IL-4 instructs TH1 responses and resistance to Leishmania major in susceptible BALB/c mice

被引:0
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作者
Tilo Biedermann
Stephan Zimmermann
Hayo Himmelrich
Alain Gumy
Oliver Egeter
Arne K. Sakrauski
Irene Seegmüller
Heike Voigt
Pascal Launois
Alan D. Levine
Hermann Wagner
Klaus Heeg
Jacques A. Louis
Martin Röcken
机构
[1] Ludwig-Maximilians-University Munich,Department of Dermatology and Allergology
[2] Technical University Munich,Department of Microbiology
[3] University of Marburg,Department of Microbiology
[4] WHO Immunology Research and Training Center,Department of Medicine
[5] Institute of Biochemistry,undefined
[6] University of Lausanne,undefined
[7] Case Western Reserve University,undefined
[8] Novartis Research Institute,undefined
[9] Pasteur Institute,undefined
来源
Nature Immunology | 2001年 / 2卷
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摘要
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.
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页码:1054 / 1060
页数:6
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