先前暴露于减毒李斯特菌疫苗不会降低免疫原性:李斯特菌疫苗在诱导针对艾滋病毒的免疫反应方面的功效的临床前评估。

James B Whitney, Saied Mirshahidi, So-Yon Lim, Lauren Goins, Chris C Ibegbu, Daniel C Anderson, Richard B Raybourne, Fred R Frankel, Judy Lieberman, Ruth M Ruprecht
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引用次数: 11

摘要

背景:我们在非人类灵长类动物中评估了一种减毒单核增生李斯特菌(Lm)候选疫苗载体,其递送方案仅依赖于口服疫苗接种。我们试图确定先前的Lm载体暴露对针对HIV抗原的新免疫反应的发展的影响。研究结果:两组恒河猴,一组是Lm新手,另一组有记录的Lm载体暴露,对口服接种表达重组HIV-1 Gag蛋白的同一载体的反应进行了评估。ELISA法检测Lm载体对抗李斯特菌抗体产生的影响;采用HIV-Gag特异性ELISpot法检测细胞反应。我们的研究结果表明,与Listeria-naïve猴子相比,先前的Lm暴露并没有减少对HIV的新生细胞反应的产生。此外,空载体暴露并没有引起有效的抗体反应,这与Lm的细胞内性质一致。结论:本研究在临床前疫苗模型中证明,事先用空的Lm载体口服免疫不会降低对Lm表达的HIV基因的免疫原性。这项工作强调了继续开发作为口服疫苗的减毒Lm的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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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.

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-naïve 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.

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