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Identification and characterization of latency-associated peptide-expressing γδ T cells
γδ T cells are a subset of lymphocytes specialized in protecting the host against pathogens and tumours. Here we describe a subset of regulatory γδ T cells that express the latency-associated peptide (LAP), a membrane-bound TGF-β1. Thymic CD27+IFN-γ+CCR9+α(4)β(7)+TCRγδ+ cells migrate to the peripher...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4686827/ https://www.ncbi.nlm.nih.gov/pubmed/26644347 http://dx.doi.org/10.1038/ncomms9726 |
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author | Rezende, Rafael M. da Cunha, Andre P. Kuhn, Chantal Rubino, Stephen M'Hamdi, Hanane Gabriely, Galina Vandeventer, Tyler Liu, Shirong Cialic, Ron Pinheiro-Rosa, Natalia Oliveira, Rafael P. Gaublomme, Jellert T. Obholzer, Nikolaus Kozubek, James Pochet, Nathalie Faria, Ana M. C. Weiner, Howard L. |
author_facet | Rezende, Rafael M. da Cunha, Andre P. Kuhn, Chantal Rubino, Stephen M'Hamdi, Hanane Gabriely, Galina Vandeventer, Tyler Liu, Shirong Cialic, Ron Pinheiro-Rosa, Natalia Oliveira, Rafael P. Gaublomme, Jellert T. Obholzer, Nikolaus Kozubek, James Pochet, Nathalie Faria, Ana M. C. Weiner, Howard L. |
author_sort | Rezende, Rafael M. |
collection | PubMed |
description | γδ T cells are a subset of lymphocytes specialized in protecting the host against pathogens and tumours. Here we describe a subset of regulatory γδ T cells that express the latency-associated peptide (LAP), a membrane-bound TGF-β1. Thymic CD27+IFN-γ+CCR9+α(4)β(7)+TCRγδ+ cells migrate to the periphery, particularly to Peyer's patches and small intestine lamina propria, where they upregulate LAP, downregulate IFN-γ via ATF-3 expression and acquire a regulatory phenotype. TCRγδ+LAP+ cells express antigen presentation molecules and function as antigen presenting cells that induce CD4+Foxp3+ regulatory T cells, although TCRγδ+LAP+ cells do not themselves express Foxp3. Identification of TCRγδ+LAP+ regulatory cells provides an avenue for understanding immune regulation and biologic processes linked to intestinal function and disease. |
format | Online Article Text |
id | pubmed-4686827 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46868272016-01-07 Identification and characterization of latency-associated peptide-expressing γδ T cells Rezende, Rafael M. da Cunha, Andre P. Kuhn, Chantal Rubino, Stephen M'Hamdi, Hanane Gabriely, Galina Vandeventer, Tyler Liu, Shirong Cialic, Ron Pinheiro-Rosa, Natalia Oliveira, Rafael P. Gaublomme, Jellert T. Obholzer, Nikolaus Kozubek, James Pochet, Nathalie Faria, Ana M. C. Weiner, Howard L. Nat Commun Article γδ T cells are a subset of lymphocytes specialized in protecting the host against pathogens and tumours. Here we describe a subset of regulatory γδ T cells that express the latency-associated peptide (LAP), a membrane-bound TGF-β1. Thymic CD27+IFN-γ+CCR9+α(4)β(7)+TCRγδ+ cells migrate to the periphery, particularly to Peyer's patches and small intestine lamina propria, where they upregulate LAP, downregulate IFN-γ via ATF-3 expression and acquire a regulatory phenotype. TCRγδ+LAP+ cells express antigen presentation molecules and function as antigen presenting cells that induce CD4+Foxp3+ regulatory T cells, although TCRγδ+LAP+ cells do not themselves express Foxp3. Identification of TCRγδ+LAP+ regulatory cells provides an avenue for understanding immune regulation and biologic processes linked to intestinal function and disease. Nature Publishing Group 2015-12-08 /pmc/articles/PMC4686827/ /pubmed/26644347 http://dx.doi.org/10.1038/ncomms9726 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Rezende, Rafael M. da Cunha, Andre P. Kuhn, Chantal Rubino, Stephen M'Hamdi, Hanane Gabriely, Galina Vandeventer, Tyler Liu, Shirong Cialic, Ron Pinheiro-Rosa, Natalia Oliveira, Rafael P. Gaublomme, Jellert T. Obholzer, Nikolaus Kozubek, James Pochet, Nathalie Faria, Ana M. C. Weiner, Howard L. Identification and characterization of latency-associated peptide-expressing γδ T cells |
title | Identification and characterization of latency-associated peptide-expressing γδ T cells |
title_full | Identification and characterization of latency-associated peptide-expressing γδ T cells |
title_fullStr | Identification and characterization of latency-associated peptide-expressing γδ T cells |
title_full_unstemmed | Identification and characterization of latency-associated peptide-expressing γδ T cells |
title_short | Identification and characterization of latency-associated peptide-expressing γδ T cells |
title_sort | identification and characterization of latency-associated peptide-expressing γδ t cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4686827/ https://www.ncbi.nlm.nih.gov/pubmed/26644347 http://dx.doi.org/10.1038/ncomms9726 |
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