Highly attenuated smallpox vaccine protects rabbits and mice against pathogenic orthopoxvirus challenge

被引:47
作者
Empig, C
Kenner, JR
Perret-Gentil, M
Youree, BE
Bell, E
Chen, A
Gurwith, M
Higgins, K
Lock, M
Rice, AD
Schriewer, J
Sinangil, F
White, E
Buller, RM
Dermody, TS
Isaacs, SN
Moyer, RW
机构
[1] VanGen Inc, San Francisco, CA 94080 USA
[2] Univ Florida, Dept Mol Genet & Microbiol, Gainesville, FL USA
[3] Vanderbilt Univ, Sch Med, Dept Med, Nashville, TN 37212 USA
[4] Vanderbilt Univ, Sch Med, Dept Pediat, Nashville, TN 37212 USA
[5] Vanderbilt Univ, Sch Med, Dept Immunol & Microbiol, Nashville, TN 37212 USA
[6] Vanderbilt Univ, Sch Med, Elizabeth B Lamb Ctr Pediat Res, Nashville, TN 37212 USA
[7] Vanderbilt Univ, Sch Med, Dept Med, Nashville, TN 37212 USA
[8] St Louis Univ, Dept Mol Microbiol & Immunol, St Louis, MO 63103 USA
关键词
smallpox; vaccine; orthopoxvirus;
D O I
10.1016/j.vaccine.2005.03.029
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 possible reemergence of smallpox through bioterrorism requires the preparation of adequate stockpiles of vaccine. Dryvax, the only US-licensed vaccinia virus smallpox vaccine, has an unacceptable safety profile in the pre-event setting. LC16m8 is a Japanese-licensed attenuated vaccinia virus strain that has been safely used in over 50,000 persons. Until now, efficacy of this vaccine was unproven. Using two animal models, we show that LC16m8 and Dryvax elicit comparable humoral immune responses after a single vaccination and equivalently protect against lethal poxvirus disease. Thus, LC16m8 shows promise as a safe and effective smallpox vaccine with the potential for replacing Dryvax. (c) 2006 Published by Elsevier Ltd.
引用
收藏
页码:3686 / 3694
页数:9
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