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首页> 外文期刊>Vaccine >Vaccine generated immunity targets an HPV16 E7 HLA-A2.1-restricted CD8(+) T cell epitope relocated to an early gene or a late gene of the cottontail rabbit papillomavirus (CRPV) genome in HLA-A2.1 transgenic rabbits
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Vaccine generated immunity targets an HPV16 E7 HLA-A2.1-restricted CD8(+) T cell epitope relocated to an early gene or a late gene of the cottontail rabbit papillomavirus (CRPV) genome in HLA-A2.1 transgenic rabbits

机译:疫苗产生的免疫力靶向HPV16 E7 HLA-A2.1限制性CD8(+)T细胞表位,其重定位到HLA-A2.1转基因兔中棉尾兔乳头瘤病毒(CRPV)基因组的早期基因或晚期基因

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摘要

The newly established HLA-A2.1 transgenic rabbit model has proven useful for testing the immunogenicity of well known and computer-predicted A2-restricted epitopes. In the current study we compared the protective immunity induced to a preferred HPV16 E7 A2-restricted epitope that has been relocated to positions within the CRPV E7 gene and the CRPV L2 gene. Epitope expression from both the E7 protein and the L2 protein resulted in increased protection against viral DNA challenge of the HLA-A2.1 transgenic rabbits as compared to control-vaccinated rabbit groups. These data indicate that proteins expressed at both early and late time points during a natural papillomavirus infection can be targeted by epitope-specific immunity and indicate this immunity is increased to early rather than late expressed proteins of papillomaviruses. This study also highlights the broad utility of the HLAA2.1 transgenic rabbit model for testing numerous immunological factors involved in vaccine generated protective immunity
机译:新建立的HLA-A2.1转基因兔模型已被证明可用于测试众所周知的和计算机预测的A2限制性表位的免疫原性。在当前的研究中,我们比较了诱导的保护性免疫与首选的HPV16 E7 A2限制性表位,该表位已重定位到CRPV E7基因和CRPV L2基因内。与对照疫苗接种的兔组相比,E7蛋白和L2蛋白的表位表达均导致针对HLA-A2.1转基因兔的病毒DNA攻击的保护作用增强。这些数据表明,在天然乳头瘤病毒感染过程中在早期和晚期时间点表达的蛋白都可以被表位特异性免疫所靶向,并且表明这种免疫力增强了乳头瘤病毒的早期而非晚期表达蛋白。这项研究还强调了HLAA2.1转基因兔模型在测试与疫苗产生的保护性免疫有关的众多免疫因素中的广泛用途

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