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Ebola-GP DNA Prime rAd5-GP Boost: Influence of Prime Frequency and Prime/Boost Time Interval on the Immune Response in Non-human Primates

机译:埃博拉-GP DNA Prime Rad5-GP提升:主要频率和素质/升压时间间隔对非人类灵长类动物的免疫应答的影响

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摘要

Heterologous prime-boost immunization regimens are a common strategy for many vaccines. DNA prime rAd5-GP boost immunization has been demonstrated to protect non-human primates against a lethal challenge of Ebola virus, a pathogen that causes fatal hemorrhagic disease in humans. This protection correlates with antibody responses and is also associated with IFNγ+ TNFα+ double positive CD8+ T-cells. In this study, we compared single DNA vs. multiple DNA prime immunizations, and short vs. long time intervals between the DNA prime and the rAd5 boost to evaluate the impact of these different prime-boost strategies on vaccine-induced humoral and cellular responses in non-human primates. We demonstrated that DNA/rAd5 prime-boost strategies can be tailored to induce either CD4+ T-cell or CD8+ T-cell dominant responses while maintaining a high magnitude antibody response. Additionally, a single DNA prime immunization generated a stable memory response that could be boosted by rAd5 3 years later. These results suggest DNA/rAd5 prime-boost provides a flexible platform that can be fine-tuned to generate desirable T-cell memory responses.
机译:异源素促升免疫方案是许多疫苗的常见策略。已经证明了DNA Prime Rad5-GP增强免疫免疫免疫,以保护非人的灵长类动物免受埃博拉病毒的致命挑战,这是一种导致人类致命出血疾病的病原体。该保护与抗体​​应答相关,也与IFNγ+TNFα+双阳性CD8 + T细胞相关。在这项研究中,我们比较了单一DNA与多个DNA Prime免疫,并且DNA Prime和RAD5之间的长时间间隔进行评估,以评估这些不同素质促进策略对疫苗诱导的体液和细胞反应的影响非人类灵长类动物。我们证明,DNA / RAD5 Prime-Boost策略可以定制以诱导CD4 + T细胞或CD8 + T细胞的显性反应,同时保持高幅度抗体应答。另外,单个DNA主要免疫产生稳定的存储器响应,该稳定存储器响应可以在3年后由RAD5升高。这些结果表明DNA / RAD5 Prime-Boost提供了一种灵活的平台,可以进行微调以产生所需的T细胞存储器响应。

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