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用红内期和红前期的啮齿动物疟原虫活全生物体免疫产生的免疫的物种特异性及其对疫苗开发的影响。

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.

机构信息

Department of Protozoology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Sakamoto, Nagasaki, Japan.

出版信息

Int J Parasitol. 2012 Aug;42(9):859-70. doi: 10.1016/j.ijpara.2012.07.001. Epub 2012 Jul 28.

Abstract

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.

摘要

一种有前景的疟疾疫苗开发策略涉及使用减毒全寄生虫,因为这些寄生虫比亚单位疫苗向免疫系统呈现出更大的抗原谱。疟原虫生命周期的复杂性为基于减毒全生物体疫苗提供了多个阶段。在设计和使用此类疫苗时,需要考虑到对人类具有感染力的寄生虫的多样性。最有价值的疫苗将是对多种疟原虫/株有效。在这里,我们比较了使用活寄生虫和抗疟药物减毒进行红细胞前和红细胞期全生物体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,以及针对一个阶段的免疫可能被同源和异源寄生虫的其他阶段暴露所消除的可能性。使用啮齿动物疟原虫 Plasmodium yoelii yoelii 和 Plasmodium vinckei lentum 来解决这些问题,因为它们在感染啮齿动物的疟原虫亚种之间提供了最大可能的遗传距离。结果发现,活减毒寄生虫疫苗接种产生的红细胞期和红细胞前期免疫都具有物种特异性成分,红细胞前期免疫提供了更广泛的泛物种保护。我们表明,在用氯喹处理的同时接种孢子后获得的保护几乎完全依赖于 CD8(+) T 细胞。还提出了红细胞期和红细胞前期疫苗接种之间的跨阶段保护证据。最后,结果表明,对于这些物种,在用红细胞前期阶段免疫接种后,同源或异源物种的红细胞期感染不会消除这种免疫。这是首次使用相同的寄生虫物种对红细胞期和红细胞前期全生物体疫苗接种策略的特异性和功效进行直接比较。

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