European Journal of Immunology · 1999 · 228 citations · 51 references
Life SciencesCell BiologyImmunologyAllergyCellular ImmunologyHypersensitivityAllergic ConditionsAllergic DiseaseCytokine BiologyImmune Cell PhysiologyImmune Gene RegulationAllergic Cytokine ResponsesAllergic Immune ResponsesAtopic PatientsCytokine SynthesisImmunologic Mechanisms Of AllergyIntracellular StainingPeripheral Blood Natural Killer CellsPhosphorothioate Chemistry
The effects of phosphorothioate oligonucleotides containing CpG motifs (CpG-ODN) on cultured cells from allergic patients and non-atopic individuals were investigated. In peripheral blood mononuclear cells (PBMC) CpG-ODN led to a significant increase of IFN-gamma. By intracellular cytokine staining, IFN-gamma production could be attributed to NK cells and inhibition experiments indicated an IL-12-dependent mechanism. Moreover, CpG-ODN increased mRNA expression of IL-12 and IL-18 in PBMC. In this respect, no significant difference between allergic and non-atopic individuals was observed. Monocyte-derived dendritic cells were identified as one IL-12- and IL-18-producing source. In addition, stimulation of PBMC derived from atopic patients with CpG-ODN led to a considerable increase of polyclonal IgG and IgM synthesis. In contrast, the production of total IgE was suppressed. CpG-ODN induced a significant rise of IgG and IgM specific for allergens to which the patients were sensitized, whereas allergen-specific IgE levels remained unchanged. Our data suggest that CpG-ODN display a strong influence on the ongoing immune response and might represent potential adjuvants for specific immunotherapy of type I allergy.
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