Cutting edge:: A murine, IL-12-independent pathway of IFN-γ induction by gram-negative:: Bacteria based on STAT4 activation by type I IFN and IL-18 signaling

被引:100
作者
Freudenberg, MA
Merlin, T
Kalis, C
Chvatchko, Y
Stübig, H
Galanos, C
机构
[1] Max Planck Inst Immunbiol, D-79108 Freiburg, Germany
[2] Serono Pharmaceut Res Inst, Geneva, Switzerland
关键词
D O I
10.4049/jimmunol.169.4.1665
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IFN-alphabeta is a potent immunoregulatory cytokine involved in the defense against viral and bacterial infections. In this study, we describe an as yet undefined IFN-alphabeta-dependent pathway of IFN-gamma induction in mice. This pathway is based on a synergism of IFN-alphabeta and IL-18, and is independent of IL-12 signaling yet dependent on STAT4. In contradiction to current dogma, we show further that IFN-alphabeta alone induces tyrosine phosphorylation of STAT4 in murine splenocytes of different mouse strains. This pathway participates in the induction of IFN-gamma by Gram-negative bacteria and. is therefore expected to play a role whenever IFN-alpha or IFN-beta and IL-18 are produced concomitantly during bacterial, viral, or other infections.
引用
收藏
页码:1665 / 1668
页数:4
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