Hansen Jonathan J, Sartor R Balfour
Department of Medicine, University of North Carolina at Chapel Hill, CB 7032, Chapel Hill, NC, 27599, USA,
Curr Treat Options Gastroenterol. 2015 Mar;13(1):105-20. doi: 10.1007/s11938-014-0042-7.
Despite recent major strides in our understanding of the genetic and microbial influences that contribute to the development of the inflammatory bowel diseases (IBDs), their etiology continues to be enigmatic. Results from experiments in animal models of IBDs overwhelmingly support a causal role of the microbiota in these diseases, though whether such a cause-effect relationship exists in human IBDs is still uncertain. Therefore, virtually all currently approved and most often prescribed treatments for IBDs are directed toward the over-active immune response in these diseases rather than the intestinal bacteria. Nevertheless, there is an important need for non-immunosuppressive therapies that may present a more favorable risk-benefit profile such as those that selectively target the disruptions in gut microbiota that accompany IBDs. This need has led to clinical trials of various microbial-directed therapies including fecal microbial transplant, antibiotics, probiotics, and prebiotics. Unfortunately, these published studies, many of which are small, have generally failed to demonstrate a consistent benefit of these agents in IBDs, thus leading to slow acceptance of microbe-focused treatments for these conditions. In this article, we review and summarize the microbial basis for IBDs and the results of the most recent trials of fecal microbial transplant, antibiotics, probiotics, and prebiotics in IBDs. We also comment on possible safety concerns with these agents, speculate on why they have failed to show efficacy in certain clinical settings, and propose strategies to improve their usefulness.
尽管我们最近在理解促成炎症性肠病(IBD)发生发展的遗传和微生物影响方面取得了重大进展,但其病因仍然成谜。IBD动物模型实验的结果压倒性地支持微生物群在这些疾病中起因果作用,尽管这种因果关系在人类IBD中是否存在仍不确定。因此,目前几乎所有获批且最常处方的IBD治疗方法都是针对这些疾病中过度活跃的免疫反应,而非肠道细菌。然而,迫切需要非免疫抑制疗法,这类疗法可能具有更有利的风险效益比,比如那些选择性针对伴随IBD出现的肠道微生物群紊乱的疗法。这种需求促使了各种微生物导向疗法的临床试验,包括粪便微生物移植、抗生素、益生菌和益生元。不幸的是,这些已发表的研究(其中许多规模较小)总体上未能证明这些药物对IBD有持续的益处,因此这些以微生物为重点的治疗方法在这些病症中的接受度进展缓慢。在本文中,我们回顾并总结了IBD的微生物学基础以及粪便微生物移植、抗生素、益生菌和益生元在IBD中最新试验的结果。我们还对这些药物可能存在的安全问题进行了评论,推测它们在某些临床环境中未能显示疗效的原因,并提出提高其效用的策略。