Suppr超能文献

神经节苷脂GD1b是一例感觉运动轴索性多神经病中一种双克隆IgM的靶抗原:N-乙酰神经氨酸参与该表位。

Ganglioside GD1b is the target antigen for a biclonal IgM in a case of sensory-motor axonal polyneuropathy: involvement of N-acetylneuraminic acid in the epitope.

作者信息

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

机构信息

INSERM Unit 134 Neurobiologie cellulaire moléculaire et clinique, Hôpital de la Salpêtrière, Paris, France.

出版信息

Ann Neurol. 1992 Jul;32(1):18-23. doi: 10.1002/ana.410320105.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验