Post-exposure efficacy of Oral T-705 (Favipiravir) against inhalational Ebola virus infection in a mouse model

被引:168
作者
Smither, Sophie J. [1 ]
Eastaugh, Lin S. [1 ]
Steward, Jackie A. [1 ]
Nelson, Michelle [1 ]
Lenk, Robert P. [2 ]
Lever, Mark S. [1 ]
机构
[1] Dstl, Dept Biomed Sci, Salisbury SP4 0JQ, Wilts, England
[2] MediVector Inc, Boston, MA 02110 USA
关键词
Ebola; Broad-spectrum; Licensed; Aerosol; Bioterrorism; Favipiravir; IN-VIVO ACTIVITIES; ADMINISTERED T-705; HEMORRHAGIC-FEVER; INFLUENZA-VIRUS; RNA-POLYMERASE; VITRO; MICE; FILOVIRUSES; ARENAVIRUS; MECHANISM;
D O I
10.1016/j.antiviral.2014.01.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Filoviruses cause disease with high case fatality rates and are considered biological threat agents. Licensed post-exposure therapies that can be administered by the oral route are desired for safe and rapid distribution and uptake in the event of exposure or outbreaks. Favipiravir or T-705 has broad antiviral activity and has already undergone phase II and is undergoing phase III clinical trials for influenza. Here we report the first use of T-705 against Ebola virus. T-705 gave 100% protection against aerosol Ebola virus E718 infection; protection was shown in immune-deficient mice after 14 days of twice-daily dosing. T-705 was also shown to inhibit Ebola virus infection in cell culture. T-705 is likely to be licensed for use against influenza in the near future and could also be used with a new indication for filovirus infection. (C) 2014 Published by Elsevier B.V.
引用
收藏
页码:153 / 155
页数:3
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