Evaluation of adenovirus vectors containing serotype 35 fibers for vaccination

被引:42
作者
DiPaolo, N
Ni, S
Gaggar, A
Strauss, R
Tuve, S
Li, ZY
Stone, D
Shayakhmetov, D
Kiviat, N
Touré, P
Sow, S
Horvat, B
Lieber, A
机构
[1] Univ Washington, Dept Med, Div Med Genet, Seattle, WA 98195 USA
[2] Univ Washington, Dept Pathol, Seattle, WA 98195 USA
[3] Univ Dakar, Dept Infect Dis, Dakar, Senegal
[4] INSERM, U404, F-69008 Lyon, France
关键词
adenovirus serotype 35; vaccination; CD46; CD46 transgenic mice;
D O I
10.1016/j.ymthe.2005.12.008
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In contrast to commonly used serotype 5-based adenovirus (Ad) vectors, Ad's containing fibers derived from B-group serotype 35 (Ad5/35) efficiently transduce human DCs ex vivo and appear to target antigen-presenting cells after intravenous injection into baboons. Based on this, Ad5/35 vectors could be valuable tools for immunotherapy and vaccination. On the other hand, a number of studies indicate that signaling through the B-group Ad receptor, CD46, can cause tolerance or immunosuppression. Since mice do not express CD46 in a human-like pattern, we studied the in vivo properties of Ad5/35 in transgenic mice that express CD46 in a pattern and at a level similar to those of humans. Hypersensitivity assays and analyses of frequencies of regulatory T cells and T cell responses did not indicate that AdS/35 injection exerts detrimental effects on the host's immune system. An Ac15/35 vector expressing a model antigen was able to trigger a strong T cell response against the test antigen after intramuscular injection. Overall, compared to Ac15 vectors, Ad5/35 vectors had a better safety profile, reflected by lower serum levels of proinflammatory cytokines.
引用
收藏
页码:756 / 765
页数:10
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