Dysregulated T helper cell differentiation in the absence of interferon regulatory factor 4

被引:198
|
作者
Lohoff, M
Mittrücker, HW
Prechtl, S
Bischof, S
Sommer, F
Kock, S
Ferrick, DA
Duncan, GS
Gessner, A
Mak, TW [1 ]
机构
[1] Amgen Res Inst, Dept Immunol, Toronto, ON, Canada
[2] Amgen Res Inst, Dept Med Biophys, Toronto, ON, Canada
[3] Inst Klin Mikrobiol, D-91054 Erlangen, Germany
[4] Inst Med Mikrobiol, D-35037 Marburg, Germany
[5] Max Planck Inst Infekt Biol, D-10117 Berlin, Germany
[6] Univ Calif Davis, Sch Vet Med, Davis, CA 95616 USA
关键词
D O I
10.1073/pnas.182425099
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Certain IFN regulatory factor (IRF) transcription factors indirectly influence T helper (Th) cell differentiation by regulating the production of IL-12. Here, we show that IRF4 directly regulates Th cell differentiation in vitro and in vivo during murine leishmaniasis. In the absence of IRF4, IL-12-induced Th1 cell differentiation was compromised, while IL-4 failed to induce Th2 cell differentiation. Instead, IL-4 tended to induce Th1 cells, defined by production of IFN-gamma and TNF. Although early IL-4 signaling was normal in IRF4(-/-) Th cells, the protein GATA-3, a transcription factor critical for Th2 development, was not up-regulated following IL-4 treatment. Retroviral overexpression of GATA-3 rescued Th2 differentiation. Therefore, IRF4 deficiency manifests itself as severely dysregulated Th cell differentiation.
引用
收藏
页码:11808 / 11812
页数:5
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