Usuku K, Nishizawa M, Osame M, Tabira T
Division of Demyelinating Disease and Aging, National Center of Neurology and Psychiatry, Tokyo, Japan.
J Neuroimmunol. 1991 Sep;33(3):199-205. doi: 10.1016/0165-5728(91)90107-i.
Since there are several immune abnormalities and autoimmune-like features in human T-cell lymphotropic virus type I (HTLV-I)-associated myelopathy/HTLV-I-associated tropical spastic paraparesis (HAM/TSP), we examined cytotoxic and suppressor cell functions in HAM/TSP. In this study, we assayed cell-mediated cytotoxicity of CD8+ T-cell lines established from cerebrospinal fluid lymphocytes of two patients with HAM and concanavalin A-induced suppressor cell activities of peripheral blood lymphocytes from five patients with HAM. Our study revealed that three of four CD8+ T-cell lines showed cytotoxic activities against autologous CD4+ T-cell lines infected with HTLV-I, and two of the three lines showed major histocompatibility complex class I-restricted cytotoxicity. We also demonstrated that the concanavalin A-induced suppressor function was not defective in HAM patients. Therefore, the immune abnormalities and autoimmune-like features observed in HAM/TSP may not result from defective cytotoxic or suppressor cell activities.
由于人类嗜T细胞病毒I型(HTLV-I)相关脊髓病/HTLV-I相关热带痉挛性截瘫(HAM/TSP)存在多种免疫异常和自身免疫样特征,我们研究了HAM/TSP患者的细胞毒性和抑制细胞功能。在本研究中,我们检测了从两名HAM患者的脑脊液淋巴细胞建立的CD8 + T细胞系的细胞介导细胞毒性,以及五名HAM患者外周血淋巴细胞的伴刀豆球蛋白A诱导的抑制细胞活性。我们的研究表明,四个CD8 + T细胞系中的三个对感染HTLV-I的自体CD4 + T细胞系表现出细胞毒性活性,并且三个细胞系中的两个表现出主要组织相容性复合体I类限制性细胞毒性。我们还证明,伴刀豆球蛋白A诱导的抑制功能在HAM患者中没有缺陷。因此,在HAM/TSP中观察到的免疫异常和自身免疫样特征可能不是由细胞毒性或抑制细胞活性缺陷引起的。