Gibson P R
University of Melbourne, Department of Medicine, Royal Melbourne Hospital, Victoria, Australia.
Baillieres Clin Gastroenterol. 1997 Mar;11(1):17-33. doi: 10.1016/s0950-3528(97)90051-8.
There is now considerable evidence that abnormalities of the structure and function of the colonic epithelium are present in patients with ulcerative colitis and that many of these may occur independently of mucosal inflammation. It is proposed that epithelial abnormalities are the central defect that underlie the development of mucosal inflammation and its chronicity. A simple model for pathogenesis is proposed in which inflammation develops only when epithelial barrier function is impaired to an extent which permits the influx of luminal pro-inflammatory molecules to the lamina propria. Several candidate hypotheses regarding the molecular basis for the abnormality are addressed. The mechanism by which the barrier function is critically impaired involves the interaction of the abnormal epithelium with luminal, mucosal and systemic factors. Focusing on the epithelium would potentially lead to a conceptually different management approach and the development of novel therapeutic strategies.
现在有大量证据表明,溃疡性结肠炎患者存在结肠上皮结构和功能异常,而且其中许多异常可能独立于黏膜炎症而发生。有人提出,上皮异常是黏膜炎症发生及其慢性化的核心缺陷。本文提出了一个简单的发病机制模型,即只有当上皮屏障功能受损到一定程度,允许腔内促炎分子流入固有层时,炎症才会发生。文中探讨了关于这种异常分子基础的几个候选假说。屏障功能严重受损的机制涉及异常上皮与腔内、黏膜和全身因素的相互作用。关注上皮可能会带来概念上不同的管理方法和新治疗策略的开发。