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Vaccination against hepatitis C virus with dendritic cells transduced with an adenovirus encoding NS3 protein

机译:用编码NS3蛋白的腺病毒转导的树突状细胞对丙型肝炎病毒进行疫苗接种

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摘要

Chronic infection by hepatitis C virus (HCV) is characterized by the absence of efficient antiviral T-cell responses. Thus, vaccination strategies to induce strong anti-HCV T-cell responses are of paramount importance for prophylactic and therapeutic purposes. Dendritic cells (DCs) are the most potent antigen presenting cells; therefore, immunization with these cells loaded with viral antigens offers a new approach for induction of antiviral immunity. Here we show that immunization with DCs transfected with an adenovirus encoding non-structural 3 protein, from HCV (AdNS3), induced multiepitopic CD4 T helper cell 1 (Th1) and CD8 T-cell responses in different mouse strains. These responses prevented the growth of a tumorexpressing HCV proteins, in short- and long-term experiments. Moreover, immunization with AdNS3-transfected DCs did not induce anti-adenoviral antibodies, as compared to direct immunization with AdNS3, but elicited T-cell responses even in the presence of pre-existing anti-adenoviral antibodies. Finally, responses induced by this protocol down-regulated the expression of HCV RNA in the liver. In conclusion, DCs transfected with AdNS3 may prove to be an efficient anti-HCV vaccine.
机译:丙型肝炎病毒(HCV)的慢性感染的特征是缺乏有效的抗病毒T细胞反应。因此,对于预防和治疗目的,诱导强烈的抗HCV T细胞应答的疫苗接种策略至关重要。树突状细胞(DC)是最有效的抗原呈递细胞。因此,用载有病毒抗原的这些细胞进行免疫提供了一种诱导抗病毒免疫的新方法。在这里,我们显示了用编码来自HCV(AdNS3)的编码非结构性3蛋白的腺病毒转染的DC进行的免疫诱导了不同小鼠品系中的多表位CD4 T辅助细胞1(Th1)和CD8 T细胞应答。在短期和长期实验中,这些反应阻止了表达肿瘤的HCV蛋白的生长。此外,与用AdNS3直接免疫相比,用AdNS3转染的DC免疫不会诱导抗腺病毒抗体,但即使在已有抗腺病毒抗体存在的情况下,也会引起T细胞反应。最后,由该方案引起的应答下调了肝脏中HCV RNA的表达。总之,用AdNS3转染的DC可能被证明是一种有效的抗HCV疫苗。

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