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Mucosal-Associated Invariant T Cells in Autoimmune Diseases
Mucosal-associated invariant T (MAIT) cells are innate T cells restricted by MHC-related molecule 1 (MR1). MAIT cells express semi-invariant T-cell receptors TRAV1-2-TRAJ33/12/20 in humans and TRAV1-TRAJ33 in mice. MAIT cells recognize vitamin B2 biosynthesis derivatives presented by MR1. Similar to...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004381/ https://www.ncbi.nlm.nih.gov/pubmed/29942318 http://dx.doi.org/10.3389/fimmu.2018.01333 |
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author | Chiba, Asako Murayama, Goh Miyake, Sachiko |
author_facet | Chiba, Asako Murayama, Goh Miyake, Sachiko |
author_sort | Chiba, Asako |
collection | PubMed |
description | Mucosal-associated invariant T (MAIT) cells are innate T cells restricted by MHC-related molecule 1 (MR1). MAIT cells express semi-invariant T-cell receptors TRAV1-2-TRAJ33/12/20 in humans and TRAV1-TRAJ33 in mice. MAIT cells recognize vitamin B2 biosynthesis derivatives presented by MR1. Similar to other innate lymphocytes, MAIT cells are also activated by cytokines in the absence of exogenous antigens. MAIT cells have the capacity to produce cytokines, such as IFNγ, TNFα, and IL-17, and cytotoxic proteins, including perforin and granzyme B. MAIT cells were originally named after their preferential location in the mucosal tissue of the gut, but they are also abundant in other peripheral organs, including the liver and lungs. In humans, the frequency of MAIT cells is high in peripheral blood, and these cells constitute approximately 5% of circulating CD3(+) cells. Their abundance in tissues and rapid activation following stimulation have led to great interest in their function in various types of immune diseases. In this review, first, we will briefly introduce key information of MAIT cell biology required for better understating their roles in immune responses, and then describe how MAIT cells are associated with autoimmune and other immune diseases in humans. Moreover, we will discuss their functions based on information from animal models of autoimmune and immunological diseases. |
format | Online Article Text |
id | pubmed-6004381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60043812018-06-25 Mucosal-Associated Invariant T Cells in Autoimmune Diseases Chiba, Asako Murayama, Goh Miyake, Sachiko Front Immunol Immunology Mucosal-associated invariant T (MAIT) cells are innate T cells restricted by MHC-related molecule 1 (MR1). MAIT cells express semi-invariant T-cell receptors TRAV1-2-TRAJ33/12/20 in humans and TRAV1-TRAJ33 in mice. MAIT cells recognize vitamin B2 biosynthesis derivatives presented by MR1. Similar to other innate lymphocytes, MAIT cells are also activated by cytokines in the absence of exogenous antigens. MAIT cells have the capacity to produce cytokines, such as IFNγ, TNFα, and IL-17, and cytotoxic proteins, including perforin and granzyme B. MAIT cells were originally named after their preferential location in the mucosal tissue of the gut, but they are also abundant in other peripheral organs, including the liver and lungs. In humans, the frequency of MAIT cells is high in peripheral blood, and these cells constitute approximately 5% of circulating CD3(+) cells. Their abundance in tissues and rapid activation following stimulation have led to great interest in their function in various types of immune diseases. In this review, first, we will briefly introduce key information of MAIT cell biology required for better understating their roles in immune responses, and then describe how MAIT cells are associated with autoimmune and other immune diseases in humans. Moreover, we will discuss their functions based on information from animal models of autoimmune and immunological diseases. Frontiers Media S.A. 2018-06-11 /pmc/articles/PMC6004381/ /pubmed/29942318 http://dx.doi.org/10.3389/fimmu.2018.01333 Text en Copyright © 2018 Chiba, Murayama and Miyake. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Chiba, Asako Murayama, Goh Miyake, Sachiko Mucosal-Associated Invariant T Cells in Autoimmune Diseases |
title | Mucosal-Associated Invariant T Cells in Autoimmune Diseases |
title_full | Mucosal-Associated Invariant T Cells in Autoimmune Diseases |
title_fullStr | Mucosal-Associated Invariant T Cells in Autoimmune Diseases |
title_full_unstemmed | Mucosal-Associated Invariant T Cells in Autoimmune Diseases |
title_short | Mucosal-Associated Invariant T Cells in Autoimmune Diseases |
title_sort | mucosal-associated invariant t cells in autoimmune diseases |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004381/ https://www.ncbi.nlm.nih.gov/pubmed/29942318 http://dx.doi.org/10.3389/fimmu.2018.01333 |
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