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作 者:许靖霞[1] 蔡仙德[1] 王立新[1] 谭剑萍[1]
机构地区:[1]南京铁道医学院微生物学教研室
出 处:《南京铁道医学院学报》1998年第4期231-234,共4页Journal of Nanjing Railway Medical College
基 金:铁道部科技基金
摘 要:目的:观察抗CD3McAb诱导人外周血单个核细胞(HPBMC)活化增殖过程中的影响因素及抗CD3McAb激活的杀伤细胞(CD3AK细胞)免疫学特性的变化。方法:采用MTT法和苔盼蓝染色法、IL-2依赖细胞株(CTLL细胞)增殖实验、TNF-α(双抗体夹心ELISA法)试剂盒以及间接免疫荧光法分别检测CD3AK细胞的增殖活性、内源性IL-2、TNF-α的产生及CD3、CD4、CD8、IL-2R等的表达。结果:抗CD3McAb对HPBMC有很强的丝裂原作用,该作用与其诱导浓度、时间及外源性IL-2的协同作用密切相关。CD3AK细胞可产生内源性IL-2、TNF-α,IL-2R表达及CD8+细胞百分率显著增多。结论:CD3AK细胞具有很强的增殖能力,但需要外源性IL-2的协同作用,增殖细胞以CD8+细胞为主。Objective:The experiment was designed to observe the effects of anti-CD 3McAb on the activating and proliferating ability of resting human peripheral blood mononuclear cells (HPBMC) in vitro .Methods:The activating effects of anti-CD 3McAb,the production of endogenous inteleukin-2(IL-2) and the tumor necrosis factors α(TNF-α),and the expression of CD 3,CD 4,CD 8 and IL-2R were obtained by using MTT method,trypan blue test,indirect immunofluorescence method and enzyme-linked immunosorbent assay(ELISA) method.Results:Anti-CD 3McAb was a good mitogenesis,depending on its concentration,time and exogenous IL-2.CD 3AK cells produce both IL-2 and TNF-α.They greatly increase IL-2R expression.There were predominently CD 8-positive cells.Conclusion: Anti-CD 3McAb has a potent mitogenesis that activates T lymphocytes with the presence of synergistic action of exogenous IL-2.
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