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CTLA4Ig修饰树突状细胞对实验动物淋巴细胞增殖及胞毒效应的影响
引用本文:邱文洪,郭凯文,朱慧芬,邵静芳,杨敬,张悦,龚非力,沈关心.CTLA4Ig修饰树突状细胞对实验动物淋巴细胞增殖及胞毒效应的影响[J].中国免疫学杂志,2004,20(11):765-767.
作者姓名:邱文洪  郭凯文  朱慧芬  邵静芳  杨敬  张悦  龚非力  沈关心
作者单位:1. 华中科技大学同济医学院免疫学系,武汉,430030
2. 华中科技大学同济医学院病原生物系,武汉,430030
基金项目:国家重点基础研究项目发展规划 (即国家 973计划 )资助项目 (No CB5 10 0 0 8),国家自然科学基金重点资助项目 (3 983 0 3 40 )
摘    要:目的:探讨CTLA4Ig修饰的DC对实验动物免疫功能的影响。方法:将经CTLA4Ig基因修饰或未修饰Dc腹腔注射C57BL/6致敏小鼠,以致敏或未致敏C57BL/6单个核细胞作为反应细胞,以未修饰DC细胞及修饰DC为刺激细胞,共培养6天,采用MTT比色法检测细胞增殖,乳酸脱氢酶法测定细胞毒活性。结果:CTLA4Ig融合蛋白对未修饰DC致敏或未致敏小鼠的同种细胞刺激的增殖反应有明显的抑制作用。CTLA4Ig修饰DC诱导不同组小鼠淋巴细胞增殖反应均明显降低,CTLA4Ig融合蛋白对CTL细胞毒活性有显著抑制作用。CTLA4Ig修饰DC对不同组小鼠CTL细胞毒活性均具有抵抗作用,未修饰DC细胞对未致敏小鼠以及未修饰DC对致敏小鼠CTL细胞毒活性敏感。结论:稳定表达CTLA4Ig融合蛋白的DC诱导显著降低同种小鼠淋巴细胞的增殖反应和对CTL细胞毒活性的抵抗。

关 键 词:树突状细胞  CTLA4Ig  单向混合淋巴细胞培养  乳酸脱氢酶法
文章编号:1000-484X(2004)11-0765-03

The influence of CTLA4Ig-modified dendritic cells on proliferation and cytotoxicity of lymphocytes in experimental animals
QIU Wen-Hong,GUO Kai-Wen,ZHU Hui-Fen,SHAO Jing-Fang,YANG Ji ng,ZHANG Yue,GONG Fei-Li,SHEN Guan-Xin.The influence of CTLA4Ig-modified dendritic cells on proliferation and cytotoxicity of lymphocytes in experimental animals[J].Chinese Journal of Immunology,2004,20(11):765-767.
Authors:QIU Wen-Hong  GUO Kai-Wen  ZHU Hui-Fen  SHAO Jing-Fang  YANG Ji ng  ZHANG Yue  GONG Fei-Li  SHEN Guan-Xin
Institution:QIU Wen-Hong,GUO Kai-Wen,ZHU Hui-Fen,SHAO Jing-Fang,YANG Ji ng,ZHANG Yue,GONG Fei-Li,SHEN Guan-Xin. Department of Immunology, Department of Pathogen ic Biology,Tonji Medical College,Huazhong University of Science and Technology,W uhan 430030,China[
Abstract:Objective:To study the influence of dendritic cells modified by CTLA4Ig on immunological f unction of experimental animals.Methods:The unmodified or modified dendritic cells were injected intraperitoneally into C57BL/6 mice to sensitize them.Peripheral blood mononuclear cells(PBMC) of sensi tized or unsensitized C57BL/6 mice as reaction cells,dendritic cells modified or unmodified by CTLA4Ig as stimulation cells.These two type cells were co-cultur ed for 6 days.MTT assay was used to detect lymphocyte proliferation.Lactate dehy drogenase release method was used to examine the cytotoxic activity.Results:The result showed that CTLA4Ig fusion protein could obviously inhibite lymphocyt e proliferation response of unsensitized or sensitized C57BL/6 mice.Lymphocyte p roliferation responses of different group mice induced by CTLA4Ig-modified de ndritic cells were significant decreased.CTLA4Ig fusion protein could obviously inhibit the cytotoxic activity of cytotoxic T lymphocyte.Modified dendritic cell s could resist the cytotoxic activity of cytotoxic T lymphocytes of different gr oup mice.Unmodified dendritic cells were susceptible to cytotoxic T lymphocytes of mice unsensitized or sensitized by unmodified dendritic cells.Conclusion:Dendritic cells stably expressing CTLA4Ig fusion protein can obviously decrease lymphocyte proliferation response of allogenic mice and reduce the cytotoxic act ivity.
Keywords:Dendritic cell  CTLA-4Ig  MLC  LDH  
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