重症肌无力患者巨细胞病毒抗体升高

Victoria Probst , Nicole H Trier , Gunnar Houen
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摘要

重症肌无力(MG)是一种自身免疫性疾病,其特征是肌肉变性和对神经肌肉连接处成分的自身抗体。MG的发生被认为是遗传和环境因素共同作用的结果,病毒感染被认为通过分子模仿和/或慢性炎症参与MG的发病。在这项工作中,我们分析了MG患者血清中对人类疱疹病毒家族成员和其他选定病原体的抗体,以确定这些患者血清中的病毒抗体状态。酶联免疫吸附试验、western blotting和line blotting分析显示,巨细胞病毒(CMV) IgG抗体滴度升高与MG存在关联。使用个体血清样本重复这些结果,并显示MG患者和健康对照组之间巨细胞病毒抗体滴度存在显著差异。其他病毒没有表现出同样的趋势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antibodies to cytomegalovirus are elevated in myasthenia gravis

Myasthenia gravis (MG) is an autoimmune disease characterised by muscular degeneration and autoantibodies to components of the neuromuscular junction. Development of MG is thought to occur from a combination of genetic and environmental factors, and viral infections have been suggested to be involved in the onset of MG through molecular mimicry and/or chronic inflammation. In this work, we analysed sera from MG patients for antibodies to members of the human herpes virus family and other selected pathogens to determine the virus antibody status in the sera of these patients. Enzyme-linked immunosorbent assay, western blotting and line blotting analyses using MG serum pools showed an association between elevated IgG antibody titers to cytomegalovirus (CMV) and MG. These results were replicated using individual serum samples, and showed significant differences in CMV antibody titer between MG patients and healthy controls. Other viruses did not show the same tendency.

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