IL-12、IL-7、IL-2体外协同诱导人PBMC增殖和PBMC杀瘤活性的实验研究  被引量:5

SYNERGISTIC INDUCEMENT OF PROLIFERATION AND ANTITUMOR ACTIVITY OF HUMAN PBMC BY IL-12,IL-7 AND IL-2 IN VITRO

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作  者:徐红薇[1,2] 吴长有[1,2] 李波[1,2] 任欢[1,2] 钟照华[1,2] 李呼伦[1,2] 邢淑贤[1,2] 田景先[1,2] 

机构地区:[1]哈尔滨医科大学免疫学教研室 [2]哈尔滨医科大学微生物学教研室

出  处:《中国免疫学杂志》1998年第5期338-341,共4页Chinese Journal of Immunology

摘  要:研究了重组IL12、IL7、IL2协同对健康人外周血单个核细胞(PBMC)的体外增殖和杀瘤活性的影响。结果表明,高浓度IL2与低浓度IL2协同可引起PBMC明显增殖,若在该培养体系中加入低浓度的IL2,可使这种增殖效应显著增强。如果加大IL12剂量时会产生更强的细胞毒活性,并呈现剂量依赖关系。在此培养条件下的培养上清中亦检出了较高水平的IFNγ。对培养3~14d的协同刺激细胞表型分析显示,CD56抗原阳性细胞百分率呈递增趋势,提示CD56+的NK细胞构成了产生增殖和杀伤效应的主要细胞群体。The synergistic effects of recombinant IL12、IL7 and IL2 on the proliferation of human normal peripheral blood mononuclear cell(PBMC) and their antitumor effect had been studied.Results showed that high dose of IL7 plus low dose of IL12 could obviously promote PBMC proliferation.The promotion could be dramatically enhanced by addition of low dose of IL2.If raised the concentration of IL12,the cytotoxic activity could also raised,it suggested that this was a dosedependent effect.High concentrations of IFNγ could be detected in the culture supernatant.According to the phenotype analysis of the synergistic treated PBMC during 3 to 14 days,the percentage of CD56 positive cells raised gradually among the total PBMC.It suggested that CD56+ NK cell was the main proliferation subset which played the cytotoxic effect.

关 键 词:白细胞介素 PBMC 增殖 细胞毒 肿瘤 免疫疗法 

分 类 号:R730.51[医药卫生—肿瘤]

 

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