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首页> 外文期刊>The FASEB Journal >Novel approaches to intervene gut microbiota in the treatment of chronic liver diseases
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Novel approaches to intervene gut microbiota in the treatment of chronic liver diseases

机译:干预肠道微生物群治疗慢性肝病的新方法

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摘要

Recent investigations of gut microbiota have contributed to understanding of the critical role of microbial community in pathophysiology. Dysbiosis not only causes disturbance directly to the gastrointestinal tract but also affects the liver through gut-liver axis. Various types of dysbiosis have been documented in alcoholic liver disease (ALD), nonalcoholic fatty liver disease, autoimmune hepatitis (AIH), primary sclerosing cholangitis, and may be crucial for the initiation, progression, or deterioration to end-stage liver disease. A few microbial species have been identified as the causal factors leading to these chronic illnesses that either do not have clear etiologies or lack effective treatment. Notably, cytolysinproducing Enterococcus faecalis, Klebsiella pneumoniae and Enterococcus gallinarum were defined for ALD, NASH, and AIH, respectively. These groundbreaking discoveries drive a rapid development in innovative therapeutics, such as fecal microbial transplantation and implementation of specific bacteriophages in addition to prebiotics, probiotics, or synbiotics for intervention of dysbiosis. Although most emerging interventions are in preclinical development or early clinical trials, a better delineation of specific dysbiosis in these disorders at metabolic, immunogenic, or molecular levels in establishing particular causal effects aids in modulating or correcting the microbial community which is the part of daily life for human being.
机译:最近对肠道微生物群的研究有助于了解微生物群落在病理生理学中的关键作用。困难不仅导致胃肠道直接扰动,而且还会通过肠轴轴线影响肝轴。在酒精性肝病(ALD),非酒精性脂肪肝疾病,自身激素肝炎(AIH),初级硬化性胆管炎中有各种类型的脱敏病,可能对终末期肝病的起始,进展或恶化至关重要。已经确定了一些微生物物种作为导致这些慢性疾病的因果因子,其无论没有明确的病因还是缺乏有效的治疗。值得注意的是,分别为ALD,NASH和AIH定义了肠球菌粪肠球菌,Klebsiella肺炎和肠球菌。这些突破性的发现能够在创新的治疗方法中推动快速发展,例如益生菌,益生菌或同步性除了脱泌症的益生物学,益生菌或同步性的粪便微生物移植和实施。虽然大多数新兴干预措施都是临床前发育或早期临床试验,但在代谢,免疫原性或分子水平时,更好地描绘这些疾病,在代谢,免疫原性或分子水平方面建立特定的因果效应助剂调节或纠正日常生活的一部分对于人类。

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