Department of Neurology, University of Texas Health Science Center, Houston, TX, USA.
Mol Med. 2011 Jan-Feb;17(1-2):95-102. doi: 10.2119/molmed.2010.00071. Epub 2010 Sep 17.
A defining feature of multiple sclerosis (MS) is the occurrence of clinical relapses separated by periods of clinical stability. Better understanding of the events underlying clinical relapse might suggest new approaches to treatment. The objective of this study was to measure changes in the expression of RNA in the blood during relapse. We used microarrays to measure mRNA expression in paired samples from 14 MS patients during clinical relapse and while stable. Seventy-one transcripts changed expression at the P < 0.001 significance level. The most notable finding was decreased expression of transcripts with regulatory function, expressed primarily in non-T cells. These decreased transcripts included the interleukin-1 receptor antagonist, which had a corresponding decrease in the protein concentration in serum. Transcripts with increased expression were expressed primarily in T cells. Pathways analysis suggested involvement of the cytokine network, coagulation and complement cascades, IL-10 signaling and NF-κB signaling. We conclude that there are alterations of mRNA expression in both T cells and non-T cells during MS relapse.
多发性硬化症(MS)的一个特征是在临床稳定期之间发生临床复发。更好地了解临床复发的潜在事件可能会提示新的治疗方法。本研究的目的是测量在复发期间血液中 RNA 表达的变化。我们使用微阵列来测量 14 名 MS 患者在临床复发和稳定期间配对样本中的 mRNA 表达。71 个转录本在 P < 0.001 显著性水平上改变了表达。最显著的发现是具有调节功能的转录本表达降低,主要在非 T 细胞中表达。这些减少的转录本包括白细胞介素-1 受体拮抗剂,其在血清中的蛋白浓度相应降低。表达增加的转录本主要在 T 细胞中表达。途径分析表明细胞因子网络、凝血和补体级联、IL-10 信号和 NF-κB 信号的参与。我们得出结论,在 MS 复发期间,T 细胞和非 T 细胞中都存在 mRNA 表达的改变。