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新生儿重症肌无力:30例病例的新临床与免疫学评估

Neonatal myasthenia gravis: a new clinical and immunologic appraisal on 30 cases.

作者信息

Morel E, Eymard B, Vernet-der Garabedian B, Pannier C, Dulac O, Bach J F

机构信息

INSERM U25-CNRS UA 122, Hôpital Necker, Paris, France.

出版信息

Neurology. 1988 Jan;38(1):138-42. doi: 10.1212/wnl.38.1.138.

Abstract

Anti-acetylcholine receptor (AChR) antibody titers, toxin binding blocking antibody, functional activity of serum on rat myotube cultures, IgG subclasses, and clinical data were studied in relation to the onset of neonatal myasthenia gravis (NMG) in 30 children of myasthenic mothers. Fourteen had NMG, including 4 atypical cases. Anti-AChR antibody titer was the best indication of NMG onset. NMG in a previous baby was also predictive. Pattern of IgG subclasses, presence of toxin-binding blocking antibodies, and serum functional activity were less predictive, but cast light on the mechanism of anti-AChR antibody pathogenicity.

摘要

在30名患有重症肌无力的母亲所生儿童中,研究了抗乙酰胆碱受体(AChR)抗体滴度、毒素结合阻断抗体、血清对大鼠肌管培养物的功能活性、IgG亚类以及临床数据与新生儿重症肌无力(NMG)发病的关系。14名儿童患有NMG,其中包括4例非典型病例。抗AChR抗体滴度是NMG发病的最佳指标。前一个婴儿患有NMG也具有预测性。IgG亚类模式、毒素结合阻断抗体的存在以及血清功能活性的预测性较差,但有助于阐明抗AChR抗体致病机制。

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