Immunogenicity of lyophilized recombinant adenovirus-based vaccine expressing HIV-1 gagpol in mice

被引:0
|
作者
Zhang, Yizhe [1 ]
Kong, Wei [2 ]
机构
[1] Zhengzhou Univ, Dept Bioengn, Zhengzhou 450001, Henan, Peoples R China
[2] Jilin Univ, Coll Life Sci, Changchun 130000, Jilin, Peoples R China
来源
LIFE SCIENCE JOURNAL-ACTA ZHENGZHOU UNIVERSITY OVERSEAS EDITION | 2009年 / 6卷 / 03期
基金
中国国家自然科学基金;
关键词
Ad-gagpol vaccine; lyophilize; stability; immunogenicity; STABILITY; VECTORS; FORMULATIONS;
D O I
暂无
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective. To evaluate the stability and immunogenicity of lyophilized recombinant adenovirus-based vaccine expressing HIV-1 gagpol (Ad-gagpol vaccine). Methods. Screening the optimal novel protector excipient according to the appearance, virus titer and thermostability of the lyophilized Ad-gagpol vaccine. Western blot analysis and IFN-gamma Elispot assay were used to detect the immunogenicity of lyophilized Ad-gagpol vaccine in mice. Results. Optimal protector excipient and buffer system of lyophilized Ad-based vaccine were identified. It was found to be fairly stable following lengthy exposure to higher temperature. The mice which administered lyophilized Ad-gagpol vaccine produced indistinguishable antibody titer and IFN-gamma ELISPOT level compared with liquid Ad-gagpol vaccine group (P > 0.05). Conclusion. Lyophilized Ad-gagpol vaccine can induce high immunogenicity in mice. The protector containing human serum albumin, trehalose, mannitol, dextran and sucrose was suitable for lyophilized Ad-gagpol vaccine. [Life Science Journal. 2009; 6(1): 13-17] (ISSN: 1097-8135).
引用
收藏
页码:13 / 17
页数:5
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