| Literature DB >> 31935422 |
Michael K Lo1, Franck Amblard2, Mike Flint3, Payel Chatterjee3, Mahesh Kasthuri2, Chengwei Li2, Olivia Russell2, Kiran Verma2, Leda Bassit2, Raymond F Schinazi2, Stuart T Nichol3, Christina F Spiropoulou4.
Abstract
Nipah virus (NiV) is a highly pathogenic zoonotic paramyxovirus that continues to cause outbreaks in humans characterized by high mortality and significant clinical sequelae in survivors. Currently, no therapeutics are approved for use in humans against NiV infection. Here, we report that 4'-chloromethyl-2'-deoxy-2'-fluorocytidine (ALS-8112) inhibits NiV. ALS-8112 is the parent nucleoside of lumicitabine, which has been evaluated in phase I and II clinical trials to treat pediatric and adult respiratory syncytial virus infection. In this study, we tested ALS-8112 against NiV and other major human respiratory pneumo- and paramyxoviruses in 2 human lung epithelial cell lines, and demonstrated the ability of ALS-8112 to reduce infectious wild-type NiV yield by over 6 orders of magnitude with no apparent cytotoxicity. However, further cytotoxicity testing in primary cells and bone marrow progenitor cells indicated cytotoxicity at higher concentrations of ALS-8112. Our results warrant the evaluation of lumicitabine against NiV infection in relevant animal models. Published by Elsevier B.V.Entities:
Keywords: ALS-8112; Henipavirus; Lumicitabine; Nipah virus; Nucleoside analog; RSV
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Year: 2020 PMID: 31935422 PMCID: PMC7054849 DOI: 10.1016/j.antiviral.2020.104712
Source DB: PubMed Journal: Antiviral Res ISSN: 0166-3542 Impact factor: 5.970