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首页> 外文期刊>Nature reviews. Gastroenterology & hepatology >The gut-liver axis and the intersection with the microbiome
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The gut-liver axis and the intersection with the microbiome

机译:肠肝轴和微生物组的交叉点

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In the past decade, an exciting realization has been that diverse liver diseases -ranging from nonalcoholic steatohepatitis, alcoholic steatohepatitis and cirrhosis to hepatocellular carcinoma - fall along a spectrum. Work on the biology of the gut-liver axis has assisted in understanding the basic biology of both alcoholic fatty liver disease and nonalcoholic fatty liver disease (NAFLD). Of immense importance is the advancement in understanding the role of the microbiome, driven by high-throughput DNA sequencing and improved computational techniques that enable the complexity of the microbiome to be interrogated, together with improved experimental designs. Here, we review gut-liver communications in liver disease, exploring the molecular, genetic and microbiome relationships and discussing prospects for exploiting the microbiome to determine liver disease stage and to predict the effects of pharmaceutical, dietary and other interventions at a population and individual level. Although much work remains to be done in understanding the relationship between the microbiome and liver disease, rapid progress towards clinical applications is being made, especially in study designs that complement human intervention studies with mechanistic work in mice that have been humanized in multiple respects, including the genetic, immunological and microbiome characteristics of individual patients. These 'avatar mice' could be especially useful for guiding new microbiome-based or microbiome-informed therapies.
机译:在过去的十年中,令人兴奋的实现一直是多元化的肝脏疾病 - 从非酒精性脱毛骨膜炎,酒精性脱毛性和肝硬化到肝细胞癌 - 沿着光谱落下。对肠肝轴生物学的工作有助于了解酒精脂肪肝病和非酒精性脂肪肝病(NAFLD)的基本生物学。巨大重要性是理解微生物组的作用的进步,由高通量DNA测序和改进的计算技术驱动,使得微生物组的复杂性与改进的实验设计一起进行询问。在这里,我们审查肝病中的肠肝通信,探索分子,遗传和微生物组的关系,并讨论利用微生物组的前景来确定肝病阶段,预测药物,膳食和其他干预措施对人群和个人水平的影响。虽然在了解微生物组和肝病之间的关系中仍有很大的工作,但正在制定临床应用的快速进展,特别是在研究设计中,使人类干预研究与在多个方面的人为化的小鼠中的机械工作,包括个体患者的遗传,免疫学和微生物细胞特征。这些“头像小鼠”可能对引导新的微生物组或微生物组织信息的疗法特别有用。

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