay nas approximately twofold higher than that by the bDNA 2.0 assay and was highly correlated to that by the Amplicor 1.5 assay. Moreover, cost analysis based on labor, disposables, and biohazardous wastes showed significant savings with the bDNA 3.0 assay as compared to the costs of the Amplicor 1.5 assay.
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页码:1113 / 1120
页数:8
相关论文
共 18 条
[1]   Absolute copy number and relative change in determinations of human immunodeficiency virus type 1 RNA in plasma: Effect of an external standard on kit comparisons [J].
Brambilla, D ;
Leung, S ;
Lew, J ;
Todd, J ;
Herman, S ;
Cronin, M ;
Shapiro, DE ;
Bremer, J ;
Hanson, C ;
Hillyer, GV ;
McSherry, GD ;
Sperling, RS ;
Coombs, RW ;
Reichelderfer, PS .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (01) :311-314
[2]   Antiretroviral therapy for HIV infection in 1998 - Updated recommendations of the International AIDS Society USA panel [J].
Carpenter, CCJ ;
Fischl, MA ;
Hammer, SM ;
Hirsch, MS ;
Jacobsen, DM ;
Katzenstein, DA ;
Montaner, JSG ;
Richman, DD ;
Saag, MS ;
Schooley, RT ;
Thompson, MA ;
Vella, S ;
Yeni, PG ;
Volberding, PA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 280 (01) :78-86
[3]   Presence of an inducible HIV-1 latent reservoir during highly active antiretroviral therapy [J].
Chun, TW ;
Stuyver, L ;
Mizell, SB ;
Ehler, LA ;
Mican, JAM ;
Baseler, M ;
Lloyd, AL ;
Nowak, MA ;
Fauci, AS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (24) :13193-13197
[4]   A branched DNA signal amplification assay for quantification of nucleic acid targets below 100 molecules/ml [J].
Collins, ML ;
Irvine, B ;
Tyner, D ;
Fine, E ;
Zayati, C ;
Chang, CA ;
Horn, T ;
Ahle, D ;
Detmer, J ;
Shen, LP ;
Kolberg, J ;
Bushnell, S ;
Urdea, MS ;
Ho, DD .
NUCLEIC ACIDS RESEARCH, 1997, 25 (15) :2979-2984
[5]   Identification of a reservoir for HIV-1 in patients on highly active antiretroviral therapy [J].
Finzi, D ;
Hermankova, M ;
Pierson, T ;
Carruth, LM ;
Buck, C ;
Chaisson, RE ;
Quinn, TC ;
Chadwick, K ;
Margolick, J ;
Brookmeyer, R ;
Gallant, J ;
Markowitz, M ;
Ho, DD ;
Richman, DD ;
Siliciano, RF .
SCIENCE, 1997, 278 (5341) :1295-1300
[6]  
Fleiss JL, 1981, STAT METHODS RATES P, Vxviii, P321
[7]  
Hodara V., 1998, Acta Physiologica Pharmacologica et Therapeutica Latinoamericana, V48, P107
[8]   An enhanced-sensitivity branched-DNA assay for quantification of human immunodeficiency virus type 1 RNA in plasma [J].
Kern, D ;
Collins, M ;
Fultz, T ;
Detmer, J ;
Hamren, S ;
Peterkin, JJ ;
Sheridan, P ;
Urdea, M ;
White, R ;
Yeghiazarian, T ;
Todd, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (12) :3196-3202
[9]   Intra-assay performance characteristics of five assays for quantification of human immunodeficiency virus type 1 RNA in plasma [J].
Lin, HJ ;
Pedneault, L ;
Hollinger, FB .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (03) :835-839
[10]   HIV-1 replication in patients with undetectable plasma virus receiving HEART [J].
Natarajan, V ;
Bosche, M ;
Metcalf, JA ;
Ward, DJ ;
Lane, HC ;
Kovacs, JA .
LANCET, 1999, 353 (9147) :119-120