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作 者:王立新[1] 许靖霞[2] 谭剑萍[2] 蔡仙德[2]
机构地区:[1]南京铁道医学院医学检验系 [2]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1期12-15,共4页Journal of Nanjing Railway Medical College
基 金:铁道部科技基金
摘 要:目的:观察并比较粘附状态抗CD3单抗和游离状态抗CD3单抗诱导人外周血单个核细胞(HPBMC)活化增殖的能力。方法:采用3H-TdR掺入淋巴细胞增殖试验、苔盼蓝拒染法、间接免疫荧光染色法以及CTLL细胞IL-2检测法,分别检测人外周血单个核细胞,经两种状态抗CD3单抗刺激后,其增殖活性、外源性IL-2的协同作用、内源性IL-2释放以及IL-2R表达等生物免疫学指标。结果:粘附状态抗CD3单抗刺激HPBMC,其增殖活性、活细胞总数以及增殖活性维持的时间均高于游离状态抗CD3单抗,且前者不依赖外源性IL-2;粘附状态抗CD3单抗诱导HPBMC释放内源性IL-2以及细胞表面IL-2R表达的能力也强于游离状态抗CD3单抗。结论:粘附状态抗CD3单抗比游离状态抗CD3单抗具有更强的诱导人T淋巴细胞活化增殖能力。Objective:To observe and compare the effects of immobile CD 3McAb and soluble CD 3McAb on the activating and proliferating ability of resting human peripheral blood T lymphocytes in vitro .Method:The activation effects of CD 3McAb were obtained by using 3H-TdR incorporation method,trypan blue test,indirect immunofluorescence method and MTT method.Results:Immobile CD 3McAb was better than soluble CD 3McAb on mitogenesis,vital total cells and potent activity.Moreover,it was active in the absence of exogenous rIL-2.Immobile CD 3McAb can also induce HPBMC to release more endogenous IL-2 and better expressive ability of IL-2R than soluble CD 3McAb.Conclusion:Immobile CD 3McAb was more potent on activating T lymphocytes than soluble CD 3McAb.
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