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增强型 Toxoplasma gondii 致密颗粒抗原 7(GRA7)对小鼠弓形虫病的保护性免疫应答:一种初免-加强型免疫接种策略。

Enhancement of protective immune responses induced by Toxoplasma gondii dense granule antigen 7 (GRA7) against toxoplasmosis in mice using a prime-boost vaccination strategy.

机构信息

Department of Parasitology, Shandong University School of Medicine, Jinan, Shandong 250012, PR China.

出版信息

Vaccine. 2012 Aug 17;30(38):5631-6. doi: 10.1016/j.vaccine.2012.06.081. Epub 2012 Jul 10.

Abstract

Effective vaccines against Toxoplasma gondii may contribute to preventing and controlling the spread of toxoplasmosis, which is important for improving outcomes of infections in humans and livestock animals. The dense granule antigen 7 (GRA7) of T. gondii might be an immunodominant antigen for a vaccine candidate. In the present study, a further exploration of its vaccine effect, a heterologous prime-boost vaccination strategy with a recombinant eukaryotic plasmid pEGFP-GRA7 and a recombinant protein GRA7 expressed from a prokaryotic plasmid pET30-GRA7, was performed in BALB/c mice. The data reveal that a DNA prime-protein boost vaccination induces both humoral and cellular immune responses against T. gondii associated with high levels of total IgG, IgG2a isotype and gamma interferon (IFN-γ). Challenge experiments further show that the DNA prime-protein boost vaccination significantly increases survival rate (60%), compared with controls in which all died within 8 days of challenge. Therefore, the DNA prime-protein boost vaccination based on GRA7 might be a promising regimen for further development of an effective vaccine against T. gondii.

摘要

有效的弓形虫疫苗可能有助于预防和控制弓形虫病的传播,这对于改善人类和家畜感染的结果非常重要。弓形虫致密颗粒抗原 7(GRA7)可能是疫苗候选物的免疫优势抗原。在本研究中,我们进一步探索了其疫苗效果,使用重组真核质粒 pEGFP-GRA7 和源自原核质粒 pET30-GRA7 的重组蛋白 GRA7 进行了异源初免-加强免疫接种策略,在 BALB/c 小鼠中进行了实验。数据显示,DNA 初免-蛋白加强免疫接种诱导了针对弓形虫的体液和细胞免疫反应,与高水平的总 IgG、IgG2a 同种型和γ干扰素(IFN-γ)相关。攻毒实验进一步表明,DNA 初免-蛋白加强免疫接种可使存活率(60%)显著提高,而对照组在攻毒后 8 天内全部死亡。因此,基于 GRA7 的 DNA 初免-蛋白加强免疫接种可能是开发有效弓形虫疫苗的有前途的方案。

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