Division of Pulmonary and Critical Care Medicine, University of Michigan Medical School, Ann Arbor, MI.
Department of Microbiology and Immunology, University of Michigan, Ann Arbor, MI.
J Immunol. 2024 Apr 15;212(8):1269-1275. doi: 10.4049/jimmunol.2300716.
Although the lungs were once considered a sterile environment, advances in sequencing technology have revealed dynamic, low-biomass communities in the respiratory tract, even in health. Key features of these communities-composition, diversity, and burden-are consistently altered in lung disease, associate with host physiology and immunity, and can predict clinical outcomes. Although initial studies of the lung microbiome were descriptive, recent studies have leveraged advances in technology to identify metabolically active microbes and potential associations with their immunomodulatory by-products and lung disease. In this brief review, we discuss novel insights in airway disease and parenchymal lung disease, exploring host-microbiome interactions in disease pathogenesis. We also discuss complex interactions between gut and oropharyngeal microbiota and lung immunobiology. Our advancing knowledge of the lung microbiome will provide disease targets in acute and chronic lung disease and may facilitate the development of new therapeutic strategies.
尽管肺部曾经被认为是一个无菌的环境,但测序技术的进步揭示了呼吸道中存在着动态的、低生物量的微生物群落,即使在健康状态下也是如此。这些群落的关键特征——组成、多样性和负担——在肺部疾病中持续发生改变,与宿主生理学和免疫相关,并可预测临床结局。尽管最初对肺部微生物组的研究是描述性的,但最近的研究利用技术进步来识别具有代谢活性的微生物,并确定它们与免疫调节副产物和肺部疾病之间的潜在关联。在这篇简短的综述中,我们探讨了气道疾病和实质肺疾病方面的新见解,探索了宿主-微生物组在疾病发病机制中的相互作用。我们还讨论了肠道和口咽微生物组与肺部免疫生物学之间的复杂相互作用。我们对肺部微生物组的不断深入的了解将为急性和慢性肺部疾病提供治疗靶点,并可能促进新的治疗策略的发展。