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肠道菌群如何影响乳糜泻,以及我们能做什么。

How the Microbiota May Affect Celiac Disease and What We Can Do.

机构信息

Pediatric Clinical Microbiomics Service, Misericordia Hospital, Via Senese 161, 58100 Grosseto, Italy.

Section of Pediatric Gastroenterology, Hepatology and Nutrition, Celiac Disease Center, University of Chicago Medicine, 5841 S. Maryland Ave. MC 4065, Chicago, IL 60637, USA.

出版信息

Nutrients. 2024 Jun 14;16(12):1882. doi: 10.3390/nu16121882.

Abstract

Celiac disease (CeD) is an autoimmune disease with a strong association with human leukocyte antigen (HLA), characterized by the production of specific autoantibodies and immune-mediated enterocyte killing. CeD is a unique autoimmune condition, as it is the only one in which the environmental trigger is known: gluten, a storage protein present in wheat, barley, and rye. How and when the loss of tolerance of the intestinal mucosa to gluten occurs is still unknown. This event, through the activation of adaptive immune responses, enhances epithelial cell death, increases the permeability of the epithelial barrier, and induces secretion of pro-inflammatory cytokines, resulting in the transition from genetic predisposition to the actual onset of the disease. While the role of gastrointestinal infections as a possible trigger has been considered on the basis of a possible mechanism of antigen mimicry, a more likely alternative mechanism appears to involve a complex disruption of the gastrointestinal microbiota ecosystem triggered by infections, rather than the specific effect of a single pathogen on intestinal mucosal homeostasis. Several lines of evidence show the existence of intestinal dysbiosis that precedes the onset of CeD in genetically at-risk subjects, characterized by the loss of protective bacterial elements that both epigenetically and functionally can influence the response of the intestinal epithelium leading to the loss of gluten tolerance. We have conducted a literature review in order to summarize the current knowledge about the complex and in part still unraveled dysbiosis that precedes and accompanies CeD and present some exciting new data on how this dysbiosis might be prevented and/or counteracted. The literature search was conducted on PubMed.gov in the time frame 2010 to March 2024 utilizing the terms "celiac disease and microbiota", "celiac disease and microbiome", and "celiac disease and probiotics" and restricting the search to the following article types: Clinical Trials, Meta-Analysis, Review, and Systematic Review. A total of 364 papers were identified and reviewed. The main conclusions of this review can be outlined as follows: (1) quantitative and qualitative changes in gut microbiota have been clearly documented in CeD patients; (2) intestinal microbiota's extensive and variable interactions with enterocytes, viral and bacterial pathogens and even gluten combine to impact the inflammatory immune response to gluten and the loss of gluten tolerance, ultimately affecting the pathogenesis, progression, and clinical expression of CeD; (3) gluten-free diet fails to restore the eubiosis of the digestive tract in CeD patients, and also negatively affects microbial homeostasis; (4) new tools allowing targeted microbiota therapy, such as the use of probiotics (a good example being precision probiotics like the novel strain of (20220303-A2) begin to show exciting potential applications.

摘要

乳糜泻(CeD)是一种自身免疫性疾病,与人类白细胞抗原(HLA)密切相关,其特征是产生特定的自身抗体和免疫介导的肠细胞杀伤。CeD 是一种独特的自身免疫性疾病,因为它是唯一已知环境触发因素的疾病:麸质,一种存在于小麦、大麦和黑麦中的储存蛋白。肠道黏膜对麸质的耐受性丧失是如何以及何时发生的仍不清楚。这一事件通过适应性免疫反应的激活,增强了上皮细胞的死亡,增加了上皮屏障的通透性,并诱导促炎细胞因子的分泌,导致从遗传易感性向实际发病的转变。虽然胃肠道感染作为可能的触发因素的作用是基于抗原模拟的可能机制,但更可能的替代机制似乎涉及由感染引发的胃肠道微生物群落生态系统的复杂破坏,而不是单一病原体对肠道黏膜稳态的具体影响。有几条证据表明,在遗传易患 CeD 的受试者中,存在肠道菌群失调,这先于 CeD 的发生,并伴有肠道菌群失调,其特征是保护性细菌元素的丧失,这些细菌元素在表观遗传和功能上都可以影响肠道上皮的反应,导致对麸质的耐受性丧失。我们进行了文献综述,以总结目前关于 CeD 发生前和发生时复杂且部分尚未阐明的菌群失调的知识,并介绍一些关于如何预防和/或对抗这种菌群失调的令人兴奋的新数据。文献检索在 PubMed.gov 上进行,时间范围为 2010 年至 2024 年 3 月,使用的术语为“乳糜泻和微生物组”、“乳糜泻和微生物群”和“乳糜泻和益生菌”,并将搜索限制为以下文章类型:临床试验、荟萃分析、综述和系统综述。共确定并审查了 364 篇论文。本综述的主要结论可以概括如下:(1)CeD 患者肠道微生物群的数量和质量发生了明显变化;(2)肠道微生物群与肠细胞、病毒和细菌病原体甚至麸质的广泛和多样的相互作用,共同影响对麸质的炎症免疫反应和对麸质的耐受性丧失,最终影响 CeD 的发病机制、进展和临床表现;(3)无麸质饮食未能恢复 CeD 患者消化道的生态平衡,也对微生物群的稳态产生负面影响;(4)新的工具允许靶向微生物群治疗,例如使用益生菌(一个很好的例子是像新型菌株 20220303-A2 这样的精准益生菌)开始显示出令人兴奋的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/537d/11206804/2c726610b02b/nutrients-16-01882-g001.jpg

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