Hirayama M, Kawai K, Iida M
Second Department of Internal Medicine, Fukui Medical School.
Rinsho Shinkeigaku. 1990 Mar;30(3):262-5.
We studied anti-oligodendrocyte antibody in sera and CSF from patients with multiple sclerosis (MS) and other neurological diseases (OND) by enzyme-linked immunosorbent assay (ELISA). Oligodendrocytes were isolated by percoll density gradient from brains of 4 week-old rat and cultured in poly-1-lysine-coated 96 well microwell plate. After overnight culture, oligodendrocytes were fixed in 0.5% glutaraldehyde and stored at -20 degrees C. ELISA was performed using peroxidase-conjugated goat anti-human IgG (Fab')2 as usual. Serum and CSF were examined at dilution of 1:400 and 1:2 respectively, and O.D. was read at 490 nM. In sera from patients with MS and OND, the titer of anti-oligodendrocyte antibody was significantly higher than those from normal controls. However, there was no significant difference between MS and OND. Significantly higher titer of anti-oligodendrocyte antibody was observed in CSF from patients with meningoencephalitis and polyradiculoneuropathy. However, comparing CSF anti-oligodendrocyte antibody per CSF IgG, there was no significant difference among each group. There was no significant correlation between the cytotoxicity index of sera and anti-oligodendrocyte antibody level. There might be additional cytotoxic factor other than anti-oligodendrocyte antibody. Our data support the idea anti-oligodendrocyte antibody is not specific to MS, and the role of anti-oligodendrocyte antibody in the pathogenesis of MS is secondary.
我们通过酶联免疫吸附测定(ELISA)研究了多发性硬化症(MS)患者以及其他神经系统疾病(OND)患者血清和脑脊液中的抗少突胶质细胞抗体。从4周龄大鼠的大脑中通过Percoll密度梯度分离少突胶质细胞,并在包被有聚-L-赖氨酸的96孔微孔板中培养。过夜培养后,将少突胶质细胞固定于0.5%戊二醛中,并储存在-20℃。像往常一样使用过氧化物酶偶联的山羊抗人IgG(Fab')2进行ELISA。血清和脑脊液分别以1:400和1:2的稀释度进行检测,在490 nM处读取光密度(O.D.)。在MS患者和OND患者的血清中,抗少突胶质细胞抗体的滴度显著高于正常对照者。然而,MS患者和OND患者之间没有显著差异。在脑膜脑炎和多神经根神经病患者的脑脊液中观察到抗少突胶质细胞抗体滴度显著更高。然而,比较每份脑脊液IgG中的脑脊液抗少突胶质细胞抗体,各组之间没有显著差异。血清的细胞毒性指数与抗少突胶质细胞抗体水平之间没有显著相关性。除抗少突胶质细胞抗体外,可能还存在其他细胞毒性因子。我们的数据支持抗少突胶质细胞抗体并非MS所特有的观点,并且抗少突胶质细胞抗体在MS发病机制中的作用是次要的。