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暴露组学:表观遗传学与自身免疫性疾病

Exposome: Epigenetics and autoimmune diseases.

作者信息

Danieli Maria Giovanna, Casciaro Marco, Paladini Alberto, Bartolucci Martina, Sordoni Martina, Shoenfeld Yehuda, Gangemi Sebastiano

机构信息

SOS Immunologia delle Malattie Rare e dei Trapianti, AOU delle Marche & Dipartimento di Scienze Cliniche e Molecolari, Università Politecnica delle Marche, via Tronto 10/A, 60126 Torrette di Ancona, Italy; Postgraduate School of Allergy and Clinical Immunology, Università Politecnica delle Marche, via Tronto 10/A, 60126 Ancona, Italy.

Operative Unit of Allergy and Clinical Immunology, Department of Clinical and Experimental Medicine, University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.

出版信息

Autoimmun Rev. 2024 Jun;23(6):103584. doi: 10.1016/j.autrev.2024.103584. Epub 2024 Aug 2.

Abstract

Systemic autoimmune diseases are complex conditions characterized by an immune system dysregulation and an aberrant activation against self-antigens, leading to tissue and organ damage. Even though genetic predisposition plays a role, it cannot fully explain the onset of these diseases, highlighting the significant impact of non-heritable influences such as environment, hormones and infections. The exposome represents all those factors, ranging from chemical pollutants and dietary components to psychological stressors and infectious agents. Epigenetics, which studies changes in gene expression without altering the DNA sequence, is a crucial link between exposome and the development of autoimmune diseases. Key epigenetic mechanisms include DNA methylation, histone modifications, and non-coding RNAs. These epigenetic modifications could provide a potential piece of the puzzle in understanding systemic autoimmune diseases and their connection with the exposome. In this work we have collected the most important and recent evidence in epigenetic changes linked to systemic autoimmune diseases (systemic lupus erythematosus, idiopathic inflammatory myopathies, ANCA-associated vasculitis, and rheumatoid arthritis), emphasizing the roles these changes may play in disease pathogenesis, their potential as diagnostic biomarkers and their prospective in the development of targeted therapies.

摘要

系统性自身免疫性疾病是复杂的病症,其特征在于免疫系统失调以及针对自身抗原的异常激活,从而导致组织和器官损伤。尽管遗传易感性起一定作用,但它无法完全解释这些疾病的发病机制,这凸显了环境、激素和感染等非遗传因素的重大影响。暴露组代表了所有这些因素,从化学污染物和饮食成分到心理压力源和传染因子。表观遗传学研究在不改变DNA序列的情况下基因表达的变化,是暴露组与自身免疫性疾病发展之间的关键联系。关键的表观遗传机制包括DNA甲基化、组蛋白修饰和非编码RNA。这些表观遗传修饰可能为理解系统性自身免疫性疾病及其与暴露组的联系提供潜在线索。在这项工作中,我们收集了与系统性自身免疫性疾病(系统性红斑狼疮、特发性炎症性肌病、抗中性粒细胞胞浆抗体相关性血管炎和类风湿性关节炎)相关的表观遗传变化的最重要和最新证据,强调了这些变化在疾病发病机制中可能发挥的作用、它们作为诊断生物标志物的潜力以及在靶向治疗开发方面的前景。

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