首页> 美国卫生研究院文献>The Korean Journal of Parasitology >Evaluation of Protective Immune Response Induced by a DNA Vaccine Encoding GRA8 against Acute Toxoplasmosis in a Murine Model
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Evaluation of Protective Immune Response Induced by a DNA Vaccine Encoding GRA8 against Acute Toxoplasmosis in a Murine Model

机译:小鼠模型中编码GRA8的DNA疫苗对急性弓形虫病引起的保护性免疫应答的评估。

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摘要

Toxoplasma gondii is an apicomplexan zoonotic protozoan parasite that infects most species of warm-blooded animals, including humans. The heavy incidence and severe or lethal damage caused by T. gondii infection clearly indicate a need for the development of an effective vaccine. T. gondii GRA8 is a member of the dense granules protein family and is used as a marker of acute infection. In the present study, we evaluated the protective immunity induced by DNA vaccination based on a recombinant eukaryotic plasmid, pDsRed2-GRA8, against acute toxoplasmosis in mice. BALB/c mice were intramuscularly immunized with the pDsRed2-GRA8 plasmid and then challenged by infection with the highly virulent GFP-RH strain of T. gondii. The specific immune responses and protective efficacy against T. gondii of this vaccine were analyzed by measuring cytokine and serum antibody titers, splenocyte proliferation assays, and the survival times of mice after challenge. Our results showed that mice immunized with pDsRed2-GRA8 demonstrated specific humoral and cellular responses, induced higher IgG antibody titers with predominant IgG2a production; increased levels of IL-10, IL-12 (p70), IFN-γ, TNF-α, and splenocyte proliferation; and prolonged survival times compared to those of control mice. The present study showed that DNA immunization with pDsRed2-GRA8 induced humoral and cellular immune responses, and all immunized mice showed greater Th1-type immune responses and longer survival times than those of control mice. These results indicated that T. gondii GRA8 DNA immunization induces a partial protective effect against acute toxoplasmosis.
机译:弓形虫是一种被感染的原生动物寄生虫,感染了大多数温血动物,包括人类。由刚地弓形虫感染引起的高发病率和严重或致命的破坏清楚地表明需要开发有效的疫苗。弓形虫GRA8是致密颗粒蛋白家族的成员,被用作急性感染的标志物。在本研究中,我们评估了基于重组真核质粒pDsRed2-GRA8的DNA疫苗诱导的小鼠抗急性弓形虫病的保护性免疫。用pDsRed2-GRA8质粒对BALB / c小鼠进行肌肉免疫,然后用弓形虫的高毒力GFP-RH株感染以攻击。通过测量细胞因子和血清抗体滴度,脾细胞增殖测定以及攻击后小鼠的存活时间,分析了该疫苗对弓形虫的特异性免疫应答和保护功效。我们的结果表明,用pDsRed2-GRA8免疫的小鼠表现出特异性的体液和细胞反应,诱导了较高的IgG抗体滴度,并主要产生IgG2a。 IL-10,IL-12(p70),IFN-γ,TNF-α和脾细胞增殖水平升高;与对照组小鼠相比,存活时间更长。本研究表明,用pDsRed2-GRA8进行的DNA免疫诱导了体液和细胞免疫反应,并且与对照小鼠相比,所有免疫小鼠均显示出更大的Th1型免疫反应和更长的存活时间。这些结果表明,弓形虫GRA8 DNA免疫诱导了针对急性弓形虫病的部分保护作用。

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