Literature DB >> 25703558

MR1-restricted mucosal associated invariant T (MAIT) cells in the immune response to Mycobacterium tuberculosis.

Marielle C Gold1, Ruth J Napier, David M Lewinsohn.   

Abstract

The intracellular pathogen Mycobacterium tuberculosis (Mtb) and its human host have long co-evolved. Although the host cellular immune response is critical to the control of the bacterium information on the specific contribution of different immune cell subsets in humans is incomplete. Mucosal associated invariant T (MAIT) cells are a prevalent and unique T-cell population in humans with the capacity to detect intracellular infection with bacteria including Mtb. MAIT cells detect bacterially derived metabolites presented by the evolutionarily conserved major histocompatibility complex-like molecule MR1. Here, we review recent advances in our understanding of this T-cell subset and address the potential roles for MR1-restricted T cells in the control, diagnosis, and therapy of tuberculosis.
© 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  MR1; mucosal associated invariant T cells (MAIT); tuberculosis

Mesh:

Substances:

Year:  2015        PMID: 25703558      PMCID: PMC4339229          DOI: 10.1111/imr.12271

Source DB:  PubMed          Journal:  Immunol Rev        ISSN: 0105-2896            Impact factor:   12.988


  127 in total

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3.  Microbial recognition via Toll-like receptor-dependent and -independent pathways determines the cytokine response of murine dendritic cell subsets to CD40 triggering.

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8.  MR1-restricted MAIT cells display ligand discrimination and pathogen selectivity through distinct T cell receptor usage.

Authors:  Marielle C Gold; James E McLaren; Joseph A Reistetter; Sue Smyk-Pearson; Kristin Ladell; Gwendolyn M Swarbrick; Yik Y L Yu; Ted H Hansen; Ole Lund; Morten Nielsen; Bram Gerritsen; Can Kesmir; John J Miles; Deborah A Lewinsohn; David A Price; David M Lewinsohn
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Journal:  J Exp Med       Date:  2013-10-07       Impact factor: 14.307

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  43 in total

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Review 6.  Integrating Lung Physiology, Immunology, and Tuberculosis.

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