Department of Internal Medicine, Division of Rheumatology, University of Michigan, SRB 3007, 109 Zina Pitcher Pl., Ann Arbor, MI 48109-2200, United States.
Clin Immunol. 2018 Jul;192:1-5. doi: 10.1016/j.clim.2018.04.005. Epub 2018 Apr 9.
Systemic lupus erythematosus flares when genetically predisposed people encounter environmental agents that cause oxidative stress, such as infections and sunlight. How these modify the immune system to initiate flares is unclear. Drug induced lupus models demonstrate that CD4+ T cells epigenetically altered with DNA methylation inhibitors cause lupus in animal models, and similar T cells are found in patients with active lupus. How infections and sun exposure inhibit T cell DNA methylation is unclear. DNA methylation patterns are replicated each time a cell divides in a process that requires DNA methyltransferase one (Dnmt1), which is upregulated as cells enter mitosis, as well as the methyl donor S-adenosylmethionine, created from dietary sources. Reactive oxygen species that inhibit Dnmt1 upregulation, and a diet poor in methyl donors, combine to cause lupus in animal models. Similar changes are found in patients with active lupus, indicating a mechanism contributing to lupus flares.
系统性红斑狼疮在易患人群接触到感染和阳光等导致氧化应激的环境因素时会发作。目前尚不清楚这些因素如何改变免疫系统引发发作。药物诱导的狼疮模型表明,用 DNA 甲基化抑制剂修饰的 CD4+T 细胞会在动物模型中引起狼疮,而在活动性狼疮患者中也发现了类似的 T 细胞。感染和阳光暴露如何抑制 T 细胞的 DNA 甲基化尚不清楚。在细胞分裂过程中,DNA 甲基转移酶 1(Dnmt1)会复制 DNA 甲基化模式,Dnmt1 在细胞进入有丝分裂时上调,甲基供体 S-腺苷甲硫氨酸(来源于饮食)也会被上调。抑制 Dnmt1 上调的活性氧和饮食中缺乏甲基供体结合在一起,会在动物模型中引起狼疮。在活动性狼疮患者中也发现了类似的变化,这表明这是一种导致狼疮发作的机制。