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Recasting Human Vδ1 Lymphocytes in an Adaptive Role

γδ T cells are unconventional lymphocytes commonly described as ‘innate-like’ in function, which can respond in both a T cell receptor (TCR)-independent and also major histocompatibility complex (MHC)-unrestricted TCR-dependent manner. While the relative importance of TCR recognition had remained un...

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Detalles Bibliográficos
Autores principales: Davey, Martin S., Willcox, Carrie R., Baker, Alfie T., Hunter, Stuart, Willcox, Benjamin E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980997/
https://www.ncbi.nlm.nih.gov/pubmed/29680462
http://dx.doi.org/10.1016/j.it.2018.03.003
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author Davey, Martin S.
Willcox, Carrie R.
Baker, Alfie T.
Hunter, Stuart
Willcox, Benjamin E.
author_facet Davey, Martin S.
Willcox, Carrie R.
Baker, Alfie T.
Hunter, Stuart
Willcox, Benjamin E.
author_sort Davey, Martin S.
collection PubMed
description γδ T cells are unconventional lymphocytes commonly described as ‘innate-like’ in function, which can respond in both a T cell receptor (TCR)-independent and also major histocompatibility complex (MHC)-unrestricted TCR-dependent manner. While the relative importance of TCR recognition had remained unclear, recent studies revealed that human Vδ1 T cells display unexpected parallels with adaptive αβ T cells. Vδ1 T cells undergo profound and highly focussed clonal expansion from an initially diverse and private TCR repertoire, most likely in response to specific immune challenges. Concomitantly, they differentiate from a Vδ1 T cell naïve (T(naïve)) to a Vδ1 T cell effector (T(effector)) phenotype, marked by the downregulation of lymphoid homing receptors and upregulation of peripheral homing receptors and effector markers. This suggests that an adaptive paradigm applies to Vδ1 T cells, likely involving TCR-dependent but MHC-unrestricted responses to microbial and non-microbial challenges.
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spelling pubmed-59809972018-06-04 Recasting Human Vδ1 Lymphocytes in an Adaptive Role Davey, Martin S. Willcox, Carrie R. Baker, Alfie T. Hunter, Stuart Willcox, Benjamin E. Trends Immunol Article γδ T cells are unconventional lymphocytes commonly described as ‘innate-like’ in function, which can respond in both a T cell receptor (TCR)-independent and also major histocompatibility complex (MHC)-unrestricted TCR-dependent manner. While the relative importance of TCR recognition had remained unclear, recent studies revealed that human Vδ1 T cells display unexpected parallels with adaptive αβ T cells. Vδ1 T cells undergo profound and highly focussed clonal expansion from an initially diverse and private TCR repertoire, most likely in response to specific immune challenges. Concomitantly, they differentiate from a Vδ1 T cell naïve (T(naïve)) to a Vδ1 T cell effector (T(effector)) phenotype, marked by the downregulation of lymphoid homing receptors and upregulation of peripheral homing receptors and effector markers. This suggests that an adaptive paradigm applies to Vδ1 T cells, likely involving TCR-dependent but MHC-unrestricted responses to microbial and non-microbial challenges. Elsevier Science Ltd 2018-06 /pmc/articles/PMC5980997/ /pubmed/29680462 http://dx.doi.org/10.1016/j.it.2018.03.003 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Davey, Martin S.
Willcox, Carrie R.
Baker, Alfie T.
Hunter, Stuart
Willcox, Benjamin E.
Recasting Human Vδ1 Lymphocytes in an Adaptive Role
title Recasting Human Vδ1 Lymphocytes in an Adaptive Role
title_full Recasting Human Vδ1 Lymphocytes in an Adaptive Role
title_fullStr Recasting Human Vδ1 Lymphocytes in an Adaptive Role
title_full_unstemmed Recasting Human Vδ1 Lymphocytes in an Adaptive Role
title_short Recasting Human Vδ1 Lymphocytes in an Adaptive Role
title_sort recasting human vδ1 lymphocytes in an adaptive role
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980997/
https://www.ncbi.nlm.nih.gov/pubmed/29680462
http://dx.doi.org/10.1016/j.it.2018.03.003
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