Dendritic Cells in Systemic Lupus Erythematosus: From Pathogenic Players to Therapeutic Tools
System lupus erythematosus (SLE) is a multifactorial systemic autoimmune disease with a wide variety of presenting features. SLE is believed to result from dysregulated immune responses, loss of tolerance of CD4 T cells and B cells to ubiquitous self-antigens, and the subsequent production of anti-n...
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2016-01-01
|
Series: | Mediators of Inflammation |
Online Access: | http://dx.doi.org/10.1155/2016/5045248 |
id |
doaj-b865d0acb9014500af9e61795070f777 |
---|---|
record_format |
Article |
spelling |
doaj-b865d0acb9014500af9e61795070f7772020-11-24T22:32:39ZengHindawi LimitedMediators of Inflammation0962-93511466-18612016-01-01201610.1155/2016/50452485045248Dendritic Cells in Systemic Lupus Erythematosus: From Pathogenic Players to Therapeutic ToolsJared Klarquist0Zhenyuan Zhou1Nan Shen2Edith M. Janssen3Division of Immunobiology, Cincinnati Children’s Hospital Medical Center and the University of Cincinnati College of Medicine, Cincinnati, OH 45229, USAShanghai Institute of Rheumatology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, ChinaShanghai Institute of Rheumatology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, ChinaDivision of Immunobiology, Cincinnati Children’s Hospital Medical Center and the University of Cincinnati College of Medicine, Cincinnati, OH 45229, USASystem lupus erythematosus (SLE) is a multifactorial systemic autoimmune disease with a wide variety of presenting features. SLE is believed to result from dysregulated immune responses, loss of tolerance of CD4 T cells and B cells to ubiquitous self-antigens, and the subsequent production of anti-nuclear and other autoreactive antibodies. Recent research has associated lupus development with changes in the dendritic cell (DC) compartment, including altered DC subset frequency and localization, overactivation of mDCs and pDCs, and functional defects in DCs. Here we discuss the current knowledge on the role of DC dysfunction in SLE pathogenesis, with the focus on DCs as targets for interventional therapies.http://dx.doi.org/10.1155/2016/5045248 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jared Klarquist Zhenyuan Zhou Nan Shen Edith M. Janssen |
spellingShingle |
Jared Klarquist Zhenyuan Zhou Nan Shen Edith M. Janssen Dendritic Cells in Systemic Lupus Erythematosus: From Pathogenic Players to Therapeutic Tools Mediators of Inflammation |
author_facet |
Jared Klarquist Zhenyuan Zhou Nan Shen Edith M. Janssen |
author_sort |
Jared Klarquist |
title |
Dendritic Cells in Systemic Lupus Erythematosus: From Pathogenic Players to Therapeutic Tools |
title_short |
Dendritic Cells in Systemic Lupus Erythematosus: From Pathogenic Players to Therapeutic Tools |
title_full |
Dendritic Cells in Systemic Lupus Erythematosus: From Pathogenic Players to Therapeutic Tools |
title_fullStr |
Dendritic Cells in Systemic Lupus Erythematosus: From Pathogenic Players to Therapeutic Tools |
title_full_unstemmed |
Dendritic Cells in Systemic Lupus Erythematosus: From Pathogenic Players to Therapeutic Tools |
title_sort |
dendritic cells in systemic lupus erythematosus: from pathogenic players to therapeutic tools |
publisher |
Hindawi Limited |
series |
Mediators of Inflammation |
issn |
0962-9351 1466-1861 |
publishDate |
2016-01-01 |
description |
System lupus erythematosus (SLE) is a multifactorial systemic autoimmune disease with a wide variety of presenting features. SLE is believed to result from dysregulated immune responses, loss of tolerance of CD4 T cells and B cells to ubiquitous self-antigens, and the subsequent production of anti-nuclear and other autoreactive antibodies. Recent research has associated lupus development with changes in the dendritic cell (DC) compartment, including altered DC subset frequency and localization, overactivation of mDCs and pDCs, and functional defects in DCs. Here we discuss the current knowledge on the role of DC dysfunction in SLE pathogenesis, with the focus on DCs as targets for interventional therapies. |
url |
http://dx.doi.org/10.1155/2016/5045248 |
work_keys_str_mv |
AT jaredklarquist dendriticcellsinsystemiclupuserythematosusfrompathogenicplayerstotherapeutictools AT zhenyuanzhou dendriticcellsinsystemiclupuserythematosusfrompathogenicplayerstotherapeutictools AT nanshen dendriticcellsinsystemiclupuserythematosusfrompathogenicplayerstotherapeutictools AT edithmjanssen dendriticcellsinsystemiclupuserythematosusfrompathogenicplayerstotherapeutictools |
_version_ |
1725732963130277888 |