1899. The Cellular Kinase Inhibitor OSU-03012 Inhibits Enterovirus 71 In Vitro. (26th November 2018)

• Record Type: Journal Article
• Authors: Chan, Jasper; Tsang, Jessica; Zou, Zijiao; Chik, Kenn; Yuan, Shuofeng; Chu, Hin; Lau, Susanna; Yuen, Kwok-Yung
• Is Part Of: Open forum infectious diseases. Volume 5(2018)Supplement 1
• Page Start: S545
• Page End: S545
• Publication Date: 2018-11-26
• Subjects: Communicable diseases -- Periodicals; Medical microbiology -- Periodicals; Infection -- Periodicals; 616.9
• DOI: 10.1093/ofid/ofy210.1555
• Languages: English
• ISSNs: 2328-8957

Abstract

Abstract: Background: Enterovirus 71 (EV-71) is a nonenveloped, single-stranded positive-sense RNA virus belonging to genus Enterovius, family Picornaviridae . EV-71 has caused recurrent outbreaks of hand, foot, and mouth disease especially among children in Asia. Some patients develop severe complications, such as meningitis, encephalitis, poliomyelitis-like paralysis, myocarditis, and pulmonary edema. There are currently limited treatment options for EV-71 infection. OSU-03012 is a celecoxib derivative cellular kinase inhibitor with no inhibiting activity on cyclooxygenase that has antiviral activities against a broad-spectrum of viruses, including flaviviruses, filoviruses, and arenaviruses. Methods: Two clinical isolates of EV-71 obtained from patients with laboratory-confirmed EV-71 infections were included in the study. We evaluated the in vitro anti-EV-71 activity of OSU-03012, using virus yield reduction assays (by quantitative reverse transcription-polymerase chain reaction), cell protection assay, and plaque reduction assay in multiple cell lines. Results: OSU-03012 inhibited both EV-71 strains in U251 (neuronal) and RD (rhabdomyosarcoma) cells. The half maximal inhibitory concentration (IC50 ) of OSU-03012 against EV-71 was consistently <2 µM in these cell lines in the virus yield reduction assay. At 2µM of OSU-03012, there was a nearly 2-log reduction in viral RNA load in both U251 and RD cells. There was a dose-dependent increase in the percentage of viable cells after the addition of 0 to 2 µM of OSU-03012 in EV-71-infected U251 and RD cells in the cell protection assay. In the plaque reduction assay, there was >70% reduction in plaque numbers with the addition of 2 µM of OSU-03012. Conclusion: OSU-03012 exhibits anti-EV-71 activity in vitro . The treatment effects of OSU-03012 should be further evaluated in representative animal models of severe EV-71 infection to provide further data for potential clinical evaluation in the future. Disclosures: J. Chan, Pfizer Corporation Hong Kong: Travel grant recipient, Grant recipient. Astellas Pharma Hong Kong Corporation Limited: Travel grant recipient, Grant recipient. Gilead Sciences Hong Kong Limited: Invited speaker, Speaker honorarium. Luminex Corporation: Invited speaker, Speaker honorarium.