Achiron Anat, Gurevich Michael, Friedman Nir, Kaminski Naftali, Mandel Mathilda
Multiple Sclerosis Center, Sheba Medical Center, Tel-Hashomer 52621, Israel.
Ann Neurol. 2004 Mar;55(3):410-7. doi: 10.1002/ana.20008.
Multiple sclerosis (MS) is a central nervous system disease with an unpredictable course and outcome. Peripheral blood mononuclear cells (PBMCs) are involved in the disease pathogenesis and induce active demyelination. Using oligonucleotide microarrays, we identified a statistically significant transcriptional signature of 1,109 genes in PBMCs from 26 MS patients, irrespective of disease activation state or immunomodulatory treatment. This signature contains genes that implicate underlying processes involved in MS pathogenesis including T-cell activation and expansion, inflammation, and apoptosis. Another transcriptional signature of 721 genes involved in cellular recruitment, epitope spreading, and escape from regulatory immune surveillance identified MS patients in acute relapse compared with remission. Our results offer new opportunity for understanding the mechanisms involved in MS and indicate that gene expression patterns in PBMCs contain information about a remote-target disease process that may be useful for diagnosis and future tailoring of therapeutic strategies for MS.
多发性硬化症(MS)是一种中枢神经系统疾病,其病程和预后不可预测。外周血单个核细胞(PBMCs)参与该疾病的发病机制并诱导活动性脱髓鞘。使用寡核苷酸微阵列,我们在26例MS患者的PBMCs中鉴定出1109个基因具有统计学意义的转录特征,而不考虑疾病激活状态或免疫调节治疗。该特征包含涉及MS发病机制的潜在过程的基因,包括T细胞激活和扩增、炎症和细胞凋亡。另一个由721个基因组成的转录特征涉及细胞募集、表位扩展和逃避调节性免疫监视,该特征可将急性复发期的MS患者与缓解期患者区分开来。我们的结果为理解MS的发病机制提供了新的契机,并表明PBMCs中的基因表达模式包含有关远程目标疾病过程的信息,这可能有助于MS的诊断和未来治疗策略的定制。