| Literature DB >> 33925713 |
Chengfeng Gao1, Chunxia Wen1, Zhifeng Li2, Shuhan Lin1, Shu Gao1, Haida Ding1, Peng Zou3, Zheng Xing1,4, Yufeng Yu1.
Abstract
Viral infections are one of the leading causes in human mortality and disease. Broad-spectrum antiviral drugs are a powerful weapon against new and re-emerging viruses. However, viral resistance to existing broad-spectrum antivirals remains a challenge, which demands development of new broad-spectrum therapeutics. In this report, we showed that fludarabine, a fluorinated purine analogue, effectively inhibited infection of RNA viruses, including Zika virus, Severe fever with thrombocytopenia syndrome virus, and Enterovirus A71, with all IC50 values below 1 μM in Vero, BHK21, U251 MG, and HMC3 cells. We observed that fludarabine has shown cytotoxicity to these cells only at high doses indicating it could be safe for future clinical use if approved. In conclusion, this study suggests that fludarabine could be developed as a potential broad-spectrum anti-RNA virus therapeutic agent.Entities:
Keywords: Enterovirus A71; Severe fever with thrombocytopenia syndrome virus; Zika virus; antiviral drugs; fludarabine
Year: 2021 PMID: 33925713 DOI: 10.3390/v13050774
Source DB: PubMed Journal: Viruses ISSN: 1999-4915 Impact factor: 5.048