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Mucosal and systemic antibody responses and protection induced by a prime/boost rotavirus-DNA vaccine in a gnotobiotic pig model

机译:初生/加强型轮状病毒-DNA疫苗在致生猪模型中引起的粘膜和全身抗体反应和保护

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A live rotavirus prime/DNA boost vaccine regimen was evaluated in a gnotobiotic pig model for human rotavirus (HRV) diarrhea. Plasmid DNA expressing rotavirus inner capsid VP6 was administered to pigs intramuscularly (IM) twice after oral priming with attenuated (Att) Wa strain HRV (AttHRV/VP6DNA2x). Other groups included: (1) VP6 DNA IM 2x then AttHRV orally (VP6DNA2x/AttHRV); (2) VP6 DNA IM 3x (VP6DNA3x) and controls. Significant protection (70%) against virus shedding, but lower protection against diarrhea (30%) was achieved only in the AttHRV/VP6DNA2x group after challenge (virulent Wa HRV). The other vaccines (VP6DNA2x/AttHRV and VP6DNA3x) were less effective. Higher protection rates were associated with the highest IgA antibody responses induced by the AttHRV/VP6DNA2x regimen. Interestingly, the VP6 DNA vaccine, although not effective when administered alone, boosted neutralizing and VP4 antibody titers in pigs previously primed with AttHRV, possibly mediated by cross-reactive T helper cells.
机译:在人类轮状病毒(HRV)腹泻的致病性猪模型中评估了活的轮状病毒初免/ DNA加强疫苗接种方案。用减毒(Att)Wa株HRV(AttHRV / VP6DNA2x)口服引发后,对猪进行两次肌肉注射(IM)表达轮状病毒内衣壳VP6的​​质粒DNA。其他组包括:(1)VP6 DNA IM 2x,然后口服AttHRV(VP6DNA2x / AttHRV); (2)VP6 DNA IM 3x(VP6DNA3x)和对照。仅在攻击后(毒性Wa HRV),才在AttHRV / VP6DNA2x组中获得了针对病毒脱落的显着保护(70%),但对腹泻的保护性较低(30%)。其他疫苗(VP6DNA2x / AttHRV和VP6DNA3x)效果较差。较高的保护率与AttHRV / VP6DNA2x方案诱导的最高IgA抗体反应相关。有趣的是,尽管单独使用VP6 DNA疫苗无效,但可以提高先前用AttHRV引发的猪的中和和VP4抗体效价,这可能是由交叉反应性T辅助细胞介导的。

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