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The location of invasion-related protein MIC3 of Toxoplasma gondii and protective effect of its DNA vaccine in mice

机译:弓形虫侵袭相关蛋白MIC3的定位及其DNA疫苗对小鼠的保护作用

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摘要

The micronemal protein MIC3 of Toxoplasma gondii plays a predominant role in the early phase of the invasion process. In this research, the expression and location of protein MIC3 and fusion protein EGFP-MIC3 were observed in host cells and in T. gondii respectively. Protective experiments of DNA vaccine pcDNA3-MIC3 (pMIC3i) in animals showed that the vaccine could significantly prolong the survival time of the mice challenged by virulent RH strains of T. gondii. All mice vaccinated with plasmid pcDNA3-MIC3 have been elicited specific humoral immunity and cellular immunity. The cellular immune response was associated with the increase of the CD4 and CD8 T lymphocytes and the decrease of the CD4/CD8 T lymphocyte ratio evidently. It indicated that the mic3 DNA vaccine could stimulate the host resisting Toxoplasma mainly by the way of CD8CTL cells. In conclusion, a potent DNA vaccine pcDNA3-MIC3 could elicit a strong specific immune response and induce effective protection against T. gondii challenge in Kunming mice, suggesting that mic3 is a potential vaccine candidate against toxoplasmosis.
机译:弓形虫的微Nemal蛋白MIC3在入侵过程的早期起主要作用。在这项研究中,分别在宿主细胞和弓形虫中观察到了蛋白MIC3和融合蛋白EGFP-MIC3的表达和定位。 DNA疫苗pcDNA3-MIC3(pMIC3i)在动物中的保护性实验表明,该疫苗可以显着延长被弓形虫RH毒株攻击的小鼠的存活时间。接种了质粒pcDNA3-MIC3的所有小鼠均被诱导产生特定的体液免疫和细胞免疫。细胞免疫应答与CD4和CD8 T淋巴细胞的增加以及CD4 / CD8 T淋巴细胞的比率的降低明显相关。说明mic3 DNA疫苗主要通过CD8CTL细胞刺激宿主抗弓形虫。总之,有效的DNA疫苗pcDNA3-MIC3可以引起强烈的特异性免疫反应,并在昆明小鼠中诱导针对弓形虫攻击的有效保护,这表明mic3是抗弓形虫病的潜在候选疫苗。

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