Rheumatology:组氨酸是系统性红斑狼疮发病机制中的生物标志物

2022-06-17 紫菀款冬 MedSci原创

研究系统性红斑狼疮(SLE)患者血浆中代谢物的变化,以识别新的生物标志物,为SLE发病机制提供线索。

目的:研究系统性红斑狼疮(SLE)患者血浆中代谢物的变化,以识别新的生物标志物,为SLE发病机制提供线索。

方法:招募SLE患者(n = 41,发现队列和 n = 37,复制队列),健康对照组(HCs,n = 30 和 n = 29),类风湿关节炎患者(n = 19,疾病对照)。采用液相色谱-飞行时间质谱(LC-TOFMS)和毛细管电泳-飞行时间质谱(CE-TOFMS)分析血浆样品的代谢谱。使用RNA-Seq分析18个免疫细胞亚群的转录组数据。用小鼠脾B细胞研究组氨酸(His)在浆母细胞分化中的重要性。

结果:包括His在内的特定氨基酸组合可以有效区分SLE患者和HCs。随机森林和偏最小二乘鉴别分析(PLS-DA)确定His是SLE患者的有效分类器。His血浆水平的降低与损伤累积相关,与泼尼松龙剂量和I型干扰素(IFN)特征无关。浆母细胞中的氧化磷酸化(OXPHOS)特征与His水平呈负相关。此外,固有免疫信号诱导的浆母细胞分化依赖于His。

结论:血浆His水平是SLE患者潜在的生物标志物,且与损伤累积有关。该研究数据表明His作为一种致病性代谢物SLE发病机制中的重要性。

 

出处:Iwasaki Y, Takeshima Y, Nakano M, et al. Combined plasma metabolomic and transcriptomic analysis identify histidine as a biomarker and potential contributor in SLE pathogenesis [published online ahead of print, 2022 Jun 11]. Rheumatology (Oxford). 2022;keac338. doi:10.1093/rheumatology/keac338

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    2022-06-17 zhouqu_8
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六种免疫细胞中的细胞水平全转录组关联研究补充了系统性红斑狼疮(SLE)基因的发现并指导了新遗传关联的识别。这些基因发现提供了对SLE遗传关联的生物学见解。 

A&R:纵向队列中与SLE亚型相关的CpG位点甲基化动态变化

在这个SLE纵向队列中确定了SLE亚型相关CpG的一个子集,它们随着时间的推移是稳定的,并且可能可用作疾病亚型的生物标志物。与全基因组甲基化组相比,另一个与SLE亚型相关的CpG子集的变化比例更高。

躲避这5大危险因素,将“复发”扼杀在摇篮!

那么哪些因素与SLE复发因素有关呢?

A&R:系统性红斑狼疮的共享和亚洲特异性基因座的鉴定以及III型干扰素信号传导和溶酶体功能在该疾病中作用的证据:一项多祖先全基因组关联研究

在这项研究中,确定了系统性红斑狼疮(SLE)的共享位点和亚洲特异性位点,功能注释提供了增加III型干扰素信号传导和降低SLE溶酶体功能参与的证据。