Institute of Pediatric Research, Children's Hospital of Soochow University, Suzhou, China.
Department of Experimental Center, Medical College of Soochow University, Suzhou, China.
Front Immunol. 2021 Oct 11;12:742542. doi: 10.3389/fimmu.2021.742542. eCollection 2021.
Viral infectious diseases pose a great challenge to human health around the world. Type I interferons (IFN-Is) function as the first line of host defense and thus play critical roles during virus infection by mediating the transcriptional induction of hundreds of genes. Nevertheless, overactive cytokine immune responses also cause autoimmune diseases, and thus, tight regulation of the innate immune response is needed to achieve viral clearance without causing excessive immune responses. Emerging studies have recently uncovered that the ubiquitin system, particularly deubiquitinating enzymes (DUBs), plays a critical role in regulating innate immune responses. In this review, we highlight recent advances on the diverse mechanisms of human DUBs implicated in IFN-I signaling. These DUBs function dynamically to calibrate host defenses against various virus infections by targeting hub proteins in the IFN-I signaling transduction pathway. We also present a future perspective on the roles of DUB-substrate interaction networks in innate antiviral activities, discuss the promises and challenges of DUB-based drug development, and identify the open questions that remain to be clarified. Our review provides a comprehensive description of DUBs, particularly their differential mechanisms that have evolved in the host to regulate IFN-I-signaling-mediated antiviral responses.
病毒传染病对全球人类健康构成了巨大挑战。I 型干扰素(IFN-Is)作为宿主防御的第一道防线,通过介导数百个基因的转录诱导,在病毒感染过程中发挥着关键作用。然而,过度活跃的细胞因子免疫反应也会导致自身免疫性疾病,因此需要严格调节先天免疫反应,以在不引起过度免疫反应的情况下清除病毒。最近的新兴研究揭示了泛素系统,特别是去泛素化酶(DUBs),在调节先天免疫反应中起着关键作用。在这篇综述中,我们强调了人类 DUBs 在 IFN-I 信号转导中涉及的多种机制的最新进展。这些 DUBs 通过靶向 IFN-I 信号转导途径中的枢纽蛋白,动态地发挥作用,针对各种病毒感染来校准宿主防御。我们还对 DUB-底物相互作用网络在先天抗病毒活性中的作用提出了未来展望,讨论了基于 DUB 的药物开发的前景和挑战,并确定了仍需澄清的开放性问题。我们的综述提供了 DUB 的全面描述,特别是它们在宿主中进化而来的调节 IFN-I 信号转导介导的抗病毒反应的不同机制。