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首页> 外文期刊>Journal of Immune Based Therapies Vaccines >Prior exposure to an attenuated Listeria vaccine does not reduce immunogenicity: pre-clinical assessment of the efficacy of a Listeria vaccine in the induction of immune responses against HIV
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Prior exposure to an attenuated Listeria vaccine does not reduce immunogenicity: pre-clinical assessment of the efficacy of a Listeria vaccine in the induction of immune responses against HIV

机译:事先接触减毒李斯特菌疫苗不会降低免疫原性:对李斯特菌疫苗在诱导针对HIV的免疫反应中的功效的临床前评估

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Background We have evaluated an attenuated Listeria monocytogenes (Lm) candidate vaccine vector in nonhuman primates using a delivery regimen relying solely on oral vaccination. We sought to determine the impact of prior Lm vector exposure on the development of new immune responses against HIV antigens. Findings Two groups of rhesus macaques one Lm naive, the other having documented prior Lm vector exposures, were evaluated in response to oral inoculations of the same vector expressing recombinant HIV-1 Gag protein. The efficacy of the Lm vector was determined by ELISA to assess the generation of anti-Listerial antibodies; cellular responses were measured by HIV-Gag specific ELISpot assay. Our results show that prior Lm exposures did not diminish the generation of de novo cellular responses against HIV, as compared to Listeria-na?ve monkeys. Moreover, empty vector exposures did not elicit potent antibody responses, consistent with the intracellular nature of Lm. Conclusions The present study demonstrates in a pre-clinical vaccine model, that prior oral immunization with an empty Lm vector does not diminish immunogenicity to Lm-expressed HIV genes. This work underscores the need for the continued development of attenuated Lm as an orally deliverable vaccine.
机译:背景技术我们已经评估了仅依靠口服疫苗接种的非人灵长类动物减毒李斯特菌候选疫苗载体。我们试图确定以前的Lm载体暴露对针对HIV抗原的新免疫反应发展的影响。研究结果评估了两只恒河猴,一组是幼稚的天真猕猴,另一组已经记录了先前的Lm载体暴露,是对表达重组HIV-1 Gag蛋白的同一载体的口服接种做出的反应。通过ELISA确定Lm载体的功效,以评估抗李斯特菌抗体的产生。通过HIV-Gag特异性ELISpot测定法测量细胞应答。我们的结果表明,与初生李斯特菌的猴子相比,以前暴露于Lm不会减少针对HIV的新生细胞反应的产生。而且,与Lm的细胞内性质一致,空载体暴露没有引起有效的抗体反应。结论本研究在临床前疫苗模型中证明,事先用空Lm载体口服免疫不会减弱对Lm表达的HIV基因的免疫原性。这项工作强调了继续开发减毒Lm作为口服可传播疫苗的必要性。

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