Department of Internal Medicine A, Ernst-Moritz-Arndt University Greifswald, Greifswald, Germany.
J Cell Mol Med. 2010 Oct;14(10):2393-403. doi: 10.1111/j.1582-4934.2009.00959.x.
Autoimmunity against type VII collagen, an adhesion molecule of the extracellular matrix in epithelial basement membranes, is causing the rare organ-specific epidermolysis bullosa acquisita (EBA). An intriguing association between EBA and inflammatory bowel disease (IBD) has been extensively documented over the last decades, but, because of the very low incidence of EBA, received little attention from physicians involved in the care of patients with IBD. More recently, autoantibodies against type VII collagen have been detected in up to 68% of IBD patients. Although these findings suggest that chronic intestinal inflammation in IBD predisposes for autoimmunity against type VII collagen, their relevance for the pathogenesis of both IBD and EBA is still unclear. In this review article, the main features of the association between IBD and EBA are presented and pathomechanistic hypotheses as well as future lines of investigation in this area are discussed. Future research should provide new pathomechanistic insights and will likely facilitate the development of more specific and effective immunotherapeutic strategies for both conditions.
自身免疫性 VII 型胶原病,一种细胞外基质的黏附分子,存在于上皮基底膜,是罕见的器官特异性获得性大疱性表皮松解症(EBA)的病因。过去几十年中,EBA 与炎症性肠病(IBD)之间存在引人关注的关联已被广泛记录,但由于 EBA 的发病率非常低,因此参与 IBD 患者治疗的医生很少关注这一问题。最近,多达 68%的 IBD 患者检测到针对 VII 型胶原的自身抗体。尽管这些发现表明 IBD 中的慢性肠道炎症易导致针对 VII 型胶原的自身免疫,但它们与 IBD 和 EBA 的发病机制的相关性仍不清楚。在这篇综述文章中,介绍了 IBD 和 EBA 之间关联的主要特征,并讨论了该领域的发病机制假说和未来的研究方向。未来的研究应提供新的发病机制见解,并可能促进这两种疾病更具体和有效的免疫治疗策略的发展。