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Antitumor immunopreventive effect in mice induced by DNA vaccine encoding a fusion protein of α-fetoprotein and CTLA4

机译:编码α-甲胎蛋白和CTLA4融合蛋白的DNA疫苗诱导的小鼠抗肿瘤免疫预防作用

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摘要

AIM: To develop a tumor DNA vaccine encoding a fusion protein of murine AFP and CTLA4, and to study its ability to induce specific CTL response and its protective effect against AFP-producing tumor. METHODS: Murine α-fetoprotein (mAFP) gene was cloned from total RNA of Hepa1-6 cells by RT-PCR. A DNA vaccine was constructed by fusion murine α-fetoprotein gene and extramembrane domain of murine CTLA4 gene. The DNA vaccine was identified by restriction enzyme analysis, sequencing and expression. EL-4 (mAFP) was developed by stable transfection of EL-4 cells with pmAFP. The frequency of cells producing IFN-γ in splenocytes harvested from the immunized mice was measured by ELISPOT. Mice immunized with DNA vaccine were inoculated with EL-4 (mAFP) cells in back to observe the protective effect of immunization on tumor. On the other hand, blood samples were collected from the immunized mice to check the functions of liver and kidney. RESULTS: 1.8 kb mAFP cDNA was cloned from total RNA of Hepal-6 cells by RT-PCR. The DNA vaccine encoding a fusion protein of mAFP-CTLA4 was constructed and confirmed by restriction enzyme analysis, sequencing and expression. The expression of mAFP mRNA in EL-4 (mAFP) was confirmed by RT-PCR. The ELISPOT results showed that the number of IFN-γ-producing cells in pmAFP-CTLA4 group was significantly higher than that in pmAFP, pcDNA3.1 and PBS group. The tumor volume in pmAFP-CTLA4 group was significantly smaller than that in pmAFP, pcDNA3.1 and PBS group, respectively. The hepatic and kidney functions in each group were not altered. CONCLUSION: AFP-CTLA4 DNA vaccine can stimulate potent specific CTL responses and has distinctive antitumor effect on AFP-producing tumor. The vaccine has no impact on the function of mouse liver and kidney.
机译:目的:开发一种编码鼠AFP和CTLA4融合蛋白的肿瘤DNA疫苗,并研究其诱导特异性CTL反应的能力及其对产生AFP的肿瘤的保护作用。方法:通过RT-PCR从Hepa1-6细胞总RNA中克隆出鼠α甲胎蛋白(mAFP)基因。通过融合鼠类α-甲胎蛋白基因和鼠类CTLA4基因的膜外结构域构建DNA疫苗。通过限制酶分析,测序和表达鉴定了DNA疫苗。 EL-4(mAFP)是通过用pmAFP稳定转染EL-4细胞而开发的。通过ELISPOT测量从免疫小鼠收获的脾细胞中产生IFN-γ的细胞的频率。将DNA疫苗免疫的小鼠背部接种EL-4(mAFP)细胞,观察免疫对肿瘤的保护作用。另一方面,从经免疫的小鼠收集血液样品以检查肝和肾的功能。结果:通过RT-PCR从Hepal-6细胞总RNA中克隆出1.8 kb mAFP cDNA。构建了编码mAFP-CTLA4融合蛋白的DNA疫苗,并通过限制酶分析,测序和表达进行了证实。 RT-PCR证实了mAFP在EL-4(mAFP)中的表达。 ELISPOT结果表明,pmAFP-CTLA4组的产生IFN-γ的细胞数量明显高于pmAFP,pcDNA3.1和PBS组。 pmAFP-CTLA4组的肿瘤体积分别明显小于pmAFP,pcDNA3.1和PBS组。每组的肝肾功能均未改变。结论:AFP-CTLA4 DNA疫苗可以刺激强效的特异性CTL反应,对产生AFP的肿瘤具有独特的抗肿瘤作用。该疫苗对小鼠肝脏和肾脏的功能没有影响。

著录项

  • 来源
    《World Journal of Gastroenterology》 |2004年第2期|p.200-204|共5页
  • 作者

    Geng Tian; Ji-Lin Yi; Ping Xiong;

  • 作者单位

    Departmentof General Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, Hubei Province, China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 消化系及腹部疾病;
  • 关键词

  • 入库时间 2022-08-17 23:37:36

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