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CTLA4Ig诱导免疫耐受的体外研究
引用本文:姜庆,吴军,易绍萱,陈希炜,罗高兴,贺伟峰.CTLA4Ig诱导免疫耐受的体外研究[J].第三军医大学学报,2003,25(21):1896-1898.
作者姓名:姜庆  吴军  易绍萱  陈希炜  罗高兴  贺伟峰
作者单位:第三军医大学附属西南医院全军烧伤研究所,重庆市器官移植基础研究所,创伤烧伤复合伤国家重点实验室,重庆,400038
基金项目:国家自然科学基金资助重大项目(39993430-2),国家自然科学基金资助面上项目(39970756),国家科技部重点项目(96-920-20-10),全军医药重点项目(98Z081)~~
摘    要:目的 观察CTLA4Ig在诱导人外周血T细胞免疫耐受中的作用。方法 以结核菌素刺激人外周血淋巴细胞,观察不同剂量CTLA4Ig对外周血淋巴细胞增殖反应的影响;观察CTLA4Ig和CsA(环孢霉素A)对再次结核菌素刺激和非相关第三者APC细胞刺激淋巴细胞增殖反应的影响,IL-2的变化,以及外源性IL-2对免疫耐受诱导的影响。结果 CTLA4Ig抑制淋巴细胞增殖呈剂量依赖关系,20μg/ml时抑制作用最强;CTLA4Ig能诱导免疫耐受并与CsA有协同作用;外源性IL-2能抑制免疫耐受的诱导。结论 CTLA4Ig能抑制淋巴细胞的增殖和IL-2的分泌释放,CTLA4Ig和CsA联合应用能更彻底抑制淋巴细胞增殖和IL-2的分泌释放,并诱导免疫耐受;外源性IL-2能逆转免疫耐受。

关 键 词:CTLA4Ig  T细胞  免疫耐受  细胞增殖
文章编号:1000-5404(2003)21-1896-03
修稿时间:2003年7月21日

Experimental study of immune tolerance induced by CTLA4Ig in vitro
JIANG Qing,WU Jun,YI Shao-xuan,CHEN Xi-wei,LUO Gao-xing,HE Wei-feng.Experimental study of immune tolerance induced by CTLA4Ig in vitro[J].Acta Academiae Medicinae Militaris Tertiae,2003,25(21):1896-1898.
Authors:JIANG Qing  WU Jun  YI Shao-xuan  CHEN Xi-wei  LUO Gao-xing  HE Wei-feng
Abstract:Objective To study the roles of cytologic T lymphocyte-associated antigen 4 immunoglobulin ( CTLA4Ig) in the induction of human T cell immune tolerance. Methods The effects of different doses of CTLA4Ig on the human T cell proliferation induced by tuberculin as well as those of CTLA4Ig and cyclosporin A (CsA) on the human lymphocyte proliferation re-stimulated by tuberculin or by the third party antigen-presenting cells (APC) were observed. The changes of IL-2 and effect of IL-2 on the immune tolerance were also observed. Results Tuberculin-induced T cell proliferation was inhibited by CTLA4Ig in a dose-dependent manner. The inhibitory effect was the strongest when the dose of CTLA4Ig was 20 fig/ml. CTLA4Ig could induce the immune tolerance and had a cooperative effect with CsA, but IL-2 could inhibit the immune tolerance. Conclusion CTLA4Ig can inhibit T cell proliferation and IL-2 excretion. Combination of CTLA4Ig and CsA can completely inhibit T cell proliferation and IL-2 excretion but can induce immune tolerance. The immune tolerance can be reversed by IL-2.
Keywords:CTLA4Ig  T cell  immune tolerance  proliferation
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