Interference without interferon: interferon-independent induction of interferon-stimulated genes and its role in cellular innate immunity

被引:3
|
作者
Swaraj, Shachee [1 ,2 ]
Tripathi, Shashank [1 ,2 ]
机构
[1] Indian Inst Sci, Ctr Infect Dis Res, Emerging Viral Pathogens Lab, Bengaluru, India
[2] Indian Inst Sci, Microbiol & Cell Biol Dept, Biol Sci Div, Bengaluru, India
来源
基金
英国惠康基金;
关键词
viral immunity; innate immunity; interferons; ISG induction; interferon-independent immunity; STAT signaling; JAK kinases; DOUBLE-STRANDED-RNA; NF-KAPPA-B; FINGER ANTIVIRAL PROTEIN; TUMOR-NECROSIS-FACTOR; INDUCED NUCLEAR FACTORS; SIMPLEX-VIRUS TYPE-1; JAK-STAT PATHWAY; CYCLIC GMP-AMP; I-INTERFERON; TRANSCRIPTION FACTOR;
D O I
10.1128/mbio.02582-24
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Interferons (IFNs) are multifaceted proteins that play pivotal roles in orchestrating robust antiviral immune responses and modulating the intricate landscape of host immunity. The major signaling pathway activated by IFNs is the JAK/STAT (Janus kinase/signal transducer and activator of transcription) pathway, which leads to the transcription of a battery of genes, collectively known as IFN-stimulated genes (ISGs). While the well-established role of IFNs in coordinating the innate immune response against viral infections is widely acknowledged, recent years have provided a more distinct comprehension of the functional significance attributed to non-canonical, IFN-independent induction of ISGs. In this review, we summarize the non-conventional signaling pathways of ISG induction. These alternative pathways offer new avenues for developing antiviral strategies or immunomodulation in various diseases.
引用
收藏
页数:20
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