Journal of Interferon & Cytokine Research · 2003 · 314 citations · 32 references
Life SciencesCell BiologyImmunologyAdaptive ImmunityCellular ImmunologyImmunoregulationCytokine BiologyImmune Cell Lineage CommitmentImmune Cell SignalingNatural Killer Cell BiologyNatural Killer Cell FunctionT Cell BiologyCd4 Positive T CellsCytokine-mediated T Cell ResponsesInterferon-gamma ResponsesNaive T CellsStat3 SignalingT Cell Lineage CommitmentTh1 Immune ResponseTh1 Responses
Interleukin-27 (IL-27) supports proliferation of naive CD4(+) T cells and enhances interferon-gamma (IFN-gamma) production by activated T cells and natural killer (NK) cells. We report here that IL-27 induces Stat1 and Stat3 phosphorylation and activation in human and murine cell lines and primary human T cells. IL-27 also induces T-Bet, a Stat1-dependent gene crucial to Th1 cell commitment. Similarly, IFN-alpha activates Stat1 and Stat3 and T-Bet expression in naive T cells. Induction of T-Bet results in upregulation of IL-12Rbeta2 on naive T cells, which is essential for responsiveness to IL-12 and differentiation to a Th1 phenotype. Both IL-27 and IFN-alpha induce expression of IL-12Rbeta2 in T cells. In contrast, IFN-gamma, which activates Stat1 but not Stat3, induces expression of T-Bet but not IL-12Rbeta2 in naive T cells. We propose that IL-27 and IFN-alpha are important for early Th1 commitment and act upstream of IL-12 and IFN-gamma in this pathway.
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A Novel Transcription Factor, T-bet, Directs Th1 Lineage Commitment
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