Papadakis K A, Targan S R
Division of Gastroenterology, University of California, Los Angeles, UCLA School of Medicine, USA.
Gastroenterol Clin North Am. 1999 Jun;28(2):283-96. doi: 10.1016/s0889-8553(05)70057-1.
The understanding of the pathogenesis of CD and UC has greatly expanded over the last decade. The combination of abnormalities in the immune system, the contribution of nonimmune cells in the intestinal mucosa, a variety of genetic risk determinants, and random environmental factors may all be necessary to induce what clinically presents as IBD. It is likely that several agents can initiate an immune response that in the intestinal microenvironment and the genetic background of the patient finally leads to pathology.
在过去十年中,对克罗恩病(CD)和溃疡性结肠炎(UC)发病机制的认识有了极大的扩展。免疫系统异常、肠道黏膜中非免疫细胞的作用、多种遗传风险决定因素以及随机环境因素的综合作用,可能都是引发临床上表现为炎症性肠病(IBD)所必需的。很可能有几种因素能够引发免疫反应,这种反应在患者的肠道微环境和遗传背景中最终导致病变。