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作 者:田子农 温端改[2] 何小舟[1] 徐仁芳[1] 许贤林[1] 侯建全[2]
机构地区:[1]常州市第一人民医院泌尿外科,213003 [2]苏州大学附属第一医院泌尿外科,215006
出 处:《中华实验外科杂志》2017年第12期2031-2034,共4页Chinese Journal of Experimental Surgery
基 金:常州市卫生局科研资助项目(QN201201);江苏省重点实验室临床免疫高技术平台培育点资助项目
摘 要:目的探讨制备小鼠白细胞介素-15(mIL-15)基因重组腺病毒载体联合RM-1前列腺癌细胞裂解产物上清共同修饰的树突状细胞(mIL-15/lysate—DC)疫苗的可行性。方法mlL.15基因的重组腺病毒联合RM-1前列腺癌细胞裂解产物上清共同修饰树突状细胞(DC)。流式细胞术检测感染效率及DC表型。结果mlL-15基因重组腺病毒载体有效感染DC,感染效率达(77.43±1.96)%;流式细胞术结果证实mIL-15/lysate—DC组与对照组比较,其CD40[(52.50±2.36)%]、CD80[(46.53±0.91)%]、CD86[(47.10±2.59)%]、CD11c[(32.07±1.72)%]和MHC—II[(53.57±2.72)%]等表面标志显著提高,具有更强的T细胞增殖能力。结论成功制备mIL-15/lysate.DC疫苗。Objective To investigate the feasibility of preparation of dentritie cell vaccine modi- fied by adenovirus - mediated mouse intedeukin (raiL) - 15 gene and cell lysate on mouse with prostate cancer. Methods Dentritic cells (DCs) are modified by adenovirus -mediated mIL - 15 gene and cell lysate on mouse with prostate cancer. The transduction efficiency and phenotypes of DCs were analyzed by flow cytometry (FCM). Results DCs are effectively infected by adenovirus - mediated mIL - 15 gene with a transduetion efficiency of (77.43 ± 1.96 ) % , which is confirmed by FCM. After modified by adeno- virus -mediated mIL - 15 gene and cell ]ysate on mouse with prostate cancer, the expresson of surface mol- ecules of DCs were up - regulated, inculding CD40 [ ( 52. 50 ± 2. 36) % ], CD80 [ (46. 53 ± 0. 91 ) % ], CD86 [(47.10 ± 2.59)%], CDllc [(32.07 ± 1.72)%] and major histocompatibility complex (MHC) - II[ (53.57 ±2. 72)% ]. Compared with control groups, the mIL- 15/lysate DC vaccine can stimulate the proliferation of T cells more strongly. Conclusion The mlL - 15/lysate DC vaccine has been successfully prepared and identified.
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