重症肌无力患者Foxp3^+CD4^+CD25^+调节性T细胞与AChRAb、Titin-Ab的相关研究  被引量:9

Research on the relationship between Foxp3^+ CD4^+ CD25^+ Treg and AChRAb or Titin-Ab in myasthenia gravis patients

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作  者:方琪[1] 冉娟娟[1] 蔡秀英[1] 薛群[1] 古彦铮[2] 王达鹏[1] 董万利[1] 

机构地区:[1]苏州大学附属第一医院神经内科,215006 [2]苏州大学生物技术研究所,215007

出  处:《中国神经免疫学和神经病学杂志》2010年第5期342-344,共3页Chinese Journal of Neuroimmunology and Neurology

基  金:江苏省自然基金资助项目(BK2006542)

摘  要:目的探讨重症肌无力(myasthenia gravis,MG)患者Foxp3^+CD4^+CD25^+调节性T细胞(Foxp3^+CD4^+CD25^+Treg)与乙酰胆碱受体抗体(AChRAb)及连接素抗体(Titin-Ab)之间的关系,进一步揭示MG的发病机制。方法采用酶联免疫吸附试验(ELISA)检测22例MG患者以及20名健康对照者血清AChRAb和Titin-Ab水平;采用流式细胞术(FCM)检测两组外周血中CD4^+CD25^+Treg的比例及其表达Foxp3的比例。结果 MG患者外周血CD4^+CD25^+Treg比例[(2.9±0.52)%]与健康对照组[(3.12±0.51)%]比较无统计学差异(P>0.05);CD4^+CD25^+Treg细胞Foxp3表达比例为(37.24±9.57)%,低于健康对照组[(58.60±4.91)%](P<0.01)。MG组CD4^+CD25^+Treg表达Foxp3比例与AChRAb、Titin-Ab水平[分别为(0.232±0.060)和(0.170±0.035)pg/mL]均呈负相关(r=-0.449,P<0.05;r=-0.691,P<0.01)。结论 Foxp3^+CD4^+CD25^+Treg细胞数目减少导致机体免疫功能缺陷是MG发病的重要环节。Objective To explore the relation between the percentage of Foxp3+ CD4+ CD25+ T regulatory cells (Foxp3+ CD4+ CD25+ Treg) in peripheral blood and the serum levels of AChRAb and Titin-Ab in myasthenia gravis (MG) patients, and further to analyze the pathogenesis of MG. Methods The levels of AChRAb and Titin-Ab in the serum of 22 patients with MG and 20 healthy controls were detected by ELISA. The percentage of CD4+ CD25+ Treg in the peripheral blood lymphocytes and that of Foxp3+ in CD4+ CD25+ Treg were detected by FCM. Results The percentage of CD4+ CD25+ Treg in peripheral blood was comparable between the MG group and the control group [(2.9±0.52) % vs. (3.12±0.51) %, respectively, P〉0. 05], but the expression of Foxp3 in CD4+ CD25+ Treg was significantly decreased in the MG group as compared to that in the control group [ (37.24±9.57)% vs. (58.60±4.91)%, respectively, P〈0.01]. There was negative correlation between the expression of Foxp3 of CD4+ CD25+ Treg in peripheral blood and the serum levels of AChRAb and Titin-Ab [ (0. 232±0. 060) pg/mL, (0. 170± 0. 035) pg/mL, respectively; r= -0. 449, P〈 0.05; r=- 0. 691, P〈0.01]. Conclusions The decreased number of Foxp3+ CD4+ CD25+ of Treg led to immune deficiency, and that might play an important role in the pathogenesis of MG.

关 键 词:重症肌无力 乙酰胆碱受体抗体 连接素抗体 Foxp3^+CD4^+XD25^+调节性T细胞 

分 类 号:R746.1[医药卫生—神经病学与精神病学]

 

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