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使用逆转录病毒载体将白细胞介素-2转导至人肝癌细胞系的作用

Effects of interleukin-2 transduction on the human hepatoma cell lines using retroviral vector.

作者信息

Kim J H, Gong S J, Yoo N C, Lee H, Shin D H, Uhm H D, Jeong S J, Cho J Y, Rha S Y, Kim Y S, Chung H C, Roh J K, Min J S, Kim B S

机构信息

Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul 120-752, Korea.

出版信息

Oncol Rep. 1999 Jan-Feb;6(1):49-54.

PMID:9864400
Abstract

Gene therapy, using cytokine gene transduction, aims to increase the antigenicity of tumor cells, and to activate the immune effector cells, and thereby inducing tumor regression. With regards to in vitro sensitivity to peripheral blood monocytes and in vivo tumorigenic activity we compared the differences between parent hepatoma cell lines and interleukin-2 (IL-2) transduced hepatoma cell lines using N2A/IL-2 and LNC/IL-2 retrovirus. IL-2 secretion was 186 pg/10(6) cells/24 h in SK-Hep1 cell line and 147 pg/106 cells/24 h in Hep-3B cell line with N2A/IL-2 retroviral vector and was 55,000 pg/10(6) cells/24 h in Hep-3B cell line with LNC/IL-2 retroviral vector. in vitro sensitivity to peripheral blood monocytes was increased by 163.8-254% in IL-2 transduced hepatoma cell lines (Hep-3B/LNC/IL-2, Hep-G2/LNC/IL-2) compared to those of the parent cell lines. The tumor was formed in 1 of 3 BALB/c mice and all 3 nude mice with the injection of 1x107 cells. Simultaneous injection of 1x10(7) cells of the parent cell line (Hep-3B) into the right flank and IL-2 transduced cell line (Hep-3B/LNC/IL-2) into the left flank of the three BALB/c mice and of 5x10(5) cells for the three nude mice resulted in a complete regression of the IL-2 modified tumor cell line (Hep-3B/LNC/IL-2) in 3 weeks and the parent cell line (Hep-3B) in 5 weeks. After injection of 1x10(7) cells into five other nude mice, the tumor of the IL-2 transduced hepatoma cells (Hep-3B/LNC/IL-2) gradually disappeared, however, the tumor of the parent hepatoma cell line initially decreased and then gradually regrew 20 days later. In conclusion, IL-2 transduced hepatoma cell lines secreting IL-2 became more sensitive to peripheral blood monocytes. IL-2 secretion by LNC/IL-2 retrovirus from the hepatoma cell lines was more prominent compared with that by N2A/IL-2 retrovirus. IL-2 transduction into the hepatoma cells resulted in increased antigenicity to the tumors formed by IL-2 transduced hepatoma cell line and parent cell line, which leads the regression of the tumors. However, the higher the tumor burden, the less efficient tumor regression by IL-2 transduction into the hepatoma cell line in nude mice was observed.

摘要

使用细胞因子基因转导的基因疗法旨在增强肿瘤细胞的抗原性,激活免疫效应细胞,从而诱导肿瘤消退。关于对外周血单核细胞的体外敏感性和体内致瘤活性,我们使用N2A/IL-2和LNC/IL-2逆转录病毒比较了亲本肝癌细胞系和白细胞介素-2(IL-2)转导的肝癌细胞系之间的差异。用N2A/IL-2逆转录病毒载体时,SK-Hep1细胞系中IL-2分泌量为186 pg/10⁶细胞/24小时,Hep-3B细胞系中为147 pg/10⁶细胞/24小时;用LNC/IL-2逆转录病毒载体时,Hep-3B细胞系中IL-2分泌量为55,000 pg/10⁶细胞/24小时。与亲本细胞系相比,IL-2转导的肝癌细胞系(Hep-3B/LNC/IL-2、Hep-G2/LNC/IL-2)对外周血单核细胞的体外敏感性提高了163.8 - 254%。注射1×10⁷个细胞后,3只BALB/c小鼠中有1只形成肿瘤,3只裸鼠均形成肿瘤。将亲本细胞系(Hep-3B)的1×10⁷个细胞同时注射到3只BALB/c小鼠的右侧腹,将IL-2转导细胞系(Hep-3B/LNC/IL-2)的1×10⁷个细胞注射到左侧腹,对于3只裸鼠则分别注射5×10⁵个细胞,结果IL-2修饰的肿瘤细胞系(Hep-3B/LNC/IL-2)在3周内完全消退,亲本细胞系(Hep-3B)在5周内完全消退。向另外5只裸鼠注射1×10⁷个细胞后,IL-2转导的肝癌细胞(Hep-3B/LNC/IL-2)的肿瘤逐渐消失,然而,亲本肝癌细胞系的肿瘤最初减小,20天后又逐渐重新生长。总之,分泌IL-2的IL-2转导肝癌细胞系对外周血单核细胞变得更敏感。与N2A/IL-2逆转录病毒相比,LNC/IL-2逆转录病毒从肝癌细胞系分泌IL-2更显著。将IL-2转导到肝癌细胞中导致由IL-2转导的肝癌细胞系和亲本细胞系形成的肿瘤的抗原性增加,从而导致肿瘤消退。然而,在裸鼠中观察到,肿瘤负荷越高,通过将IL-2转导到肝癌细胞系中实现肿瘤消退的效率越低。

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