Vincent A, Newsom-Davis J
Clin Exp Immunol. 1982 Aug;49(2):266-72.
Anti-acetylcholine receptor (anti-AChR) antibody characteristics including light chain, IgG subclass, avidity for denervated human acetylcholine receptor and reaction with various human and mammalian AChR preparations were examined in 11 patients who developed myasthenia during penicillamine treatment of rheumatoid arthritis. Results were compared with those already reported in 35 patients with generalized idiopathic myasthenia gravis (MG). We found significant differences in the avidity and the light chain of the anti-AChR. However, anti-AChR characteristics in 12 patients with recent onset (less than 4 months' duration) idiopathic MG did not differ significantly from those in patients with penicillamine-induced MG. In the patients with generalized MG a trend was found towards higher percentage of kappa light chain and higher anti-AChR avidity with duration of disease. Anti-acetylcholine receptor antibodies in penicillamine-induced myasthenia gravis therefore appear to be similar to those of idiopathic myasthenia gravis of recent onset.
在11例类风湿关节炎患者接受青霉胺治疗期间发生重症肌无力的患者中,检测了抗乙酰胆碱受体(anti-AChR)抗体的特征,包括轻链、IgG亚类、对失神经支配的人乙酰胆碱受体的亲和力以及与各种人和哺乳动物AChR制剂的反应。将结果与35例全身型特发性重症肌无力(MG)患者已报道的结果进行比较。我们发现抗AChR的亲和力和轻链存在显著差异。然而,12例近期发病(病程少于4个月)的特发性MG患者的抗AChR特征与青霉胺诱导的MG患者没有显著差异。在全身型MG患者中,发现κ轻链百分比和抗AChR亲和力随病程有升高趋势。因此,青霉胺诱导的重症肌无力中的抗乙酰胆碱受体抗体似乎与近期发病的特发性重症肌无力的抗体相似。