The Journal of Experimental Medicine · 2004 · 771 citations · 42 references
Life SciencesImmunologyPathobiologyHypersensitivityImmunoregulationInflammationAdaptive Immune ModulationAllergic DiseaseDendritic Cell BiologyDendritic Cell RegulationEffector T Cell FunctionRespiratory AllergyAllergic Airway InflammationDendritic Cell Tolerogenic FunctionDendritic Cell TolerogenicityInflammatory Cytokine ProductionInflammatory T Cell ResponsesT Cell Cytokine ProductionT Helper CellsTolerogenic Dendritic Cells
Tolerance is the usual outcome of inhalation of harmless antigen, yet T helper (Th) type 2 cell sensitization to inhaled allergens induced by dendritic cells (DCs) is common in atopic asthma. Here, we show that both myeloid (m) and plasmacytoid (p) DCs take up inhaled antigen in the lung and present it in an immunogenic or tolerogenic form to draining node T cells. Strikingly, depletion of pDCs during inhalation of normally inert antigen led to immunoglobulin E sensitization, airway eosinophilia, goblet cell hyperplasia, and Th2 cell cytokine production, cardinal features of asthma. Furthermore, adoptive transfer of pDCs before sensitization prevented disease in a mouse asthma model. On a functional level, pDCs did not induce T cell division but suppressed the generation of effector T cells induced by mDCs. These studies show that pDCs provide intrinsic protection against inflammatory responses to harmless antigen. Therapies exploiting pDC function might be clinically effective in preventing the development of asthma.
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