Screening methods for influenza antiviral drug discovery
| Autor: | Colm Atkins, James W. Noah, Carrie W. Evans, E. Lucile White |
|---|---|
| Rok vydání: | 2012 |
| Předmět: |
medicine.drug_class
Drug Evaluation Preclinical Computational biology Biology medicine.disease_cause Virus Replication Antiviral Agents Viral Proteins Dogs High-Throughput Screening Assays Drug Discovery Influenza Human Influenza A virus medicine Screening method Animals Humans Drug discovery Extramural Virology HEK293 Cells Influenza Vaccines Expert opinion Antiviral drug |
| Zdroj: | Expert opinion on drug discovery. 7(5) |
| ISSN: | 1746-045X |
| Popis: | Influenza antiviral high-throughput screens have been extensive, and yet no approved influenza antivirals have been identified through high-throughput screening. This underscores the idea that development of successful screens should focus on the exploitation of the underrepresented viral targets and novel, therapeutic host targets.The authors review conventional screening applications and emerging technologies with the potential to enhance influenza antiviral discovery. Real-world examples from the authors' work in biocontained environments are also provided. Future innovations are discussed, including the use of targeted libraries, multiplexed assays, proximity-based endpoint methods, non-laboratory-adapted virus strains, and primary cells, for immediate physiological relevance and translational applications.The lack of successful anti-influenza drug discovery using high-throughput screening should not deter future efforts. Increased understanding of the functions of viral targets and host-pathogen interactions has broadened the target reservoir. Future screening efforts should focus on identifying new drugs against unexploited viral and host targets using currently developed assays, and on the development of novel, innovative assays to discover new drugs with novel mechanisms. Innovative screens must be designed to identify compounds that specifically inhibit protein-protein or protein-RNA interactions or other virus/host factor interactions that are crucial for viral replication. Finally, the use of recent viral isolates, increased biocontainment (for highly-pathogenic strains), primary cell lines, and targeted compound libraries must converge in efficient high-throughput primary screens to generate high-content, physiologically-relevant data on compounds with robust antiviral activity. |
| Databáze: | OpenAIRE |
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