Immunomodulation
IL-4-mediated fine tuning of IL-12p70 production by human DC
Article first published online: 16 OCT 2008
DOI: 10.1002/eji.200838463
Copyright © 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Guenova, E., Volz, T., Sauer, K., Kaesler, S., Müller, M. R., Wölbing, F., Chen, K., Schwärzler, C., Brossart, P., Röcken, M. and Biedermann, T. (2008), IL-4-mediated fine tuning of IL-12p70 production by human DC. Eur. J. Immunol., 38: 3138–3149. doi: 10.1002/eji.200838463
Publication History
- Issue published online: 7 NOV 2008
- Article first published online: 16 OCT 2008
- Manuscript Accepted: 27 AUG 2008
- Manuscript Revised: 17 AUG 2008
- Manuscript Received: 27 APR 2008
Funded by
- Deutsche Forschungsgemeinschaft. Grant Number: DFG Bi 696/3-1; SFB 685
- Landesstiftung Baden-Württemberg. Grant Number: P-LS-AL/17
- Fortüne Program of the University of Tübingen. Grant Numbers: F126810, 1261150)
- Abstract
- Article
- References
- Cited By
Keywords:
- Cytokines;
- DC;
- Human;
- Inflammation;
- Skin
Abstract
IL-4 is expressed at high levels in allergic diseases and dominates the early phases of multiple acquired immune responses. However, the precise role of IL-4 during early inflammation and its impact on the differentiation of newly recruited DC precursors remains elusive. In order to characterize the impact of IL-4 on the differentiation of human DC, we investigated the role of IL-4 on the differentiation of monocytes into DC. Human DC were differentiated from peripheral blood precursors under either low or high concentrations of IL–4. We analyzed their cytokine profile and capacity to polarize T-cell differentiation. Concentrations of 5 (low) and 50 (high) ng/mL IL-4 induced two distinct types of DC. DC differentiated under low-dose IL-4 (5 ng/mL) produced almost no IL–12p70, and primed naïve CD4+ T cells allowing IL-4 secretion and Th2 induction. In contrast, DC generated under high concentrations of IL-4 (50 ng/mL) produced large amounts of IL-12p70, low IL-10 and primed naïve CD4+ T cells to become Th1 cells. Thus, we demonstrate that the Th2 cell cytokine IL-4 decisively determines the phenotype of ongoing immune responses by orchestrating the functional phenotype of newly immigrating DC precursors.

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