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Combination of nanoparticle-based therapeutic vaccination and transient ablation of regulatory T cells enhances anti-viral immunity during chronic retroviral infection

机译:纳米颗粒治疗性疫苗和调节性T细胞的短暂消融相结合可增强慢性逆转录病毒感染过程中的抗病毒免疫力

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摘要

BackgroundRegulatory T cells (Tregs) have been shown to limit anti-viral immunity during chronic retroviral infection and to restrict vaccine-induced T cell responses. The objective of the study was to assess whether a combinational therapy of nanoparticle-based therapeutic vaccination and concomitant transient ablation of Tregs augments anti-viral immunity and improves virus control in chronically retrovirus-infected mice. Therefore, chronically Friend retrovirus (FV)-infected mice were immunized with calcium phosphate (CaP) nanoparticles functionalized with TLR9 ligand CpG and CD8+ or CD4+ T cell epitope peptides (GagL85–93 or Env gp70123–141) of FV. In addition, Tregs were ablated during the immunization process. Reactivation of CD4+ and CD8+ effector T cells was analysed and the viral loads were determined.
机译:背景技术调节性T细胞(Tregs)已显示出在慢性逆转录病毒感染期间限制抗病毒免疫力并限制疫苗诱导的T细胞应答。这项研究的目的是评估基于纳米颗粒的治疗性疫苗和Tregs的短暂消融的联合治疗是否能增强抗病毒免疫力并改善慢性逆转录病毒感染小鼠的病毒控制。因此,用经TLR9配体CpG和CD8 + 或CD4 + T细胞表位肽功能化的磷酸钙(CaP)纳米颗粒免疫慢性Friend逆转录病毒(FV)感染的小鼠( FV的GagL85–93或Env gp70123–141)。另外,在免疫过程中Treg被消融。分析了CD4 + 和CD8 + 效应T细胞的活化,并确定了病毒载量。

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