Richman D P, Patrick J, Arnason B G
N Engl J Med. 1976 Mar 25;294(13):694-8. doi: 10.1056/NEJM197603252941304.
To determine the potential importance of an immune response directed against the acetylcholine receptor in myasthenia gravis, we studied cell-mediated immunity to receptor as measured by lymphocyte stimulation in 21 myasthenic patients and 21 controls, including five with amyotrophic lateral sclerosis. The mean (+/- S.E.M.) stimulation index was 5.3 +/- 1.3 for patients and 1.2 +/- 0.3 for controls (P less than 0.005). Fourteen patients had indexes greater than 2.0 (nine of 11 males, five of 10 females, 10 of 11 elderly patients, and five of six with thymoma). Stimulation index correlated with disease activity (rs = 0.71, P less than 0.01). Peripheral blood lymphocytes from one of three young female myasthenic patients responded to autologous thymocytes but not to receptor; peripheral blood lymphocytes from the other two responded to receptor but not to autologous thymocytes. Our findings are further evidence that autoimmunity to the acetylcholine receptor plays a central part in myasthenia gravis.
为了确定针对重症肌无力中乙酰胆碱受体的免疫反应的潜在重要性,我们通过淋巴细胞刺激来研究对受体的细胞介导免疫,对21例重症肌无力患者和21名对照者进行了检测,其中包括5例肌萎缩侧索硬化症患者。患者的平均(±标准误)刺激指数为5.3±1.3,对照者为1.2±0.3(P<0.005)。14例患者的指数大于2.0(11例男性中的9例,10例女性中的5例,11例老年患者中的10例,6例胸腺瘤患者中的5例)。刺激指数与疾病活动度相关(rs=0.71,P<0.01)。3例年轻女性重症肌无力患者中,1例患者的外周血淋巴细胞对自身胸腺细胞有反应,但对受体无反应;另外2例患者的外周血淋巴细胞对受体有反应,但对自身胸腺细胞无反应。我们的研究结果进一步证明,对乙酰胆碱受体的自身免疫在重症肌无力中起核心作用。