| Literature DB >> 11600887 |
T Biedermann1, S Zimmermann, H Himmelrich, A Gumy, O Egeter, A K Sakrauski, I Seegmüller, H Voigt, P Launois, A D Levine, H Wagner, K Heeg, J A Louis, M Röcken.
Abstract
Immunity to infection with intracellular pathogens is regulated by interleukin 12 (IL-12), which mediates protective T helper type 1 (TH1) responses, or IL-4, which induces TH2 cells and susceptibility. Paradoxically, we show here that when present during the initial activation of dendritic cells (DCs) by infectious agents, IL-4 instructed DCs to produce IL-12 and promote TH1 development. This TH1 response established resistance to Leishmania major in susceptible BALB/c mice. When present later, during the period of T cell priming, IL-4 induced TH2 differentiation and progressive leishmaniasis in resistant mice. Because immune responses developed via the consecutive activation of DCs and then T cells, the contrasting effects of IL-4 on DC development and T cell differentiation led to immune responses that had opposing functional phenotypes.Entities:
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Year: 2001 PMID: 11600887 DOI: 10.1038/ni725
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606