摘要
探讨胸腺内插指状细胞(IDC)在重症肌无力(MG)发病中的作用。方法采用S-100蛋白抗体用免疫组织化学方法对30例MG患者非瘤性胸腺内S-100蛋白阳性IDC的分布和数量观察研究。同时取10例不同年龄的正常胸腺作对照。结果MG非瘤性胸腺内IDC数目明显增多(P<0.05),且IDC数目的多少和胸腺髓质上皮细胞的增生程度呈正相关。结论IDC可能参与MG的发病,胸腺髓质内增生的上皮细胞在MG自身免疫过程中起一定作用。
Objective The authors made a study of the role of interdigitating cells (IDC) in the pathogenesis of myasthenia gravis (MG) study. Method The distribution and number of S 100 protein positive interdigitating cells in nonneoplastic thymus were examined in 30 patients with mysthenia gravis, using the ABC immunohistochemical methods. The specimens of thymus taken from 10 cases of non myasthenic patients of various ages were taken as controls.Results Showed that IDC were distributed in the medullary as well as in the corticomedullay junction areas in the nonneoplastic thymus of the myasthenic patients. The number of IDC in the medulla of myasthenic thymus was increased significantly as compared with that in the non myasthenic patients. The increase was more prominent in those areas the hyperplasia of the medullary epithelial cells were found. Conclusion The authors considered that IDC might participate in the pathogenesis of MG and the medullary epithelial cells might trigger off the cascade of the autoimmune process in myasthenia.
出处
《中华神经科杂志》
CAS
CSCD
1997年第2期81-83,共3页
Chinese Journal of Neurology
关键词
重症肌无力
胸腺
插指状细胞
Myasthenia gravis Thymus Immunohistochemitry S 100 protein Interdigitating cells