微吸入和失调的气消化微生物群在肺部疾病中的潜在作用的叙述性回顾

Abdullah Althuwaybi, A. Alamer, M. McDonnell, M. Brennan, R. Rutherford, M. Wilcox, P. Chater, J. Pearson, C. Ward
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引用次数: 1

摘要

人类微生物组项目在启动时没有将肺和气道纳入其采样点,这表明对人类肺部微生物组在健康和疾病中的作用的认识不足。最近,通过使用与培养无关的方法来表征人类肺部微生物组,这种模式发生了变化。原来的想法是,正常的肺基本上是无菌的,之前在正常志愿者和意识水平下降的患者中发现了微吸,这一想法受到了挑战。肺移植受者的临床隐匿性感染标志物也对无菌肺提出了质疑。可以说是对人类肺部微生物组重要性的“重新发现”,可能仍然低估了器官系统之间的生理和病理生理相互关系,这些关系是在不同的研究学科中研究的。特别是,微吸入可能是调节肺微生物组的一个重要的直接机制。除了与胃食管反流和微吸入相关的吸入外,作者认为慢性肺部疾病中吞咽困难的重要性将越来越多地认识到与口咽部与肺部之间的虚弱相关的微生物组交换。因此,本综述讨论了人类微生物组的相互联系,重点关注气消化病理生理和微吸的潜力。与人类肺部疾病的潜在联系进行了讨论,并在发展中的文献背景。因此,这篇综述强调了肺病理生理学翻译干预急需的新靶点,并强调了未来混合学科团队方法的重要性。
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A narrative review of the potential role of microaspiration and a dysregulated aerodigestive microbiome in lung disease
: When initiated the human microbiome project did not include the lungs and airways in its sampling sites, indicating an under appreciation of the role of the human lung microbiome in health and disease. This paradigm has recently changed through the use of culture independent methods to characterise the human lung microbiome. The original thinking, that the normal lung was essentially sterile, had previously been challenged by findings of microaspiration in normal volunteers and in patients with decreased levels of consciousness. The sterile lung was also questioned by findings of clinically occult infection markers in lung allograft recipients. What is arguably a “rediscovery” of the importance of the human lung microbiome may still underappreciate physiological and patho-physiological inter-relationships between organ systems, studied in separate research disciplines. In particular, microaspiration may be an important, direct mechanism through which the lung microbiome is modulated. As well as aspiration related to gastro-oesophageal reflux and microaspiration the authors feel that the importance of dysphagia in chronic lung disease, will be increasingly recognised in frailty related microbiome exchange between the oropharynx into the lung. This review therefore discusses interconnections in the human microbiome, with a focus on the potential for aerodigestive pathophysiology and microaspiration. Potential connections with human lung disease are discussed and contextualised within a developing literature. This review therefore highlights much needed new targets for translational intervention in lung pathophysiology and underlies the importance of a mixed disciplinary team approach for the future.
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