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pubmed-article:15210741pubmed:abstractTextClassical studies have demonstrated that in vitro priming of naive CD4 T cells to become T helper (Th)2 cells is strikingly dependent on interleukin (IL)-4, whereas priming for interferon (IFN)gamma production is IL-12/IFNgamma-dependent. Therefore, it was quite surprising when we noted that priming of naive C57BL/6 CD4(+) cells to become IL-4 producers was substantially inhibited by the addition of anti-IFNgamma antibodies. This was true using immobilized anti-CD3 and anti-CD28 antibodies or soluble anti-CD3/anti-CD28 and antigen-presenting cells in the presence or absence of added IL-4. Priming of CD4 T cells from IFNgamma(-/-) C57BL/6 mice with immobilized anti-CD3 and anti-CD28 resulted in limited production of IL-4, even with the addition of 1,000 U/ml of IL-4. Titrating IFNgamma into such cultures showed a striking increase in the proportion of T cells that secreted IL-4 upon challenge; this effect was completely IL-4-dependent in that it was blocked with anti-IL-4 antibody. Thus, IFNgamma plays an unanticipated but substantial role in Th2 priming, although it is an important Th1 cytokine, and under certain circumstances a Th1 inducer.lld:pubmed
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pubmed-article:15210741pubmed:authorpubmed-author:PaulWilliam...lld:pubmed
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pubmed-article:15210741pubmed:dateRevised2009-11-18lld:pubmed
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pubmed-article:15210741pubmed:articleTitleInterferon gamma enhances both in vitro and in vivo priming of CD4+ T cells for IL-4 production.lld:pubmed
pubmed-article:15210741pubmed:affiliationDivision of Allergy, LAboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 6610 Rockledge Dr., Rm. 3060, Bethesda, MD 20892, USA. pbocek@niaid.nih.govlld:pubmed
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