Yamamoto T, Sato T, Sugita H
Neurology. 1987 Aug;37(8):1329-33. doi: 10.1212/wnl.37.8.1329.
Antifilamin, antivinculin, and antitropomyosin antibody activities were investigated in sera from 43 patients with myasthenia gravis (MG). Antifilamin and antivinculin antibody activities are significantly higher in MG patients compared with normal controls and patients with Duchenne muscular dystrophy (DMD), Parkinson's disease, and spinocerebellar degeneration. The antifilamin antibody was highly positive (100%) in ocular myasthenia. Antitropomyosin antibody activity was similar to that in DMD patients. No correlation was observed between these antibody activities and the antiacetylcholine receptor antibody titers, the duration of the disease, and thymic pathology.
研究了43例重症肌无力(MG)患者血清中的抗细丝蛋白、抗纽蛋白和抗原肌球蛋白抗体活性。与正常对照组以及杜氏肌营养不良症(DMD)、帕金森病和脊髓小脑变性患者相比,MG患者的抗细丝蛋白和抗纽蛋白抗体活性显著更高。抗细丝蛋白抗体在眼肌型重症肌无力中呈高度阳性(100%)。抗原肌球蛋白抗体活性与DMD患者相似。未观察到这些抗体活性与抗乙酰胆碱受体抗体滴度、病程及胸腺病理之间存在相关性。