Strony L P, Wagner K, Keshgegian A A
Clin Chim Acta. 1982 Jul 1;122(2):203-12. doi: 10.1016/0009-8981(82)90279-0.
Demonstration of an oligoclonal immunoglobulin pattern in cerebrospinal fluid by a commercial agarose gel electrophoresis system and immunofixation were evaluated in the service clinical laboratory of a university hospital. In 303 patients, 45 with clinically definite multiple sclerosis and 209 with other neurologic diseases, the sensitivity of oligoclonal banding for multiple sclerosis was 71%, and the specificity, 83%. Oligoclonal banding was frequent in inflammatory disease, tumor/pseudotumor or vascular diseases of the central nervous system (35%, 36% and 26%, respectively) and less frequent in degenerative central nervous system disease and peripheral neuropathy (5.2% and 15%). No patient with non-neurologic disease had oligoclonal banding. The addition of an immunochemical step (immunofixation) did not increase sensitivity and only minimally increased specificity. It did permit distinction in selected cases between immunoglobulin and other molecules with identical electrophoretic mobility.
在一所大学医院的临床检验实验室中,对一种商用琼脂糖凝胶电泳系统及免疫固定法检测脑脊液中寡克隆免疫球蛋白模式的情况进行了评估。在303例患者中,45例为临床确诊的多发性硬化症患者,209例患有其他神经系统疾病,寡克隆带对多发性硬化症的敏感性为71%,特异性为83%。寡克隆带在中枢神经系统的炎症性疾病、肿瘤/假瘤或血管疾病中很常见(分别为35%、36%和26%),而在中枢神经系统退行性疾病和周围神经病变中较少见(分别为5.2%和15%)。没有非神经系统疾病患者出现寡克隆带。增加免疫化学步骤(免疫固定)并未提高敏感性,仅略微提高了特异性。它确实能在某些病例中区分免疫球蛋白和具有相同电泳迁移率的其他分子。