Dr. B.C. Roy College of Pharmacy and Allied Health Sciences, Durgapur, India. bhu
Int Rev Immunol. 2010;29(1):4-37. doi: 10.3109/08830180903437212.
Current advances in understanding of the pathogenesis of inflammatory bowel disease have encouraged the development of many new therapies targeted at specific and non-specific mediators of the inflammatory bowel disease inflammatory pathway. Crohn's disease and ulcerative colitis, two common inflammatory bowel diseases likely result from interaction of multiple genetic and environmental risk and protective factors, deregulation of mucosal immunity in gut and breakdown of delicate balance of proinflammatory and anti-inflammatory cytokines. Immunobiologic agents targeted against TNF, leukocyte adhesion, Th1 polarization, T cell activation, nuclear factor-kappaB (NF-kappaB), and others are being assessed and will open exciting perspectives on development of therapies for inflammatory bowel disease.
目前,人们对炎症性肠病发病机制的理解取得了一些进展,这促进了许多新疗法的发展,这些疗法针对炎症性肠病炎症途径的特定和非特定介质。克罗恩病和溃疡性结肠炎是两种常见的炎症性肠病,可能是由多种遗传和环境风险和保护因素相互作用、肠道黏膜免疫失调以及促炎和抗炎细胞因子之间微妙平衡的破坏引起的。目前正在评估针对 TNF、白细胞黏附、Th1 极化、T 细胞激活、核因子-κB(NF-κB)等的免疫生物制剂,这些制剂为炎症性肠病的治疗方法的发展开辟了令人兴奋的前景。