Stendahl L, Link H, Möller E, Norrby E
J Neurol Sci. 1976 Jan;27(1):93-8. doi: 10.1016/0022-510x(76)90237-9.
Thirty patients with acute, unilateral optic neuritis (ON), where re-examination after a mean observation period of 5 years did not reveal any aetiology, were investigated with regard to laboratory abnormalities frequently observed in multiple sclerosis. Eleven patients had oligoclonal IgG in CSF. In 5 of these a measles virus antibody response within the CNS was demonstrable. The remaining 19 patients did not display oligoclonal CSF IgG, nor an antibody response. The major histocompatibility antigens HL-A3 and HL-A7 occurred at similar frequencies in ON and in controls, irrespective of the presence of oligoclonal CSF IgG. The HL-A7 associated MLC determinant LD-7a occurred in ON at a frequency between that observed in controls and in MS. However, an association of the same magnitude as observed in MS was found between ON with oligoclonal CSF IgG and the presence of LD-7a. This association was absent in those ON patients who lacked oligoclonal CSF IgG. The present data indicate that the finding of oligoclonal CSF IgG may increase the risk of developing MS.
对30例急性单侧视神经炎(ON)患者进行了研究,这些患者在平均5年的观察期后复查未发现任何病因,研究内容为多发性硬化中常见的实验室异常情况。11例患者脑脊液中有寡克隆IgG。其中5例在中枢神经系统内可显示麻疹病毒抗体反应。其余19例患者未显示脑脊液寡克隆IgG,也未显示抗体反应。主要组织相容性抗原HL-A3和HL-A7在视神经炎患者和对照组中的出现频率相似,与脑脊液中是否存在寡克隆IgG无关。与HL-A7相关的混合淋巴细胞培养决定簇LD-7a在视神经炎患者中的出现频率介于对照组和多发性硬化患者之间。然而,在伴有脑脊液寡克隆IgG的视神经炎患者与LD-7a的存在之间发现了与多发性硬化中观察到的相同程度的关联。在缺乏脑脊液寡克隆IgG的视神经炎患者中不存在这种关联。目前的数据表明,脑脊液中发现寡克隆IgG可能会增加患多发性硬化的风险。