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Resident CD141 (BDCA3)(+) dendritic cells in human skin produce IL-10 and induce regulatory T cells that suppress skin inflammation

Human skin immune homeostasis, and its regulation by specialized subsets of tissue-residing immune sentinels, is poorly understood. In this study, we identify an immunoregulatory tissue-resident dendritic cell (DC) in the dermis of human skin that is characterized by surface expression of CD141, CD1...

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Autores principales: Chu, Chung-Ching, Ali, Niwa, Karagiannis, Panagiotis, Di Meglio, Paola, Skowera, Ania, Napolitano, Luca, Barinaga, Guillermo, Grys, Katarzyna, Sharif-Paghaleh, Ehsan, Karagiannis, Sophia N., Peakman, Mark, Lombardi, Giovanna, Nestle, Frank O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3348099/
https://www.ncbi.nlm.nih.gov/pubmed/22547651
http://dx.doi.org/10.1084/jem.20112583
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author Chu, Chung-Ching
Ali, Niwa
Karagiannis, Panagiotis
Di Meglio, Paola
Skowera, Ania
Napolitano, Luca
Barinaga, Guillermo
Grys, Katarzyna
Sharif-Paghaleh, Ehsan
Karagiannis, Sophia N.
Peakman, Mark
Lombardi, Giovanna
Nestle, Frank O.
author_facet Chu, Chung-Ching
Ali, Niwa
Karagiannis, Panagiotis
Di Meglio, Paola
Skowera, Ania
Napolitano, Luca
Barinaga, Guillermo
Grys, Katarzyna
Sharif-Paghaleh, Ehsan
Karagiannis, Sophia N.
Peakman, Mark
Lombardi, Giovanna
Nestle, Frank O.
author_sort Chu, Chung-Ching
collection PubMed
description Human skin immune homeostasis, and its regulation by specialized subsets of tissue-residing immune sentinels, is poorly understood. In this study, we identify an immunoregulatory tissue-resident dendritic cell (DC) in the dermis of human skin that is characterized by surface expression of CD141, CD14, and constitutive IL-10 secretion (CD141(+) DDCs). CD141(+) DDCs possess lymph node migratory capacity, induce T cell hyporesponsiveness, cross-present self-antigens to autoreactive T cells, and induce potent regulatory T cells that inhibit skin inflammation. Vitamin D(3) (VitD3) promotes certain phenotypic and functional properties of tissue-resident CD141(+) DDCs from human blood DCs. These CD141(+) DDC-like cells can be generated in vitro and, once transferred in vivo, have the capacity to inhibit xeno-graft versus host disease and tumor alloimmunity. These findings suggest that CD141(+) DDCs play an essential role in the maintenance of skin homeostasis and in the regulation of both systemic and tumor alloimmunity. Finally, VitD3-induced CD141(+) DDC-like cells have potential clinical use for their capacity to induce immune tolerance.
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spelling pubmed-33480992012-11-07 Resident CD141 (BDCA3)(+) dendritic cells in human skin produce IL-10 and induce regulatory T cells that suppress skin inflammation Chu, Chung-Ching Ali, Niwa Karagiannis, Panagiotis Di Meglio, Paola Skowera, Ania Napolitano, Luca Barinaga, Guillermo Grys, Katarzyna Sharif-Paghaleh, Ehsan Karagiannis, Sophia N. Peakman, Mark Lombardi, Giovanna Nestle, Frank O. J Exp Med Brief Definitive Report Human skin immune homeostasis, and its regulation by specialized subsets of tissue-residing immune sentinels, is poorly understood. In this study, we identify an immunoregulatory tissue-resident dendritic cell (DC) in the dermis of human skin that is characterized by surface expression of CD141, CD14, and constitutive IL-10 secretion (CD141(+) DDCs). CD141(+) DDCs possess lymph node migratory capacity, induce T cell hyporesponsiveness, cross-present self-antigens to autoreactive T cells, and induce potent regulatory T cells that inhibit skin inflammation. Vitamin D(3) (VitD3) promotes certain phenotypic and functional properties of tissue-resident CD141(+) DDCs from human blood DCs. These CD141(+) DDC-like cells can be generated in vitro and, once transferred in vivo, have the capacity to inhibit xeno-graft versus host disease and tumor alloimmunity. These findings suggest that CD141(+) DDCs play an essential role in the maintenance of skin homeostasis and in the regulation of both systemic and tumor alloimmunity. Finally, VitD3-induced CD141(+) DDC-like cells have potential clinical use for their capacity to induce immune tolerance. The Rockefeller University Press 2012-05-07 /pmc/articles/PMC3348099/ /pubmed/22547651 http://dx.doi.org/10.1084/jem.20112583 Text en © 2012 Chu et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Brief Definitive Report
Chu, Chung-Ching
Ali, Niwa
Karagiannis, Panagiotis
Di Meglio, Paola
Skowera, Ania
Napolitano, Luca
Barinaga, Guillermo
Grys, Katarzyna
Sharif-Paghaleh, Ehsan
Karagiannis, Sophia N.
Peakman, Mark
Lombardi, Giovanna
Nestle, Frank O.
Resident CD141 (BDCA3)(+) dendritic cells in human skin produce IL-10 and induce regulatory T cells that suppress skin inflammation
title Resident CD141 (BDCA3)(+) dendritic cells in human skin produce IL-10 and induce regulatory T cells that suppress skin inflammation
title_full Resident CD141 (BDCA3)(+) dendritic cells in human skin produce IL-10 and induce regulatory T cells that suppress skin inflammation
title_fullStr Resident CD141 (BDCA3)(+) dendritic cells in human skin produce IL-10 and induce regulatory T cells that suppress skin inflammation
title_full_unstemmed Resident CD141 (BDCA3)(+) dendritic cells in human skin produce IL-10 and induce regulatory T cells that suppress skin inflammation
title_short Resident CD141 (BDCA3)(+) dendritic cells in human skin produce IL-10 and induce regulatory T cells that suppress skin inflammation
title_sort resident cd141 (bdca3)(+) dendritic cells in human skin produce il-10 and induce regulatory t cells that suppress skin inflammation
topic Brief Definitive Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3348099/
https://www.ncbi.nlm.nih.gov/pubmed/22547651
http://dx.doi.org/10.1084/jem.20112583
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