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Mixing Signals: Molecular Turn Ons and Turn Offs for Innate γδ T-Cells
Lymphocytes of the gamma delta (γδ) T-cell lineage are evolutionary conserved and although they express rearranged antigen-specific receptors, a large proportion respond as innate effectors. γδ T-cells are poised to combat infection by responding rapidly to cytokine stimuli similar to innate lymphoi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270187/ https://www.ncbi.nlm.nih.gov/pubmed/25566265 http://dx.doi.org/10.3389/fimmu.2014.00654 |
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author | Bekiaris, Vasileios Šedý, John R. Ware, Carl F. |
author_facet | Bekiaris, Vasileios Šedý, John R. Ware, Carl F. |
author_sort | Bekiaris, Vasileios |
collection | PubMed |
description | Lymphocytes of the gamma delta (γδ) T-cell lineage are evolutionary conserved and although they express rearranged antigen-specific receptors, a large proportion respond as innate effectors. γδ T-cells are poised to combat infection by responding rapidly to cytokine stimuli similar to innate lymphoid cells. This potential to initiate strong inflammatory responses necessitates that inhibitory signals are balanced with activation signals. Here, we discuss some of the key mechanisms that regulate the development, activation, and inhibition of innate γδ T-cells in light of recent evidence that the inhibitory immunoglobulin-superfamily member B and T lymphocyte attenuator restricts their differentiation and effector function. |
format | Online Article Text |
id | pubmed-4270187 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-42701872015-01-06 Mixing Signals: Molecular Turn Ons and Turn Offs for Innate γδ T-Cells Bekiaris, Vasileios Šedý, John R. Ware, Carl F. Front Immunol Immunology Lymphocytes of the gamma delta (γδ) T-cell lineage are evolutionary conserved and although they express rearranged antigen-specific receptors, a large proportion respond as innate effectors. γδ T-cells are poised to combat infection by responding rapidly to cytokine stimuli similar to innate lymphoid cells. This potential to initiate strong inflammatory responses necessitates that inhibitory signals are balanced with activation signals. Here, we discuss some of the key mechanisms that regulate the development, activation, and inhibition of innate γδ T-cells in light of recent evidence that the inhibitory immunoglobulin-superfamily member B and T lymphocyte attenuator restricts their differentiation and effector function. Frontiers Media S.A. 2014-12-18 /pmc/articles/PMC4270187/ /pubmed/25566265 http://dx.doi.org/10.3389/fimmu.2014.00654 Text en Copyright © 2014 Bekiaris, Šedý and Ware. http://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) or licensor 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 Bekiaris, Vasileios Šedý, John R. Ware, Carl F. Mixing Signals: Molecular Turn Ons and Turn Offs for Innate γδ T-Cells |
title | Mixing Signals: Molecular Turn Ons and Turn Offs for Innate γδ T-Cells |
title_full | Mixing Signals: Molecular Turn Ons and Turn Offs for Innate γδ T-Cells |
title_fullStr | Mixing Signals: Molecular Turn Ons and Turn Offs for Innate γδ T-Cells |
title_full_unstemmed | Mixing Signals: Molecular Turn Ons and Turn Offs for Innate γδ T-Cells |
title_short | Mixing Signals: Molecular Turn Ons and Turn Offs for Innate γδ T-Cells |
title_sort | mixing signals: molecular turn ons and turn offs for innate γδ t-cells |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270187/ https://www.ncbi.nlm.nih.gov/pubmed/25566265 http://dx.doi.org/10.3389/fimmu.2014.00654 |
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