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先天宿主对肠道细菌病原体的反应:抵抗和耐受之间的平衡。

Innate host responses to enteric bacterial pathogens: a balancing act between resistance and tolerance.

机构信息

Division of Gastroenterology, BC's Children's Hospital, the Child and Family Research Institute and the University of British Columbia, Vancouver, BC, Canada.

出版信息

Cell Microbiol. 2012 Apr;14(4):475-84. doi: 10.1111/j.1462-5822.2012.01750.x. Epub 2012 Feb 15.

Abstract

Infection by enteric bacterial pathogens activates pathogen recognition receptors, leading to innate responses that promote host defence. While responses that promote host 'resistance' to infection, through the release of antimicrobial mediators, or the recruitment of inflammatory cells aimed at clearing the infection are best known, recent studies have begun to identify additional innate driven responses that instead promote intestinal tissue repair and host survival. Described as infection 'tolerance' responses, we and others have primarily studied these responses in the Citrobacter rodentium infection model. In this review we discuss the impact of innate resistance mechanisms on host defence, and describe how 'tolerance' responses act primarily on the intestinal epithelium, triggering epithelial cell proliferation, repair or promoting barrier function. Resistance and tolerance responses appear to work together, with tolerance repairing the tissue injury caused by resistance driven inflammation. Tolerance responses fit a pattern where innate immunity and inflammation are tightly regulated in the gastrointestinal tract. Moreover, tolerance may have developed due to the successful subversion and avoidance of host resistance by enteric bacterial pathogens. Further studies are needed to clarify the contribution of different pathogen recognition receptors to tolerance and resistance responses against bacterial pathogens, in the gut or in other host tissues.

摘要

肠细菌病原体的感染激活病原体识别受体,导致促进宿主防御的先天反应。虽然通过释放抗菌介质或招募旨在清除感染的炎症细胞来促进宿主对感染的“抵抗力”的反应是最广为人知的,但最近的研究已经开始识别出另外一些促进肠道组织修复和宿主存活的先天驱动反应。这些反应被描述为感染“耐受”反应,我们和其他人主要在柠檬酸杆菌感染模型中研究了这些反应。在这篇综述中,我们讨论了先天抵抗机制对宿主防御的影响,并描述了“耐受”反应如何主要作用于肠上皮细胞,触发上皮细胞增殖、修复或促进屏障功能。抵抗和耐受反应似乎共同作用,耐受反应修复由抵抗驱动的炎症引起的组织损伤。耐受反应符合一种模式,即胃肠道中先天免疫和炎症受到严格调控。此外,耐受反应可能是由于肠道细菌病原体成功地颠覆和避免了宿主的抵抗。需要进一步的研究来阐明不同的病原体识别受体对肠道或其他宿主组织中针对细菌病原体的耐受和抵抗反应的贡献。

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