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作 者:郜恒骏[1] 童菊芳[1] 朱红音[1] 顾伟齐[1] 任卫平[1] 萧树东[1]
机构地区:[1]上海第二医科大学附属仁济医院,上海市消化疾病研究所200001
出 处:《胃肠病学》2001年第3期161-165,共5页Chinese Journal of Gastroenterology
基 金:国家自然科学基金(No.39770345)资助
摘 要:目的:构建表达人白细胞介素-2(hIL-2)的重组痘苗病毒,为肿瘤免疫基因治疗作必要准备。方法:应用分子克隆基因重组技术构建重组hIL-2痘苗病毒真核表达载体PMJ601(MJ601hlL-2)。在此基础上,应用分子病毒学同源重组技术构建能表达hIL-2的重组痘苗病毒(VMJ601hIL-2)。制备hIL-2探针,用DNA杂交技术鉴定VMJ601hIL-2,并用聚丙烯酰胺凝胶电泳(SDS-PAGE)检测VMJ601hIL-2的基因产物。结果:成功构建了MJ601hIL-2和VMJ601hIL-2,VMJ601hIL-2感染的SGC7901胃癌细胞能分泌具有生物活性的hIL-2蛋白。结论:VMJ601hIL-2的构建与鉴定为进一步实施体内恶性肿瘤免疫基因治疗打下了坚实的基础。BackgroundiAims: To construct the recombinant vaccinia virus expressing human interleukin-2 (hIL-2) to form the essential prerequisite of gene therapy for cancer. Methods: Recombinant hIL-2 pMJ6Ol cukaryotic expression vector of vaccinia virus (MJ6O1hIL-2) was constructed using recombi- nant DNA technique with molecular cloning, and recombinant vaccinia virus expressing hIL-2 (VMJ 6O1hIL-2) was constructed by homologous recornbination using molecular virology. Then hIL-2 probe was prepared to detect VMJ6O1hIL.2 using DNA hybridization technique. Eventually the recombinant gene product was detected by polvacrylamide gel electrophoresis (SDS.PAGE). Results: MJ6O1hIL-2 and VMJ6O1hIL-2 were successfully constructed and hIL-2 protein with biological activity could be secreted by SGC79O1 gastric cancer cells infected by VMJ601hIL-2. Conclusions: It is one of the crucial steps in the construction and identification of VMJ6O1hJL-2 since it is the firm basis for further in vivo gene therapy in the treatment of malignant tumor.
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