Protection against lethal challenge by Ebola virus-like particles produced in insect cells

被引:70
|
作者
Sun, Yuliang [1 ,2 ]
Carrion, Ricardo, Jr. [3 ,4 ]
Ye, Ling [1 ,2 ]
Wen, Zhiyuan [1 ,2 ]
Ro, Young-Tae [3 ,5 ]
Brasky, Kathleen [4 ]
Ticer, Anysha E. [3 ]
Schwegler, E. Ellen [3 ]
Patterson, Jean L. [3 ]
Compans, Richard W. [1 ,2 ]
Yang, Chinglai [1 ,2 ]
机构
[1] Emory Univ, Sch Med, Rollins Res Ctr, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Rollins Res Ctr, Emory Vaccine Ctr, Atlanta, GA 30322 USA
[3] SW Fdn Biomed Res, Dept Virol & Immunol, San Antonio, TX 78227 USA
[4] SW Fdn Biomed Res, SW Natl Primate Res Ctr, San Antonio, TX 78227 USA
[5] Konkuk Univ, Grad Sch Med, Biochem Lab, Chungju 380701, South Korea
基金
美国国家卫生研究院;
关键词
Ebola virus; Virus like particle; Antibody; Lethal challenge; Vaccine; NONHUMAN-PRIMATES; IMMUNE-RESPONSES; VACCINE; IMMUNOGENICITY; IMMUNIZATION; EXPRESSION; INFECTION; EFFICACY; MUCOSAL; DNA;
D O I
10.1016/j.virol.2008.09.020
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Ebola virus-like particles (VLPs) were produced in insect cells using a recombinant baculovirus expression system and their efficacy for protection against Ebola virus infection was investigated. Two immunizations with 50 mu g Ebola VLPs (high dose) induced a high level of antibodies against Ebola GP that exhibited strong neutralizing activity against GP-mediated virus infection and conferred complete protection of vaccinated mice against lethal challenge by a high dose of mouse-adapted Ebola virus. In contrast, two immunizations with 10 mu g Ebola VLPs (low dose) induced 5-fold lower levels of antibodies against GP and these mice were not protected against lethal Ebola virus challenge, similar to control mice that were immunized with 50 mu g SIV Gag VLPs. However. the antibody responses against GP were boosted significantly after a third immunization with 10 mu g Ebola VLPs to similar levels as those induced by two immunizations with 50 mu g Ebola VLPs, and vaccinated mice were also effectively protected against lethal Ebola virus challenge. Furthermore, serum viremia levels in protected mice were either below the level of detection or significantly lower compared to the viremia levels in control mice. These results show that effective protection can be achieved by immunization with Ebola VLPs produced in insect cells, which give high production yields, and lend further Support to their development as an effective vaccine strategy against Ebola virus. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:12 / 21
页数:10
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