摘要
利用逆转录病毒中介的基因转移技术,将重组人TNF-αcDNA功能片断导入小鼠脾LAK细胞中,然后用此细胞对荷瘤小鼠局部治疗,并以导入NeoR基因的LAK细胞做对照。结果,经导有TNF-α基因的LAK细胞治疗的小鼠肿瘤明显变小,甚至消失,小鼠寿命亦明显高于对照组。
Using retrovirus mediated gene transfer technique, we transduced the recombinant TNF α cDNA into murine LAK cells. With these transduced LAK cells, we treated the tumor bearing mice implanted by S180 cells.The results were:(1)The tumor of the mice treated with TNF α transduced LAK cells became obviously smaller or even disapeared; (2)The life span of the mice treated with TNF α trnsduced LAK cells was much longer than that of those traeated with Neo R gene transduced LAK cells or with N S. These demonstrated that the transduction of TNF α gene into mice could convey an obvious antitumor effect in vivo, and testified the feasibility for clinical application of TNF α gene therapy for cancer. [WT5”HZ〗
出处
《中国医科大学学报》
CAS
CSCD
北大核心
1997年第3期224-226,共3页
Journal of China Medical University