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Enhancement of CD4 and CD8 immunity by anti-CD137 (4-1BB) monoclonal antibodies during hepatitis C vaccination with recombinant adenovirus

机译:在重组腺病毒丙型肝炎疫苗接种过程中,抗CD137(4-1BB)单克隆抗体增强了CD4和CD8免疫

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摘要

The induction of protective or therapeutic cellular immunity against hepatitis C virus (HCV) is a difficult goal. In a previous work we showed that immunization with a recombinant adenovirus encoding HCV-NS3 (RAdNS3) could partially protect mice from challenge with a vaccinia virus encoding HCV antigens. We sought to investigate whether systemic administration of an immunostimulatory monoclonal antibody directed against the lymphocyte surface molecule CD137 could enhance the immunity elicited by RAdNS3. It was found that treatment with anti-CD137 mAb after the administration of a suboptimal dose of RAdNS3 enhanced cytotoxic and T helper cell responses against HCV NS3. Importantly, the ability of RAdNS3 to induce protective immunity against challenge with a recombinant vaccinia virus expressing HCV proteins was markedly augmented. Thus, combination of immunostimulatory anti-CD137 mAb with recombinant adenoviruses expressing HCV proteins might be useful in strategies of immunization against HCV.
机译:诱导针对丙型肝炎病毒(HCV)的保护性或治疗性细胞免疫是一个困难的目标。在以前的工作中,我们表明,用编码HCV-NS3的重组腺病毒(RAdNS3)进行免疫可以部分保护小鼠免受编码HCV抗原的牛痘病毒的攻击。我们寻求研究全身施用针对淋巴细胞表面分子CD137的免疫刺激性单克隆抗体是否可以增强RAdNS3引发的免疫力。发现在给予次最佳剂量的RAdNS3后用抗CD137mAb治疗增强了针对HCV NS3的细胞毒性和T辅助细胞应答。重要的是,RAdNS3诱导针对表达HCV蛋白的重组牛痘病毒的攻击产生保护性免疫的能力显着增强。因此,免疫刺激性抗CD137 mAb与表达HCV蛋白的重组腺病毒的结合可能在针对HCV的免疫策略中有用。

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