Rohowsky-Kochan C, Troiano R, Cook S D
University of Medicine and Dentistry of New Jersey, New Jersey Medical School, Newark 07103.
J Immunogenet. 1989 Dec;16(6):437-44. doi: 10.1111/j.1744-313x.1989.tb00492.x.
Multiple sclerosis is a demyelinating disease of the central nervous system with genetic, viral and autoimmune characteristics. Myelin basic protein (MBP) is a suspected target autoantigen since it induces experimental autoimmune encephalomyelitis, an animal model closely resembling multiple sclerosis. The disease is mediated by Class II restricted, MBP-reactive T cells possessing the T helper/inducer phenotype. In the present study, we have isolated MBP-reactive T cell clones from the peripheral blood of a chronic progressive multiple sclerosis patient. The clones displayed blastogenic memory responses when rechallenged with the autoantigen and irradiated autologous lymphocytes. MBP recognition by the autoantigen-reactive T lymphocytes was restricted by major histocompatibility complex Class II antigens. Both CD4+8- and CD4-8+ MBP-reactive T cell clones were obtained.
多发性硬化症是一种具有遗传、病毒和自身免疫特征的中枢神经系统脱髓鞘疾病。髓鞘碱性蛋白(MBP)是一种可疑的靶自身抗原,因为它可诱发实验性自身免疫性脑脊髓炎,这是一种与多发性硬化症极为相似的动物模型。该疾病由具有辅助性T/诱导性T细胞表型的Ⅱ类限制性、MBP反应性T细胞介导。在本研究中,我们从一名慢性进行性多发性硬化症患者的外周血中分离出了MBP反应性T细胞克隆。当用自身抗原和经照射的自体淋巴细胞再次刺激时,这些克隆表现出母细胞化的记忆反应。自身抗原反应性T淋巴细胞对MBP的识别受主要组织相容性复合体Ⅱ类抗原的限制。我们获得了CD4+8-和CD4-8+两种MBP反应性T细胞克隆。