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早期囊性纤维化肺病中的气道微生物群

The airway microbiota in early cystic fibrosis lung disease.

作者信息

Frayman Katherine B, Armstrong David S, Grimwood Keith, Ranganathan Sarath C

机构信息

Department of Respiratory and Sleep Medicine, Royal Children's Hospital, Melbourne, Victoria, Australia.

Respiratory Diseases Group, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.

出版信息

Pediatr Pulmonol. 2017 Nov;52(11):1384-1404. doi: 10.1002/ppul.23782. Epub 2017 Aug 16.

Abstract

Infection plays a critical role in the pathogenesis of cystic fibrosis (CF) lung disease. Over the past two decades, the application of molecular and extended culture-based techniques to microbial analysis has changed our understanding of the lungs in both health and disease. CF lung disease is a polymicrobial disorder, with obligate and facultative anaerobes recovered alongside traditional pathogens in varying proportions, with some differences observed to correlate with disease stage. While healthy lungs are not sterile, differences between the lower airway microbiota of individuals with CF and disease-controls are already apparent in childhood. Understanding the evolution of the CF airway microbiota, and its relationship with clinical treatments and outcome at each disease stage, will improve our understanding of the pathogenesis of CF lung disease and potentially inform clinical management. This review summarizes current knowledge of the early development of the respiratory microbiota in healthy children and then discusses what is known about the airway microbiota in individuals with CF, including how it evolves over time and where future research priorities lie.

摘要

感染在囊性纤维化(CF)肺部疾病的发病机制中起着关键作用。在过去二十年中,分子技术和基于扩展培养的技术应用于微生物分析,改变了我们对健康和患病肺部的认识。CF肺部疾病是一种多微生物紊乱疾病,专性和兼性厌氧菌与传统病原体一起以不同比例被检出,观察到一些差异与疾病阶段相关。虽然健康的肺部并非无菌,但CF患者与疾病对照者的下呼吸道微生物群之间的差异在儿童期就已很明显。了解CF气道微生物群的演变及其在每个疾病阶段与临床治疗和结果的关系,将增进我们对CF肺部疾病发病机制的理解,并可能为临床管理提供依据。本综述总结了目前关于健康儿童呼吸道微生物群早期发育的知识,然后讨论了CF患者气道微生物群的已知情况,包括其随时间的演变以及未来的研究重点所在。

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