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High IFN-γ Release and Impaired Capacity of Multi-Cytokine Secretion in IGRA Supernatants Are Associated with Active Tuberculosis

Interferon gamma (IFN-γ) release assays (IGRAs) detect Mycobacterium tuberculosis (Mtb) infection regardless of the active (ATB) or latent (LTBI) forms of tuberculosis (TB). In this study, Mtb-specific T cell response against region of deletion 1 (RD1) antigens were explored by a microbead multiplex...

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Autores principales: Carrère-Kremer, Séverine, Rubbo, Pierre-Alain, Pisoni, Amandine, Bendriss, Sophie, Marin, Grégory, Peries, Marianne, Bolloré, Karine, Terru, Dominique, Godreuil, Sylvain, Bourdin, Arnaud, Van de Perre, Philippe, Tuaillon, Edouard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5014470/
https://www.ncbi.nlm.nih.gov/pubmed/27603919
http://dx.doi.org/10.1371/journal.pone.0162137
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author Carrère-Kremer, Séverine
Rubbo, Pierre-Alain
Pisoni, Amandine
Bendriss, Sophie
Marin, Grégory
Peries, Marianne
Bolloré, Karine
Terru, Dominique
Godreuil, Sylvain
Bourdin, Arnaud
Van de Perre, Philippe
Tuaillon, Edouard
author_facet Carrère-Kremer, Séverine
Rubbo, Pierre-Alain
Pisoni, Amandine
Bendriss, Sophie
Marin, Grégory
Peries, Marianne
Bolloré, Karine
Terru, Dominique
Godreuil, Sylvain
Bourdin, Arnaud
Van de Perre, Philippe
Tuaillon, Edouard
author_sort Carrère-Kremer, Séverine
collection PubMed
description Interferon gamma (IFN-γ) release assays (IGRAs) detect Mycobacterium tuberculosis (Mtb) infection regardless of the active (ATB) or latent (LTBI) forms of tuberculosis (TB). In this study, Mtb-specific T cell response against region of deletion 1 (RD1) antigens were explored by a microbead multiplex assay performed in T-SPOT TB assay (T-SPOT) supernatants from 35 patients with ATB and 115 patients with LTBI. T-SPOT is positive when over 7 IFN-γ secreting cells (SC)/250 000 peripheral blood mononuclear cells (PBMC) are enumerated. However, over 100 IFN-γ SC /250 000 PBMC were more frequently observed in the ATB group compared to the LTBI group. By contrast, lower cytokine concentrations and lower cytokine productions relative to IFN-γ secretion were observed for IL 4, IL-12, TNF-α, GM-CSF, Eotaxin and IFN-α when compared to LTBI. Thus, high IFN-γ release and low cytokine secretions in relation with IFN-γ production appeared as signatures of ATB, corroborating that multicytokine Mtb-specific response against RD1 antigens reflects host capacity to contain TB reactivation. In this way, testing cytokine profile in IGRA supernatants would be helpful to improve ATB screening strategy including immunologic tests.
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spelling pubmed-50144702016-09-27 High IFN-γ Release and Impaired Capacity of Multi-Cytokine Secretion in IGRA Supernatants Are Associated with Active Tuberculosis Carrère-Kremer, Séverine Rubbo, Pierre-Alain Pisoni, Amandine Bendriss, Sophie Marin, Grégory Peries, Marianne Bolloré, Karine Terru, Dominique Godreuil, Sylvain Bourdin, Arnaud Van de Perre, Philippe Tuaillon, Edouard PLoS One Research Article Interferon gamma (IFN-γ) release assays (IGRAs) detect Mycobacterium tuberculosis (Mtb) infection regardless of the active (ATB) or latent (LTBI) forms of tuberculosis (TB). In this study, Mtb-specific T cell response against region of deletion 1 (RD1) antigens were explored by a microbead multiplex assay performed in T-SPOT TB assay (T-SPOT) supernatants from 35 patients with ATB and 115 patients with LTBI. T-SPOT is positive when over 7 IFN-γ secreting cells (SC)/250 000 peripheral blood mononuclear cells (PBMC) are enumerated. However, over 100 IFN-γ SC /250 000 PBMC were more frequently observed in the ATB group compared to the LTBI group. By contrast, lower cytokine concentrations and lower cytokine productions relative to IFN-γ secretion were observed for IL 4, IL-12, TNF-α, GM-CSF, Eotaxin and IFN-α when compared to LTBI. Thus, high IFN-γ release and low cytokine secretions in relation with IFN-γ production appeared as signatures of ATB, corroborating that multicytokine Mtb-specific response against RD1 antigens reflects host capacity to contain TB reactivation. In this way, testing cytokine profile in IGRA supernatants would be helpful to improve ATB screening strategy including immunologic tests. Public Library of Science 2016-09-07 /pmc/articles/PMC5014470/ /pubmed/27603919 http://dx.doi.org/10.1371/journal.pone.0162137 Text en © 2016 Carrère-Kremer 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
Carrère-Kremer, Séverine
Rubbo, Pierre-Alain
Pisoni, Amandine
Bendriss, Sophie
Marin, Grégory
Peries, Marianne
Bolloré, Karine
Terru, Dominique
Godreuil, Sylvain
Bourdin, Arnaud
Van de Perre, Philippe
Tuaillon, Edouard
High IFN-γ Release and Impaired Capacity of Multi-Cytokine Secretion in IGRA Supernatants Are Associated with Active Tuberculosis
title High IFN-γ Release and Impaired Capacity of Multi-Cytokine Secretion in IGRA Supernatants Are Associated with Active Tuberculosis
title_full High IFN-γ Release and Impaired Capacity of Multi-Cytokine Secretion in IGRA Supernatants Are Associated with Active Tuberculosis
title_fullStr High IFN-γ Release and Impaired Capacity of Multi-Cytokine Secretion in IGRA Supernatants Are Associated with Active Tuberculosis
title_full_unstemmed High IFN-γ Release and Impaired Capacity of Multi-Cytokine Secretion in IGRA Supernatants Are Associated with Active Tuberculosis
title_short High IFN-γ Release and Impaired Capacity of Multi-Cytokine Secretion in IGRA Supernatants Are Associated with Active Tuberculosis
title_sort high ifn-γ release and impaired capacity of multi-cytokine secretion in igra supernatants are associated with active tuberculosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5014470/
https://www.ncbi.nlm.nih.gov/pubmed/27603919
http://dx.doi.org/10.1371/journal.pone.0162137
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