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High-dimensional single-cell analysis reveals the immune signature of narcolepsy

机译:高维单细胞分析揭示了发作性睡病的免疫特征

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摘要

Narcolepsy type 1 is a devastating neurological sleep disorder resulting from the destruction of orexin-producing neurons in the central nervous system (CNS). Despite its striking association with the HLA-DQB1*06:02 allele, the autoimmune etiology of narcolepsy has remained largely hypothetical. Here, we compared peripheral mononucleated cells from narcolepsy patients with HLA-DQB1*06:02-matched healthy controls using high-dimensional mass cytometry in combination with algorithm-guided data analysis. Narcolepsy patients displayed multifaceted immune activation in CD4(+) and CD8(+) T cells dominated by elevated levels of B cell-supporting cytokines. Additionally, T cells from narcolepsy patients showed increased production of the proinflammatory cytokines IL-2 and TNF. Although it remains to be established whether these changes are primary to an autoimmune process in narcolepsy or secondary to orexin deficiency, these findings are indicative of inflammatory processes in the pathogenesis of this enigmatic disease.
机译:发作性睡病1型是毁灭性的神经系统睡眠障碍,由破坏中枢神经系统(CNS)中产生食欲素的神经元引起。尽管发作性睡病的自身免疫病因学与HLA-DQB1 * 06:02等位基因有着惊人的联系,但在很大程度上仍是假说。在这里,我们比较了嗜睡症患者与HLA-DQB1 * 06:02匹配的健康对照者的外周单核细胞,使用高维质量细胞仪结合算法指导的数据分析。发作性睡病患者在以B细胞支持细胞因子水平升高为主的CD4(+)和CD8(+)T细胞中表现出多方面的免疫激活。另外,来自发作性睡病患者的T细胞显示促炎细胞因子IL-2和TNF的产生增加。尽管这些改变是发作性睡病中自身免疫过程的主要原因还是食欲素缺乏症的原因尚待确定,但这些发现表明该神秘疾病发病机理中存在炎症过程。

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