Gomes Andreia C, Jönsson Gun, Mjörnheim Susanna, Olsson Tomas, Hillert Jan, Grandien Alf
Department of Neurology, Neurotec Department, Karolinska Institute at Huddinge University Hospital, R54, SE-141 86, Stockholm, Sweden.
J Neuroimmunol. 2003 Feb;135(1-2):126-34. doi: 10.1016/s0165-5728(02)00437-x.
Multiple sclerosis (MS) is a chronic disease involving an inflammatory reaction within the white matter of the CNS, mediated by T cells, B cells and macrophages. The pathogenesis of MS may involve impaired activation-induced cell death of activated myelin-specific mature T cells. We investigated the mRNA expression of the apoptosis mediators cellular FLICE-inhibitory protein (cFLIP), caspase-8, CD95 and CD95L in peripheral blood mononuclear cells (PB MNCs) from MS patients using real-time PCR. The overall increased expression of the four key players in the CD95 pathway in relapsing-remitting MS suggests their involvement in the inflammatory process in this disease.
多发性硬化症(MS)是一种慢性疾病,涉及中枢神经系统白质内由T细胞、B细胞和巨噬细胞介导的炎症反应。MS的发病机制可能涉及活化的髓鞘特异性成熟T细胞的活化诱导细胞死亡受损。我们使用实时PCR研究了MS患者外周血单核细胞(PB MNCs)中凋亡介质细胞FLICE抑制蛋白(cFLIP)、半胱天冬酶-8、CD95和CD95L的mRNA表达。复发缓解型MS中CD95途径四个关键因子的总体表达增加,表明它们参与了该疾病的炎症过程。