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以H22自体肿瘤作为全肿瘤细胞疫苗诱导特异性免疫治疗的实验研究

Experimental study of specific immunotherapy induced by H22 autologous tumor as whole tumor cell vaccine.

作者信息

Yang Wei, Guo Cheng, Liu Qing-guang, Pan Chengen

机构信息

Hepatobiliary Department, First Hospital, Xi'an Jiaotong University, Xi'an, PR China.

出版信息

Biomed Pharmacother. 2009 Jul;63(6):404-8. doi: 10.1016/j.biopha.2008.08.020. Epub 2008 Sep 18.

DOI:10.1016/j.biopha.2008.08.020
PMID:18849136
Abstract

This study explores the novel H22 whole-cell vaccine of active specific immunotherapy in the treatment of hepatocellular carcinoma. H22 hepatoma tumor vaccine modified by human interleukin-2 (hIL-2) and mouse granulocyte-monocyte colony-stimulating factor (mGM-CSF) fusion gene was prepared to study its specific anti-tumor immunity. Mice were inoculated by these vaccines. Then tumor cells were injected into mouse models. The (51)Cr release assay was used to examine the cytotoxicities of the splenocytes to H22 hepatoma cells in immunized mice, tumor-bearing mice and control mice. The blood was needed to test the level of IL-10 and interferon (IFN)-gamma in serum. Survival time of mice was calculated. Specific cytotoxicity rate of splenocytes from the immunized mice to H22 cancer cell was 38%, significantly higher than 13.6% in the tumor-bearing group, 7.5% in the control group, and 9.1% in S180 cells (p<0.05). Serum IFN-gamma in the immunized group was significantly increased compared with other groups (p<0.01), and serum IL-10 in the immunized group was significantly decreased compared with other groups (p<0.01). The survival time of the transgenic vaccinated group was significantly longer.

摘要

本研究探讨新型H22全细胞疫苗主动特异性免疫疗法治疗肝细胞癌的效果。制备了经人白细胞介素-2(hIL-2)和小鼠粒细胞-巨噬细胞集落刺激因子(mGM-CSF)融合基因修饰的H22肝癌肿瘤疫苗,以研究其特异性抗肿瘤免疫。用这些疫苗接种小鼠。然后将肿瘤细胞注入小鼠模型。采用(51)Cr释放试验检测免疫小鼠、荷瘤小鼠和对照小鼠脾细胞对H22肝癌细胞的细胞毒性。采集血液检测血清中IL-10和干扰素(IFN)-γ水平。计算小鼠存活时间。免疫小鼠脾细胞对H22癌细胞的特异性细胞毒性率为38%,显著高于荷瘤组的13.6%、对照组的7.5%和S180细胞组的9.1%(p<0.05)。免疫组血清IFN-γ水平与其他组相比显著升高(p<0.01),免疫组血清IL-10水平与其他组相比显著降低(p<0.01)。转基因疫苗接种组的存活时间显著延长。

相似文献

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Experimental study of specific immunotherapy induced by H22 autologous tumor as whole tumor cell vaccine.以H22自体肿瘤作为全肿瘤细胞疫苗诱导特异性免疫治疗的实验研究
Biomed Pharmacother. 2009 Jul;63(6):404-8. doi: 10.1016/j.biopha.2008.08.020. Epub 2008 Sep 18.
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[Application of a tumor cell vaccine transfected with GM-CSF/IL-2 fusion gene for specific immunotherapy of hepatocellular carcinoma].GM-CSF/IL-2融合基因转染的肿瘤细胞疫苗在肝癌特异性免疫治疗中的应用
Nan Fang Yi Ke Da Xue Xue Bao. 2008 Feb;28(2):188-92.
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[Application of fusion gene mGM-CSF/hIL-2 to specific immunotherapy induced by hepatic tumor cell vaccine].融合基因mGM-CSF/hIL-2在肝癌细胞疫苗诱导的特异性免疫治疗中的应用
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[Construction of a DNA vaccine against extracellular domain 1-3 of Flk1 and its inhibitory effect on growth of liver cancer cell line H22].[抗Flk1胞外结构域1-3的DNA疫苗构建及其对肝癌细胞系H22生长的抑制作用]
Ai Zheng. 2004 Dec;23(12):1616-21.

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ACS Nano. 2019 Jun 25;13(6):6477-6490. doi: 10.1021/acsnano.8b09613. Epub 2019 May 17.
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The tumor protection effect of high-frequency administration of whole tumor cell vaccine and enhanced efficacy by the protein component from Agrocybe aegerita.高频接种全肿瘤细胞疫苗的肿瘤保护作用及杨树菇蛋白成分增强疗效的作用
Int J Clin Exp Med. 2015 May 15;8(5):6914-25. eCollection 2015.
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New progress of non-surgical treatments for hepatocellular carcinoma.
肝细胞癌非手术治疗的新进展。
Med Oncol. 2013 Mar;30(1):381. doi: 10.1007/s12032-012-0381-y. Epub 2013 Jan 6.
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ProtEx technology for the generation of novel therapeutic cancer vaccines.用于生成新型治疗性癌症疫苗的ProtEx技术。
Exp Mol Pathol. 2009 Jun;86(3):198-207. doi: 10.1016/j.yexmp.2009.01.010. Epub 2009 Jan 31.