| Literature DB >> 31494195 |
George R Painter1, Richard A Bowen2, Gregory R Bluemling3, John DeBergh4, Vindhya Edpuganti4, Prabhakar R Gruddanti4, David B Guthrie4, Michael Hager4, Damien L Kuiper4, Mark A Lockwood4, Deborah G Mitchell4, Michael G Natchus4, Zachary M Sticher4, Alexander A Kolykhalov5.
Abstract
The New World alphaviruses Venezuelan, Eastern, and Western equine encephalitis viruses (VEEV, EEEV and WEEV, respectively) commonly cause a febrile disease that can progress to meningoencephalitis, resulting in significant morbidity and mortality. To address the need for a therapeutic agent for the treatment of Alphavirus infections, we identified and pursued preclinical characterization of a ribonucleoside analog EIDD-1931 (β-D-N4-hydroxycytidine, NHC), which has shown broad activity against alphaviruses in vitro and has a very high genetic barrier for development of resistance. To be truly effective as a therapeutic agent for VEEV infection a drug must penetrate the blood brain barrier and arrest virus replication in the brain. High plasma levels of EIDD-1931 are rapidly achieved in mice after oral dosing. Once in the plasma EIDD-1931 is efficiently distributed into organs, including brain, where it is rapidly converted to its active 5'-triphosphate. EIDD-1931 showed a good safety profile in mice after 7-day repeated dosing with up to 1000 mg/kg/day doses. In mouse model studies, EIDD-1931 was 90-100% effective in protecting mice against lethal intranasal infection when therapeutic treatment was started as late as 24 h post-infection, and partial protection was achieved when treatment was delayed for 48 h post-infection. These results support further preclinical development of EIDD-1931 as a potential anti-alphavirus drug.Entities:
Keywords: Alphavirus; CNS penetration; Murine model; Ribonucleoside analog; Therapeutic treatment
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Year: 2019 PMID: 31494195 DOI: 10.1016/j.antiviral.2019.104597
Source DB: PubMed Journal: Antiviral Res ISSN: 0166-3542 Impact factor: 5.970