Strong and persistent CD4+ T-cell response in healthy adults immunized with a candidate HIV-1 vaccine containing gp120, Nef and Tat antigens formulated in three Adjuvant Systems

被引:67
作者
Leroux-Roels, Isabel [5 ]
Koutsoukos, Marguerite [1 ]
Clement, Frederic [5 ]
Steyaert, Sophia [5 ]
Janssens, Michel [1 ]
Bourguignon, Patricia [1 ]
Cohen, Kristen [2 ,3 ,4 ]
Altfeld, Marcus [2 ,3 ,4 ]
Vandepapeliere, Pierre [1 ]
Pedneault, Louise [1 ]
McNally, Lisa [1 ]
Leroux-Roels, Geert [5 ]
Voss, Gerald [1 ]
机构
[1] GlaxoSmithKline Biol, Rixensart, Belgium
[2] Massachusetts Gen Hosp, Partners AIDS Res Ctr, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Div Aids, Boston, MA USA
[5] Ghent Univ & Hosp, Ctr Vaccinol, Ghent, Belgium
关键词
Human immunodeficiency virus; HIV-1; vaccine; Adjuvant; CD4(+) T-cell response; CENTRAL MEMORY; VIRAL BURDEN; DOUBLE-BLIND; VIRUS; INFECTION; VIREMIA; ANTIBODY; EFFICACY; DISEASE; RTS; S/AS02A;
D O I
10.1016/j.vaccine.2010.08.035
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
This randomized double-blind study aimed to determine the safety and immunogenicity of a gp120/NefTat candidate human immunodeficiency virus type 1 (HIV-1) vaccine formulated with one of three different Adjuvant Systems (ASO2(A), ASO2(V) and ASO1(B)) in healthy HIV-seronegative adults. All vaccine formulations induced strong HIV-specific CD4(+) T-cell responses characterized by high lympho-proliferative capacity and IL-2 production that were still detectable 18 months after last immunization, with strongest responses seen in the AS01(B) group. Broad coverage was demonstrated against gp120, and to a lesser extent Nef, derived from the most common circulating clades (B, C and circulating recombinant form [CRF]-01). All vaccine formulations exhibited acceptable safety and reactogenicity profiles. The demonstration of superior CIA T-cell induction by AS01(B) provides important guidance for future HIV vaccine development. (C) 2010 Published by Elsevier Ltd.
引用
收藏
页码:7016 / 7024
页数:9
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