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Breakdown of Immune Tolerance in Systemic Lupus Erythematosus by Dendritic Cells
Dendritic cells (DC) play an important role in the pathogenesis of systemic lupus erythematosus (SLE), an autoimmune disease with multiple tissue manifestations. In this review, we summarize recent studies on the roles of conventional DC and plasmacytoid DC in the development of both murine lupus an...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4789470/ https://www.ncbi.nlm.nih.gov/pubmed/27034965 http://dx.doi.org/10.1155/2016/6269157 |
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author | Liao, Xiaofeng Reihl, Alec M. Luo, Xin M. |
author_facet | Liao, Xiaofeng Reihl, Alec M. Luo, Xin M. |
author_sort | Liao, Xiaofeng |
collection | PubMed |
description | Dendritic cells (DC) play an important role in the pathogenesis of systemic lupus erythematosus (SLE), an autoimmune disease with multiple tissue manifestations. In this review, we summarize recent studies on the roles of conventional DC and plasmacytoid DC in the development of both murine lupus and human SLE. In the past decade, studies using selective DC depletions have demonstrated critical roles of DC in lupus progression. Comprehensive in vitro and in vivo studies suggest activation of DC by self-antigens in lupus pathogenesis, followed by breakdown of immune tolerance to self. Potential treatment strategies targeting DC have been developed. However, many questions remain regarding the mechanisms by which DC modulate lupus pathogenesis that require further investigations. |
format | Online Article Text |
id | pubmed-4789470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-47894702016-03-31 Breakdown of Immune Tolerance in Systemic Lupus Erythematosus by Dendritic Cells Liao, Xiaofeng Reihl, Alec M. Luo, Xin M. J Immunol Res Review Article Dendritic cells (DC) play an important role in the pathogenesis of systemic lupus erythematosus (SLE), an autoimmune disease with multiple tissue manifestations. In this review, we summarize recent studies on the roles of conventional DC and plasmacytoid DC in the development of both murine lupus and human SLE. In the past decade, studies using selective DC depletions have demonstrated critical roles of DC in lupus progression. Comprehensive in vitro and in vivo studies suggest activation of DC by self-antigens in lupus pathogenesis, followed by breakdown of immune tolerance to self. Potential treatment strategies targeting DC have been developed. However, many questions remain regarding the mechanisms by which DC modulate lupus pathogenesis that require further investigations. Hindawi Publishing Corporation 2016 2016-02-29 /pmc/articles/PMC4789470/ /pubmed/27034965 http://dx.doi.org/10.1155/2016/6269157 Text en Copyright © 2016 Xiaofeng Liao et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Liao, Xiaofeng Reihl, Alec M. Luo, Xin M. Breakdown of Immune Tolerance in Systemic Lupus Erythematosus by Dendritic Cells |
title | Breakdown of Immune Tolerance in Systemic Lupus Erythematosus by Dendritic Cells |
title_full | Breakdown of Immune Tolerance in Systemic Lupus Erythematosus by Dendritic Cells |
title_fullStr | Breakdown of Immune Tolerance in Systemic Lupus Erythematosus by Dendritic Cells |
title_full_unstemmed | Breakdown of Immune Tolerance in Systemic Lupus Erythematosus by Dendritic Cells |
title_short | Breakdown of Immune Tolerance in Systemic Lupus Erythematosus by Dendritic Cells |
title_sort | breakdown of immune tolerance in systemic lupus erythematosus by dendritic cells |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4789470/ https://www.ncbi.nlm.nih.gov/pubmed/27034965 http://dx.doi.org/10.1155/2016/6269157 |
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