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
论文数: 0引用数: 0
h-index: 0
机构:Fox Chase Canc Ctr, Program Viral Pathogenesis, Div Basic Sci, Philadelphia, PA 19111 USA
Fang, M
Cheng, H
论文数: 0引用数: 0
h-index: 0
机构:Fox Chase Canc Ctr, Program Viral Pathogenesis, Div Basic Sci, Philadelphia, PA 19111 USA
Cheng, H
Dai, ZP
论文数: 0引用数: 0
h-index: 0
机构:Fox Chase Canc Ctr, Program Viral Pathogenesis, Div Basic Sci, Philadelphia, PA 19111 USA
Dai, ZP
Bu, ZM
论文数: 0引用数: 0
h-index: 0
机构:Fox Chase Canc Ctr, Program Viral Pathogenesis, Div Basic Sci, Philadelphia, PA 19111 USA
Bu, ZM
Sigal, LJ
论文数: 0引用数: 0
h-index: 0
机构:Fox Chase Canc Ctr, Program Viral Pathogenesis, Div Basic Sci, Philadelphia, PA 19111 USA
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
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.