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Single-cell characterization and quantification of translation-competent viral reservoirs in treated and untreated HIV infection

The phenotypic characterization of the cells in which HIV persists during antiretroviral therapy (ART) remains technically challenging. We developed a simple flow cytometry-based assay to quantify and characterize infected cells producing HIV proteins during untreated and treated HIV infection. By c...

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Autores principales: Pardons, Marion, Baxter, Amy E., Massanella, Marta, Pagliuzza, Amélie, Fromentin, Rémi, Dufour, Caroline, Leyre, Louise, Routy, Jean-Pierre, Kaufmann, Daniel E., Chomont, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411230/
https://www.ncbi.nlm.nih.gov/pubmed/30811499
http://dx.doi.org/10.1371/journal.ppat.1007619
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author Pardons, Marion
Baxter, Amy E.
Massanella, Marta
Pagliuzza, Amélie
Fromentin, Rémi
Dufour, Caroline
Leyre, Louise
Routy, Jean-Pierre
Kaufmann, Daniel E.
Chomont, Nicolas
author_facet Pardons, Marion
Baxter, Amy E.
Massanella, Marta
Pagliuzza, Amélie
Fromentin, Rémi
Dufour, Caroline
Leyre, Louise
Routy, Jean-Pierre
Kaufmann, Daniel E.
Chomont, Nicolas
author_sort Pardons, Marion
collection PubMed
description The phenotypic characterization of the cells in which HIV persists during antiretroviral therapy (ART) remains technically challenging. We developed a simple flow cytometry-based assay to quantify and characterize infected cells producing HIV proteins during untreated and treated HIV infection. By combining two antibodies targeting the HIV capsid in a standard intracellular staining protocol, we demonstrate that p24-producing cells can be detected with high specificity and sensitivity in the blood from people living with HIV. In untreated individuals, the frequency of productively infected cells strongly correlated with plasma viral load. Infected cells preferentially displayed a transitional memory phenotype and were enriched in Th17, peripheral Tfh and regulatory T cells subsets. These cells also preferentially expressed activation markers (CD25, HLA-DR, Ki67), immune checkpoint molecules (PD-1, LAG-3, TIGIT, Tim-3) as well as the integrins α4β7 and α4β1. In virally suppressed individuals on ART, p24-producing cells were only detected upon stimulation (median frequency of 4.3 p24+ cells/10(6) cells). These measures correlated with other assays assessing the size of the persistent reservoir including total and integrated HIV DNA, Tat/rev Induced Limiting Dilution Assay (TILDA) and quantitative viral outgrowth assay (QVOA). In ART-suppressed individuals, p24-producing cells preferentially displayed a transitional and effector memory phenotype, and expressed immune checkpoint molecules (PD-1, TIGIT) as well as the integrin α4β1. Remarkably, α4β1 was expressed by more than 70% of infected cells both in untreated and ART-suppressed individuals. Altogether, these results highlight a broad diversity in the phenotypes of HIV-infected cells in treated and untreated infection and suggest that strategies targeting multiple and phenotypically distinct cellular reservoirs will be needed to exert a significant impact on the size of the reservoir.
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spelling pubmed-64112302019-04-02 Single-cell characterization and quantification of translation-competent viral reservoirs in treated and untreated HIV infection Pardons, Marion Baxter, Amy E. Massanella, Marta Pagliuzza, Amélie Fromentin, Rémi Dufour, Caroline Leyre, Louise Routy, Jean-Pierre Kaufmann, Daniel E. Chomont, Nicolas PLoS Pathog Research Article The phenotypic characterization of the cells in which HIV persists during antiretroviral therapy (ART) remains technically challenging. We developed a simple flow cytometry-based assay to quantify and characterize infected cells producing HIV proteins during untreated and treated HIV infection. By combining two antibodies targeting the HIV capsid in a standard intracellular staining protocol, we demonstrate that p24-producing cells can be detected with high specificity and sensitivity in the blood from people living with HIV. In untreated individuals, the frequency of productively infected cells strongly correlated with plasma viral load. Infected cells preferentially displayed a transitional memory phenotype and were enriched in Th17, peripheral Tfh and regulatory T cells subsets. These cells also preferentially expressed activation markers (CD25, HLA-DR, Ki67), immune checkpoint molecules (PD-1, LAG-3, TIGIT, Tim-3) as well as the integrins α4β7 and α4β1. In virally suppressed individuals on ART, p24-producing cells were only detected upon stimulation (median frequency of 4.3 p24+ cells/10(6) cells). These measures correlated with other assays assessing the size of the persistent reservoir including total and integrated HIV DNA, Tat/rev Induced Limiting Dilution Assay (TILDA) and quantitative viral outgrowth assay (QVOA). In ART-suppressed individuals, p24-producing cells preferentially displayed a transitional and effector memory phenotype, and expressed immune checkpoint molecules (PD-1, TIGIT) as well as the integrin α4β1. Remarkably, α4β1 was expressed by more than 70% of infected cells both in untreated and ART-suppressed individuals. Altogether, these results highlight a broad diversity in the phenotypes of HIV-infected cells in treated and untreated infection and suggest that strategies targeting multiple and phenotypically distinct cellular reservoirs will be needed to exert a significant impact on the size of the reservoir. Public Library of Science 2019-02-27 /pmc/articles/PMC6411230/ /pubmed/30811499 http://dx.doi.org/10.1371/journal.ppat.1007619 Text en © 2019 Pardons 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
Pardons, Marion
Baxter, Amy E.
Massanella, Marta
Pagliuzza, Amélie
Fromentin, Rémi
Dufour, Caroline
Leyre, Louise
Routy, Jean-Pierre
Kaufmann, Daniel E.
Chomont, Nicolas
Single-cell characterization and quantification of translation-competent viral reservoirs in treated and untreated HIV infection
title Single-cell characterization and quantification of translation-competent viral reservoirs in treated and untreated HIV infection
title_full Single-cell characterization and quantification of translation-competent viral reservoirs in treated and untreated HIV infection
title_fullStr Single-cell characterization and quantification of translation-competent viral reservoirs in treated and untreated HIV infection
title_full_unstemmed Single-cell characterization and quantification of translation-competent viral reservoirs in treated and untreated HIV infection
title_short Single-cell characterization and quantification of translation-competent viral reservoirs in treated and untreated HIV infection
title_sort single-cell characterization and quantification of translation-competent viral reservoirs in treated and untreated hiv infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411230/
https://www.ncbi.nlm.nih.gov/pubmed/30811499
http://dx.doi.org/10.1371/journal.ppat.1007619
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