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Infected site-restricted Foxp3(+) natural regulatory T cells are specific for microbial antigens
Natural regulatory T (T reg) cells are involved in control of the immune response, including response to pathogens. Previous work has demonstrated that the repertoire of natural T reg cells may be biased toward self-antigen recognition. Whether they also recognize foreign antigens and how this recog...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118233/ https://www.ncbi.nlm.nih.gov/pubmed/16533885 http://dx.doi.org/10.1084/jem.20052056 |
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author | Suffia, Isabelle J. Reckling, Stacie K. Piccirillo, Ciriaco A. Goldszmid, Romina S. Belkaid, Yasmine |
author_facet | Suffia, Isabelle J. Reckling, Stacie K. Piccirillo, Ciriaco A. Goldszmid, Romina S. Belkaid, Yasmine |
author_sort | Suffia, Isabelle J. |
collection | PubMed |
description | Natural regulatory T (T reg) cells are involved in control of the immune response, including response to pathogens. Previous work has demonstrated that the repertoire of natural T reg cells may be biased toward self-antigen recognition. Whether they also recognize foreign antigens and how this recognition contributes to their function remain unknown. Our studies addressed the antigenic specificity of natural T reg cells that accumulate at sites of chronic infection with Leishmania major in mice. Our results support the idea that natural T reg cells are able to respond specifically to foreign antigens in that they strongly proliferate in response to Leishmania-infected dendritic cells, they maintain Foxp3 expression, and Leishmania-specific T reg cell lines can be generated from infected mice. Surprisingly, the majority of natural T reg cells at the infected site are Leishmania specific. Further, we showed that parasite-specific natural T reg cells are restricted to sites of infection and that their survival is strictly dependent on parasite persistence. |
format | Text |
id | pubmed-2118233 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21182332007-12-13 Infected site-restricted Foxp3(+) natural regulatory T cells are specific for microbial antigens Suffia, Isabelle J. Reckling, Stacie K. Piccirillo, Ciriaco A. Goldszmid, Romina S. Belkaid, Yasmine J Exp Med Articles Natural regulatory T (T reg) cells are involved in control of the immune response, including response to pathogens. Previous work has demonstrated that the repertoire of natural T reg cells may be biased toward self-antigen recognition. Whether they also recognize foreign antigens and how this recognition contributes to their function remain unknown. Our studies addressed the antigenic specificity of natural T reg cells that accumulate at sites of chronic infection with Leishmania major in mice. Our results support the idea that natural T reg cells are able to respond specifically to foreign antigens in that they strongly proliferate in response to Leishmania-infected dendritic cells, they maintain Foxp3 expression, and Leishmania-specific T reg cell lines can be generated from infected mice. Surprisingly, the majority of natural T reg cells at the infected site are Leishmania specific. Further, we showed that parasite-specific natural T reg cells are restricted to sites of infection and that their survival is strictly dependent on parasite persistence. The Rockefeller University Press 2006-03-20 /pmc/articles/PMC2118233/ /pubmed/16533885 http://dx.doi.org/10.1084/jem.20052056 Text en Copyright © 2006, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Suffia, Isabelle J. Reckling, Stacie K. Piccirillo, Ciriaco A. Goldszmid, Romina S. Belkaid, Yasmine Infected site-restricted Foxp3(+) natural regulatory T cells are specific for microbial antigens |
title | Infected site-restricted Foxp3(+) natural regulatory T cells are specific for microbial antigens |
title_full | Infected site-restricted Foxp3(+) natural regulatory T cells are specific for microbial antigens |
title_fullStr | Infected site-restricted Foxp3(+) natural regulatory T cells are specific for microbial antigens |
title_full_unstemmed | Infected site-restricted Foxp3(+) natural regulatory T cells are specific for microbial antigens |
title_short | Infected site-restricted Foxp3(+) natural regulatory T cells are specific for microbial antigens |
title_sort | infected site-restricted foxp3(+) natural regulatory t cells are specific for microbial antigens |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118233/ https://www.ncbi.nlm.nih.gov/pubmed/16533885 http://dx.doi.org/10.1084/jem.20052056 |
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