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The dual-target approach in viral HIV-1 viremia testing: An added value to virological monitoring?

New methods of HIV-1 RNA quantification based on dual-target detection are increasingly used in HIV viral load monitoring, but clinical implications and impact of dual-target detection on HIV-1 infection management are not established. Aptima HIV-1 Quant Dx assay is a last generation HIV viral load...

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Autores principales: Amendola, Alessandra, Sberna, Giuseppe, Forbici, Federica, Abbate, Isabella, Lorenzini, Patrizia, Pinnetti, Carmela, Antinori, Andrea, Capobianchi, Maria Rosaria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7001951/
https://www.ncbi.nlm.nih.gov/pubmed/32023284
http://dx.doi.org/10.1371/journal.pone.0228192
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author Amendola, Alessandra
Sberna, Giuseppe
Forbici, Federica
Abbate, Isabella
Lorenzini, Patrizia
Pinnetti, Carmela
Antinori, Andrea
Capobianchi, Maria Rosaria
author_facet Amendola, Alessandra
Sberna, Giuseppe
Forbici, Federica
Abbate, Isabella
Lorenzini, Patrizia
Pinnetti, Carmela
Antinori, Andrea
Capobianchi, Maria Rosaria
author_sort Amendola, Alessandra
collection PubMed
description New methods of HIV-1 RNA quantification based on dual-target detection are increasingly used in HIV viral load monitoring, but clinical implications and impact of dual-target detection on HIV-1 infection management are not established. Aptima HIV-1 Quant Dx assay is a last generation HIV viral load method, that uses pol and LTR as simultaneous target, providing quantitative results based mainly on pol target, while LTR target is used to report the results when pol signal is absent. In our laboratory, about 6% of results of all HIV-1 viral load tests performed with this platform in one year period resulted from LTR signal. Interestingly, LTR-based viremia (sometimes exceeding 1,000 copies/mL) was observed in a small proportion (up to 1%) of patients under ART, considered for long time virologically suppressed on the basis of a single target (pol-based) assay. Male gender, >700 vs <200 CD4 cell/mL and dual therapy including NRTI plus either NNRTI, or PI/b or INSTI were independently associated with increased risk of LTR-based HIV-1 viral load detection by multivariable logistic regression. A significant linear correlation was observed between LTR-based HIV-1 RNA levels and PBMC-associated proviral DNA. Moreover, in a small group of patients with HIV-1 RNA levels >200 copies/mL, longitudinal assessments showed parallel kinetics between plasma viremia and proviral DNA. Sequencing of pol region for drug resistance assessment in patients with LTR-based viremia failed on plasma HIV-1 RNA, while it was successful on proviral DNA. The detection/quantification of HIV-1 viremia based only on LTR signal with a dual target assay in samples resulting undetectable with the more conventional target pol needs accurate evaluation; unravelling the biological basis of this phenomenon, here described for the first time, is mandatory to establish relevance and implication by both pathogenetic (i.e. infectivity of LTR-detected viruses, reservoir turnover, immune activation, etc.) and clinical standpoint.
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spelling pubmed-70019512020-02-18 The dual-target approach in viral HIV-1 viremia testing: An added value to virological monitoring? Amendola, Alessandra Sberna, Giuseppe Forbici, Federica Abbate, Isabella Lorenzini, Patrizia Pinnetti, Carmela Antinori, Andrea Capobianchi, Maria Rosaria PLoS One Research Article New methods of HIV-1 RNA quantification based on dual-target detection are increasingly used in HIV viral load monitoring, but clinical implications and impact of dual-target detection on HIV-1 infection management are not established. Aptima HIV-1 Quant Dx assay is a last generation HIV viral load method, that uses pol and LTR as simultaneous target, providing quantitative results based mainly on pol target, while LTR target is used to report the results when pol signal is absent. In our laboratory, about 6% of results of all HIV-1 viral load tests performed with this platform in one year period resulted from LTR signal. Interestingly, LTR-based viremia (sometimes exceeding 1,000 copies/mL) was observed in a small proportion (up to 1%) of patients under ART, considered for long time virologically suppressed on the basis of a single target (pol-based) assay. Male gender, >700 vs <200 CD4 cell/mL and dual therapy including NRTI plus either NNRTI, or PI/b or INSTI were independently associated with increased risk of LTR-based HIV-1 viral load detection by multivariable logistic regression. A significant linear correlation was observed between LTR-based HIV-1 RNA levels and PBMC-associated proviral DNA. Moreover, in a small group of patients with HIV-1 RNA levels >200 copies/mL, longitudinal assessments showed parallel kinetics between plasma viremia and proviral DNA. Sequencing of pol region for drug resistance assessment in patients with LTR-based viremia failed on plasma HIV-1 RNA, while it was successful on proviral DNA. The detection/quantification of HIV-1 viremia based only on LTR signal with a dual target assay in samples resulting undetectable with the more conventional target pol needs accurate evaluation; unravelling the biological basis of this phenomenon, here described for the first time, is mandatory to establish relevance and implication by both pathogenetic (i.e. infectivity of LTR-detected viruses, reservoir turnover, immune activation, etc.) and clinical standpoint. Public Library of Science 2020-02-05 /pmc/articles/PMC7001951/ /pubmed/32023284 http://dx.doi.org/10.1371/journal.pone.0228192 Text en © 2020 Amendola et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Amendola, Alessandra
Sberna, Giuseppe
Forbici, Federica
Abbate, Isabella
Lorenzini, Patrizia
Pinnetti, Carmela
Antinori, Andrea
Capobianchi, Maria Rosaria
The dual-target approach in viral HIV-1 viremia testing: An added value to virological monitoring?
title The dual-target approach in viral HIV-1 viremia testing: An added value to virological monitoring?
title_full The dual-target approach in viral HIV-1 viremia testing: An added value to virological monitoring?
title_fullStr The dual-target approach in viral HIV-1 viremia testing: An added value to virological monitoring?
title_full_unstemmed The dual-target approach in viral HIV-1 viremia testing: An added value to virological monitoring?
title_short The dual-target approach in viral HIV-1 viremia testing: An added value to virological monitoring?
title_sort dual-target approach in viral hiv-1 viremia testing: an added value to virological monitoring?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7001951/
https://www.ncbi.nlm.nih.gov/pubmed/32023284
http://dx.doi.org/10.1371/journal.pone.0228192
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