Development of Peptide Vaccines in Dengue

被引:29
作者
Reginald, Kavita [1 ,2 ]
Chan, Yanqi [1 ]
Plebanski, Magdalena [3 ]
Poh, Chit Laa [1 ]
机构
[1] Sunway Univ, Res Ctr Biomed Sci, Subang Jaya, Selangor, Malaysia
[2] Sunway Univ, Sch Sci & Technol, Dept Biol Sci, Subang Jaya, Selangor, Malaysia
[3] Monash Univ, Dept Immunol & Pathol, Melbourne, Vic, Australia
关键词
Dengue; peptide vaccine; multi-epitope; synthetic peptides; HLA; cell mediated immunity; T-CELL RESPONSES; ANTIBODY-DEPENDENT ENHANCEMENT; INCOMPLETE FREUNDS-ADJUVANT; COLONY-STIMULATING FACTOR; ORIGINAL ANTIGENIC SIN; CLASS-I BINDING; VIRUS-INFECTION; HEMORRHAGIC-FEVER; IMMUNE-RESPONSES; SYNTHETIC PEPTIDES;
D O I
10.2174/1381612823666170913163904
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dengue is one of the most important arboviral infections worldwide, infecting up to 390 million people and causing 25,000 deaths annually. Although a licensed dengue vaccine is available, it is not efficacious against dengue serotypes that infect people living in South East Asia, where dengue is an endemic disease. Hence, there is an urgent need to develop an efficient dengue vaccine for this region. Data from different clinical trials indicate that a successful dengue vaccine must elicit both neutralizing antibodies and cell mediated immunity. This can be achieved by designing a multi-epitope peptide vaccine comprising B, CD8(+) and CD4(+) T cell epitopes. As recognition of T cell epitopes are restricted by human leukocyte antigens (HLA), T cell epitopes which are able to recognize several major HLAs will be preferentially included in the vaccine design. While peptide vaccines are safe, biocompatible and cost-effective, it is poorly immunogenic. Strategies to improve its immunogenicity by the use of long peptides, adjuvants and nanoparticle delivery mechanisms are discussed.
引用
收藏
页码:1157 / 1173
页数:17
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