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Distinct and complementary roles for Aspergillus fumigatus-specific Tr1 and Foxp3(+) regulatory T cells in humans and mice

Unlike induced Foxp3(+) regulatory T cells (Foxp3(+) iT(reg)) that have been shown to play an essential role in the development of protective immunity to the ubiquitous mold Aspergillus fumigatus, type-(1)-regulatory T cells (Tr1) cells have, thus far, not been implicated in this process. Here, we e...

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Autores principales: Bedke, Tanja, Iannitti, Rossana G, De Luca, Antonella, Giovannini, Gloria, Fallarino, Francesca, Berges, Carsten, Latgé, Jean-Paul, Einsele, Hermann, Romani, Luigina, Topp, Max S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168117/
https://www.ncbi.nlm.nih.gov/pubmed/24820384
http://dx.doi.org/10.1038/icb.2014.34
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author Bedke, Tanja
Iannitti, Rossana G
De Luca, Antonella
Giovannini, Gloria
Fallarino, Francesca
Berges, Carsten
Latgé, Jean-Paul
Einsele, Hermann
Romani, Luigina
Topp, Max S
author_facet Bedke, Tanja
Iannitti, Rossana G
De Luca, Antonella
Giovannini, Gloria
Fallarino, Francesca
Berges, Carsten
Latgé, Jean-Paul
Einsele, Hermann
Romani, Luigina
Topp, Max S
author_sort Bedke, Tanja
collection PubMed
description Unlike induced Foxp3(+) regulatory T cells (Foxp3(+) iT(reg)) that have been shown to play an essential role in the development of protective immunity to the ubiquitous mold Aspergillus fumigatus, type-(1)-regulatory T cells (Tr1) cells have, thus far, not been implicated in this process. Here, we evaluated the role of Tr1 cells specific for an epitope derived from the cell wall glucanase Crf-1 of A. fumigatus (Crf-1/p41) in antifungal immunity. We identified Crf-1/p41-specific latent-associated peptide(+) Tr1 cells in healthy humans and mice after vaccination with Crf-1/p41+zymosan. These cells produced high amounts of interleukin (IL)-10 and suppressed the expansion of antigen-specific T cells in vitro and in vivo. In mice, in vivo differentiation of Tr1 cells was dependent on the presence of the aryl hydrocarbon receptor, c-Maf and IL-27. Moreover, in comparison to Tr1 cells, Foxp3(+) iT(reg) that recognize the same epitope were induced in an interferon gamma-type inflammatory environment and more potently suppressed innate immune cell activities. Overall, our data show that Tr1 cells are involved in the maintenance of antifungal immune homeostasis, and most likely play a distinct, yet complementary, role compared with Foxp3(+) iT(reg).
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spelling pubmed-41681172014-09-24 Distinct and complementary roles for Aspergillus fumigatus-specific Tr1 and Foxp3(+) regulatory T cells in humans and mice Bedke, Tanja Iannitti, Rossana G De Luca, Antonella Giovannini, Gloria Fallarino, Francesca Berges, Carsten Latgé, Jean-Paul Einsele, Hermann Romani, Luigina Topp, Max S Immunol Cell Biol Original Article Unlike induced Foxp3(+) regulatory T cells (Foxp3(+) iT(reg)) that have been shown to play an essential role in the development of protective immunity to the ubiquitous mold Aspergillus fumigatus, type-(1)-regulatory T cells (Tr1) cells have, thus far, not been implicated in this process. Here, we evaluated the role of Tr1 cells specific for an epitope derived from the cell wall glucanase Crf-1 of A. fumigatus (Crf-1/p41) in antifungal immunity. We identified Crf-1/p41-specific latent-associated peptide(+) Tr1 cells in healthy humans and mice after vaccination with Crf-1/p41+zymosan. These cells produced high amounts of interleukin (IL)-10 and suppressed the expansion of antigen-specific T cells in vitro and in vivo. In mice, in vivo differentiation of Tr1 cells was dependent on the presence of the aryl hydrocarbon receptor, c-Maf and IL-27. Moreover, in comparison to Tr1 cells, Foxp3(+) iT(reg) that recognize the same epitope were induced in an interferon gamma-type inflammatory environment and more potently suppressed innate immune cell activities. Overall, our data show that Tr1 cells are involved in the maintenance of antifungal immune homeostasis, and most likely play a distinct, yet complementary, role compared with Foxp3(+) iT(reg). Nature Publishing Group 2014-09 2014-05-13 /pmc/articles/PMC4168117/ /pubmed/24820384 http://dx.doi.org/10.1038/icb.2014.34 Text en Copyright © 2014 Australasian Society for Immunology Inc. http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported 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-nc-nd/3.0/
spellingShingle Original Article
Bedke, Tanja
Iannitti, Rossana G
De Luca, Antonella
Giovannini, Gloria
Fallarino, Francesca
Berges, Carsten
Latgé, Jean-Paul
Einsele, Hermann
Romani, Luigina
Topp, Max S
Distinct and complementary roles for Aspergillus fumigatus-specific Tr1 and Foxp3(+) regulatory T cells in humans and mice
title Distinct and complementary roles for Aspergillus fumigatus-specific Tr1 and Foxp3(+) regulatory T cells in humans and mice
title_full Distinct and complementary roles for Aspergillus fumigatus-specific Tr1 and Foxp3(+) regulatory T cells in humans and mice
title_fullStr Distinct and complementary roles for Aspergillus fumigatus-specific Tr1 and Foxp3(+) regulatory T cells in humans and mice
title_full_unstemmed Distinct and complementary roles for Aspergillus fumigatus-specific Tr1 and Foxp3(+) regulatory T cells in humans and mice
title_short Distinct and complementary roles for Aspergillus fumigatus-specific Tr1 and Foxp3(+) regulatory T cells in humans and mice
title_sort distinct and complementary roles for aspergillus fumigatus-specific tr1 and foxp3(+) regulatory t cells in humans and mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168117/
https://www.ncbi.nlm.nih.gov/pubmed/24820384
http://dx.doi.org/10.1038/icb.2014.34
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