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重症肌无力是一种自身免疫性疾病,患病率为77~150/100万,患者神经-肌肉接头处传递功能障碍,部分或全身骨骼肌表现出易疲劳和无力,常伴有斜视、眼皮下垂、表情淡漠、吞咽困难、软颈、构音困难等症状,严重者可出现呼吸肌麻痹或球麻痹,危害患者的生命健康。本研究观察了免疫抑制剂对55例重症肌无力患者调节性T细胞及辅助性T细胞水平的影响。1资料与方法1.1一般资料选本院2012年2月至2016年5月
Myasthenia gravis is an autoimmune disease with a prevalence of 77-150 / 1 million. Transmission dysfunction occurs at the neuromuscular junction of patients, and some or all of the skeletal muscles exhibit fatigue and weakness, often associated with strabismus, eyelids Drooping, apathetic, dysphagia, soft neck, dysarthria and other symptoms, severe paralysis or paralysis of respiratory muscles may occur, endanger the life and health of patients. This study looked at the effects of immunosuppressive agents on the levels of regulatory T cells and helper T cells in 55 patients with myasthenia gravis. 1 Materials and Methods 1.1 General Information Selected hospital from February 2012 to May 2016