Department of Pediatrics and Communicable Diseases, Ann Arbor, MI.
Division of Pulmonary and Critical Care Medicine, Department of Medicine, Ann Arbor, MI.
Chest. 2019 Aug;156(2):376-382. doi: 10.1016/j.chest.2019.05.011. Epub 2019 May 30.
COPD, asthma, and cystic fibrosis (CF) are obstructive lung diseases with distinct pathophysiologies and clinical phenotypes. In this paper, we highlight recent advances in our understanding of relationships between clinical phenotypes, host inflammatory response, and lung microbiota in these diseases. Although COPD, asthma, and CF largely have distinct lung microbiota and inflammatory profiles, certain commonalities exist. In all three of these lung diseases, and in healthy persons, anaerobic taxa that are typically associated with oral microbiota (eg, Prevotella species, Veillonella species) are present in the airways and associated with increased host inflammatory response. Similarly, across all three diseases, members of the Proteobacteria phylum are associated with more advanced disease. Finally, we highlight challenges in translating these findings into advances in clinical care, including continued knowledge gaps regarding the causal relationships between host inflammatory response, lung microbiota, medication effects, and clinical phenotypes.
慢性阻塞性肺疾病(COPD)、哮喘和囊性纤维化(CF)是具有不同病理生理学和临床表型的阻塞性肺疾病。在本文中,我们强调了在理解这些疾病的临床表型、宿主炎症反应和肺部微生物组之间关系方面的最新进展。尽管 COPD、哮喘和 CF 在很大程度上具有不同的肺部微生物组和炎症特征,但仍存在某些共同之处。在所有这三种肺部疾病中,以及在健康人群中,通常与口腔微生物组相关的厌氧分类群(例如,普雷沃氏菌属、韦荣球菌属)存在于气道中,并与宿主炎症反应增加相关。同样,在所有三种疾病中,变形菌门的成员与更严重的疾病相关。最后,我们强调了将这些发现转化为临床护理进展所面临的挑战,包括宿主炎症反应、肺部微生物组、药物作用和临床表型之间因果关系的持续知识差距。