Epigenetic mechanisms driving the pathogenesis of systemic lupus erythematosus, systemic sclerosis and dermatomyositis

被引:3
|
作者
Zhang, Yusheng [1 ]
Bermudez, Narges Maskan [1 ]
Sa, Brianna [1 ]
Maderal, Andrea D. [1 ]
Jimenez, Joaquin J. [1 ]
机构
[1] Univ Miami, Miller Sch Med, Dr Phillip Frost Dept Dermatol & Cutaneous Surg, Miami, FL 33124 USA
关键词
autoimmunity; connective tissue disorders; dermatomyositis; epigenetics; lupus; scleroderma; systemic lupus erythematosus; systemic sclerosis; WIDE DNA METHYLATION; CD4(+) T-CELLS; GENE-EXPRESSION; OXIDATIVE STRESS; AUTOIMMUNITY; ACTIVATION; HYPOMETHYLATION; FIBROBLASTS; CHROMATIN; DISEASE;
D O I
10.1111/exd.14986
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Autoimmune connective tissue disorders, including systemic lupus erythematosus, systemic sclerosis (SSc) and dermatomyositis (DM), often manifest with debilitating cutaneous lesions and can result in systemic organ damage that may be life-threatening. Despite recent therapeutic advancements, many patients still experience low rates of sustained remission and significant treatment toxicity. While genetic predisposition plays a role in these connective tissue disorders, the relatively low concordance rates among monozygotic twins (ranging from approximately 4% for SSc to about 11%-50% for SLE) have prompted increased scrutiny of the epigenetic factors contributing to these diseases. In this review, we explore some seminal studies and key findings to provide a comprehensive understanding of how dysregulated epigenetic mechanisms can contribute to the development of SLE, SSc and DM.
引用
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页数:14
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