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共济失调性多发性神经病与抗Pr2 IgM κ M蛋白血症。

Ataxic polyneuropathy and anti-Pr2 IgM kappa M proteinemia.

作者信息

Arai M, Yoshino H, Kusano Y, Yazaki Y, Ohnishi Y, Miyatake T

机构信息

Department of Neurology, Niigata University, Japan.

出版信息

J Neurol. 1992 Mar;239(3):147-51. doi: 10.1007/BF00833915.

Abstract

A case of ataxic neuropathy associated with IgM kappa M proteinemia is reported. Double filtration plasmapheresis effectively treated the neuropathy. The IgM kappa antibody had anti-Pr2 cold agglutinin activity. We demonstrated reactivities of the IgM kappa antibody to sialosyl paragloboside, sialosyl lactosaminyl paragloboside, GT1b, GD1a, GD1b, GM3 and GD3 on high-performance thin-layer chromatography immunostaining and enzyme-linked immunosorbent assay, which is previously unreported antigenic specificity of the M proteins in cases of paraproteinemic neuropathy. IgM M protein with anti-Pr2 cold agglutinin activity may play a pathogenetic role in peripheral nerve demyelination, because the target antigens of the M protein are present in myelin and possibly in endothelial cells of the peripheral nervous system.

摘要

报告了1例与IgM κ型M蛋白血症相关的共济失调性神经病。双重过滤血浆置换有效治疗了该神经病。IgM κ抗体具有抗Pr2冷凝集素活性。我们通过高效薄层色谱免疫染色和酶联免疫吸附测定证明了IgM κ抗体对唾液酸化副球蛋白、唾液酸化乳糖胺基副球蛋白、GT1b、GD1a、GD1b、GM3和GD3的反应性,这是副蛋白血症性神经病病例中M蛋白以前未报道的抗原特异性。具有抗Pr2冷凝集素活性的IgM M蛋白可能在周围神经脱髓鞘中起致病作用,因为M蛋白的靶抗原存在于髓鞘中,也可能存在于周围神经系统的内皮细胞中。

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