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Factors Influencing Functional Heterogeneity in Human Mucosa-Associated Invariant T Cells

Mucosa-associated invariant T (MAIT) cells are unconventional innate-like T cells that recognize microbial riboflavin metabolites presented by the monomorphic MHC class I-related (MR1) molecule. Despite the high level of evolutionary conservation of MR1 and the limited diversity of known antigens, h...

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Autores principales: Dias, Joana, Boulouis, Caroline, Sobkowiak, Michał J., Lal, Kerri G., Emgård, Johanna, Buggert, Marcus, Parrot, Tiphaine, Gorin, Jean-Baptiste, Leeansyah, Edwin, Sandberg, Johan K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052907/
https://www.ncbi.nlm.nih.gov/pubmed/30050537
http://dx.doi.org/10.3389/fimmu.2018.01602
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author Dias, Joana
Boulouis, Caroline
Sobkowiak, Michał J.
Lal, Kerri G.
Emgård, Johanna
Buggert, Marcus
Parrot, Tiphaine
Gorin, Jean-Baptiste
Leeansyah, Edwin
Sandberg, Johan K.
author_facet Dias, Joana
Boulouis, Caroline
Sobkowiak, Michał J.
Lal, Kerri G.
Emgård, Johanna
Buggert, Marcus
Parrot, Tiphaine
Gorin, Jean-Baptiste
Leeansyah, Edwin
Sandberg, Johan K.
author_sort Dias, Joana
collection PubMed
description Mucosa-associated invariant T (MAIT) cells are unconventional innate-like T cells that recognize microbial riboflavin metabolites presented by the monomorphic MHC class I-related (MR1) molecule. Despite the high level of evolutionary conservation of MR1 and the limited diversity of known antigens, human MAIT cells and their responses may not be as homogeneous as previously thought. Here, we review recent findings indicating that MAIT cells display microbe-specific response patterns with multiple layers of heterogeneity. The natural killer cell receptor CD56 marks a MAIT cell subset with distinct response profile, and the T cell receptor β-chain diversity influences responsiveness at the single cell level. The MAIT cell tissue localization also influences their response profiles with higher IL-17 in tissue-resident MAIT cells. Furthermore, there is emerging evidence that the type of antigen-presenting cells, and innate cytokines produced by such cells, influence the quality of the ensuing MAIT cell response. On the microbial side, the expression patterns of MR1-presented antigenic and non-antigenic compounds, expression of other bioactive microbial products, and of innate pattern recognition ligands all influence downstream MAIT cell responses. These recent findings deepen our understanding of MAIT cell functional diversity and adaptation to the type and location of microbial challenge.
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spelling pubmed-60529072018-07-26 Factors Influencing Functional Heterogeneity in Human Mucosa-Associated Invariant T Cells Dias, Joana Boulouis, Caroline Sobkowiak, Michał J. Lal, Kerri G. Emgård, Johanna Buggert, Marcus Parrot, Tiphaine Gorin, Jean-Baptiste Leeansyah, Edwin Sandberg, Johan K. Front Immunol Immunology Mucosa-associated invariant T (MAIT) cells are unconventional innate-like T cells that recognize microbial riboflavin metabolites presented by the monomorphic MHC class I-related (MR1) molecule. Despite the high level of evolutionary conservation of MR1 and the limited diversity of known antigens, human MAIT cells and their responses may not be as homogeneous as previously thought. Here, we review recent findings indicating that MAIT cells display microbe-specific response patterns with multiple layers of heterogeneity. The natural killer cell receptor CD56 marks a MAIT cell subset with distinct response profile, and the T cell receptor β-chain diversity influences responsiveness at the single cell level. The MAIT cell tissue localization also influences their response profiles with higher IL-17 in tissue-resident MAIT cells. Furthermore, there is emerging evidence that the type of antigen-presenting cells, and innate cytokines produced by such cells, influence the quality of the ensuing MAIT cell response. On the microbial side, the expression patterns of MR1-presented antigenic and non-antigenic compounds, expression of other bioactive microbial products, and of innate pattern recognition ligands all influence downstream MAIT cell responses. These recent findings deepen our understanding of MAIT cell functional diversity and adaptation to the type and location of microbial challenge. Frontiers Media S.A. 2018-07-10 /pmc/articles/PMC6052907/ /pubmed/30050537 http://dx.doi.org/10.3389/fimmu.2018.01602 Text en Copyright © 2018 Dias, Boulouis, Sobkowiak, Lal, Emgård, Buggert, Parrot, Gorin, Leeansyah and Sandberg. 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(s) 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
Dias, Joana
Boulouis, Caroline
Sobkowiak, Michał J.
Lal, Kerri G.
Emgård, Johanna
Buggert, Marcus
Parrot, Tiphaine
Gorin, Jean-Baptiste
Leeansyah, Edwin
Sandberg, Johan K.
Factors Influencing Functional Heterogeneity in Human Mucosa-Associated Invariant T Cells
title Factors Influencing Functional Heterogeneity in Human Mucosa-Associated Invariant T Cells
title_full Factors Influencing Functional Heterogeneity in Human Mucosa-Associated Invariant T Cells
title_fullStr Factors Influencing Functional Heterogeneity in Human Mucosa-Associated Invariant T Cells
title_full_unstemmed Factors Influencing Functional Heterogeneity in Human Mucosa-Associated Invariant T Cells
title_short Factors Influencing Functional Heterogeneity in Human Mucosa-Associated Invariant T Cells
title_sort factors influencing functional heterogeneity in human mucosa-associated invariant t cells
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052907/
https://www.ncbi.nlm.nih.gov/pubmed/30050537
http://dx.doi.org/10.3389/fimmu.2018.01602
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