Viral MicroRNAs: Interfering the Interferon Signaling

被引:14
作者
Ahmad, Imran [1 ]
Valverde, Araceli [1 ]
Siddiqui, Hasan [1 ]
Schaller, Samantha [1 ]
Naqvi, Afsar R. [1 ]
机构
[1] Univ Illinois, Coll Dent, Mucosa Immunol Lab, Chicago, IL 60612 USA
关键词
Viruses; viral microRNA; interferons; post-transcriptional silencing; immune response; JAK-STAT; EPSTEIN-BARR-VIRUS; NF-KAPPA-B; DNA-BINDING; TYROSINE PHOSPHORYLATION; TRANSCRIPTION FACTOR; REGULATORY FACTOR-3; HUMAN CYTOKINE; IFN-GAMMA; PATHWAY; EBV;
D O I
10.2174/1381612826666200109181238
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Interferons are secreted cytokines with potent antiviral, antitumor and immunomodulatory functions. As the first line of defense against viruses, this pathway restricts virus infection and spread. On the contrary, viruses have evolved ingenious strategies to evade host immune responses including the interferon pathway. Multiple families of viruses, in particular, DNA viruses, encode microRNA (miR) that are small, non-protein coding, regulatory RNAs. Virus-derived miRNAs (v-miR) function by targeting host and virus-encoded transcripts and are critical in shaping host-pathogen interaction. The role of v-miRs in viral pathogenesis is emerging DOI as demonstrated by their function in subverting host defense mechanisms and regulating fundamental biological : processes such as cell survival, proliferation, modulation of viral life-cycle phase. In this review, we will discuss the role of v-miRs in the suppression of host genes involved in the viral nucleic acid detection, JAK-STAT pathway, and cytokine-mediated antiviral gene activation to favor viral replication and persistence. This information has yielded new insights into our understanding of how v-miRs promote viral evasion of host immunity and likely provide novel antiviral therapeutic targets.
引用
收藏
页码:446 / 454
页数:9
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