Department of Women's and Children's Health, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
Department of Paediatric Rheumatology, Alder Hey Children's NHS Foundation Trust Hospital, Liverpool, United Kingdom.
Front Immunol. 2019 Jul 4;10:1525. doi: 10.3389/fimmu.2019.01525. eCollection 2019.
Historically, systemic self-inflammatory conditions were classified as either autoinflammatory and caused by the innate immune system or autoimmune and driven by adaptive immune responses. However, it became clear that reality is much more complex and that autoimmune/inflammatory conditions range along an "inflammatory spectrum" with primarily autoinflammatory vs. autoimmune conditions resembling extremes at either end. Epigenetic modifications influence gene expression and alter cellular functions without modifying the genomic sequence. Methylation of CpG DNA dinucleotides and/or their hydroxymethylation, post-translational modifications to amino termini of histone proteins, and non-coding RNA expression are main epigenetic events. The pathophysiology of autoimmune/inflammatory diseases has been closely linked with disease causing gene mutations (rare) or a combination of genetic susceptibility and epigenetic modifications arising from exposure to the environment (more common). Over recent years, progress has been made in understanding molecular mechanisms involved in systemic inflammation and the contribution of innate and adaptive immune responses. Epigenetic events have been identified as (i) central pathophysiological factors in addition to genetic disease predisposition and (ii) as co-factors determining clinical pictures and outcomes in individuals with monogenic disease. Thus, a complete understanding of epigenetic contributors to autoimmune/inflammatory disease will result in approaches to predict individual disease outcomes and the introduction of effective, target-directed, and tolerable therapies. Here, we summarize recent findings that signify the importance of epigenetic modifications in autoimmune/inflammatory disorders along the inflammatory spectrum choosing three examples: the autoinflammatory bone condition chronic nonbacterial osteomyelitis (CNO), the "mixed pattern" disorder psoriasis, and the autoimmune disease systemic lupus erythematosus (SLE).
从历史上看,系统性自炎症性疾病被分为自身炎症性疾病和由先天免疫系统引起的疾病,或自身免疫性疾病和由适应性免疫反应驱动的疾病。然而,事实证明,情况要复杂得多,自身免疫/炎症性疾病沿着“炎症谱”分布,主要的自身炎症性疾病与自身免疫性疾病的情况相似,处于极端的两端。表观遗传修饰影响基因表达并改变细胞功能,而不会改变基因组序列。CpG DNA 二核苷酸的甲基化和/或它们的羟甲基化、组蛋白氨基末端的翻译后修饰以及非编码 RNA 的表达是主要的表观遗传事件。自身免疫/炎症性疾病的病理生理学与致病基因突变(罕见)或遗传易感性与暴露于环境引起的表观遗传修饰(更为常见)密切相关。近年来,人们在理解系统性炎症中涉及的分子机制以及先天和适应性免疫反应的贡献方面取得了进展。表观遗传事件已被确定为(i)除遗传疾病易感性之外的主要病理生理因素,以及(ii)作为决定个体具有单基因疾病的临床特征和结局的共同因素。因此,对自身免疫/炎症性疾病的表观遗传贡献有一个全面的了解,将导致能够预测个体疾病结局并引入有效、靶向和耐受的治疗方法。在这里,我们总结了最近的发现,这些发现表明了在炎症谱上的自身免疫/炎症性疾病中表观遗传修饰的重要性,选择了三个例子:自身炎症性骨病慢性非细菌性骨髓炎(CNO)、“混合模式”疾病银屑病和自身免疫性疾病系统性红斑狼疮(SLE)。