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Molecular Determinants of Target Cell Recognition by Human γδ T Cells

The unique capabilities of gamma-delta (γδ) T cells to recognize cells under stressed conditions, particularly infected or transformed cells, and killing them or regulating the immune response against them, paved the way to the development of promising therapeutic strategies for cancer and infectiou...

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Autores principales: Simões, André E., Di Lorenzo, Biagio, Silva-Santos, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934422/
https://www.ncbi.nlm.nih.gov/pubmed/29755480
http://dx.doi.org/10.3389/fimmu.2018.00929
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author Simões, André E.
Di Lorenzo, Biagio
Silva-Santos, Bruno
author_facet Simões, André E.
Di Lorenzo, Biagio
Silva-Santos, Bruno
author_sort Simões, André E.
collection PubMed
description The unique capabilities of gamma-delta (γδ) T cells to recognize cells under stressed conditions, particularly infected or transformed cells, and killing them or regulating the immune response against them, paved the way to the development of promising therapeutic strategies for cancer and infectious diseases. From a mechanistic standpoint, numerous studies have unveiled a remarkable flexibility of γδ T cells in employing their T cell receptor and/or NK cell receptors for target cell recognition, even if the relevant ligands often remain uncertain. Here, we review the accumulated knowledge on the diverse mechanisms of target cell recognition by γδ T cells, focusing on human γδ T cells, to provide an integrated perspective of their therapeutic potential in cancer and infectious diseases.
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spelling pubmed-59344222018-05-11 Molecular Determinants of Target Cell Recognition by Human γδ T Cells Simões, André E. Di Lorenzo, Biagio Silva-Santos, Bruno Front Immunol Immunology The unique capabilities of gamma-delta (γδ) T cells to recognize cells under stressed conditions, particularly infected or transformed cells, and killing them or regulating the immune response against them, paved the way to the development of promising therapeutic strategies for cancer and infectious diseases. From a mechanistic standpoint, numerous studies have unveiled a remarkable flexibility of γδ T cells in employing their T cell receptor and/or NK cell receptors for target cell recognition, even if the relevant ligands often remain uncertain. Here, we review the accumulated knowledge on the diverse mechanisms of target cell recognition by γδ T cells, focusing on human γδ T cells, to provide an integrated perspective of their therapeutic potential in cancer and infectious diseases. Frontiers Media S.A. 2018-04-27 /pmc/articles/PMC5934422/ /pubmed/29755480 http://dx.doi.org/10.3389/fimmu.2018.00929 Text en Copyright © 2018 Simões, Di Lorenzo and Silva-Santos. 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
Simões, André E.
Di Lorenzo, Biagio
Silva-Santos, Bruno
Molecular Determinants of Target Cell Recognition by Human γδ T Cells
title Molecular Determinants of Target Cell Recognition by Human γδ T Cells
title_full Molecular Determinants of Target Cell Recognition by Human γδ T Cells
title_fullStr Molecular Determinants of Target Cell Recognition by Human γδ T Cells
title_full_unstemmed Molecular Determinants of Target Cell Recognition by Human γδ T Cells
title_short Molecular Determinants of Target Cell Recognition by Human γδ T Cells
title_sort molecular determinants of target cell recognition by human γδ t cells
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934422/
https://www.ncbi.nlm.nih.gov/pubmed/29755480
http://dx.doi.org/10.3389/fimmu.2018.00929
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