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The Biology and Role of Interleukin-32 in Tuberculosis

Tuberculosis, caused by Mycobacterium tuberculosis, remains a leading cause of morbidity and mortality globally, with nearly 10.4 million new cases of incidence and over 1.7 million deaths annually. Drug-resistant M. tuberculosis strains, especially multidrug-resistant or extensively drug-resistant...

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Detalles Bibliográficos
Autores principales: Li, Wu, Deng, Wanyan, Xie, Jianping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217754/
https://www.ncbi.nlm.nih.gov/pubmed/30426023
http://dx.doi.org/10.1155/2018/1535194
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author Li, Wu
Deng, Wanyan
Xie, Jianping
author_facet Li, Wu
Deng, Wanyan
Xie, Jianping
author_sort Li, Wu
collection PubMed
description Tuberculosis, caused by Mycobacterium tuberculosis, remains a leading cause of morbidity and mortality globally, with nearly 10.4 million new cases of incidence and over 1.7 million deaths annually. Drug-resistant M. tuberculosis strains, especially multidrug-resistant or extensively drug-resistant strains, have further intensified the problem associated with tuberculosis control. Host-directed therapy is a promising alternative for tuberculosis control. IL-32 is increasingly recognized as an important host molecule against tuberculosis. In this review, we highlight the proinflammatory properties of IL-32 and the mode of action of IL-32 in mycobacterial infections to inspire the development of novel immunity-based countermeasures and host-directed therapies against tuberculosis.
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spelling pubmed-62177542018-11-13 The Biology and Role of Interleukin-32 in Tuberculosis Li, Wu Deng, Wanyan Xie, Jianping J Immunol Res Review Article Tuberculosis, caused by Mycobacterium tuberculosis, remains a leading cause of morbidity and mortality globally, with nearly 10.4 million new cases of incidence and over 1.7 million deaths annually. Drug-resistant M. tuberculosis strains, especially multidrug-resistant or extensively drug-resistant strains, have further intensified the problem associated with tuberculosis control. Host-directed therapy is a promising alternative for tuberculosis control. IL-32 is increasingly recognized as an important host molecule against tuberculosis. In this review, we highlight the proinflammatory properties of IL-32 and the mode of action of IL-32 in mycobacterial infections to inspire the development of novel immunity-based countermeasures and host-directed therapies against tuberculosis. Hindawi 2018-10-22 /pmc/articles/PMC6217754/ /pubmed/30426023 http://dx.doi.org/10.1155/2018/1535194 Text en Copyright © 2018 Wu Li et al. http://creativecommons.org/licenses/by/4.0/ 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 Review Article
Li, Wu
Deng, Wanyan
Xie, Jianping
The Biology and Role of Interleukin-32 in Tuberculosis
title The Biology and Role of Interleukin-32 in Tuberculosis
title_full The Biology and Role of Interleukin-32 in Tuberculosis
title_fullStr The Biology and Role of Interleukin-32 in Tuberculosis
title_full_unstemmed The Biology and Role of Interleukin-32 in Tuberculosis
title_short The Biology and Role of Interleukin-32 in Tuberculosis
title_sort biology and role of interleukin-32 in tuberculosis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217754/
https://www.ncbi.nlm.nih.gov/pubmed/30426023
http://dx.doi.org/10.1155/2018/1535194
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