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
相关论文
共 48 条
[1]   MORPHOGENESIS OF HEPATITIS-A VIRUS - ISOLATION AND CHARACTERIZATION OF SUBVIRAL PARTICLES [J].
ANDERSON, DA ;
ROSS, BC .
JOURNAL OF VIROLOGY, 1990, 64 (11) :5284-5289
[2]  
Andre Francis, 2002, Expert Rev Vaccines, V1, P9, DOI 10.1586/14760584.1.1.9
[3]   PATHOGENESIS OF HEPATITIS-A IN ORALLY INOCULATED OWL MONKEYS (AOTUS-TRIVIRGATUS) [J].
ASHER, LVS ;
BINN, LN ;
MENSING, TL ;
MARCHWICKI, RH ;
VASSELL, RA ;
YOUNG, GD .
JOURNAL OF MEDICAL VIROLOGY, 1995, 47 (03) :260-268
[4]   Structural analysis of the epitope of the Anti-HIV antibody 2F5 sheds light into its mechanism of neutralization and HIV fusion [J].
Barbato, G ;
Bianchi, E ;
Ingallinella, P ;
Hurni, WH ;
Miller, MD ;
Cilibertol, G ;
Cortese, R ;
Bazzo, R ;
Shiver, JW ;
Pessi, A .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 330 (05) :1101-1115
[5]   Chimeric hepatitis A virus particles presenting a foreign epitope (HIV gp41) at their surface [J].
Beneduce, F ;
Kusov, Y ;
Klinger, M ;
Gauss-Müller, V ;
Morace, G .
ANTIVIRAL RESEARCH, 2002, 55 (02) :369-377
[6]   SYNTHESIS AND ASSEMBLY OF HEPATITIS-A VIRUS-SPECIFIC PROTEINS IN BS-C-1 CELLS [J].
BOROVEC, SV ;
ANDERSON, DA .
JOURNAL OF VIROLOGY, 1993, 67 (06) :3095-3102
[7]  
BRADLEY DW, 1977, J CLIN MICROBIOL, V5, P521
[8]   Analysis of deletion mutants indicates that the 2A polypeptide of hepatitis A virus participates in virion morphogenesis [J].
Cohen, L ;
Bénichou, D ;
Martin, A .
JOURNAL OF VIROLOGY, 2002, 76 (15) :7495-7505
[9]   IgA-coated particles of Hepatitis A virus are translocalized antivectorially from the apical to the basolateral site of polarized epithelial cells via the polymeric immunoglobulin receptor [J].
Dotauer, A ;
Brenner, M ;
Gebhardt, U ;
Vallbracht, A .
JOURNAL OF GENERAL VIROLOGY, 2005, 86 :2747-2751
[10]   Hepatitis A virus-specific immunoglobulin a mediates infection of hepatocytes with hepatitis A virus via the asialoglycoprotein receptor [J].
Dotzauer, A ;
Gebhardt, U ;
Bieback, K ;
Göttke, U ;
Kracke, A ;
Mages, J ;
Lemon, SM ;
Vallbracht, A .
JOURNAL OF VIROLOGY, 2000, 74 (23) :10950-10957