数字农科院2.0

Strategies for improving the efficacy of a H6 subtype avian influenza DNA vaccine in chickens

文献类型： 外文期刊

作者： Jiang, Yongping;Bu, Zhigao;Zeng, Xianying;Tian, Guobin;Li, Yanbing;Ge, Jinying;Chen, Hualan;Shan, Songhua;Ellis, Trevor;Edwards, John;Fenwick, Stan

作者机构：

关键词： pCAGGS: vector;H6 subtype avian influenza DNA vaccine: immunologic-drug;immunostimulant-drug;vaccine;pharmacodyn;immune response;seroconversion rate

期刊名称： JOURNAL OF VIROLOGICAL METHODS

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收录情况： SCI

摘要： A low-pathogenicity avian influenza H6N2 virus was used to investigate approaches to improve DNA vaccine efficacy. The viral hemagglutinin (HA) gene or its chicken biased HA gene, incorporating a Kozak sequence, was cloned into a pCAGGS vector to produce the pCAG-HAk and pCAG-optiHAk constructs. Following two intramuscular injections, the seroconversion rate in vaccinated chickens with 10, 100 or 300 mu g pCAG-HAk were 87.5%, 75% and 75%, respectively. The profile of H6 hemagglutination inhibition (HI) antibodies induced by different doses of pCAG-HAk during the 8-week study period was similar. The HI titer rose significantly in the three different dose groups following the booster and reached a plateau 2-3 weeks post-booster. In a single dose vaccination group with 100 mu g pCAG-HAk, a maximum seroconversion rate reached 53.3% at 5 weeks post-vaccination. The earliest time of seroconversion appeared two weeks after DNA immunization. Following two electroporation (EP) vaccinations with 100 mu g pCAG-HAk, all birds seroconverted and the HI antibody titers were significantly higher than those using intramuscular immunization, suggesting that EP was more efficient than intramuscular delivery of the DNA vaccines. In comparison, chickens immunized with 10 or 100 mu g pCAG-optiHAk showed 37.5% and 87.5% seroconversion rates, respectively, at 3 weeks following the booster. The pCAG-HAk was not significantly different from the pCAG-optiHAk in either the seroconversion rate or H6 H1 titer, suggesting that the codon-optimized HA DNA vaccine did not achieve significantly better immunogenicity than the pCAG-HAk vaccine

分类号： R37

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