A chimeric Sindbis-based vaccine protects cynomolgus macaques against a lethal aerosol challenge of eastern equine encephalitis virus

被引:33
作者
Roy, Chad J. [1 ]
Adams, A. Paige [2 ,3 ]
Wang, Eryu [2 ,3 ]
Leal, Grace [2 ,3 ]
Seymour, Robert L. [2 ,3 ]
Sivasubramani, Satheesh K. [1 ]
Mega, William [4 ]
Frolov, Ilya [5 ]
Didier, Peter J. [6 ]
Weaver, Scott C. [2 ,3 ]
机构
[1] Tulane Natl Primate Res Ctr, Div Microbiol, Covington, LA 70433 USA
[2] Univ Texas Med Branch, Sealy Ctr Vaccine Dev, Inst Human Infect & Immun, Galveston, TX 77555 USA
[3] Univ Texas Med Branch, Dept Pathol, Galveston, TX 77555 USA
[4] Lovelace Resp Res Inst, Albuquerque, NM 87108 USA
[5] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35294 USA
[6] Tulane Natl Primate Res Ctr, Div Comparat Pathol, Covington, LA 70433 USA
基金
美国国家卫生研究院;
关键词
Encephalitis; Aerosol; Nonhuman primate; Alphavirus; Vaccine; EMBRYO CELL-CULTURE; INTERFERON SENSITIVITY; INFECTION; VARICELLA; STRAINS;
D O I
10.1016/j.vaccine.2013.01.014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Eastern equine encephalitis virus (EEEV) is a mosquito-borne alphavirus that causes sporadic, often fatal disease outbreaks in humans and equids, and is also a biological threat agent. Two chimeric vaccine candidates were constructed using a cDNA clone with a Sindbis virus (SINV) backbone and structural protein genes from either a North (SIN/NAEEEV) or South American (SIN/SAEEEV) strain of EEEV. The vaccine candidates were tested in a nonhuman primate (NHP) model of eastern equine encephalitis (EEE). Cynomolgus macaques were either sham-vaccinated, or vaccinated with a single dose of either SIN/NAEEEV or SIN/SAEEEV. After vaccination, animals were challenged by aerosol with a virulent North American strain of EEEV (NA EEEV). The SIN/NAEEEV vaccine provided significant protection, and most vaccinated animals survived EEEV challenge (82%) with little evidence of disease, whereas most SIN/SAEEEV-vaccinated (83%) and control (100%) animals died. Protected animals exhibited minimal changes in temperature and cardiovascular rhythm, whereas unprotected animals showed profound hyperthermia and changes in heart rate postexposure. Acute inflammation and neuronal necrosis were consistent with EEEV-induced encephalitis in unprotected animals, whereas no encephalitis-related histopathologic changes were observed in the SIN/NAEEEV-vaccinated animals. These results demonstrate that the chimeric SIN/NAEEEV vaccine candidate protects against an aerosol EEEV exposure. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1464 / 1470
页数:7
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