Zhou Xin, Liao Youxia
Department of ICU/Emergency, Wuhan University, Wuhan Third Hospital, Wuhan, China.
Front Microbiol. 2021 Dec 23;12:779620. doi: 10.3389/fmicb.2021.779620. eCollection 2021.
Acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) are common acute and severe cases of the respiratory system with complicated pathogenesis and high mortality. Sepsis is the leading indirect cause of ALI/ARDS in the intensive care unit (ICU). The pathogenesis of septic ALI/ARDS is complex and multifactorial. In the development of sepsis, the disruption of the intestinal barrier function, the alteration of gut microbiota, and the translocation of the intestinal microbiome can lead to systemic and local inflammatory responses, which further alter the immune homeostasis in the systemic environment. Disruption of homeostasis may promote and propagate septic ALI/ARDS. In turn, when ALI occurs, elevated levels of inflammatory cytokines and the shift of the lung microbiome may lead to the dysregulation of the intestinal microbiome and the disruption of the intestinal mucosal barrier. Thus, the interaction between the lung and the gut can initiate and potentiate sepsis-induced ALI/ARDS. The gut-lung crosstalk may be a promising potential target for intervention. This article reviews the underlying mechanism of gut-lung crosstalk in septic ALI/ARDS.
急性肺损伤(ALI)和急性呼吸窘迫综合征(ARDS)是呼吸系统常见的急重症,发病机制复杂,死亡率高。脓毒症是重症监护病房(ICU)中ALI/ARDS的主要间接病因。脓毒症相关性ALI/ARDS的发病机制复杂且具有多因素性。在脓毒症的发展过程中,肠道屏障功能的破坏、肠道微生物群的改变以及肠道微生物组的易位可导致全身和局部炎症反应,进而进一步改变全身环境中的免疫稳态。稳态的破坏可能促进和加剧脓毒症相关性ALI/ARDS。反过来,当发生ALI时,炎症细胞因子水平升高和肺部微生物组的变化可能导致肠道微生物组失调和肠道黏膜屏障破坏。因此,肺与肠道之间的相互作用可引发并增强脓毒症诱导的ALI/ARDS。肠-肺串扰可能是一个有前景的潜在干预靶点。本文综述了脓毒症相关性ALI/ARDS中肠-肺串扰的潜在机制。