van Noort J M, van Sechel A C, Bajramovic J J, el Ouagmiri M, Polman C H, Lassmann H, Ravid R
Division of Immunological and Infectious Diseases, TNO Prevention and Health, Leiden, The Netherlands.
Nature. 1995 Jun 29;375(6534):798-801. doi: 10.1038/375798a0.
The identification of key antigens in human autoimmune diseases is a crucial step towards the development of specific intervention. The autoantigen(s) relevant to multiple sclerosis (MS) probably reside in myelin of the central nervous system, the target of the disease. Here we examine proliferative responses of human peripheral blood T cells to the complete collection of myelin proteins fractionated by reversed-phase high-performance liquid chromatography. Myelin isolated from MS-affected brain contained a single protein fraction to which T cells from MS patients and from healthy controls showed dominant responses. This highly immunogenic protein was identified as alpha B-crystallin, a small heat-shock protein. Immunohistochemical examination of MS lesions revealed the presence of oligodendrocytes and astrocytes with raised alpha B-crystallin expression, which were not found in unaffected myelin. Our findings indicate that alpha B-crystallin serves as immunodominant myelin antigen to human T cells when expressed at the elevated levels found in active MS lesions.
确定人类自身免疫性疾病中的关键抗原是开发特异性干预措施的关键一步。与多发性硬化症(MS)相关的自身抗原可能存在于中枢神经系统的髓磷脂中,而髓磷脂正是该疾病的靶标。在此,我们检测了人类外周血T细胞对通过反相高效液相色谱法分离的完整髓磷脂蛋白集合的增殖反应。从受MS影响的大脑中分离出的髓磷脂含有单一蛋白质组分,MS患者和健康对照者的T细胞对该组分均表现出主要反应。这种高度免疫原性的蛋白质被鉴定为αB-晶状体蛋白,一种小分子热休克蛋白。对MS病变的免疫组织化学检查显示,少突胶质细胞和星形胶质细胞中αB-晶状体蛋白表达升高,而在未受影响的髓磷脂中未发现这种情况。我们的研究结果表明,当αB-晶状体蛋白在活动性MS病变中以升高的水平表达时,它作为人类T细胞的免疫显性髓磷脂抗原发挥作用。