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针对肠道治疗多发性硬化症。

Targeting the gut to treat multiple sclerosis.

机构信息

Department of Neurology, School of Medicine, Washington University in St. Louis, St. Louis, Missouri, USA.

University of Milan, Milan, Italy.

出版信息

J Clin Invest. 2021 Jul 1;131(13). doi: 10.1172/JCI143774.

Abstract

The gut-brain axis (GBA) refers to the complex interactions between the gut microbiota and the nervous, immune, and endocrine systems, together linking brain and gut functions. Perturbations of the GBA have been reported in people with multiple sclerosis (pwMS), suggesting a possible role in disease pathogenesis and making it a potential therapeutic target. While research in the area is still in its infancy, a number of studies revealed that pwMS are more likely to exhibit altered microbiota, altered levels of short chain fatty acids and secondary bile products, and increased intestinal permeability. However, specific microbes and metabolites identified across studies and cohorts vary greatly. Small clinical and preclinical trials in pwMS and mouse models, in which microbial composition was manipulated through the use of antibiotics, fecal microbiota transplantation, and probiotic supplements, have provided promising outcomes in preventing CNS inflammation. However, results are not always consistent, and large-scale randomized controlled trials are lacking. Herein, we give an overview of how the GBA could contribute to MS pathogenesis, examine the different approaches tested to modulate the GBA, and discuss how they may impact neuroinflammation and demyelination in the CNS.

摘要

肠脑轴(Gut-Brain Axis,GBA)是指肠道微生物群与神经系统、免疫系统和内分泌系统之间的复杂相互作用,共同连接大脑和肠道的功能。在多发性硬化症(Multiple Sclerosis,MS)患者中,已经报道了 GBA 的紊乱,这表明它可能在疾病发病机制中起作用,使其成为一个潜在的治疗靶点。尽管该领域的研究仍处于起步阶段,但许多研究表明,MS 患者更有可能表现出微生物群的改变、短链脂肪酸和次级胆汁产物水平的改变以及肠道通透性的增加。然而,不同研究和队列中确定的特定微生物和代谢物差异很大。在 MS 患者和小鼠模型中进行的小型临床和临床前试验中,通过使用抗生素、粪便微生物群移植和益生菌补充剂来操纵微生物组成,在预防中枢神经系统炎症方面提供了有希望的结果。然而,结果并不总是一致的,并且缺乏大规模的随机对照试验。本文概述了 GBA 如何有助于 MS 的发病机制,检查了测试过的不同调节 GBA 的方法,并讨论了它们如何影响中枢神经系统中的神经炎症和脱髓鞘。

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