Potent immune responses and in vitro pro-inflammatory cytokine suppression by a novel adenovirus vaccine vector based on rare human serotype 28

被引:39
|
作者
Kahl, Christoph A. [1 ]
Bonnell, Jessica [1 ]
Hiriyanna, Suja [1 ]
Fultz, Megan [1 ]
Nyberg-Hoffman, Cassandra [1 ]
Chen, Ping [1 ]
King, C. Richter [1 ]
Gall, Jason G. D. [1 ]
机构
[1] GenVec Inc, Gaithersburg, MD 20878 USA
关键词
Adenovirus; Vector; Human vaccine; Seroprevalence; PRIME-BOOST REGIMENS; CELLULAR RECEPTOR; GENE-TRANSFER; PROTECTIVE EFFICACY; HIV-1; VACCINE; DNA; IMMUNOGENICITY; VIRUS; ANTIBODIES; INFECTION;
D O I
10.1016/j.vaccine.2010.06.050
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Adenovirus vaccine vectors derived from rare human serotypes have been shown to be less potent than serotype 5 (Ad5) at inducing immune responses to encoded antigens. To identify highly immunogenic adenovirus vectors, we assessed pro-inflammatory cytokine expression, binding to the CD46 receptor, and immunogenicity Species D adenoviruses uniquely suppressed pro-inflammatory cytokines and induced high levels of type I interferon. Thus, it was unexpected that a vector derived from a representative serotype, Ad28, induced significantly higher transgene-specific T cell responses than an Ad35 vector. Prime-boost regimens with Ad28, Ad35, Ad 14, or Ad5 significantly boosted T cell and antibody responses. The seroprevalence of Ad28 was confirmed to be <10% in the United States. Together, this shows that a rare human serotype-based vector can elicit strong immune responses, which was not predicted by in vitro results (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5691 / 5702
页数:12
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