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首页> 外文期刊>International Journal for Parasitology >The species specificity of immunity generated by live whole organism immunisation with erythrocytic and pre-erythrocytic stages of rodent malaria parasites and implications for vaccine development
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The species specificity of immunity generated by live whole organism immunisation with erythrocytic and pre-erythrocytic stages of rodent malaria parasites and implications for vaccine development

机译:在啮齿类疟原虫的促红细胞生成期和促红细胞生成前阶段进行全活体生物免疫所产生的免疫的物种特异性及其对疫苗开发的意义

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摘要

A promising strategy for the development of a malaria vaccine involves the use of attenuated whole parasites, as these present a greater repertoire of antigens to the immune system than subunit vaccines. The complexity of the malaria parasite's life cycle offers multiple stages on which to base an attenuated whole organism vaccine. An important consideration in the design and employment of such vaccines is the diversity of the parasites that are infective to humans. The most valuable vaccine would be one that was effective against multiple species/strains of malaria parasite. Here we compare the species specificity of pre-erythrocytic and erythrocytic whole organism vaccination using live parasites with anti-malarial drug attenuation. The cross-stage protection afforded by each vaccination strategy, and the possibility that immunity against one stage may be abrogated by exposure to other stages of both homologous and heterologous parasites was also assessed. The rodent malaria parasites Plasmodium yoelii yoelii and Plasmodium vinckei lentum are to address these questions, as they offer the widest possible genetic distance between sub-species of malaria parasites infectious to rodents. It was found that both erythrocytic and pre-erythrocytic stage immunity generated by live, attenuated parasite vaccination have species-specific components, with pre-erythrocytic stage immunity offering a much broader pan-species protection. We show that the protection achieved following sporozoite inoculation with concurrent mefloquine treatment is almost entirely dependent of CD8 + T-cells. Evidence is presented for cross-stage protection between erythrocytic and pre-erythrocytic stage vaccination. Finally, it is shown that, with these species, an erythrocytic stage infection of either a homologous or heterologous species following immunisation with pre-erythrocytic stages does not abrogate this immunity. This is the first direct comparison of the specificity and efficacy of erythrocytic and pre-erythrocytic stage whole organism vaccination strategies utilising the same parasite species pair.
机译:开发疟疾疫苗的一种有前途的策略涉及使用减毒的完整寄生虫,因为与亚单位疫苗相比,它们对免疫系统的抗原组成更大。疟疾寄生虫生命周期的复杂性为减毒的全生物疫苗提供了多个阶段。设计和使用此类疫苗的重要考虑因素是对人类具有感染力的寄生虫的多样性。最有价值的疫苗是对多种物种/株的疟原虫有效的疫苗。在这里,我们比较了使用抗疟疾药物减毒活寄生虫进行的红细胞前和红细胞全生物疫苗接种的物种特异性。还评估了每种疫苗接种策略提供的跨阶段保护,以及通过暴露于其他阶段的同源和异源寄生虫而可以消除针对某一阶段的免疫的可能性。啮齿动物疟原虫疟原虫yoelii yoelii和温氏疟原虫要解决这些问题,因为它们提供了对啮齿动物具有感染力的疟原虫亚种之间的最大遗传距离。已发现,通过活的,减毒的寄生虫疫苗接种产生的促红细胞生成前和促红细胞生成前阶段免疫均具有物种特异性成分,而促红细胞生成前阶段免疫提供了更为广泛的泛物种保护。我们显示,同时进行甲氧喹治疗后,子孢子接种后获得的保护几乎完全依赖于CD8 + T细胞。提出了在红细胞阶段和前红细胞阶段疫苗之间进行跨阶段保护的证据。最后,显示出对于这些物种,在用促红细胞前阶段免疫后,同源或异源物种的促红细胞阶段感染都不会消除这种免疫力。这是首次直接比较使用相同寄生物对的红细胞阶段和红细胞阶段前全生物疫苗接种策略的特异性和功效。

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