Article ID Journal Published Year Pages File Type
3199964 Journal of Allergy and Clinical Immunology 2010 10 Pages PDF
Abstract

BackgroundDendritic cells (DCs) regulate the immune response to allergens in the lung; they induce either effector or regulatory T cells, which promote or suppress, respectively, the development of allergy. IL-10 is a potent immunosuppressive cytokine that induces type 1 regulatory (Tr1) T cells.ObjectiveTo generate allergen-specific Tr1 cells in vitro from children with allergy.MethodsMonocyte-derived DCs from children with allergy to house dust mites (HDM) were generated by incubating the cells with IL-10 and pulsing them with Der p 2, a major HDM allergen, or by pulsing them with Der p 2 and incubating them with IL-10 during their last 2 days of differentiation.ResultsDer p 2–specific T-cell proliferation and TH2 cytokine production were significantly reduced when T cells from patients with allergy to HDM were activated with autologous Der p 2–pulsed DCs that had been differentiated or incubated with IL-10. T-cell lines generated with Der p 2–pulsed DCs that were differentiated with IL-10 were hyporesponsive to reactivation with Der p 2 and able to suppress Der p 2–specific TH2 effector cells.ConclusionDendritic cells differentiated in the presence of IL-10 and pulsed with allergen gave rise to a population of tolerogenic DCs that induced allergen-specific Tr1 cells. This finding represents an important step forward to the prospective clinical application of tolerogenic DCs to modulate allergen-specific T-cell responses.

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