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[系统性硬化症的病理生理学]

[Pathophysiology of systemic sclerosis].

作者信息

Allanore Yannick

机构信息

Inserm U1016, institut Cochin, rhumatologie A, université Paris Descartes, hôpital Cochin, 27, rue du Faubourg-Saint-Jacques, 75014 Paris, France.

出版信息

Med Sci (Paris). 2016 Feb;32(2):183-91. doi: 10.1051/medsci/20163202012. Epub 2016 Mar 2.

Abstract

Systemic sclerosis (SSc) is an orphan disease affecting the connective tissue. The cause of SSc remains unknown but is likely to involve environmental factors in a genetically primed individual with SSc belonging to the multigenic disorders. Pathogenesis is dominated by early microvascular changes targeting endothelial cells and with the release of several mediators promoting an inflammatory response and vascular remodelling. Several lines of evidence position autoimmunity as a key perpetuating event with activation of both innate and adaptive immunity and with the production of distinct autoantibodies. The cascade ultimates with the fibrosis defined by accumulation of extra-cellular matrix through an imbalance between synthesis and degradation of several components and mesenchymal cell activation and differentiation controlled by a large number of autocrine and paracrine factors.

摘要

系统性硬化症(SSc)是一种影响结缔组织的罕见病。SSc的病因尚不清楚,但可能涉及环境因素,在具有遗传易感性的个体中引发该病,SSc属于多基因疾病。发病机制主要由早期针对内皮细胞的微血管变化主导,并伴有多种介质的释放,促进炎症反应和血管重塑。多条证据表明自身免疫是关键的持续事件,涉及固有免疫和适应性免疫的激活以及独特自身抗体的产生。这一连串事件最终导致纤维化,其特征是细胞外基质通过几种成分合成与降解之间的失衡而积累,以及由大量自分泌和旁分泌因子控制的间充质细胞激活和分化。

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