4.8 Article

Mast-Cell-Derived TNF Amplifies CD+ Dendritic Cell Functionality and CDir T Cell Priming

期刊

CELL REPORTS
卷 13, 期 2, 页码 399-411

出版社

CELL PRESS
DOI: 10.1016/j.celrep.2015.08.078

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资金

  1. German Research foundation (DFG) [DU1172/2, 14681, DU1172/3, 1394]
  2. Technische Universitat Dresden
  3. Russian Science Foundation [14-50-00060]
  4. DFG [NE1466/2-1]
  5. German Research foundation [DU548/2-1, SFB643-TPA7]
  6. BayGene
  7. Russian Science Foundation [14-50-00060] Funding Source: Russian Science Foundation

向作者/读者索取更多资源

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 CDS' 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.

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