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丙酮酸脱氢酶复合物E2亚单位重组蛋白体外刺激PBC患者PBMCs实验研究
引用本文:赵军,王业东,辛绍杰,迟淑平,李靖,舒翠莉,李伯安,程云. 丙酮酸脱氢酶复合物E2亚单位重组蛋白体外刺激PBC患者PBMCs实验研究[J]. 医学争鸣, 2005, 26(13): 1185-1188
作者姓名:赵军  王业东  辛绍杰  迟淑平  李靖  舒翠莉  李伯安  程云
作者单位:解放军302医院传染病研究所免疫室、感染二科,北京,100039;解放军302医院传染病研究所免疫室、感染二科,北京,100039;解放军302医院传染病研究所免疫室、感染二科,北京,100039;解放军302医院传染病研究所免疫室、感染二科,北京,100039;解放军302医院传染病研究所免疫室、感染二科,北京,100039;解放军302医院传染病研究所免疫室、感染二科,北京,100039;解放军302医院传染病研究所免疫室、感染二科,北京,100039;解放军302医院传染病研究所免疫室、感染二科,北京,100039
基金项目:国家自然科学基金,军队科研项目
摘    要:目的:初步探讨丙酮酸脱氢酶复合物的E2亚单位(PDC-E2)与原发性胆汁性肝硬化(PBC)发病机制间的关系.方法:用纯化的PDC-E2重组蛋白体外刺激PBC患者外周血单个核细胞(PBMCs);3H-TdR掺入法检测PBMCs增殖情况;ELASA法检测细胞上清中TNF-α含量.结果:11例M2抗体阳性和1例AMA阳性的PBC患者中有8例出现不同程度PBMCs增殖,而2例AMA和M2抗体均阴性的PBC患者和4例AIH患者PBMCs均无增殖.11例M2抗体阳性的PBC患者刺激后TNF-α分泌均明显增加.结论:PBC患者外周血中存在针对PDC-E2的自身反应性T细胞;TNF-α可能在PBC的病理损伤中发挥重要作用.

关 键 词:胆汁性肝硬化  外周血单个核细胞  丙酮酸脱氢酶复合物  肿瘤坏死因子
文章编号:1000-2790(2005)13-1185-04
修稿时间:2005-04-05

Peripheral blood T cell responses to recombinant PDC-E2 in primary biliary cirrhosis
ZHAO Jun,WANG Ye-Dong,XIN Shao-jie,CHI Shu-ping,LI Jing,SHU Cui-li,LI Bo-an,CHENG Yun. Peripheral blood T cell responses to recombinant PDC-E2 in primary biliary cirrhosis[J]. Negative, 2005, 26(13): 1185-1188
Authors:ZHAO Jun  WANG Ye-Dong  XIN Shao-jie  CHI Shu-ping  LI Jing  SHU Cui-li  LI Bo-an  CHENG Yun
Abstract:AIM: To evaluate the peripheral blood T cell responses to PDC-E2 and its possible role in the pathogenesis of primary biliary cirrhosis (PBC). METHODS: Fourteen patients with PBC and four patients with autoimmune hepatitis (AIH) were enrolled in this study. Peripheral blood mononuclear cells (PBMCs) were stimulated by purified recombinant PDC-E2. Stimulation index was measured by ~3H-TdR incorporation assay and TNF-a was detected in the supernatant of culture by ELISA. RESULTS: The proliferation of PBMCs was observed in 8 out of the 14 PBC patients, who were antimitochomdrial antibody (AMA) or anti-M2 positive. AMA positivity or anti-M2 positivity was not observed in AIH patients. TNF-a secretion increased significantly after stimulation in all the 11 anti-M2 positive PBC patients. CONCLUSION: The results suggest the possibility of using PDC-E2 as a target antigen to induce autoimmune damage in PBC and that TNF-a may play an important role in this damage.
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