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Analysis of Th17 and Tc17 Frequencies and Antiviral Defenses in Gut-Associated Lymphoid Tissue of Chronic HIV-1 Positive Patients

The complex relationship between both the Th1/Th17 and Tc1/Tc17 axis and innate defences in the intestinal mucosa during HIV-1 infection has not been well characterized. This study examined the frequency, phenotype, and functional status of T cell populations in the gut-associated lymphoid tissue an...

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Autores principales: d'Ettorre, Gabriella, Ceccarelli, Giancarlo, Andreotti, Mauro, Selvaggi, Carla, Giustini, Noemi, Serafino, Sara, Schietroma, Ivan, Nunnari, Giuseppe, Antonelli, Guido, Vullo, Vincenzo, Scagnolari, Carolina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499407/
https://www.ncbi.nlm.nih.gov/pubmed/26221062
http://dx.doi.org/10.1155/2015/395484
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author d'Ettorre, Gabriella
Ceccarelli, Giancarlo
Andreotti, Mauro
Selvaggi, Carla
Giustini, Noemi
Serafino, Sara
Schietroma, Ivan
Nunnari, Giuseppe
Antonelli, Guido
Vullo, Vincenzo
Scagnolari, Carolina
author_facet d'Ettorre, Gabriella
Ceccarelli, Giancarlo
Andreotti, Mauro
Selvaggi, Carla
Giustini, Noemi
Serafino, Sara
Schietroma, Ivan
Nunnari, Giuseppe
Antonelli, Guido
Vullo, Vincenzo
Scagnolari, Carolina
author_sort d'Ettorre, Gabriella
collection PubMed
description The complex relationship between both the Th1/Th17 and Tc1/Tc17 axis and innate defences in the intestinal mucosa during HIV-1 infection has not been well characterized. This study examined the frequency, phenotype, and functional status of T cell populations in the gut-associated lymphoid tissue and peripheral blood of virologically suppressed HIV-1-infected patients on therapy, focusing on the Th1, Th17, Tc1, and Tc17 cell subsets. We found a persistent immune cell activation (CD38 and HLADR expression) into the GALT despite the higher levels of Th17 and Tc17 in respect to peripheral blood. An upregulation of type I IFN response in GALT compared to the peripheral blood compartment was also recorded. Furthermore, IFN-α/β levels were negatively related to the frequencies of Th1 naïve cells and Tc1 cell subsets (naïve, central memory, and effector memory) in the GALT. In contrast, no relationships between type I IFN response and Th1 or Tc1 cell subsets in peripheral blood compartment and between IFN-α/β and Th17/Tc17 in both GALT and peripheral blood district were recorded. These data indicate that prolonged antiretroviral treatment improves GALT immune function despite the persistence of immune activation and type I IFN response in chronic HIV-1 positive patients.
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spelling pubmed-44994072015-07-28 Analysis of Th17 and Tc17 Frequencies and Antiviral Defenses in Gut-Associated Lymphoid Tissue of Chronic HIV-1 Positive Patients d'Ettorre, Gabriella Ceccarelli, Giancarlo Andreotti, Mauro Selvaggi, Carla Giustini, Noemi Serafino, Sara Schietroma, Ivan Nunnari, Giuseppe Antonelli, Guido Vullo, Vincenzo Scagnolari, Carolina Mediators Inflamm Research Article The complex relationship between both the Th1/Th17 and Tc1/Tc17 axis and innate defences in the intestinal mucosa during HIV-1 infection has not been well characterized. This study examined the frequency, phenotype, and functional status of T cell populations in the gut-associated lymphoid tissue and peripheral blood of virologically suppressed HIV-1-infected patients on therapy, focusing on the Th1, Th17, Tc1, and Tc17 cell subsets. We found a persistent immune cell activation (CD38 and HLADR expression) into the GALT despite the higher levels of Th17 and Tc17 in respect to peripheral blood. An upregulation of type I IFN response in GALT compared to the peripheral blood compartment was also recorded. Furthermore, IFN-α/β levels were negatively related to the frequencies of Th1 naïve cells and Tc1 cell subsets (naïve, central memory, and effector memory) in the GALT. In contrast, no relationships between type I IFN response and Th1 or Tc1 cell subsets in peripheral blood compartment and between IFN-α/β and Th17/Tc17 in both GALT and peripheral blood district were recorded. These data indicate that prolonged antiretroviral treatment improves GALT immune function despite the persistence of immune activation and type I IFN response in chronic HIV-1 positive patients. Hindawi Publishing Corporation 2015 2015-06-28 /pmc/articles/PMC4499407/ /pubmed/26221062 http://dx.doi.org/10.1155/2015/395484 Text en Copyright © 2015 Gabriella d'Ettorre et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
d'Ettorre, Gabriella
Ceccarelli, Giancarlo
Andreotti, Mauro
Selvaggi, Carla
Giustini, Noemi
Serafino, Sara
Schietroma, Ivan
Nunnari, Giuseppe
Antonelli, Guido
Vullo, Vincenzo
Scagnolari, Carolina
Analysis of Th17 and Tc17 Frequencies and Antiviral Defenses in Gut-Associated Lymphoid Tissue of Chronic HIV-1 Positive Patients
title Analysis of Th17 and Tc17 Frequencies and Antiviral Defenses in Gut-Associated Lymphoid Tissue of Chronic HIV-1 Positive Patients
title_full Analysis of Th17 and Tc17 Frequencies and Antiviral Defenses in Gut-Associated Lymphoid Tissue of Chronic HIV-1 Positive Patients
title_fullStr Analysis of Th17 and Tc17 Frequencies and Antiviral Defenses in Gut-Associated Lymphoid Tissue of Chronic HIV-1 Positive Patients
title_full_unstemmed Analysis of Th17 and Tc17 Frequencies and Antiviral Defenses in Gut-Associated Lymphoid Tissue of Chronic HIV-1 Positive Patients
title_short Analysis of Th17 and Tc17 Frequencies and Antiviral Defenses in Gut-Associated Lymphoid Tissue of Chronic HIV-1 Positive Patients
title_sort analysis of th17 and tc17 frequencies and antiviral defenses in gut-associated lymphoid tissue of chronic hiv-1 positive patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4499407/
https://www.ncbi.nlm.nih.gov/pubmed/26221062
http://dx.doi.org/10.1155/2015/395484
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