| Literature DB >> 33171339 |
Anthony D Kelleher1, Christina Cortez-Jugo2, Francesca Cavalieri3, Yijiao Qu2, Allan R Glanville4, Frank Caruso2, Geoff Symonds5, Chantelle L Ahlenstiel6.
Abstract
Gene silencing induced by RNAi represents a promising antiviral development strategy. This review will summarise the current state of RNAi therapeutics for treating acute and chronic human virus infections. The gene silencing pathways exploited by RNAi therapeutics will be described and include both classic RNAi, inducing cytoplasmic mRNA degradation post-transcription and novel RNAi, mediating epigenetic modifications at the transcription level in the nucleus. Finally, the challenge of delivering gene modifications via RNAi will be discussed, along with the unique characteristics of respiratory versus systemic administration routes to highlight recent advances and future potential of RNAi antiviral treatment strategies.Entities:
Year: 2020 PMID: 33171339 DOI: 10.1016/j.coph.2020.09.011
Source DB: PubMed Journal: Curr Opin Pharmacol ISSN: 1471-4892 Impact factor: 5.547