Comparative evaluation of the Abbott HIV-1 RealTime~(TM) assay with the Standard Roche COBAS~R Amplicor~(TM) HIV-1 Monitor~R Test, vl.5 for determining HIV-1 RNA levels in plasma specimens from Pune, India

摘要

The implementation of cost effective HIV-1 viral load assays in resource-limited settings have been an impediment for monitoring HIV-1 therapy. A study involving the comparative analytical performance of two HIV-1 viral load assays - Standard Roche COBAS~R Amplicor~(TM) HIV-1 Monitor~R Test, version 1.5 (Roche Diagnostics, Basel, Switzerland) and Abbott HIV-1 RealTime~(TM) assay (Abbott Molecular, Wiesbaden, Germany) was performed using 125 specimens in Pune, India. A strong correlation was observedbetween the manual endpoint reverse transcriptase polymerase chain reaction assay and the recent real time polymerase chain reaction assay [r-0.989, p value < 0.0001) and agreement was 94.4%. Results of the study indicate a higher sensitivity of the Abbott HIV-1 RealTime~(TM) assay for HIV-1 Virology Quality Assurance copy controls as compared to the Standard Roche COBAS~R Amplicor~(TM) HIV-1 Monitor~R Test, version 1.5. Furthermore, features of the Abbott m2000rt RealTime~(TM) PCR assay platform such as higher analytical sensitivity, automated/manual extraction platforms for high/low sample throughputs and ability to quantify a variety of infectious agents (Hepatitis B virus, Hepatitis C virus, Human Papillomavirus and Neisseria gonorrhoeae/Chlamydiatrachomatis) justify its suitability in resource-limited Indian settings. Besides, the study also highlights utility of the precise Virology Quality Assurance validation template in performance evaluation of various quantitative viral load assays.