Shanahan Fergus
Alimentary Pharmabiotic Centre, Department of Medicine, Clinical Science Bldg., Cork University Hospital, Cork, Ireland.
Am J Physiol Gastrointest Liver Physiol. 2005 Mar;288(3):G417-21. doi: 10.1152/ajpgi.00421.2004.
Mechanisms underlying the conditioning influence of the intestinal flora on mucosal homeostasis, including development and function of immune responses, are attracting increasing scientific scrutiny. The intestinal flora is a positive asset to host defense, but some of its components may, in genetically susceptible hosts, become a risk factor for development of inflammatory bowel disease (IBD). It follows that strategies to enhance assets or offset microbial liabilities represent a therapeutic option; therein lies the rationale for manipulation of the flora in IBD. In addition, the diversity of regulatory signalling among the flora and host epithelum, lymphoid tissue, and neuromuscular apparatus is an untapped reservoir from which novel therapeutics may be mined. Moreover, the capacity to engineer food-grade or commensal bacteria to deliver therapeutic molecules to the intestinal mucosa promises to extend the scope of microbial manipulation for the benefit of mankind.
肠道菌群对黏膜稳态(包括免疫反应的发育和功能)产生调节影响的潜在机制,正吸引着越来越多的科学关注。肠道菌群是宿主防御的一项积极资产,但在基因易感性宿主中,其某些成分可能成为炎性肠病(IBD)发病的一个风险因素。因此,增强有益成分或抵消微生物有害影响的策略代表了一种治疗选择;这就是在IBD中操控菌群的基本原理。此外,菌群与宿主上皮、淋巴组织及神经肌肉装置之间调节信号的多样性是一个尚未开发的宝库,从中或许可以挖掘出新的治疗方法。而且,改造食品级或共生细菌以将治疗分子递送至肠道黏膜的能力,有望扩大微生物操控的范围,造福人类。