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生物疗法在新发克罗恩病治疗中的应用:为何、何时及如何应用?

Biological therapy in the management of recent-onset Crohn's disease: why, when and how?

作者信息

Löwenberg Mark, Peppelenbosch Maikel, Hommes Daniel

机构信息

Department of Gastroenterology and Hepatology, Academic Medical Center, Amsterdam, The Netherlands.

出版信息

Drugs. 2006;66(11):1431-9. doi: 10.2165/00003495-200666110-00002.

Abstract

Crohn's disease is a chronic inflammatory bowel disease that may involve any part of the gastrointestinal tract. Conventional therapy consists of corticosteroids, azathioprine or methotrexate, but the clinical management of Crohn's disease is significantly hampered by adverse effects. With the introduction of biological agents (such as infliximab), the goals of therapy have advanced, including induction of remission with bowel healing as well as reduction in the rate of complications, surgeries and mortality. Current therapy for moderate to severe Crohn's disease is based on 'step-up' algorithms, which initiate treatment with corticosteroids followed by immunomodulatory agents, and defer therapy with biological agents until patients become refractory to conventional therapeutics. Recently, it has been shown that induction therapy with infliximab and azathioprine in recent-onset Crohn's disease (i.e. 'top-down' approach) is superior to current step-up algorithms to induce clinical remission. The underlying molecular mechanisms responsible for these differences in clinical outcome remain to be defined. Experimental studies have demonstrated that corticosteroids are able to induce impaired apoptosis of immune cells, including T cells and dendritic cells, resulting in loss of tolerance and subsequent autoimmunity. Further research will have to determine whether corticosteroid therapy augments the mechanism of loss of tolerance in Crohn's disease, which could complicate future clinical management.

摘要

克罗恩病是一种慢性炎症性肠病,可累及胃肠道的任何部位。传统疗法包括使用皮质类固醇、硫唑嘌呤或甲氨蝶呤,但克罗恩病的临床治疗因不良反应而受到显著阻碍。随着生物制剂(如英夫利昔单抗)的引入,治疗目标有所提高,包括诱导缓解并实现肠道愈合,以及降低并发症、手术和死亡率。目前中重度克罗恩病的治疗基于“逐步升级”方案,即先用皮质类固醇开始治疗,随后使用免疫调节剂,将生物制剂的治疗推迟到患者对传统疗法产生耐药性时。最近研究表明,在新发克罗恩病中使用英夫利昔单抗和硫唑嘌呤进行诱导治疗(即“自上而下”方法)优于目前的逐步升级方案,能诱导临床缓解。导致这些临床结果差异的潜在分子机制仍有待确定。实验研究表明,皮质类固醇能够诱导免疫细胞(包括T细胞和树突状细胞)凋亡受损,导致耐受性丧失及随后的自身免疫。进一步的研究将必须确定皮质类固醇疗法是否会加剧克罗恩病中耐受性丧失的机制,这可能会使未来的临床管理复杂化。

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