Obi T, Kusunoki S, Takatsu M, Mizoguchi K, Nishimura Y
Department of Neurology, National Shizuoka Hospital, Japan.
Acta Neurol Scand. 1992 Aug;86(2):215-8. doi: 10.1111/j.1600-0404.1992.tb05069.x.
A 77-year-old man presented sensory-dominant neuropathy associated with IgM M-protein reacting with various gangliosides. The M-protein bound to gangliosides with polysialosyl residue, such as GD1b, GD3, GT1b, GT3, GQ1b, and GQ1c. In addition, GD1a, GM3 and LM1, having a terminal monosialosyl epitope, were also recognized. Previously, Ilyas et al. described a similar case in which sensory symptoms were associated with IgM M-protein reacting with gangliosides containing a disialosyl group, such as GD3, GD1b, and GT1b, but not GM3 and GD1a. It is suggested that the reactivity of IgM M-protein with polysialogangliosides may be associated with the pathogenesis of sensory-dominant neuropathy.
一名77岁男性出现了以感觉为主的神经病变,伴有与多种神经节苷脂发生反应的IgM M蛋白。该M蛋白与带有多唾液酸残基的神经节苷脂结合,如GD1b、GD3、GT1b、GT3、GQ1b和GQ1c。此外,还识别出具有末端单唾液酸基表位的GD1a、GM3和LM1。此前,伊利亚斯等人描述了一个类似病例,其中感觉症状与IgM M蛋白有关,该蛋白与含有二唾液酸基的神经节苷脂(如GD3、GD1b和GT1b)发生反应,但不与GM3和GD1a发生反应。提示IgM M蛋白与多唾液酸神经节苷脂的反应性可能与以感觉为主的神经病变的发病机制有关。