Krishnareddy Suneeta, Swaminath Arun
Suneeta Krishnareddy, Arun Swaminath, Mount Sinai School of Medicine, Columbia University Medical Center, New York, NY 10029, United States.
World J Gastroenterol. 2014 Feb 7;20(5):1139-46. doi: 10.3748/wjg.v20.i5.1139.
Although antagonists of tumor necrosis factor have resulted in major therapeutic benefits in inflammatory bowel disease, the magnitude and durability of response are variable. Similar to previously available drugs such as 5-aminosalicylates and immunomodulators, the therapeutic effect is not universal leaving many people searching for options. The development of newer agents has benefited from advances in the understanding of the pathophysiology of the disease. Uncontrolled activation of the acquired immune system has an important role, and lymphocytes, cytokines, and adhesion molecules are broadly targeted for therapeutic intervention. There is increasing evidence of an important role of the innate immune system and the intestinal epithelium, and the therapeutic paradigm is also shifting from immunosuppression to the reinforcement of the intestinal barrier, and modification of the disease process. In this review, we explore the limitation of current therapy as well as mechanisms of actions of new drugs and the efficacy and adverse events from data from clinical trials.
尽管肿瘤坏死因子拮抗剂已在炎症性肠病中带来了重大治疗益处,但反应的程度和持久性各不相同。与先前可用的药物如5-氨基水杨酸酯和免疫调节剂类似,治疗效果并非普遍适用,这使得许多人在寻找其他选择。新型药物的研发受益于对该疾病病理生理学认识的进展。获得性免疫系统的失控激活起着重要作用,淋巴细胞、细胞因子和黏附分子广泛成为治疗干预的靶点。越来越多的证据表明先天性免疫系统和肠上皮具有重要作用,治疗模式也正从免疫抑制转向增强肠道屏障以及改变疾病进程。在本综述中,我们从临床试验数据探讨了当前治疗的局限性、新药的作用机制、疗效及不良事件。