Adenovirus-Vectored Drug-Vaccine Duo as a Rapid-Response Tool for Conferring Seamless Protection against Influenza

被引:19
|
作者
Zhang, Jianfeng [1 ]
Tarbet, E. Bart [2 ]
Feng, Tsungwei [1 ]
Shi, Zhongkai [1 ]
Van Kampen, Kent R. [1 ]
Tang, De-chu C. [1 ]
机构
[1] Vaxin Inc, Birmingham, AL 35203 USA
[2] Utah State Univ, Inst Antiviral Res, Logan, UT 84322 USA
来源
PLOS ONE | 2011年 / 6卷 / 07期
基金
美国国家卫生研究院;
关键词
IMMUNE-RESPONSES; VIRUS; NASAL; H5N1; IMMUNOGENICITY; FORMULATIONS; IMMUNIZATION; REPLICATION; INTERFERON; ANTIBODIES;
D O I
10.1371/journal.pone.0022605
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Few other diseases exert such a huge toll of suffering as influenza. We report here that intranasal (i.n.) administration of E1/E3-defective (Delta E1E3) adenovirus serotype 5 (Ad5) particles rapidly induced an anti-influenza state as a means of prophylactic therapy which persisted for several weeks in mice. By encoding an influenza virus (IFV) hemagglutinin (HA) HA1 domain, an Ad5-HA1 vector conferred rapid protection as a prophylactic drug followed by elicitation of sustained protective immunity as a vaccine for inducing seamless protection against influenza as a drug-vaccine duo (DVD) in a single package. Since Ad5 particles induce a complex web of host responses, which could arrest influenza by activating a specific arm of innate immunity to impede IFV growth in the airway, it is conceivable that this multi-pronged influenza DVD may escape the fate of drug resistance that impairs the current influenza drugs.
引用
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页数:8
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