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- W4366425573 endingPage "7448" @default.
- W4366425573 startingPage "7448" @default.
- W4366425573 abstract "Invading pathogens have developed weapons that subvert physiological conditions to weaken the host and permit the spread of infection. Cells, on their side, have thus developed countermeasures to maintain cellular physiology and counteract pathogenesis. The cyclic GMP-AMP (cGAMP) synthase (cGAS) is a pattern recognition receptor that recognizes viral DNA present in the cytosol, activating the stimulator of interferon genes (STING) protein and leading to the production of type I interferons (IFN-I). Given its role in innate immunity activation, STING is considered an interesting and innovative target for the development of broad-spectrum antivirals. In this review, we discuss the function of STING; its modulation by the cellular stimuli; the molecular mechanisms developed by viruses, through which they escape this defense system; and the therapeutical strategies that have been developed to date to inhibit viral replication restoring STING functionality." @default.
- W4366425573 created "2023-04-21" @default.
- W4366425573 creator A5037425032 @default.
- W4366425573 creator A5074496733 @default.
- W4366425573 date "2023-04-18" @default.
- W4366425573 modified "2023-10-05" @default.
- W4366425573 title "Unlocking STING as a Therapeutic Antiviral Strategy" @default.
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