Hansson L O, Link H, Sandlund L, Einarsson R
Department of Clinical Chemistry, Karolinska Hospital, Stockholm, Sweden.
Scand J Clin Lab Invest. 1993 Aug;53(5):487-92. doi: 10.1080/00365519309092544.
Identification of oligoclonal immunoglobulin G (IgG) in cerebrospinal fluid (CSF) is one of the major laboratory signs in multiple sclerosis (MS). Oligoclonal IgG can also be seen in other immunostimulating central nervous system diseases, e.g. meningitis caused by Borrelia spirochetes. A convenient isoelectric focusing (IEF) method combined with polyethyleneglycol-enhanced (PEG) immunofixation and silverstaining using PhastSystem for detection of oligoclonal IgG bands in serum and unconcentrated spinal fluid was developed. Serum and cerebrospinal fluid samples earlier investigated using agarose IEF combined with immunoblotting and avidin-biotin amplified double-antibody peroxidase staining (= A-IEF) were blindly re-analysed using PhastGel IEF 3-9 modified with addition of Pharmalyte 8-10.5 followed by immunofixation and silver staining (= PhastIEF). PhastSystem IEF using PhastGel had the same capability to separate and visualize oligoclonal IgG bands as the conventional agarose IEF. However, PhastIEF was more convenient and less time-consuming than A-IEF. PhastIEF combined with immunofixation and silver staining using application of standardized amounts of IgG for both the serum and CSF samples (40-60 ng IgG/lane is fast, well-standardized and reproducible. The method is sensitive and uses only a minute volume of unconcentrated cerebrospinal fluid for the investigation of CSF IgG pattern.
脑脊液(CSF)中寡克隆免疫球蛋白G(IgG)的鉴定是多发性硬化症(MS)的主要实验室指标之一。寡克隆IgG也可见于其他免疫刺激性中枢神经系统疾病,例如由疏螺旋体引起的脑膜炎。开发了一种便捷的等电聚焦(IEF)方法,该方法结合聚乙二醇增强(PEG)免疫固定和使用PhastSystem的银染,用于检测血清和未浓缩脑脊液中的寡克隆IgG条带。对早期使用琼脂糖IEF结合免疫印迹和抗生物素蛋白-生物素放大双抗体过氧化物酶染色(=A-IEF)研究的血清和脑脊液样本,使用添加了Pharmalyte 8-10.5改良的PhastGel IEF 3-9进行等电聚焦,随后进行免疫固定和银染(=PhastIEF),进行盲法重新分析。使用PhastGel的PhastSystem IEF与传统琼脂糖IEF分离和可视化寡克隆IgG条带的能力相同。然而,PhastIEF比A-IEF更便捷且耗时更少。PhastIEF结合免疫固定和银染,对血清和脑脊液样本均使用标准化量的IgG(40-60 ng IgG/泳道),快速、标准化良好且可重复。该方法灵敏,仅使用微量未浓缩脑脊液来研究脑脊液IgG模式。