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Role of Microbiota and Innate Immunity in Recurrent Clostridium difficile Infection

机译:微生物群和先天免疫在艰难梭菌反复感染中的作用

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摘要

Recurrent Clostridium difficile infection represents a burdensome clinical issue whose epidemiology is increasing worldwide. The pathogenesis is not yet completely known. Recent observations suggest that the alteration of the intestinal microbiota and impaired innate immunity may play a leading role in the development of recurrent infection. Various factors can cause dysbiosis. The causes most involved in the process are antibiotics, NSAIDs, acid suppressing therapies, and age. Gut microbiota impairment can favor Clostridium difficile infection through several mechanisms, such as the alteration of fermentative metabolism (especially SCFAs), the alteration of bile acid metabolism, and the imbalance of antimicrobial substances production. These factors alter the intestinal homeostasis promoting the development of an ecological niche for Clostridium difficile and of the modulation of immune response. Moreover, the intestinal dysbiosis can promote a proinflammatory environment, whereas Clostridium difficile itself modulates the innate immunity through both toxin-dependent and toxin-independent mechanisms. In this narrative review, we discuss how the intestinal microbiota modifications and the modulation of innate immune response can lead to and exacerbate Clostridium difficile infection.
机译:难辨梭状芽孢杆菌的反复感染代表了一个繁重的临床问题,其流行病学在世界范围内正在增加。发病机理尚不完全清楚。最近的观察表明,肠道菌群的改变和先天免疫力的下降可能在复发性感染的发展中起主要作用。各种因素都可能导致营养不良。该过程中最涉及的原因是抗生素,非甾体抗炎药,抑酸疗法和衰老。肠道菌群损害可通过多种机制促进艰难梭菌感染,例如发酵代谢的改变(尤其是SCFA),胆汁酸代谢的改变以及抗菌物质产生的不平衡。这些因素改变了肠道的稳态,从而促进了艰难梭菌生态位的发展和免疫应答的调节。此外,肠道营养不良可促进促炎环境,而艰难梭菌本身通过毒素依赖性和毒素非依赖性机制调节先天免疫。在这篇叙述性综述中,我们讨论了肠道菌群的修饰和先天免疫应答的调节如何导致和加剧艰难梭菌感染。

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