Institute for Immunology, Technische Universität Dresden, Medical Faculty Carl Gustav Carus, 01307 Dresden, Germany.
Department of Dermatology, Laboratories of DC Biology, University Hospital of Erlangen, Friedrich-Alexander-University of Erlangen-Nürnberg, 91054 Erlangen, Germany.
Cell Rep. 2015 Oct 13;13(2):399-411. doi: 10.1016/j.celrep.2015.08.078. Epub 2015 Sep 24.
Mast cells are critical promoters of adaptive immunity in the contact hypersensitivity model, but the mechanism of allergen sensitization is poorly understood. Using Mcpt5-CreTNF(FL/FL) mice, we show here that the absence of TNF exclusively in mast cells impaired the expansion of CD8(+) T cells upon sensitization and the T-cell-driven adaptive immune response to elicitation. T cells primed in the absence of mast cell TNF exhibited a diminished efficiency to transfer sensitization to naive recipients. Specifically, mast cell TNF promotes CD8(+) dendritic cell (DC) maturation and migration to draining lymph nodes. The peripherally released mast cell TNF further critically boosts the CD8(+) T-cell-priming efficiency of CD8(+) DCs, thereby linking mast cell effects on T cells to DC modulation. Collectively, our findings identify the distinct potential of mast cell TNF to amplify CD8(+) DC functionality and CD8(+) T-cell-dominated adaptive immunity, which may be of great importance for immunotherapy and vaccination approaches.
肥大细胞是接触性超敏反应模型中适应性免疫的关键促进剂,但过敏原致敏的机制尚不清楚。在这里,我们使用 Mcpt5-CreTNF(FL/FL) 小鼠表明,肥大细胞中 TNF 的缺失专门会损害致敏时 CD8(+)T 细胞的扩增和 T 细胞驱动的适应性免疫反应。在没有肥大细胞 TNF 的情况下被激活的 T 细胞向幼稚受者转移致敏的效率降低。具体而言,肥大细胞 TNF 促进 CD8(+)树突状细胞 (DC) 的成熟和迁移到引流淋巴结。外周释放的肥大细胞 TNF 进一步极大地增强了 CD8(+)DC 对 CD8(+)T 细胞的启动效率,从而将肥大细胞对 T 细胞的作用与 DC 调节联系起来。总的来说,我们的发现确定了肥大细胞 TNF 放大 CD8(+)DC 功能和 CD8(+)T 细胞主导的适应性免疫的独特潜力,这对于免疫治疗和疫苗接种方法可能非常重要。