Cutaneous lupus erythematosus: recent lessons from animal models

被引:11
|
作者
Ghoreishi, M.
Dutz, J. P.
机构
[1] Univ British Columbia, Dept Dermatol & Skin Sci, Vancouver, BC V5Z 1M9, Canada
[2] Univ British Columbia, Child & Family Res Inst, Vancouver, BC V5Z 1M9, Canada
关键词
apoptosis; B cell; BSXB mouse; cutaneous lupus erythematosus; CSF-1; CXCR3; HMGB1; ICAM-1; IFN alpha; IL-1; IL-6; IL-18; MrL/lpr mouse; NZB/W mouse; T cell; TNF alpha; UV light; ENDOTHELIAL CELL-INTERACTIONS; SYSTEMIC AUTOIMMUNITY; SKIN-LESIONS; MURINE LUPUS; MRL-FAS(LPR) MICE; APOPTOTIC CELLS; MRL/LPR MICE; TNF-ALPHA; PROLONGS SURVIVAL; IPR/IPR MICE;
D O I
10.1177/0961203310370045
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cutaneous lupus erythematosus (CLE) may present as a clinically heterogeneous group of lupus-specific skin lesions that have common histopathological findings. Determination of the immunopathological sequence of events in this group of disorders has been challenging for dermatologists and immunologists but is vital for therapeutic targeting. We review animal models in which different aspects of immune alteration in CLE have been addressed. The MRL/lpr mouse develops spontaneous skin disease with some features of CLE. Study of this strain and related gene-manipulated strains has revealed roles for multiple cytokines, including interleukin (IL)-6, IL-18, and IL-21, in disease pathogenesis. A role for the growth factor colony stimulating factor 1 and the inflammatory protein high-mobility group box 1 has also been suggested. We discuss potential novel treatment options suggested by these models. Lupus (2010) 19, 1029-1035.
引用
收藏
页码:1029 / 1035
页数:7
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