论文部分内容阅读
本文报告202例重症肌无力（Myastheniagrauis,MG）患者的TGA、TMA放射免疫分析结果,并探讨其临床意义。 对象和方法 一、对象:重症肌无力患者为1995年1月～1996年12月本院神经内科确诊的住院病人,均无肝、肾或甲状腺疾病。 二、方法:TGA、TMA试剂盒由上海放射免疫分析技术研究所提供。测量仪器为北京二六一厂生产的FT-6306型γ计数器带微机数据自动处理系统。 结果 结果见表1。 讨论 目前普遍认为,MG是自身乙酰胆碱受体（AchR）致敏的自身免疫病,2/3MG患者血清免疫球蛋白增高,大多数MG病人血清中AchR抗体增高。
This article reports 202 patients with myasthenia grauis (MG) TGA, TMA radioimmunoassay results, and to explore its clinical significance. Subjects and methods First, the object: Myasthenia gravis patients for in January 1995 ~ December 1996 hospital neurology diagnosed inpatients, no liver, kidney or thyroid disease. Second, methods: TGA, TMA kit by the Shanghai radioimmunoassay Institute of Technology. The measuring instrument is the FT-6306 type γ counter produced by Beijing No. 261 Plant with automatic data processing system of microcomputer. The results in Table 1. DISCUSSION It is now generally accepted that MG is an autoimmune disease sensitized by its own acetylcholine receptor (AchR). Serum immunoglobulins are elevated in 2/3 of 3MG patients, and elevated serum AchR antibodies in most MG patients.