Niu G, Gong Y, Dong J
Department of Pathology, CAMS, School of Basic Medicine, Peking Union Medical College.
Zhonghua Bing Li Xue Za Zhi. 1996 Oct;25(5):280-3.
In order to investigate the antitumor effect of IL2 gene transfected tumor vaccine, gene transfected tumor cells which secrete IL2 in a comparatively sustained manner must be obtained. Their growth and metastatic characteristics must be identified. This study used the retrovirus infection method to introduce human IL2 cDNA into mouse B16 melanoma cells. Southern blot analysis confirmed the establishment of IL2-integrated B16 cells (B16-IL2). Northern blot also showed the expression of IL2 gene in mRNA level. IL2 secretion of B16-IL2 was comparatively stable for a period of 6 months with the highest production rate of 53u/ml. No obvious influence was observed on the morphology and growth of the tumor cells in vitro after the transfection of IL2-cDNA. But, their oncogenicity in vivo was reduced and the tumor growth induced by B16-IL2 cells was inhibited. Lung metastasis rate and extent was also reduced. This study laid the foundation for the preparation of an IL2-secreting tumor vaccine.
为了研究IL2基因转染肿瘤疫苗的抗肿瘤作用,必须获得能相对持续分泌IL2的基因转染肿瘤细胞。必须鉴定它们的生长和转移特性。本研究采用逆转录病毒感染法将人IL2 cDNA导入小鼠B16黑色素瘤细胞。Southern印迹分析证实了IL2整合B16细胞(B16-IL2)的建立。Northern印迹也显示了IL2基因在mRNA水平的表达。B16-IL2的IL2分泌在6个月内相对稳定,最高生产率为53u/ml。转染IL2-cDNA后,体外肿瘤细胞的形态和生长未观察到明显影响。但是,它们在体内的致癌性降低,B16-IL2细胞诱导的肿瘤生长受到抑制。肺转移率和转移程度也降低。本研究为制备分泌IL2的肿瘤疫苗奠定了基础。