The roles of immune memory and aging in protective immunity and endogenous reactivation of tuberculosis.

Finding more effective vaccines against tuberculosis (TB) and improved preventive treatments against endogenous reactivation of latent TB is strategic to block transmission and reach the WHO goal of eliminating TB by 2050. Key related open questions in TB research include: i) what are the determinan...

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Autores principales: Giorgio Guzzetta, Denise Kirschner
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Publicado: Public Library of Science (PLoS) 2013
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Acceso en línea:https://doaj.org/article/658fc6e66a944935a596df5f64211964
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spelling oai:doaj.org-article:658fc6e66a944935a596df5f642119642021-11-18T07:50:16ZThe roles of immune memory and aging in protective immunity and endogenous reactivation of tuberculosis.1932-620310.1371/journal.pone.0060425https://doaj.org/article/658fc6e66a944935a596df5f642119642013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23580062/?tool=EBIhttps://doaj.org/toc/1932-6203Finding more effective vaccines against tuberculosis (TB) and improved preventive treatments against endogenous reactivation of latent TB is strategic to block transmission and reach the WHO goal of eliminating TB by 2050. Key related open questions in TB research include: i) what are the determinants of a strong memory response upon primary infection? ii) what is the role of cytokines towards protective memory response against a secondary infection? iii) what are the mechanisms responsible for the increased risk of reactivation in elderly individuals? To address these questions, we explored a computational model of the immune response to Mycobacterium tuberculosis including a mathematical description of immunosenescence and the generation and maintenance of immune memory. Sensitivity analysis techniques, together with extensive model characterization and in silico experiments, were applied to identify key mechanisms controlling TB reactivation and immunological memory. Key findings of this study are summarized by the following model predictions: i) increased strength and duration of memory protection is associated with higher levels of Tumor Necrosis Factor-[Formula: see text] (TNF) during primary infection; ii) production of TNF, but not of interferon-[Formula: see text], by memory T cells during secondary infection is a major determinant of effective protection; iii) impaired recruitment of CD4+ T cells may promote reactivation of latent TB infections in aging hosts. This study is a first attempt to consider the immune dynamics of a persistent infection throughout the lifetime of the host, taking into account immunosenescence and memory. While the model is TB specific, the results are applicable to other persistent bacterial infections and can aid in the development, evaluation and refinement of TB treatment and/or vaccine protocols.Giorgio GuzzettaDenise KirschnerPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 4, p e60425 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Giorgio Guzzetta
Denise Kirschner
The roles of immune memory and aging in protective immunity and endogenous reactivation of tuberculosis.
description Finding more effective vaccines against tuberculosis (TB) and improved preventive treatments against endogenous reactivation of latent TB is strategic to block transmission and reach the WHO goal of eliminating TB by 2050. Key related open questions in TB research include: i) what are the determinants of a strong memory response upon primary infection? ii) what is the role of cytokines towards protective memory response against a secondary infection? iii) what are the mechanisms responsible for the increased risk of reactivation in elderly individuals? To address these questions, we explored a computational model of the immune response to Mycobacterium tuberculosis including a mathematical description of immunosenescence and the generation and maintenance of immune memory. Sensitivity analysis techniques, together with extensive model characterization and in silico experiments, were applied to identify key mechanisms controlling TB reactivation and immunological memory. Key findings of this study are summarized by the following model predictions: i) increased strength and duration of memory protection is associated with higher levels of Tumor Necrosis Factor-[Formula: see text] (TNF) during primary infection; ii) production of TNF, but not of interferon-[Formula: see text], by memory T cells during secondary infection is a major determinant of effective protection; iii) impaired recruitment of CD4+ T cells may promote reactivation of latent TB infections in aging hosts. This study is a first attempt to consider the immune dynamics of a persistent infection throughout the lifetime of the host, taking into account immunosenescence and memory. While the model is TB specific, the results are applicable to other persistent bacterial infections and can aid in the development, evaluation and refinement of TB treatment and/or vaccine protocols.
format article
author Giorgio Guzzetta
Denise Kirschner
author_facet Giorgio Guzzetta
Denise Kirschner
author_sort Giorgio Guzzetta
title The roles of immune memory and aging in protective immunity and endogenous reactivation of tuberculosis.
title_short The roles of immune memory and aging in protective immunity and endogenous reactivation of tuberculosis.
title_full The roles of immune memory and aging in protective immunity and endogenous reactivation of tuberculosis.
title_fullStr The roles of immune memory and aging in protective immunity and endogenous reactivation of tuberculosis.
title_full_unstemmed The roles of immune memory and aging in protective immunity and endogenous reactivation of tuberculosis.
title_sort roles of immune memory and aging in protective immunity and endogenous reactivation of tuberculosis.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/658fc6e66a944935a596df5f64211964
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