Abstract
Th cells producing IL-17 play a pro-inflammatory role atmucosal surfaces. Treg at the same sites dampen inflammation and prevent immunopathology. Th cells producing IL-17 (Th17) and Treg are thought to be distinct populations defined by expression of the transcription factors ROR-γt and Foxp3, respectively. Here, we show thatmouse CD25+Foxp3+ Treg can be converted into a hybrid T-cell population characterized by the expression of Foxp3 and ROR-γt and the production of IL-17. Conversion was observed upon coculture with DC selectively activated via dectin-1, a C-type lectin receptor involved in fungal recognition, and depended on IL-23 produced by DC.Within the Foxp3+ population, only Foxp3+ROR-γt+ T cells but not Foxp3+ROR-γt--T cells become Foxp3+IL-17+ T cells. These results indicate that some Foxp3+ T cells can produce IL-17 while retaining Foxp3 expression and suggest that Treg could play an unexpected pro-inflammatory role in some settings. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.
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CITATION STYLE
Osorio, F., LeibundGut-Landmann, S., Lochner, M., Lahl, K., Sparwaser, T., Eberl, G., & Reis e Sousa, C. (2008). DC activated via dectin-1 convert Treg into IL-17 producers. European Journal of Immunology, 38(12), 3274–3281. https://doi.org/10.1002/eji.200838950
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