Fine-Tuning of Type I Interferon Response by STAT3

被引:81
作者
Tsai, Ming-Hsun [1 ]
Pai, Li-Mei [2 ,3 ,4 ]
Lee, Chien-Kuo [1 ]
机构
[1] Natl Taiwan Univ, Grad Inst Immunol, Coll Med, Taipei, Taiwan
[2] Chang Gung Univ, Dept Biochem & Mol Biol, Taoyuan, Taiwan
[3] Chang Gung Univ, Mol Med Res Ctr, Taoyuan, Taiwan
[4] Chang Gung Mem Hosp, Liver Res Ctr, Taoyuan, Taiwan
关键词
type I interferon (IFN-I); STAT3; phospholipid scramblese 2; antiviral immunity; SOCS3; EPIDERMAL-GROWTH-FACTOR; TRANSCRIPTION; 3; STAT3; FISH SIGNAL TRANSDUCER; ACUTE-PHASE RESPONSE; TARGETED DISRUPTION; NEGATIVE REGULATION; IFN-ALPHA; ANTIVIRAL ACTIVITY; FOLLICULAR HELPER; EPITHELIAL-CELLS;
D O I
10.3389/fimmu.2019.01448
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Type I interferon (IFN-I) is induced during innate immune response and is required for initiating antiviral activity, growth inhibition, and immunomodulation. STAT1, STAT2, and STAT3 are activated in response to IFN-I stimulation. STAT1, STAT2, and IRF9 form ISGF3 complex which transactivates downstream IFN-stimulated genes and mediates antiviral response. However, the role of STAT3 remains to be characterized. Here, we review the multiple actions of STAT3 on suppressing IFN-I responses, including blocking IFN-I signaling, downregulating the expression of ISGF3 components, and antagonizing the transcriptional activity of ISGF3. Finally, we discuss the evolution of the suppressive activity of STAT3 and the therapeutic potential of STAT3 inhibitors in host defense against viral infections and IFN-I-associated diseases.
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页数:10
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