Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, UK.
J Immunol. 2010 Sep 1;185(5):2808-18. doi: 10.4049/jimmunol.1000844. Epub 2010 Aug 2.
We characterized vaccine-induced cellular responses to rabies virus in naive adult volunteers. Contrary to current paradigms, we observed potent and prolonged in vitro NK cell cytokine production and degranulation responses after restimulation of PBMCs with inactivated rabies virus in vaccinated, but not in unvaccinated, individuals. This "recall" NK cell response was absolutely dependent on Ag-specific IL-2 from CD45RO(+) CD4(+) T cells as well as IL-12 and IL-18 from accessory cells. Importantly, NK cells represented over 70% of all IFN-gamma-secreting and degranulating cells in the first 12-18 h after virus rechallenge indicating they may be required for rapid control of infection after vaccination. Activation of NK cells may be a critical function of IL-2-secreting effector memory T cells. Although IL-2-dependent postvaccination NK cell activation has been reported previously, this is the first time the magnitude of this effect and its contribution to the overall vaccine-induced response has been appreciated and the mechanisms of NK activation postvaccination have been elucidated. Our data will allow standard protocols for evaluating vaccine-induced immunity to be adapted to assess NK cell effector responses.
我们对初次成年志愿者中狂犬病病毒疫苗诱导的细胞反应进行了特征描述。与目前的模式相反,我们观察到,在接种疫苗的个体而非未接种疫苗的个体中,用狂犬病病毒灭活物再次刺激 PBMC 后,会产生强烈且持久的体外 NK 细胞细胞因子产生和脱颗粒反应。这种“回忆”NK 细胞反应绝对依赖于 Ag 特异性的 CD45RO(+)CD4(+)T 细胞产生的 IL-2,以及辅助细胞产生的 IL-12 和 IL-18。重要的是,NK 细胞占病毒再挑战后 12-18 小时内 IFN-γ分泌和脱颗粒细胞的 70%以上,表明它们可能是疫苗接种后快速控制感染所必需的。NK 细胞的激活可能是分泌 IL-2 的效应记忆 T 细胞的关键功能。尽管之前已经报道过 IL-2 依赖性的接种后 NK 细胞激活,但这是首次评估这种效应的幅度及其对整体疫苗诱导反应的贡献,并阐明了接种后 NK 细胞激活的机制。我们的数据将使评估疫苗诱导免疫的标准方案得以适应,以评估 NK 细胞效应器反应。