首页> 外文OA文献 >Evaluation of the Abbott m2000 RealTime Human Immunodeficiency Virus Type 1 (HIV-1) Assay for HIV Load Monitoring in South Africa Compared to the Roche Cobas AmpliPrep-Cobas Amplicor, Roche Cobas AmpliPrep-Cobas TaqMan HIV-1, and BioMerieux NucliSENS EasyQ HIV-1 Assays▿
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Evaluation of the Abbott m2000 RealTime Human Immunodeficiency Virus Type 1 (HIV-1) Assay for HIV Load Monitoring in South Africa Compared to the Roche Cobas AmpliPrep-Cobas Amplicor, Roche Cobas AmpliPrep-Cobas TaqMan HIV-1, and BioMerieux NucliSENS EasyQ HIV-1 Assays▿

机译:与南非的Roche Cobas AmpliPrep-Cobas Amplicor,Roche Cobas AmpliPrep-Cobas TaqMan HIV-1和BioMerieux NucliSENS EasyQ HIV- 1种测定▿

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摘要

The implementation of antiretroviral therapy demands the need for increased access to viral load (VL) monitoring. Newer real-time VL testing technologies are faster and have larger dynamic ranges and fully automated extraction to benefit higher throughputs in resource-poor environments. The Abbott RealTime human immunodeficiency virus type 1 (HIV-1) assay was evaluated as a new option for testing for HIV-1 subtype C in South Africa, and its performance was compared to the performance of existing assays (the Cobas AmpliPrep-Cobas TaqMan HIV-1, version 1, assay; the AmpliPrep-Cobas Monitor standard HIV-1 assay; and the NucliSENS EasyQ-EasyMag HIV-1 assay) in a high-throughput laboratory. The total precision of the RealTime HIV-1 assay was acceptable over all viral load ranges. This assay compared most favorably with the Cobas AmpliPrep-Cobas TaqMan HIV-1 assay (R2 = 0.904), with a low standard deviation of difference being detected (0.323 copies/ml). The bias against comparator assays ranged from −0.001 copies/ml to −0.228 copies/ml. Variability in the reporting of VLs for a 20-member subtype panel compared to the variability of other assays was noted with subtypes G and CRF02-AG. The RealTime HIV-1 assay can test 93 samples per day with minimal manual preparation, less staff, and the minimization of contamination through automation. This assay is suitable for HIV-1 subtype C VL quantification in South Africa.
机译:抗逆转录病毒疗法的实施需要增加对病毒载量(VL)监测的访问。较新的实时VL测试技术更快,具有更大的动态范围和全自动提取功能,从而在资源匮乏的环境中提高了吞吐量。评估了Abbott RealTime 1型人类免疫缺陷病毒(HIV-1)检测方法作为南非检测HIV-1亚型C的新选择,并将其性能与现有检测方法进行了比较(Cobas AmpliPrep-Cobas TaqMan在高通量实验室中进行HIV-1版本1检测,AmpliPrep-Cobas Monitor标准HIV-1检测以及NucliSENS EasyQ-EasyMag HIV-1检测)。在所有病毒载量范围内,实时HIV-1检测的总精度是可以接受的。该测定法与Cobas AmpliPrep-Cobas TaqMan HIV-1测定法(R2 = 0.904)相比最有利,检测到的差异标准差低(0.323拷贝/ ml)。对比较分析的偏倚范围为-0.001拷贝/ ml至-0.228拷贝/ ml。与亚型G和CRF02-AG相比,报告了20个成员亚型组的VLs报告的变异性与其他测定的变异性。 RealTime HIV-1分析每天可以测试93个样品,而无需进行人工操作,工作人员更少,并且可以通过自动化将污染最小化。该测定适用于南非的HIV-1亚型C VL定量。

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