More HIV-1 RNA detected and quantified with the Cobas 6800 system in patients on antiretroviral therapy

Author:

Wirden Marc12,Palich Romain123ORCID,Abdi Basma12ORCID,Valantin Marc Antoine123,Tubiana Roland123,Schneider Luminita123,Seang Sophie123,Faycal Antoine123,Sellem Baptiste123,Katlama Christine123,Calvez Vincent12,Marcelin Anne Geneviève12

Affiliation:

1. Sorbonne Université, INSERM, Institut Pierre Louis d’Epidémiologie et de Santé Publique, (IPLESP) , F75013, Paris , France

2. AP-HP, Pitié Salpêtrière Hospital, Department of Virology , Paris , France

3. AP-HP, Pitié Salpêtrière Hospital, Department of Infectious Diseases , Paris , France

Abstract

Abstract Background Target-detected (TD) results or low-level viraemia (LLV) can be observed in HIV-1 patients on ART, which regularly raises questions. Objectives We describe here the impact on HIV-1 RNA quantification of switching from the COBAS AmpliPrep/COBAS TaqMan (CAP/CTM) to the Cobas 6800 system (C6800), based on analyses of viraemia close to the lower limit of quantification (LLoQ). Patients and methods We retrospectively selected two groups of patients: 200 individuals whose viral loads (VLs) were consistently <50 copies/mL with CAP/CTM for at least 3 years before switching to C6800 (group 1), and 35 other patients with confirmed LLV when C6800 was in use (group 2). In both groups, we compared several consecutive VL results performed before and after the change of quantification assay. Analyses were performed with McNemar’s paired tests or Fisher’s exact tests. Results In group 1, the frequency of TD results (below or above the LLoQ) increased significantly after the switch to C6800 for patients with <25% of results being TD for VLs performed with CAP/CTM (P < 0.0001). Significantly more patients had at least one VL ≥20 or ≥50 copies/mL with C6800, in both group 1 (37.0% versus 18.5%; P < 0.0001 and 6.5% versus 0%; P = 0.0009, respectively) and group 2 (100% versus 66%; P = 0.0015 and 97% versus 40%; P < 0.0001, respectively). Conclusions C6800 revealed residual or low-level HIV-1 RNA that was not detected with CAP/CTM, resulting in twice as many patients being found to have a VL ≥20 copies/mL. Physicians and patients should be aware of possible differences in results between assays, and it is crucial to specify the quantitative assay used in studies.

Funder

Agence Nationale de la Recherche sur le SIDA et les Maladies Infectieuses Emergentes

ANRS

MIE

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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