表观遗传学
免疫系统
免疫学
自身免疫
生物
原发性硬化性胆管炎
自身免疫性肝炎
背景(考古学)
自身免疫性疾病
细胞代谢
免疫失调
疾病
医学
肝炎
抗体
遗传学
基因
细胞
病理
古生物学
作者
Ya‐Fei Xu,Zhibin Zhao,Ethan P. Yan,Zhe‐Xiong Lian,Weici Zhang
出处
期刊:
[Wiley]
日期:2023-06-01
卷期号:1 (2): 97-114
被引量:18
摘要
Abstract Autoimmune liver diseases (ALDs) are chronic inflammatory hepatobiliary diseases in which the autoimmune responses directed against liver tissue result in inflammation and tissue damage. There are several types of ALDs, including autoimmune hepatitis, primary biliary cholangitis, primary sclerosing cholangitis, immunoglobulin G4‐related sclerosing cholangitis, and overlap syndromes. Metabolism and epigenetics are both critical components of the development and progression of ALDs. Immunometabolism addresses how metabolic processes influence immune cell development, fate and behavior, and how immune responses impact metabolism. In the context of immunity, epigenetics involves regulating gene expression without altering the DNA sequence. Epigenetic modifications can ultimately result in changes in the immunophenotype. The interplay between the immune system, metabolism, and epigenetic factors is highly complex. A better understanding of this interplay and the regulatory mechanisms involved is crucial to uncover the disease pathogenesis of ALDs and exploring novel therapeutic options. This article provides a comprehensive review of the dysregulation of immunometabolism and epigenetics, as well as the multilevel regulatory mechanisms, underlying the autoimmunity in ALDs.
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