Key result
Despite identification of potential targets for blocking viral replication, there is currently no virus-specific drug in clinical use for Coxsackievirus-induced myocarditis.
Why the study?
Despite advances in understanding CVB3-induced myocarditis, no virus-specific drug is in clinical use, highlighting an urgent need for diverse molecular libraries for antiviral screening.
Highlights the lack of specific antiviral therapies for CVB3-induced myocarditis and the potential of natural products and high-throughput screening to identify novel treatments.
Supportive care remains the clinical standard for CVB3 myocarditis; leaves open the.
Coxsackievirus B3 (CVB3), a member of the Picornaviridae family, is considered to be one of the most important infectious agents to cause virus-induced myocarditis. Despite improvements in studying viral pathology, structure and molecular biology, as well as diagnosis of this disease, there is still no virus-specific drug in clinical use. Structural and nonstructural proteins produced during the coxsackievirus life cycle have been identified as potential targets for blocking viral replication at the step of attachment, entry, uncoating, RNA and protein synthesis by synthetic or natural compounds. Moreover, WIN (for Winthrop) compounds and application of nucleic-acid based strategies were shown to target viral capsid, entry and viral proteases, but have not reached to the clinical trials as a successful antiviral agent. There is an urgent need for diverse molecular libraries for phenotype-selective and high-throughput screening.
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Khanna et al. (2020) conducted a review in Coxsackievirus-induced Myocarditis. Natural Products and WIN compounds was evaluated. Despite identification of potential targets for blocking viral replication, there is currently no virus-specific drug in clinical use for Coxsackievirus-induced myocarditis.
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