Immunogenicity of a chimeric hepatitis A virus (HAV) carrying the HIV gp41 epitope 2F5

被引:16
作者
Kusov, Yuri Y.
Zamjatina, Natalja A.
Poleschuk, Valentina F.
Michailov, Michail I.
Morace, Graziella
Eberle, Josef
Gauss-Mueller, Verena
机构
[1] Med Univ Lubeck, Inst Med Mol Biol, D-23538 Lubeck, Germany
[2] MP Chumakov Inst Poliomyelitis, Moscow, Russia
[3] Viral Encephalitides Acad Med Sci, Moscow, Russia
[4] Ist Super Sanita, I-00161 Rome, Italy
[5] Univ Munich, Max Von Pettenkofer Inst, Munich, Germany
关键词
anti-HIV; vaccine; virus replication; marmoset; guinea pig; IMMUNE-RESPONSES; 3C PROTEINASE; B VIRUS; PARTICLES; INFECTION; ANTIBODY; VACCINE; 2A; TYPE-1; CELLS;
D O I
10.1016/j.antiviral.2006.08.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Its stable particle structure combined with its high immunogenicity makes the hepatitis A virus (HAV) a perfect carrier to expose foreign epitopes to the host immune system. In an earlier report [Beneduce, F., Kusov, Y., Klinger, M., Gauss-Miller, V., Morace, G., 2002. Chimeric hepatitis A virus particles presenting a foreign epitope (HIV gp41) at their surface. Antiviral Res. 55, 369-377] chimeric virus-like particles (HAV-gp41) were described that carried at their surface the dominant gp41 epitope 2175 (2F5e) of the human immunodeficiency virus HIV-1. Extending this work, we now report that chimeric virus HAV-gp41 replicates in HAV-susceptible cells as well as in non-human primates. Infected marmosets developed both an anti-HAV and anti-2F5 epitope immune response. Furthermore, an HIV-neutralizing antibody response was elicited in guinea pigs immunized with HAV-gp41 chimeric particles. The results demonstrate that the replication-competent chimeric HAV-gp41 can serve as either a live or a subunit vaccine for eliciting of antibodies directed against a foreign antigenic epitope. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:101 / 111
页数:11
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