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ICOS, SLAM and PD-1 expression and regulation on T lymphocytes reflect the immune dysregulation in patients with HIV-related illness with pulmonary tuberculosis
BACKGROUND: Tuberculosis (TB) continues to be the most frequent cause of illness and death from an infectious agent globally, and its interaction with HIV is having devastating effects. To investigate how HIV alters the immune response to Mycobacterium tuberculosis (Mtb), we assessed basal and Mtb-i...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International AIDS Society
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499801/ https://www.ncbi.nlm.nih.gov/pubmed/22713261 http://dx.doi.org/10.7448/IAS.15.2.17428 |
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author | Jurado, Javier Oscar Pasquinelli, Virginia Alvarez, Ivana Belén Martínez, Gustavo Javier Laufer, Natalia Sued, Omar Cahn, Pedro Musella, Rosa María Abbate, Eduardo Salomón, Horacio Quiroga, María Florencia |
author_facet | Jurado, Javier Oscar Pasquinelli, Virginia Alvarez, Ivana Belén Martínez, Gustavo Javier Laufer, Natalia Sued, Omar Cahn, Pedro Musella, Rosa María Abbate, Eduardo Salomón, Horacio Quiroga, María Florencia |
author_sort | Jurado, Javier Oscar |
collection | PubMed |
description | BACKGROUND: Tuberculosis (TB) continues to be the most frequent cause of illness and death from an infectious agent globally, and its interaction with HIV is having devastating effects. To investigate how HIV alters the immune response to Mycobacterium tuberculosis (Mtb), we assessed basal and Mtb-induced proliferation, cytokine production, and expression of signalling lymphocytic activation molecule (SLAM), inducible costimulator (ICOS) and programmed death-1 (PD-1) on T lymphocytes from HIV-positive individuals coinfected with TB, HIV-positive subjects, TB patients and healthy donors (HD). FINDINGS: HIV-TB patients showed increased ICOS, SLAM and PD-1 basal levels on T lymphocytes, whereas HIV-positive individuals displayed elevated levels of SLAM and PD-1, TB patients high levels of SLAM, and HD low levels of the three proteins. Mtb-stimulation enhanced ICOS expression in the four groups, but only TB and HD increased SLAM and PD-1 levels. CONCLUSIONS: These data show the immune deregulation that takes place during the immune response against TB in different study populations. |
format | Online Article Text |
id | pubmed-3499801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International AIDS Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-34998012012-11-26 ICOS, SLAM and PD-1 expression and regulation on T lymphocytes reflect the immune dysregulation in patients with HIV-related illness with pulmonary tuberculosis Jurado, Javier Oscar Pasquinelli, Virginia Alvarez, Ivana Belén Martínez, Gustavo Javier Laufer, Natalia Sued, Omar Cahn, Pedro Musella, Rosa María Abbate, Eduardo Salomón, Horacio Quiroga, María Florencia J Int AIDS Soc Short Report BACKGROUND: Tuberculosis (TB) continues to be the most frequent cause of illness and death from an infectious agent globally, and its interaction with HIV is having devastating effects. To investigate how HIV alters the immune response to Mycobacterium tuberculosis (Mtb), we assessed basal and Mtb-induced proliferation, cytokine production, and expression of signalling lymphocytic activation molecule (SLAM), inducible costimulator (ICOS) and programmed death-1 (PD-1) on T lymphocytes from HIV-positive individuals coinfected with TB, HIV-positive subjects, TB patients and healthy donors (HD). FINDINGS: HIV-TB patients showed increased ICOS, SLAM and PD-1 basal levels on T lymphocytes, whereas HIV-positive individuals displayed elevated levels of SLAM and PD-1, TB patients high levels of SLAM, and HD low levels of the three proteins. Mtb-stimulation enhanced ICOS expression in the four groups, but only TB and HD increased SLAM and PD-1 levels. CONCLUSIONS: These data show the immune deregulation that takes place during the immune response against TB in different study populations. International AIDS Society 2012-06-14 /pmc/articles/PMC3499801/ /pubmed/22713261 http://dx.doi.org/10.7448/IAS.15.2.17428 Text en © 2012 Jurado JO et al; licensee International AIDS Society http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Report Jurado, Javier Oscar Pasquinelli, Virginia Alvarez, Ivana Belén Martínez, Gustavo Javier Laufer, Natalia Sued, Omar Cahn, Pedro Musella, Rosa María Abbate, Eduardo Salomón, Horacio Quiroga, María Florencia ICOS, SLAM and PD-1 expression and regulation on T lymphocytes reflect the immune dysregulation in patients with HIV-related illness with pulmonary tuberculosis |
title | ICOS, SLAM and PD-1 expression and regulation on T lymphocytes reflect the immune dysregulation in patients with HIV-related illness with pulmonary tuberculosis |
title_full | ICOS, SLAM and PD-1 expression and regulation on T lymphocytes reflect the immune dysregulation in patients with HIV-related illness with pulmonary tuberculosis |
title_fullStr | ICOS, SLAM and PD-1 expression and regulation on T lymphocytes reflect the immune dysregulation in patients with HIV-related illness with pulmonary tuberculosis |
title_full_unstemmed | ICOS, SLAM and PD-1 expression and regulation on T lymphocytes reflect the immune dysregulation in patients with HIV-related illness with pulmonary tuberculosis |
title_short | ICOS, SLAM and PD-1 expression and regulation on T lymphocytes reflect the immune dysregulation in patients with HIV-related illness with pulmonary tuberculosis |
title_sort | icos, slam and pd-1 expression and regulation on t lymphocytes reflect the immune dysregulation in patients with hiv-related illness with pulmonary tuberculosis |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499801/ https://www.ncbi.nlm.nih.gov/pubmed/22713261 http://dx.doi.org/10.7448/IAS.15.2.17428 |
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