Th1 and Th17 Cells in Tuberculosis: Protection, Pathology, and Biomarkers

The outcome of Mycobacterium tuberculosis (Mtb) infection ranges from a complete pathogen clearance through asymptomatic latent infection (LTBI) to active tuberculosis (TB) disease. It is now understood that LTBI and active TB represent a continuous spectrum of states with different degrees of patho...

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Main Authors: I. V. Lyadova, A. V. Panteleev
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2015/854507
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author I. V. Lyadova
A. V. Panteleev
author_facet I. V. Lyadova
A. V. Panteleev
author_sort I. V. Lyadova
collection DOAJ
description The outcome of Mycobacterium tuberculosis (Mtb) infection ranges from a complete pathogen clearance through asymptomatic latent infection (LTBI) to active tuberculosis (TB) disease. It is now understood that LTBI and active TB represent a continuous spectrum of states with different degrees of pathogen “activity,” host pathology, and immune reactivity. Therefore, it is important to differentiate LTBI and active TB and identify active TB stages. CD4+ T cells play critical role during Mtb infection by mediating protection, contributing to inflammation, and regulating immune response. Th1 and Th17 cells are the main effector CD4+ T cells during TB. Th1 cells have been shown to contribute to TB protection by secreting IFN-γ and activating antimycobacterial action in macrophages. Th17 induce neutrophilic inflammation, mediate tissue damage, and thus have been implicated in TB pathology. In recent years new findings have accumulated that alter our view on the role of Th1 and Th17 cells during Mtb infection. This review discusses these new results and how they can be implemented for TB diagnosis and monitoring.
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issn 0962-9351
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spelling doaj-art-1102dffec49242b69efdc0dad575c4352025-02-03T05:57:07ZengWileyMediators of Inflammation0962-93511466-18612015-01-01201510.1155/2015/854507854507Th1 and Th17 Cells in Tuberculosis: Protection, Pathology, and BiomarkersI. V. Lyadova0A. V. Panteleev1Immunology Department, Central Tuberculosis Research Institute, Yauza Alley 2, Moscow 107564, RussiaImmunology Department, Central Tuberculosis Research Institute, Yauza Alley 2, Moscow 107564, RussiaThe outcome of Mycobacterium tuberculosis (Mtb) infection ranges from a complete pathogen clearance through asymptomatic latent infection (LTBI) to active tuberculosis (TB) disease. It is now understood that LTBI and active TB represent a continuous spectrum of states with different degrees of pathogen “activity,” host pathology, and immune reactivity. Therefore, it is important to differentiate LTBI and active TB and identify active TB stages. CD4+ T cells play critical role during Mtb infection by mediating protection, contributing to inflammation, and regulating immune response. Th1 and Th17 cells are the main effector CD4+ T cells during TB. Th1 cells have been shown to contribute to TB protection by secreting IFN-γ and activating antimycobacterial action in macrophages. Th17 induce neutrophilic inflammation, mediate tissue damage, and thus have been implicated in TB pathology. In recent years new findings have accumulated that alter our view on the role of Th1 and Th17 cells during Mtb infection. This review discusses these new results and how they can be implemented for TB diagnosis and monitoring.http://dx.doi.org/10.1155/2015/854507
spellingShingle I. V. Lyadova
A. V. Panteleev
Th1 and Th17 Cells in Tuberculosis: Protection, Pathology, and Biomarkers
Mediators of Inflammation
title Th1 and Th17 Cells in Tuberculosis: Protection, Pathology, and Biomarkers
title_full Th1 and Th17 Cells in Tuberculosis: Protection, Pathology, and Biomarkers
title_fullStr Th1 and Th17 Cells in Tuberculosis: Protection, Pathology, and Biomarkers
title_full_unstemmed Th1 and Th17 Cells in Tuberculosis: Protection, Pathology, and Biomarkers
title_short Th1 and Th17 Cells in Tuberculosis: Protection, Pathology, and Biomarkers
title_sort th1 and th17 cells in tuberculosis protection pathology and biomarkers
url http://dx.doi.org/10.1155/2015/854507
work_keys_str_mv AT ivlyadova th1andth17cellsintuberculosisprotectionpathologyandbiomarkers
AT avpanteleev th1andth17cellsintuberculosisprotectionpathologyandbiomarkers