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作 者:何向锋[1] 王净[2] 余方流[1] 赵枫姝[1] 蔡凯[1] 张洪义[1] 陈峻崧[1] 陈登宇[1] 窦骏[1]
机构地区:[1]东南大学医学院病原生物学与免疫学系,南京210009 [2]东南大学附属中大医院妇产科,南京210009
出 处:《中国免疫学杂志》2011年第9期779-782,共4页Chinese Journal of Immunology
基 金:国家自然科学基金(No.81071769)
摘 要:目的:评估B16F10/ESAT-6-GPI-IL-21瘤苗用于C57BL/6小鼠的安全性及其诱导的抗肿瘤免疫效应。方法:应用免疫荧光、FCM检测瘤苗细胞ESAT-6-GPI的表达情况;以Western blot方法检测瘤苗细胞IL-21的表达情况;动物实验检测瘤苗体内应用的安全性;制备荷瘤鼠术后免疫模型,评价瘤苗免疫效果。结果:B16F10/ESAT-6-GPI-IL-21瘤苗细胞表面有靶抗原ESAT-6-GPI表达,并分泌IL-21。于C57BL/6小鼠皮下接种2×105个B16F10/ESAT-6-GPI-IL-21瘤苗细胞,60天内未见致瘤,但能够诱导小鼠产生有效的抗肿瘤免疫效应。结论:B16F10/ESAT-6-GPI-IL-21瘤苗致瘤性明显下降,低剂量应用具有安全性,能够诱导小鼠产生有效的抗肿瘤免疫效应。Objective:The safety and anti-tumor efficacy of B16F10/ESAT-6-GPI-IL-21 tumour vaccine in mouse model was evaluated.Methods:Expressions of ESAT-6-GPI antigen of tumour vaccine were detected by immunofluorescence and flow cytometry,respectively.Expression of IL-21 of tumour vaccine were detected by Western blot.The biological safety of tumour vaccine was evaluated by animal experiments.The developed postoperative bearing-tumor mice were immunized with the tumour vaccine and the efficacy of B16F10/ESAT-6-GPI-IL-21 vaccine against B16F10 cell challenge was also evaluated.Results:Target antigen of ESAT-6-glycosyl phosphatidyl inositol(gpi) was expressed on the surface of B16F10/ESAT-6-GPI-IL-21 tumour vaccine that secreted IL-21 simultaneouly.There were no tumour formation in mice vaccinated with 2×105 B16F10/ESAT-6-GPI-IL-21 tumour vaccine after 60 days into the observation.The vaccine could generate a powerful immune efficiency against the B16F10 tumor cell challenge.Conclusion:B16F10/ESAT-6-GPI-IL-21 tumour vaccine oncogenicity is very low and has a safety characteristic when it is applied into mouse model in low dose.
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