论文部分内容阅读
现已公认 ,重症肌无力 (ｍａｙａｓｔｈｅｎｉａｇｒａｖｉｓ ,ＭＧ)是一种体液免疫反应介导的自身免疫性疾病 ,但其免疫病理学机制尚未完全明了。迄今为止 ,大多数学者均认为乙酰胆碱受体抗体 (ａｃｅｔｙｌ ｃｈｏｌｉｎｅｒｅｃｅｐｔｏｒａｎｔｉｂｏｄｙ ,ＡｃｈＲａｂ)与
It is recognized that mayastheniagravis (MG) is a humoral immune response mediated autoimmune disease, but its immunopathological mechanism is not fully understood. So far, most scholars think that acetylcholine receptor antibody (AchRab) and