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In Vivo Induction of Tr1 Cells via Mucosal Dendritic Cells and AHR Signaling

BACKGROUND: Type 1 regulatory T (Tr1) cells, characterized by the secretion of high levels of the anti-inflammatory cytokine interleukin-10 (IL-10), play an important role in the regulation of autoimmune diseases and transplantation. However, effective strategies that specifically induce Tr1 cells i...

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Autores principales: Wu, Henry Yim, Quintana, Francisco J., da Cunha, Andre Pires, Dake, Benjamin T., Koeglsperger, Thomas, Starossom, Sarah C., Weiner, Howard L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160310/
https://www.ncbi.nlm.nih.gov/pubmed/21886804
http://dx.doi.org/10.1371/journal.pone.0023618
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author Wu, Henry Yim
Quintana, Francisco J.
da Cunha, Andre Pires
Dake, Benjamin T.
Koeglsperger, Thomas
Starossom, Sarah C.
Weiner, Howard L.
author_facet Wu, Henry Yim
Quintana, Francisco J.
da Cunha, Andre Pires
Dake, Benjamin T.
Koeglsperger, Thomas
Starossom, Sarah C.
Weiner, Howard L.
author_sort Wu, Henry Yim
collection PubMed
description BACKGROUND: Type 1 regulatory T (Tr1) cells, characterized by the secretion of high levels of the anti-inflammatory cytokine interleukin-10 (IL-10), play an important role in the regulation of autoimmune diseases and transplantation. However, effective strategies that specifically induce Tr1 cells in vivo are limited. Furthermore, the pathways controlling the induction of these cells in vivo are not well understood. METHODOLOGY/PRINCIPAL FINDINGS: Here we report that nasal administration of anti-CD3 antibody induces suppressive Tr1 cells in mice. The in vivo induction of Tr1 cells by nasal anti-CD3 is dependent on IL-27 produced by upper airway resident dendritic cells (DCs), and is controlled by the transcription factors aryl hydrocarbon receptor (AHR) and c-Maf. Subsequently, IL-21 acts in an autocrine fashion to expand and maintain the Tr1 cells induced in vivo by nasally administered anti-CD3. CONCLUSIONS/SIGNIFICANCE: Our findings identify a unique approach to generate Tr1 cells in vivo and provide insights into the mechanisms by which these cells are induced.
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spelling pubmed-31603102011-08-30 In Vivo Induction of Tr1 Cells via Mucosal Dendritic Cells and AHR Signaling Wu, Henry Yim Quintana, Francisco J. da Cunha, Andre Pires Dake, Benjamin T. Koeglsperger, Thomas Starossom, Sarah C. Weiner, Howard L. PLoS One Research Article BACKGROUND: Type 1 regulatory T (Tr1) cells, characterized by the secretion of high levels of the anti-inflammatory cytokine interleukin-10 (IL-10), play an important role in the regulation of autoimmune diseases and transplantation. However, effective strategies that specifically induce Tr1 cells in vivo are limited. Furthermore, the pathways controlling the induction of these cells in vivo are not well understood. METHODOLOGY/PRINCIPAL FINDINGS: Here we report that nasal administration of anti-CD3 antibody induces suppressive Tr1 cells in mice. The in vivo induction of Tr1 cells by nasal anti-CD3 is dependent on IL-27 produced by upper airway resident dendritic cells (DCs), and is controlled by the transcription factors aryl hydrocarbon receptor (AHR) and c-Maf. Subsequently, IL-21 acts in an autocrine fashion to expand and maintain the Tr1 cells induced in vivo by nasally administered anti-CD3. CONCLUSIONS/SIGNIFICANCE: Our findings identify a unique approach to generate Tr1 cells in vivo and provide insights into the mechanisms by which these cells are induced. Public Library of Science 2011-08-23 /pmc/articles/PMC3160310/ /pubmed/21886804 http://dx.doi.org/10.1371/journal.pone.0023618 Text en Wu et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wu, Henry Yim
Quintana, Francisco J.
da Cunha, Andre Pires
Dake, Benjamin T.
Koeglsperger, Thomas
Starossom, Sarah C.
Weiner, Howard L.
In Vivo Induction of Tr1 Cells via Mucosal Dendritic Cells and AHR Signaling
title In Vivo Induction of Tr1 Cells via Mucosal Dendritic Cells and AHR Signaling
title_full In Vivo Induction of Tr1 Cells via Mucosal Dendritic Cells and AHR Signaling
title_fullStr In Vivo Induction of Tr1 Cells via Mucosal Dendritic Cells and AHR Signaling
title_full_unstemmed In Vivo Induction of Tr1 Cells via Mucosal Dendritic Cells and AHR Signaling
title_short In Vivo Induction of Tr1 Cells via Mucosal Dendritic Cells and AHR Signaling
title_sort in vivo induction of tr1 cells via mucosal dendritic cells and ahr signaling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160310/
https://www.ncbi.nlm.nih.gov/pubmed/21886804
http://dx.doi.org/10.1371/journal.pone.0023618
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