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Emerging PCR-Based Techniques to Study HIV-1 Reservoir Persistence

While current antiretroviral therapies are able to halt HIV-1 progression, they are not curative, as an interruption of treatment usually leads to viral rebound. The persistence of this stable HIV-1 latent reservoir forms the major barrier in HIV-1 cure research. The need for a better understanding...

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Autores principales: Lambrechts, Laurens, Cole, Basiel, Rutsaert, Sofie, Trypsteen, Wim, Vandekerckhove, Linos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7077278/
https://www.ncbi.nlm.nih.gov/pubmed/32012811
http://dx.doi.org/10.3390/v12020149
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author Lambrechts, Laurens
Cole, Basiel
Rutsaert, Sofie
Trypsteen, Wim
Vandekerckhove, Linos
author_facet Lambrechts, Laurens
Cole, Basiel
Rutsaert, Sofie
Trypsteen, Wim
Vandekerckhove, Linos
author_sort Lambrechts, Laurens
collection PubMed
description While current antiretroviral therapies are able to halt HIV-1 progression, they are not curative, as an interruption of treatment usually leads to viral rebound. The persistence of this stable HIV-1 latent reservoir forms the major barrier in HIV-1 cure research. The need for a better understanding of the mechanisms behind reservoir persistence resulted in the development of several novel assays allowing to perform an extensive in-depth characterization. The objective of this review is to present an overview of the current state-of-the-art PCR-based technologies to study the replication-competent HIV-1 reservoir. Here, we outline the advantages, limitations, and clinical relevance of different approaches. Future HIV-1 eradication studies would benefit from information-rich, high-throughput assays as they provide a more efficient and standardized way of characterizing the persisting HIV-1 reservoir.
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spelling pubmed-70772782020-03-20 Emerging PCR-Based Techniques to Study HIV-1 Reservoir Persistence Lambrechts, Laurens Cole, Basiel Rutsaert, Sofie Trypsteen, Wim Vandekerckhove, Linos Viruses Review While current antiretroviral therapies are able to halt HIV-1 progression, they are not curative, as an interruption of treatment usually leads to viral rebound. The persistence of this stable HIV-1 latent reservoir forms the major barrier in HIV-1 cure research. The need for a better understanding of the mechanisms behind reservoir persistence resulted in the development of several novel assays allowing to perform an extensive in-depth characterization. The objective of this review is to present an overview of the current state-of-the-art PCR-based technologies to study the replication-competent HIV-1 reservoir. Here, we outline the advantages, limitations, and clinical relevance of different approaches. Future HIV-1 eradication studies would benefit from information-rich, high-throughput assays as they provide a more efficient and standardized way of characterizing the persisting HIV-1 reservoir. MDPI 2020-01-28 /pmc/articles/PMC7077278/ /pubmed/32012811 http://dx.doi.org/10.3390/v12020149 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Lambrechts, Laurens
Cole, Basiel
Rutsaert, Sofie
Trypsteen, Wim
Vandekerckhove, Linos
Emerging PCR-Based Techniques to Study HIV-1 Reservoir Persistence
title Emerging PCR-Based Techniques to Study HIV-1 Reservoir Persistence
title_full Emerging PCR-Based Techniques to Study HIV-1 Reservoir Persistence
title_fullStr Emerging PCR-Based Techniques to Study HIV-1 Reservoir Persistence
title_full_unstemmed Emerging PCR-Based Techniques to Study HIV-1 Reservoir Persistence
title_short Emerging PCR-Based Techniques to Study HIV-1 Reservoir Persistence
title_sort emerging pcr-based techniques to study hiv-1 reservoir persistence
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7077278/
https://www.ncbi.nlm.nih.gov/pubmed/32012811
http://dx.doi.org/10.3390/v12020149
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