接种疫苗
病毒学
效价
生物
抗体
病毒
重组DNA
抗体效价
血凝试验
H5N1亚型流感病毒
免疫学
基因
生物化学
作者
Haroldo Toro,David L. Suarez,De-chu C. Tang,Frederik W. van Ginkel,Cassandra Breedlove
出处
期刊:Avian Diseases
[American Association of Avian Pathologists]
日期:2011-03-01
卷期号:55 (1): 43-47
被引量:14
标识
DOI:10.1637/9516-090210-reg.1
摘要
We evaluated protection conferred by mucosal vaccination with replication-competent adenovirus-free recombinant adenovirus expressing a codon-optimized avian influenza (AI) H5 gene from A/turkey/WI/68 (AdTW68.H5ck). Commercial, layer-type chicken groups were either singly vaccinated ocularly at 5 days of age, singly vaccinated via spray at 5 days of age, or ocularly primed at 5 days and ocularly boosted at 15 days of age. Only chickens primed and boosted via the ocular route developed AI systemic antibodies with maximum hemagglutination inhibition mean titers of 3.9 log2 at 32 days of age. In contrast, single vaccination via the ocular or spray routes maintained an antibody status similar to unvaccinated controls. All chickens (16/16) subjected to ocular priming and boosting with AdTW68.H5ck survived challenge with highly pathogenic AI virus A/chicken/Queretaro/14588-19/95 (H5N2). Single ocular vaccination resulted in 63% (10/16) of birds surviving the challenge followed by a 44% (7/16) survival of single-sprayed vaccinated birds. Birds vaccinated twice via the ocular route also showed significantly lower (P < 0.05) AI virus RNA concentrations in oropharyngeal swabs compared to unvaccinated–challenged controls.
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