| Literature DB >> 26411682 |
Jan Dudeck1, Shanawaz Mohammed Ghouse1, Christian H K Lehmann2, Anja Hoppe1, Nadja Schubert1, Sergei A Nedospasov3, Diana Dudziak2, Anne Dudeck4.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26411682 DOI: 10.1016/j.celrep.2015.08.078
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423