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Immunological biomarkers predict HIV-1 viral rebound after treatment interruption

Treatment of HIV-1 infection with antiretroviral therapy (ART) in the weeks following transmission may induce a state of ‘post-treatment control' (PTC) in some patients, in whom viraemia remains undetectable when ART is stopped. Explaining PTC could help our understanding of the processes that...

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Autores principales: Hurst, Jacob, Hoffmann, Matthias, Pace, Matthew, Williams, James P., Thornhill, John, Hamlyn, Elizabeth, Meyerowitz, Jodi, Willberg, Chris, Koelsch, Kersten K., Robinson, Nicola, Brown, Helen, Fisher, Martin, Kinloch, Sabine, Cooper, David A., Schechter, Mauro, Tambussi, Giuseppe, Fidler, Sarah, Babiker, Abdel, Weber, Jonathan, Kelleher, Anthony D., Phillips, Rodney E., Frater, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633715/
https://www.ncbi.nlm.nih.gov/pubmed/26449164
http://dx.doi.org/10.1038/ncomms9495
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author Hurst, Jacob
Hoffmann, Matthias
Pace, Matthew
Williams, James P.
Thornhill, John
Hamlyn, Elizabeth
Meyerowitz, Jodi
Willberg, Chris
Koelsch, Kersten K.
Robinson, Nicola
Brown, Helen
Fisher, Martin
Kinloch, Sabine
Cooper, David A.
Schechter, Mauro
Tambussi, Giuseppe
Fidler, Sarah
Babiker, Abdel
Weber, Jonathan
Kelleher, Anthony D.
Phillips, Rodney E.
Frater, John
author_facet Hurst, Jacob
Hoffmann, Matthias
Pace, Matthew
Williams, James P.
Thornhill, John
Hamlyn, Elizabeth
Meyerowitz, Jodi
Willberg, Chris
Koelsch, Kersten K.
Robinson, Nicola
Brown, Helen
Fisher, Martin
Kinloch, Sabine
Cooper, David A.
Schechter, Mauro
Tambussi, Giuseppe
Fidler, Sarah
Babiker, Abdel
Weber, Jonathan
Kelleher, Anthony D.
Phillips, Rodney E.
Frater, John
author_sort Hurst, Jacob
collection PubMed
description Treatment of HIV-1 infection with antiretroviral therapy (ART) in the weeks following transmission may induce a state of ‘post-treatment control' (PTC) in some patients, in whom viraemia remains undetectable when ART is stopped. Explaining PTC could help our understanding of the processes that maintain viral persistence. Here we show that immunological biomarkers can predict time to viral rebound after stopping ART by analysing data from a randomized study of primary HIV-1 infection incorporating a treatment interruption (TI) after 48 weeks of ART (the SPARTAC trial). T-cell exhaustion markers PD-1, Tim-3 and Lag-3 measured prior to ART strongly predict time to the return of viraemia. These data indicate that T-cell exhaustion markers may identify those latently infected cells with a higher proclivity to viral transcription. Our results may open new avenues for understanding the mechanisms underlying PTC, and eventually HIV-1 eradication.
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spelling pubmed-46337152015-11-25 Immunological biomarkers predict HIV-1 viral rebound after treatment interruption Hurst, Jacob Hoffmann, Matthias Pace, Matthew Williams, James P. Thornhill, John Hamlyn, Elizabeth Meyerowitz, Jodi Willberg, Chris Koelsch, Kersten K. Robinson, Nicola Brown, Helen Fisher, Martin Kinloch, Sabine Cooper, David A. Schechter, Mauro Tambussi, Giuseppe Fidler, Sarah Babiker, Abdel Weber, Jonathan Kelleher, Anthony D. Phillips, Rodney E. Frater, John Nat Commun Article Treatment of HIV-1 infection with antiretroviral therapy (ART) in the weeks following transmission may induce a state of ‘post-treatment control' (PTC) in some patients, in whom viraemia remains undetectable when ART is stopped. Explaining PTC could help our understanding of the processes that maintain viral persistence. Here we show that immunological biomarkers can predict time to viral rebound after stopping ART by analysing data from a randomized study of primary HIV-1 infection incorporating a treatment interruption (TI) after 48 weeks of ART (the SPARTAC trial). T-cell exhaustion markers PD-1, Tim-3 and Lag-3 measured prior to ART strongly predict time to the return of viraemia. These data indicate that T-cell exhaustion markers may identify those latently infected cells with a higher proclivity to viral transcription. Our results may open new avenues for understanding the mechanisms underlying PTC, and eventually HIV-1 eradication. Nature Pub. Group 2015-10-09 /pmc/articles/PMC4633715/ /pubmed/26449164 http://dx.doi.org/10.1038/ncomms9495 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Hurst, Jacob
Hoffmann, Matthias
Pace, Matthew
Williams, James P.
Thornhill, John
Hamlyn, Elizabeth
Meyerowitz, Jodi
Willberg, Chris
Koelsch, Kersten K.
Robinson, Nicola
Brown, Helen
Fisher, Martin
Kinloch, Sabine
Cooper, David A.
Schechter, Mauro
Tambussi, Giuseppe
Fidler, Sarah
Babiker, Abdel
Weber, Jonathan
Kelleher, Anthony D.
Phillips, Rodney E.
Frater, John
Immunological biomarkers predict HIV-1 viral rebound after treatment interruption
title Immunological biomarkers predict HIV-1 viral rebound after treatment interruption
title_full Immunological biomarkers predict HIV-1 viral rebound after treatment interruption
title_fullStr Immunological biomarkers predict HIV-1 viral rebound after treatment interruption
title_full_unstemmed Immunological biomarkers predict HIV-1 viral rebound after treatment interruption
title_short Immunological biomarkers predict HIV-1 viral rebound after treatment interruption
title_sort immunological biomarkers predict hiv-1 viral rebound after treatment interruption
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633715/
https://www.ncbi.nlm.nih.gov/pubmed/26449164
http://dx.doi.org/10.1038/ncomms9495
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