Immunization with a single extracellular enveloped virus protein produced in bacteria provides partial protection from a lethal orthopoxvirus infection in a natural host

被引:68
作者
Fang, M
Cheng, H
Dai, ZP
Bu, ZM
Sigal, LJ
机构
[1] Fox Chase Canc Ctr, Program Viral Pathogenesis, Div Basic Sci, Philadelphia, PA 19111 USA
[2] Fox Chase Canc Ctr, Program Biomol Struct & Funct, Div Basic Sci, Philadelphia, PA 19111 USA
关键词
rodent; viral; immunization; poxvirus; vaccinia virus; ectromelia virus; smallpox; subunit vaccine;
D O I
10.1016/j.virol.2005.09.056
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Subunit vaccines that use the vaccinia virus extracellular envelope protein A33R alone or combined with other structural proteins are excellent candidates for a new smallpox vaccine. Since a new smallpox vaccine would be used in humans, who are the natural hosts for the Orthopoxvirus variola, the agent of smallpox, it would be important to determine whether a prospective smallpox vaccine can protect from a lethal Orthopoxvirus infection in a natural host. We addressed this question using the mouse-specific Orthopoxvirus ectromelia virus. We demonstrate that immunization with recombinant ectromelia virus envelope protein EVM135 or its ortholog vaccinia virus A33R produced in E. coli protects susceptible mice from a lethal ectromelia virus infection. This is the first report that a subunit vaccine can provide protection to a lethal Orthopoxvirus infection in its natural host. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:231 / 243
页数:13
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