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使用抗表皮生长因子受体抗体将治疗性基因体内靶向递送至实验性鳞状细胞癌:免疫基因方法

Targeted in vivo delivery of therapeutic gene into experimental squamous cell carcinomas using anti-epidermal growth factor receptor antibody: immunogene approach.

作者信息

Chen J, Gamou S, Takayanagi A, Ohtake Y, Ohtsubo M, Shimizu N

机构信息

Department of Molecular Biology, Keio University School of Medicine, Tokyo, Japan.

出版信息

Hum Gene Ther. 1998 Dec 10;9(18):2673-81. doi: 10.1089/hum.1998.9.18-2673.

Abstract

The "Fab immunogene" is a novel gene transfer vehicle in which the Fab fragment of anti-human epidermal growth factor (EGF) receptor antibody B4G7 is conjugated with poly-L-lysine to form an affinity complex with DNA. It was developed to target delivery of therapeutic genes into EGF receptor-hyperproducing tumor cells. Various characteristic features of the immunogene have been documented (Chen et al., 1998). Here we add further evidence to prove that in vitro transfer of beta-galactosidase/Fab immunogene is exclusively to EGF receptor-positive cells and that the herpes simplex virus thymidine kinase (TK)/Fab immunogene induces substantial suicide effects on A431 tumor cells when treated together with ganciclovir. The in vivo specificity of the immunogene transfer was examined using A431 tumor-bearing nude mice. When these nude mice were injected intraperitoneally with the chloramphenicol acetyltransferase (CAT)/Fab immunogene, CAT DNA was detected in the tumors as well as in liver and kidney but not brain, whereas CAT mRNA and enzyme activity were detected only in the tumors. Local and intraperitoneal injection of the TK/Fab immunogene and subsequent administration of ganciclovir effectively suppressed the growth of A431 tumors transplanted on the backs of nude mice. These observations suggest a possible application of the Fab immunogene system in cancer gene therapy.

摘要

“Fab免疫基因”是一种新型基因传递载体,其中抗人表皮生长因子(EGF)受体抗体B4G7的Fab片段与聚-L-赖氨酸偶联,形成与DNA的亲和复合物。它被开发用于将治疗性基因靶向递送至EGF受体高表达的肿瘤细胞。免疫基因的各种特征已有文献记载(Chen等人,1998年)。在此,我们补充进一步的证据,以证明β-半乳糖苷酶/Fab免疫基因在体外仅向EGF受体阳性细胞转移,并且单纯疱疹病毒胸苷激酶(TK)/Fab免疫基因与更昔洛韦一起处理时对A431肿瘤细胞诱导显著的自杀效应。使用荷A431肿瘤的裸鼠检测免疫基因转移的体内特异性。当向这些裸鼠腹腔注射氯霉素乙酰转移酶(CAT)/Fab免疫基因时,在肿瘤以及肝脏和肾脏中检测到CAT DNA,但在脑中未检测到,而仅在肿瘤中检测到CAT mRNA和酶活性。局部和腹腔注射TK/Fab免疫基因并随后给予更昔洛韦有效地抑制了移植在裸鼠背部的A431肿瘤的生长。这些观察结果提示Fab免疫基因系统在癌症基因治疗中的可能应用。

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