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The Emerging Complexity of γδT17 Cells

Preprogrammed IL-17-producing γδ T cells constitute a poorly understood class of lymphocytes that express rearranged antigen receptors but appear to make little use of them. γδT17 cells were first characterized as tissue-resident sentinels with innate effector function. However, ongoing research con...

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Autores principales: McKenzie, Duncan R., Comerford, Iain, Silva-Santos, Bruno, McColl, Shaun R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919943/
https://www.ncbi.nlm.nih.gov/pubmed/29731754
http://dx.doi.org/10.3389/fimmu.2018.00796
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author McKenzie, Duncan R.
Comerford, Iain
Silva-Santos, Bruno
McColl, Shaun R.
author_facet McKenzie, Duncan R.
Comerford, Iain
Silva-Santos, Bruno
McColl, Shaun R.
author_sort McKenzie, Duncan R.
collection PubMed
description Preprogrammed IL-17-producing γδ T cells constitute a poorly understood class of lymphocytes that express rearranged antigen receptors but appear to make little use of them. γδT17 cells were first characterized as tissue-resident sentinels with innate effector function. However, ongoing research continues to reveal unexpected complexity to this unusual subset, including phenotypic plasticity, memory-like activity and unique migratory behavior. Despite these advances, at the core of γδT17 cell biology remain fundamental gaps in knowledge: Are γδT17 cells truly innate or has the importance of the T cell receptor been overlooked? How unique are they among IL-17-producing lymphocytes? How similar are these cells between mice and humans? We speculate that answering these unresolved questions is key to successful manipulation of γδ T cells in clinical settings.
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spelling pubmed-59199432018-05-04 The Emerging Complexity of γδT17 Cells McKenzie, Duncan R. Comerford, Iain Silva-Santos, Bruno McColl, Shaun R. Front Immunol Immunology Preprogrammed IL-17-producing γδ T cells constitute a poorly understood class of lymphocytes that express rearranged antigen receptors but appear to make little use of them. γδT17 cells were first characterized as tissue-resident sentinels with innate effector function. However, ongoing research continues to reveal unexpected complexity to this unusual subset, including phenotypic plasticity, memory-like activity and unique migratory behavior. Despite these advances, at the core of γδT17 cell biology remain fundamental gaps in knowledge: Are γδT17 cells truly innate or has the importance of the T cell receptor been overlooked? How unique are they among IL-17-producing lymphocytes? How similar are these cells between mice and humans? We speculate that answering these unresolved questions is key to successful manipulation of γδ T cells in clinical settings. Frontiers Media S.A. 2018-04-20 /pmc/articles/PMC5919943/ /pubmed/29731754 http://dx.doi.org/10.3389/fimmu.2018.00796 Text en Copyright © 2018 McKenzie, Comerford, Silva-Santos and McColl. 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
McKenzie, Duncan R.
Comerford, Iain
Silva-Santos, Bruno
McColl, Shaun R.
The Emerging Complexity of γδT17 Cells
title The Emerging Complexity of γδT17 Cells
title_full The Emerging Complexity of γδT17 Cells
title_fullStr The Emerging Complexity of γδT17 Cells
title_full_unstemmed The Emerging Complexity of γδT17 Cells
title_short The Emerging Complexity of γδT17 Cells
title_sort emerging complexity of γδt17 cells
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919943/
https://www.ncbi.nlm.nih.gov/pubmed/29731754
http://dx.doi.org/10.3389/fimmu.2018.00796
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