Nucleic acid (DNA) immunization as a platform for dengue vaccine development

被引:21
作者
Porter, Kevin R. [1 ]
Raviprakash, Kanakatte [1 ]
机构
[1] Naval Med Res Ctr, Infect Dis Directorate, Silver Spring, MD 20910 USA
关键词
Dengue; DNA vaccines; Clinical trials; Non-human primates; Shuffled DNA vaccine; Plasmid; Biojector; NEUTRALIZING ANTIBODY-RESPONSE; CLASS-II COMPARTMENTS; GM-CSF GENE; IMMUNE-RESPONSES; PLASMID DNA; VIRUS TYPE-1; PROTECTIVE EFFICACY; EBOLA-VIRUS; SEROTYPES; COMPLEX;
D O I
10.1016/j.vaccine.2015.09.102
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Since the early 1990s, DNA immunization has been used as a platform for developing a tetravalent dengue vaccine in response to the high priority need for protecting military personnel deployed to dengue endemic regions of the world. Several approaches have been explored ranging from naked DNA immunization to the use of live virus vectors to deliver the targeted genes for expression. Pre-clinical animal studies were largely successful in generating anti-dengue cellular and humoral immune responses that were protective either completely or partially against challenge with live dengue virus. However, Phase 1 clinical evaluation of a prototype monovalent dengue 1 DNA vaccine expressing prM and E genes revealed anti-dengue T cell IFN gamma responses, but poor neutralizing antibody responses. These less than optimal results are thought to be due to poor uptake and expression of the DNA vaccine plasmids. Because DNA immunization as a vaccine platform has the advantages of ease of manufacture, flexible genetic manipulation and enhanced stability, efforts continue to improve the immunogenicity of these vaccines using a variety of methods. Published by Elsevier Ltd.
引用
收藏
页码:7135 / 7140
页数:6
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