The Immune Pathogenesis of Scleroderma: Context Is Everything

被引:36
作者
Greenblatt, Matthew B. [1 ,2 ]
Aliprantis, Antonios O. [2 ,3 ]
机构
[1] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Brigham & Womens Hosp, Dept Med, Div Rheumatol Allergy & Immunol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
Scleroderma; Systemic sclerosis; Animal models; Interleukin-13; Interleukin-33; Toll-like receptor 3; Interferon; Immune; Pathogenesis; VERSUS-HOST-DISEASE; GENOME-WIDE ASSOCIATION; SYSTEMIC-SCLEROSIS; GENE-EXPRESSION; IL-13; RECEPTOR; ALTERNATIVE ACTIVATION; ANIMAL-MODELS; GROWTH-FACTOR; UP-REGULATION; INTERLEUKIN-13;
D O I
10.1007/s11926-012-0297-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The fundamental mechanisms that drive the pathogenesis of systemic sclerosis (SSc) remain elusive, despite over 50 years of investigation. Here, we review recent progress in the understanding of the immunopathogenesis of SSc. In particular, we consider interleukin-13 (IL13), and its upstream and downstream pathways, as an example of an immune system-derived mediator involved in fibrotic and vascular pathology. Emerging results linking pattern-recognition receptors and interferon pathways to SSc are also stressed. We discuss genetic data linking the immune system to SSc risk and efforts to apply animal models to subsets of patients recently resolved by gene expression profiling. These developments will help build a context for better understanding of previous observations and design of the next generation of studies that may eventually lead to effective treatment.
引用
收藏
页数:9
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