Segurado O G, Krüger H, Mertens H G
J Neurol. 1986 Aug;233(4):202-8. doi: 10.1007/BF00314019.
Clinical data and the serum and cerebrospinal fluid (CSF) findings of 71 patients with Guillain-Barré syndrome (GBS), 7 with Fisher syndrome and 24 with chronic inflammatory polyradiculoneuropathy (CIP), were analysed. Isoelectric focusing of serum and CSF together with different formulae and diagrams were applied to study blood-CSF barrier (BCB) function and possible intrathecal IgG synthesis. The CSF total protein concentration and its IgG percentage depended mainly on the degree of BCB damage, which correlated with the clinical course. Our investigations suggest that oligoclonal IgG of CSF from these patients comes essentially from serum. In the group of GBS patients, oligoclonal IgG was transitory and correlated significantly with the development of BCB damage, cranial neuritis and severity of the disease. CIP patients showed a stable IgG pattern, which varied slightly after immunosuppressive therapy.
分析了71例吉兰-巴雷综合征(GBS)患者、7例费舍尔综合征患者和24例慢性炎症性多发性神经根神经病(CIP)患者的临床资料以及血清和脑脊液(CSF)检查结果。采用血清和脑脊液等电聚焦结合不同公式和图表来研究血脑屏障(BCB)功能及可能的鞘内IgG合成。脑脊液总蛋白浓度及其IgG百分比主要取决于BCB损伤程度,而BCB损伤程度与临床病程相关。我们的研究表明,这些患者脑脊液中的寡克隆IgG主要来自血清。在GBS患者组中,寡克隆IgG是短暂性的,且与BCB损伤、颅神经炎及疾病严重程度的发展显著相关。CIP患者表现出稳定的IgG模式,在免疫抑制治疗后略有变化。