Jurewicz A, Biddison W E, Antel J P
Department of Neurology and Neurosurgery, McGill University, Montréal Neurological Institute, Québec, Canada.
J Immunol. 1998 Mar 15;160(6):3056-9.
Multiple sclerosis (MS) is considered to be an autoimmune disease that is directed either at myelin or at its cell of origin, the oligodendrocytes (OL). The inflammatory lesions in the central nervous system contain multiple myelin Ag-restricted and nonrestricted cell populations with the potential to mediate tissue injury. Previous studies indicate that it is possible to generate MHC class I-restricted myelin peptide-specific cytotoxic CD8 T cells, and that human adult OLs express MHC class I molecules in vitro. The purpose of this study was to demonstrate that myelin basic protein peptide-specific CD8 T cells could induce OL injury. We generated CD8 T cell lines from six healthy donors and five MS patients, and all cell lines were HLA-A2 positive. The obtained CD8 cell lines induced lysis of HLA-A2- but not HLA-A3-transfected HMy2.C1R cells in the presence of myelin basic protein peptide 110-118. In the absence of exogenous peptide, the CD8 T cell lines were cytotoxic to HLA-A2 but not to non-HLA-A2 OLs. Cytotoxicity was blocked with anti-MHC class I-blocking Ab. These results support the postulate that autoreactive CD8 cytotoxic T cells can contribute to the tissue injury in MS.
多发性硬化症(MS)被认为是一种自身免疫性疾病,其针对的要么是髓磷脂,要么是其起源细胞,即少突胶质细胞(OL)。中枢神经系统中的炎性病变包含多个髓磷脂抗原限制性和非限制性细胞群体,它们有可能介导组织损伤。先前的研究表明,有可能产生MHC I类限制性髓磷脂肽特异性细胞毒性CD8 T细胞,并且人类成年OLs在体外表达MHC I类分子。本研究的目的是证明髓磷脂碱性蛋白肽特异性CD8 T细胞可诱导OL损伤。我们从六名健康供体和五名MS患者中产生了CD8 T细胞系,所有细胞系均为HLA-A2阳性。在存在髓磷脂碱性蛋白肽110-118的情况下,获得的CD8细胞系可诱导HLA-A2转染而非HLA-A3转染的HMy2.C1R细胞裂解。在没有外源性肽的情况下,CD8 T细胞系对HLA-A2细胞具有细胞毒性,但对非HLA-A2的OLs没有细胞毒性。细胞毒性被抗MHC I类阻断抗体阻断。这些结果支持自身反应性CD8细胞毒性T细胞可导致MS组织损伤这一假设。