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The interaction between environmental triggers and epigenetics in autoimmunity

机译:自身免疫环境触发器与表观遗传学之间的相互作用

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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.
机译:Systemic Lupus红斑狼疮在遗传倾斜的人遇到导致氧化应激的环境代理,例如感染和阳光。这些如何修改免疫系统以启动耀斑尚不清楚。药物诱导的狼疮模型表明,随着DNA甲基化抑制剂的表现出近致表明的CD4 + T细胞导致动物模型中的狼疮,并且在活性狼疮患者中发现了类似的T细胞。如何感染和阳光暴露抑制T细胞DNA甲基化尚不清楚。每次在需要DNA甲基转移酶一(DNMT1)的过程中,每次将细胞分开(DNMT1)的过程中的方法复制DNA甲基化图案,这是由膳食来源产生的细胞,以及甲基供体S-腺苷甲基乙硫醚。抑制DNMT1上调的活性氧物质,甲基供体中的饮食差,组合在动物模型中引起狼疮。活性狼疮的患者中发现了类似的变化,表明对狼疮耀斑有助于的机制。

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