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Postexposure Protective Efficacy of T-705 (Favipiravir) Against Sudan Virus Infection in Guinea Pigs.
Rahim, Md N; Zhang, Zirui; He, Shihua; Zhu, Wenjun; Banadyga, Logan; Safronetz, David; Qiu, Xiangguo.
Afiliación
  • Rahim MN; Special Pathogens Program, National Microbiology laboratory, Public Health Agency of Canada.
  • Zhang Z; Department of Medical Microbiology, University of Manitoba, Winnipeg, Canada.
  • He S; Special Pathogens Program, National Microbiology laboratory, Public Health Agency of Canada.
  • Zhu W; Department of Medical Microbiology, University of Manitoba, Winnipeg, Canada.
  • Banadyga L; Special Pathogens Program, National Microbiology laboratory, Public Health Agency of Canada.
  • Safronetz D; Special Pathogens Program, National Microbiology laboratory, Public Health Agency of Canada.
  • Qiu X; Department of Medical Microbiology, University of Manitoba, Winnipeg, Canada.
J Infect Dis ; 218(suppl_5): S649-S657, 2018 11 22.
Article en En | MEDLINE | ID: mdl-29982696
ABSTRACT
Filoviruses such as Ebola virus (EBOV), Marburg virus (MARV), and Sudan virus (SUDV) cause deadly viral hemorrhagic fever in humans, with high case-fatality rates; however, no licensed therapeutic agent or vaccine has been clinically approved to treat or prevent infection. T-705 (favipiravir) is a novel antiviral drug that has been approved for the treatment of influenza in Japan. T-705 exhibits broad-spectrum antiviral activity against different viruses, including MARV and EBOV, and here, we are the first to report the in vitro and in vivo antiviral activity of T-705 against SUDV. T-705 treatment reduced SUDV replication in Vero E6 cells. Subcutaneous administration of T-705, beginning 1-4 days after infection and continuing for 7 days, significantly protected SUDV-infected guinea pigs, with a survival rate of 83%-100%. Viral RNA replication and infectious virus production were also significantly reduced in the blood, spleen, liver, lungs, and kidney. Moreover, early administration of low-dose T-705 and late administration (at 5 days after infection) of higher-dose T-705 also showed partial protection. Overall, our study is the first to demonstrate the antiviral activity of T-705 against SUDV, suggesting that T-705 may be a potential drug candidate for use during outbreaks.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Antivirales / Pirazinas / Infecciones por Filoviridae / Amidas Límite: Animals Idioma: En Revista: J Infect Dis Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Antivirales / Pirazinas / Infecciones por Filoviridae / Amidas Límite: Animals Idioma: En Revista: J Infect Dis Año: 2018 Tipo del documento: Article