The novel Capripoxvirus vector lumpy skin disease virus efficiently boosts modified vaccinia Ankara human immunodeficiency virus responses in rhesus macaques

被引:14
|
作者
Burgers, Wendy A. [1 ,2 ]
Ginbot, Zekarias [1 ,2 ]
Shen, Yen-Ju [1 ,2 ]
Chege, Gerald K. [1 ,2 ]
Soares, Andreia P. [1 ,2 ]
Mueller, Tracey L. [1 ,2 ]
Bunjun, Rubina [1 ,2 ]
Kiravu, Agano [1 ,2 ]
Munyanduki, Henry [1 ,2 ]
Douglass, Nicola [1 ,2 ]
Williamson, Anna-Lise [1 ,2 ,3 ]
机构
[1] Univ Cape Town, Fac Hlth Sci, Div Med Virol, ZA-7700 Rondebosch, South Africa
[2] Univ Cape Town, Fac Hlth Sci, Inst Infect Dis & Mol Med, ZA-7700 Rondebosch, South Africa
[3] Groote Schuur Hosp, Natl Hlth Lab Serv, ZA-7925 Cape Town, South Africa
来源
基金
新加坡国家研究基金会;
关键词
TYPE-1; SUBTYPE-C; T-CELLS; IMMUNE-RESPONSES; HIV-1; GENES; DNA; IMMUNOGENICITY; MAGNITUDE; CANDIDATE; INFECTION;
D O I
10.1099/vir.0.067835-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Poxvirus vectors represent promising human immunodeficiency virus (HIV) vaccine candidates and were a component of the only successful HIV vaccine efficacy trial to date. We tested the immunogenicity of a novel recombinant capripoxvirus vector, lumpy skin disease virus (LSDV), in combination with modified vaccinia Ankara (MVA), both expressing genes from HIV-1. Here, we demonstrated that the combination regimen was immunogenic in rhesus macaques, inducing high-magnitude, broad and balanced CD4(+) and CD8(+) T-cell responses, and transient activation of the immune response. These studies support further development of LSDV as a vaccine vector.
引用
收藏
页码:2267 / 2272
页数:6
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