Origin and function of anti-interferon type I viral proteins

被引:0
作者
Acchioni, Marta [1 ]
Acchioni, Chiara [1 ]
Hiscott, John [2 ]
Sgarbanti, Marco [1 ]
机构
[1] Ist Super Sanita, Dept Infect Dis, Viale Regina Elena 299, I-00161 Rome, Italy
[2] Fdn Cenci Bolognetti, Ist Pasteur Italia, Viale Regina Elena 291, I-00161 Rome, Italy
关键词
Interferon type I; Innate immunity; Viruses; Viral proteins; Immune evasion; Pathogen recognition receptors; Virus evolution; INFLUENZA-A VIRUS; DOUBLE-STRANDED-RNA; NF-KAPPA-B; INTERFERON REGULATORY FACTOR-3; PML NUCLEAR-BODIES; NS1; PROTEIN; RIG-I; EBOLA-VIRUS; VP35; IKK-EPSILON;
D O I
10.1016/j.virol.2025.110456
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Type I interferons (IFN-I) are the most important innate immune cytokines produced by vertebrate host cells following, virus infection. Broadly speaking, detection of infecting viral nucleic acids by pattern recognition receptors (PRR) and subsequent downstream signaling triggers synthesis of a large number of IFN-I-stimulated genes (ISGs), endowed with diverse antiviral effector function. The co-evolution of virus-host interactions over million years has resulted in the emergence of viral strategies that target and inhibit host PRR-mediated detection, signal transduction pathways and IFN-I-mediated stimulation of ISGs. In this review, we illustrate the multiple mechanisms of viral immune evasion and discuss the co-evolution of anti-IFN-I viral proteins by summarizing key examples from recent literature. Due to the large number of anti-IFN-I proteins described, we provide here an evaluation of the prominent examples from different virus families. Understanding the unrelenting evolution of viral evasion strategies will provide mechanistic detail concerning these evolving interactions but will further enhance the development of tailored antiviral approaches.
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