siRNAs and Viruses: The good, the Bad and the Way Forward

被引:4
|
作者
Soobramoney, Cassandra [1 ]
Parboosing, Raveen [2 ]
机构
[1] Univ KwaZulu Natal, Durban, South Africa
[2] Univ KwaZulu Natal, Dept Virol, Natl Hlth Lab Serv, Durban, South Africa
关键词
RNAi; siRNAs; antiviral siRNAs; delivery vector; siRNA modification; combination siRNAs; CORONAVIRUS MEMBRANE GENE; DOUBLE-STRANDED-RNA; IN-VIVO DELIVERY; CARBOSILANE DENDRIMERS; NONHUMAN-PRIMATES; VIRAL REPLICATION; SARS CORONAVIRUS; HIV-1; INFECTION; INTERFERENCE; INHIBITION;
D O I
10.2174/1874467214666210420113427
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There are no available antivirals for many viruses or strains, while current antivirals are limited by toxicity and drug resistance. Therefore, alternative strategies, such as RNA interference (RNAi) are required. RNAi suppresses gene expression of any mRNA, making it an attractive candidate for antiviral therapeutics. Studies have evaluated siRNAs in a range of viruses, with some showing promising results. However, issues with stability and delivery of siRNAs remain. These issues may be minimized by modifying the siRNA structure, using an efficient delivery vector and targeting multiple regions of a virus's genome in a single dose. Finding these solutions could accelerate the progress of RNAi-based antivirals. This review highlights selected examples of antiviral siRNAs, limitations of RNAi and strategies to overcome these limitations.
引用
收藏
页码:143 / 158
页数:16
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