Mast Cell-Mediated Antigen Presentation Regulates CD8+ T Cell Effector Functions

Summary The characteristics, importance, and molecular requirements for interactions between mast cells (MCs) and CD8 + T cells have not been elucidated. Here, we demonstrated that MCs induced antigen-specific CD8 + T cell activation and proliferation. This process required direct cell contact and MHC class I-dependent antigen cross-presentation by MCs and induced the secretion of interleukin-2, interferon-γ, and macrophage inflammatory protein-1α by CD8 + T cells. MCs regulated antigen-specific CD8 + T cell cytotoxicity by increasing granzyme B expression and by promoting CD8 + T cell degranulation. Because MCs also upregulated their expression of costimulatory molecules (4-1BB) and released osteopontin upon direct T cell contact, MC-T cell interactions probably are bidirectional. In vivo, adoptive transfer of antigen-pulsed MCs induced MHC class I-dependent, antigen-specific CD8 + T cell proliferation, and MCs regulated CD8 + T cell-specific priming in experimental autoimmune encephalomyelitis. Thus, MCs are important players in antigen-specific regulation of CD8 + T cells.