Adenovirus-based vaccine prevents pneumonia in ferrets challenged with the SARS coronavirus and stimulates robust immune responses in macaques

被引:54
作者
Kobinger, Gary P.
Figueredo, Joanita M.
Rowe, Thomas
Zhi, Yan
Gao, Guangping
Sanmiguel, Julio C.
Bell, Peter
Wivel, Nelson A.
Zitzow, Lois A.
Flieder, Douglas B.
Hogan, Robert J.
Wilson, James M.
机构
[1] Univ Manitoba, Canadian Sci Ctr Human & Anim Hlth, Hlth Canada, Dept Med Microbiol, Winnipeg, MB, Canada
[2] Univ Manitoba, Canadian Sci Ctr Human & Anim Hlth, Natl Microbiol Lab, Sect Pathogens Program, Winnipeg, MB, Canada
[3] Univ Penn, Sch Med, Dept Pathol & Lab Med, Gene Therapy Program, Philadelphia, PA 19104 USA
[4] So Res Inst, Emerging Pathogens Dept, Birmingham, AL 35255 USA
[5] Fox Chase Canc Ctr, Dept Pathol, Philadelphia, PA 19111 USA
关键词
SARS; adenovirus; vaccine; ACUTE RESPIRATORY SYNDROME; REPLICATION; INFECTION; VIRUS; RESERVOIRS; SELECTION; ANTIBODY; VECTORS; TRACT; GREEN;
D O I
10.1016/j.vaccine.2007.04.065
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A ferret model of severe acute respiratory syndrome (SARS)-CoV infection was used to evaluate the efficacy of an adenovirus vaccine. Animals were subjected to heterologous prime-boost using vectors from human serotype 5 and chimpanzee derived adenoviruses (human AdHu5 and chimpanzee AdC7) expressing spike protein followed by intranasal challenge with SARS-CoV Vaccination led to a substantial reduction in viral load and prevented the severe pneumonia seen in unvaccinated animals. The same prime-boost strategy was effective in rhesus macaques in eliciting SARS-CoV specific immune responses. These data indicate that a heterologous adenovirus-based prime-boost vaccine strategy could safely stimulate strong immunity that may be needed for complete protection against SARS-CoV infection. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5220 / 5231
页数:12
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