Author: Zong, Zhi; Zhang, Zhengkui; Wu, Liming; Zhang, Long; Zhou, Fangfang
                    Title: The Functional Deubiquitinating Enzymes in Control of Innate Antiviral Immunity  Cord-id: 057yy33u  Document date: 2020_12_15
                    ID: 057yy33u
                    
                    Snippet: Innate antiviral immunity is the first line of host defense against invading viral pathogens. Immunity activation primarily relies on the recognition of pathogenâ€associated molecular patterns (PAMPs) by pattern recognition receptors (PRRs). Viral proteins or nucleic acids mainly engage three classes of PRRs: Tollâ€like receptors (TLRs), retinoic acidâ€inducible gene I (RIGâ€I)â€like receptors (RLRs), and DNA sensor cyclic GMPâ€AMP (cGAMP) synthase (cGAS). These receptors initiate a series
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: Innate antiviral immunity is the first line of host defense against invading viral pathogens. Immunity activation primarily relies on the recognition of pathogenâ€associated molecular patterns (PAMPs) by pattern recognition receptors (PRRs). Viral proteins or nucleic acids mainly engage three classes of PRRs: Tollâ€like receptors (TLRs), retinoic acidâ€inducible gene I (RIGâ€I)â€like receptors (RLRs), and DNA sensor cyclic GMPâ€AMP (cGAMP) synthase (cGAS). These receptors initiate a series of signaling cascades that lead to the production of proinflammatory cytokines and type I interferon (IFNâ€I) in response to viral infection. This system requires precise regulation to avoid aberrant activation. Emerging evidence has unveiled the crucial roles that the ubiquitin system, especially deubiquitinating enzymes (DUBs), play in controlling immune responses. In this review, an overview of the most current findings on the function of DUBs in the innate antiviral immune pathways is provided. Insights into the role of viral DUBs in counteracting host immune responses are also provided. Furthermore, the prospects and challenges of utilizing DUBs as therapeutic targets for infectious diseases are discussed.
 
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