Elsevier

Journal of Clinical Virology

Volume 77, April 2016, Pages 46-54
Journal of Clinical Virology

Aptima HIV-1 Quant Dx—A fully automated assay for both diagnosis and quantification of HIV-1

https://doi.org/10.1016/j.jcv.2016.02.002Get rights and content
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Highlights

  • Aptima was more sensitive than COBAS Ampliprep TaqMan HIV-1 version 2.0 (CAP/CTM).

  • In seroconversion panels Aptima detected HIV earlier than antigen/antibody tests.

  • Diagnostic agreement was 100% with Procleix® Ultrio Elite™ blood screening assay.

  • Viral load measurements in Aptima showed good agreement with CAP/CTM.

  • Aptima demonstrated equivalent subtype quantification and good precision.

Abstract

Background

Separate assays are available for diagnosis and viral load (VL) monitoring of HIV-1. Studies have shown that using a single test for both confirmatory diagnosis and VL increases linkage to care.

Objective

To validate a single assay for both diagnosis and VL monitoring of HIV-1 on the fully automated Panther platform.

Study design

Validate the assay by assessing specificity, sensitivity, subtype detection, seroconversion, reproducibility and linearity. Also assess diagnostic agreement with the Procleix® Ultrio Elite™ discriminatory assay (Procleix), and agreement of VL results (method comparison) with Ampliprep/COBAS TaqMan HIV-1 version 2.0 (CAP/CTM), using clinical samples.

Results

The assay was specific (100%) and sensitive with a 95% limit of detection of 12 copies/mL with the 3rd WHO standards. Aptima detected HIV in seroconversion panels 6 and 11 days before p24 antigen and antibody tests, respectively. Diagnostic agreement with Procleix, was 100%. Regression analysis showed good agreement of VL results between Aptima and CAP/CTM with a slope of 1.02, intercept of 0.07, and correlation coefficient (R2) of 0.97. Aptima was more sensitive than CAP/CTM. Equivalent quantification was seen on testing clinical samples and isolates belonging to HIV group M, N, O and P and commercially available subtype panels. Assay results were linear (R2 0.9994) with standard deviation of <0.17 log copies across assay range.

Conclusions

The good specificity, sensitivity, precision, subtype performance and clinical agreement with other assays demonstrated by Aptima combined with the complete automation provided by the Panther platform makes Aptima a good candidate for both VL monitoring and diagnosis of HIV-1.

Abbreviations

Aptima
Aptima HIV-1 Quant Dx Assay
VL
viral load
CAP/CTM
COBAS® AmpliPrep/COBAS® TaqMan® HIV-1 Test v2.0
Abbott RT
Abbott RealTime HIV-1 Assay
Procleix
Procleix® Ultrio Elite™ discriminatory assay
LOD
limit of detection
LOQ
limit of quantification
LLOQ
lower limit of quantification
ART
anti retroviral therapy
NAAT
nucleic acid amplification test
SD
standard deviation

Keywords

HIV
Diagnosis
Viral load
Aptima
Panther
CAP/CTM

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