Krüger H, Englert D, Pflughaupt K W
J Neurol. 1981;226(1):15-24. doi: 10.1007/BF00313314.
Isoelectric focusing (IEF) of serum and CSF revealed oligoclonal IgG in 13 out of 16 patients with the Guillain-Barré syndrome (GBS), in 10 of them in serum only and in 3 in serum and CSF. Seventeen out of 19 patients with lymphocytic meningoradiculitis (LMR) showed oligoclonal IgG, 12 of them in CSF only. These findings, together with additional results, mean that in GBS oligoclonal IgG is synthesized mainly outside the CNS and in LMR within the CNS. Follow-up studies revealed changes in the oligoclonal IgG during the course of GBS and LMR. After treatment by plasma exchange the disappearance of oligoclonal IgG bands was followed by an improvement of GBS symptoms. The oligoclonal IgG bands returned in correlation with worsening of the disease. We were not able to elucidate the antibody character of oligoclonal IgG in GBS or LMR. No antibodies against the myelin basic protein (fragment 89-169) were detectable in the sera and CSF in any of the patients tested.
血清和脑脊液的等电聚焦(IEF)显示,16例格林-巴利综合征(GBS)患者中有13例存在寡克隆IgG,其中10例仅血清中有,3例血清和脑脊液中均有。19例淋巴细胞性脑膜炎神经根炎(LMR)患者中有17例显示寡克隆IgG,其中12例仅脑脊液中有。这些发现以及其他结果表明,GBS中的寡克隆IgG主要在中枢神经系统外合成,而LMR中的则在中枢神经系统内合成。随访研究显示,GBS和LMR病程中寡克隆IgG会发生变化。血浆置换治疗后,寡克隆IgG条带消失,随后GBS症状改善。寡克隆IgG条带随着疾病恶化而复现。我们无法阐明GBS或LMR中寡克隆IgG的抗体特性。在所检测的任何患者的血清和脑脊液中均未检测到抗髓鞘碱性蛋白(片段89 - 169)的抗体。