Ince M Nedim, Elliott David E
Division of Gastroenterology and Hepatology, Department of Internal Medicine, University of Iowa, Carver College of Medicine, 4611 JCP, 200 Hawkins Drive, Iowa City, IA 52242, USA.
Surg Clin North Am. 2007 Jun;87(3):681-96. doi: 10.1016/j.suc.2007.03.005.
Molecular and immunologic mechanisms underlying inflammation in inflammatory bowel disease (IBD) are largely unknown. Recent studies have helped better characterize genetic and environmental factors associated with colitis. Discoveries of genetic variants have confirmed that IBD is a bacteria and cytokine-driven pathologic immune response. Data have demonstrated that certain T cell subsets are important in executing the inflammatory cascade. Insufficient regulatory cell activity or modulatory cytokine production results in unrestrained inflammation. Biologic agents that block inflammatory cytokines (anti-TNFalpha antibodies) have been used successfully to treat IBD. Recent advances have also identified mucosal regulatory pathways.
炎症性肠病(IBD)中炎症背后的分子和免疫机制在很大程度上尚不清楚。最近的研究有助于更好地描述与结肠炎相关的遗传和环境因素。基因变异的发现证实,IBD是一种由细菌和细胞因子驱动的病理性免疫反应。数据表明,某些T细胞亚群在引发炎症级联反应中很重要。调节细胞活性不足或调节性细胞因子产生不足会导致炎症不受控制。阻断炎性细胞因子的生物制剂(抗TNFα抗体)已成功用于治疗IBD。最近的进展还确定了黏膜调节途径。