Gut microbiome and metabolomics in systemic sclerosis: feature, link and mechanisms.

IF 5.7 2区 医学 Q1 IMMUNOLOGY Frontiers in Immunology Pub Date : 2024-11-04 eCollection Date: 2024-01-01 DOI:10.3389/fimmu.2024.1475528
Qicen Yao, Wenfeng Tan, Feihu Bai
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Abstract

Systemic sclerosis (SSc) is a rare and highly heterogeneous chronic autoimmune disease characterized by multi-organ and tissue fibrosis, often accompanied by a poor prognosis and high mortality rates. The primary pathogenic mechanisms of SSc are considered to involve tissue fibrosis, autoimmune dysfunction, and microvascular abnormalities. Recent studies have shed light on the gut microbiota (GM) and metabolites in SSc patients, revealing their association with gastrointestinal symptoms and disease phenotypes. However, further elucidation is needed on the specific mechanisms underlying the interactions between GM, metabolites, and the immune system and their roles in the pathogenesis of SSc. This review outlines the characteristics of GM and metabolites in SSc patients, exploring their interrelationships and analyzing their correlations with the clinical phenotypes of SSc. The findings indicate that while the α-diversity of GM in SSc patients resembles that of healthy individuals, notable differences exist in the β-diversity and the abundance of specific bacterial genera, which are closely linked to gastrointestinal symptoms. Moreover, alterations in the levels of amino acids and lipid metabolites in SSc patients are prominently observed and significantly associated with clinical phenotypes. Furthermore, this review delves into the potential immunopathological mechanisms of GM and metabolites in SSc, emphasizing the critical role of interactions between GM, metabolites, and the immune system in comprehending the immunopathological processes of SSc. These insights may offer new scientific evidence for the development of future treatment strategies.

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系统性硬化症中的肠道微生物组和代谢组学:特征、联系和机制。
系统性硬化症(SSc)是一种罕见、高度异质性的慢性自身免疫性疾病,以多器官和组织纤维化为特征,通常预后不良,死亡率高。SSc 的主要致病机制被认为涉及组织纤维化、自身免疫功能障碍和微血管异常。最近的研究揭示了 SSc 患者的肠道微生物群(GM)和代谢物,揭示了它们与胃肠道症状和疾病表型的关系。然而,还需要进一步阐明肠道微生物群、代谢物和免疫系统之间相互作用的具体机制及其在 SSc 发病机制中的作用。本综述概述了 SSc 患者体内 GM 和代谢物的特征,探讨了它们之间的相互关系,并分析了它们与 SSc 临床表型的相关性。研究结果表明,虽然 SSc 患者体内 GM 的 α 多样性与健康人相似,但特定细菌属的β多样性和丰度存在明显差异,而这与胃肠道症状密切相关。此外,SSc 患者体内氨基酸和脂质代谢物水平的变化也很明显,并与临床表型密切相关。此外,本综述还深入探讨了转基因和代谢物在 SSc 中的潜在免疫病理机制,强调了转基因、代谢物和免疫系统之间的相互作用在理解 SSc 免疫病理过程中的关键作用。这些见解可为未来治疗策略的开发提供新的科学依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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