Systemic sclerosis: current views of its pathogenesis

被引:107
作者
Derk, CT [1 ]
Jimenez, SA [1 ]
机构
[1] Thomas Jefferson Univ, Div Rheumatol, Dept Med, Philadelphia, PA 19107 USA
关键词
systemic sclerosis; scleroderma; fibrosis; autoantibodies; transforming growth factor beta; collagen genes; transcription factors; COLLAGEN GENE-EXPRESSION; TGF-BETA; TOPOISOMERASE-I; SCLERODERMA; SKIN; CELLS; IDENTIFICATION; ASSOCIATION; FIBROSIS; MICROCHIMERISM;
D O I
10.1016/S1568-9972(03)00005-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Systemic sclerosis (SSc) is an autoimmune disorder of unknown etiology characterized by severe and often progressive cutaneous and visceral fibrosis, pronounced alterations in the microvasculature and numerous cellular and humoral immune abnormalities. Clinically, SSc is very heterogenous encompassing a spectrum ranging from mild limited forms of skin sclerosis with minimal internal organ involvement to severe skin and multiple internal organ fibrosis. Mortality and morbidity in SSc are very high and are directly related to the extent of the fibrotic and microvascular alterations. A better understanding of the pathogenesis of this incurable disorder will help to better target and design effective therapy in the future. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:181 / 191
页数:11
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