Human gamma delta T cells modulate the mite allergen-specific T-helper type 2-skewed immunity
Background gamma delta T cells have been described as one of immune regulators in patients with infection, malignancy, and allergy. ObjectiveTo elucidate the ability of gamma delta T cells as an allergen immunotherapy candidate, the effectiveness of human gamma delta T cells in allergen-specific T-h...
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Veröffentlicht in: | Clinical and experimental allergy 2007-11, Vol.37 (11), p.1681-1687 |
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Sprache: | eng |
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Zusammenfassung: | Background gamma delta T cells have been described as one of immune regulators in patients with infection, malignancy, and allergy. ObjectiveTo elucidate the ability of gamma delta T cells as an allergen immunotherapy candidate, the effectiveness of human gamma delta T cells in allergen-specific T-helper type 2 (Th2)-type T cells was evaluated in vitro. MethodsHouse dust mite-specific Th2-type T cell clones, Bacillus Calmette-Guerin (BCG)-specific Th1-type T cell clones, and gamma delta T cell lines were established from the peripheral blood mononuclear cells of two patients with allergic rhinitis. The effectiveness of gamma delta T cells and BCG-specific Th1-type T cell clones in the modulation of allergen-specific Th2 cells in terms of their cytokine productions was evaluated. ResultsIn response to cognate antigens, the gamma delta T cell lines demonstrated a proliferation and production of IFN- gamma that exceeded that of BCG-specific Th1-type T cell clones (mean stimulation index: 14.5 vs. 2.8, mean IFN- gamma : 130.5 vs. 10.0 pg-mL). When the gamma delta T cell lines and mite-allergen-specific Th2 clones were co-cultured with each other, only the levels of IL-4 (mean, -87%) decreased, but not the levels of IL-5 and IL-13, with an increasing concentration of gamma delta T cell antigen and IFN- gamma production (mean, +730%). ConclusionThese results demonstrated that gamma delta T cells derived from allergic patients might thus have a partial ability to modulate allergen-specific Th2-skewed immunity. |
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ISSN: | 0954-7894 1365-2222 |
DOI: | 10.1111/j.1365-2222.2007.02826.x |