Recombinant Vesicular Stomatitis Virus-Based Vaccines Against Ebola and Marburg Virus Infections

被引:157
作者
Geisbert, Thomas W. [1 ,2 ]
Feldmann, Heinz [3 ,4 ,5 ]
机构
[1] Univ Texas Med Branch, Galveston Natl Lab, Galveston, TX 77550 USA
[2] Univ Texas Med Branch, Dept Microbiol & Immunol, Galveston, TX 77550 USA
[3] NIAID, Virol Lab, Div Intramural Res, NIH,Rocky Mt Labs, Hamilton, MT USA
[4] Publ Hlth Agcy Canada, Natl Microbiol Lab, Winnipeg, MB, Canada
[5] Univ Manitoba, Dept Med Microbiol, Winnipeg, MB, Canada
基金
美国国家卫生研究院;
关键词
PROTECTS NONHUMAN-PRIMATES; HEMORRHAGIC-FEVER; POSTEXPOSURE PROTECTION; GUINEA-PIGS; VECTORS; LIVE; GLYCOPROTEINS; IMMUNOGENICITY; VACCINATION;
D O I
10.1093/infdis/jir349
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The filoviruses, Marburg virus and Ebola virus, cause severe hemorrhagic fever with a high mortality rate in humans and nonhuman primates. Among the most-promising filovirus vaccines under development is a system based on recombinant vesicular stomatitis virus (rVSV) that expresses a single filovirus glycoprotein (GP) in place of the VSV glycoprotein (G). Importantly, a single injection of blended rVSV-based filovirus vaccines was shown to completely protect nonhuman primates against Marburg virus and 3 different species of Ebola virus. These rVSV-based vaccines have also shown utility when administered as a postexposure treatment against filovirus infections, and a rVSV-based Ebola virus vaccine was recently used to treat a potential laboratory exposure. Here, we review the history of rVSV-based vaccines and pivotal animal studies showing their utility in combating Ebola and Marburg virus infections.
引用
收藏
页码:S1075 / S1081
页数:7
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