Younes-Chennoufi A B, Léger J M, Hauw J J, Preud'homme J L, Bouche P, Aucouturier P, Ratinahirana H, Lubetzki C, Lyon-Caen O, Baumann N
INSERM Unit 134 Neurobiologie cellulaire moléculaire et clinique, Hôpital de la Salpêtrière, Paris, France.
Ann Neurol. 1992 Jul;32(1):18-23. doi: 10.1002/ana.410320105.
We report on a 54-year-old man with a sensory-motor polyneuropathy associated with a biclonal IgM-kappa gammopathy, which reacted with the ganglioside GD1b. Examination of nerve biopsy specimens showed some reduction in the density of myelinated fibers and axonal degeneration with a loss of large fibers and a relative increase in the density of small fibers. Immunodetection on thin-layer chromatography of the glycolipid antigens showed strong reactivity of the patient's serum IgM-kappa with GD1b ganglioside and weak binding to GD1a. biclonal IgM antibodies did not react with GM1, asialo-GM1, GT1b, GD2, or GD3. Indirect immunofluorescence staining showed binding of IgM-kappa mainly in a crescent-like pattern on the internal side of myelin sheaths, which could correspond either to an enlarged periaxonal (adaxonal) space or to the internal mesaxon or to both. The immunostaining was abolished after absorption of the serum with GD1b.
我们报告了一名54岁男性,患有与双克隆IgM-κ型丙种球蛋白病相关的感觉运动性多神经病,该丙种球蛋白病与神经节苷脂GD1b发生反应。神经活检标本检查显示,有髓纤维密度有所降低,轴突变性,大纤维丢失,小纤维密度相对增加。对糖脂抗原进行薄层色谱免疫检测显示,患者血清IgM-κ与GD1b神经节苷脂有强反应性,与GD1a结合较弱。双克隆IgM抗体与GM1、脱唾液酸GM1、GT1b、GD2或GD3无反应。间接免疫荧光染色显示,IgM-κ主要以新月形模式结合于髓鞘内侧,这可能对应于扩大的轴周(轴内)间隙或内系膜,或两者皆有。用GD1b吸收血清后,免疫染色消失。