Universal influenza A M2e-HBc vaccine protects against disease even in the presence of pre-existing anti-HBc antibodies

被引:89
作者
De Filette, Marina [1 ,2 ]
Martens, Wouter [1 ,2 ]
Smet, Anouk [1 ,2 ]
Schotsaert, Michael [1 ,2 ]
Birkett, Ashley [3 ]
Londono-Arcila, Patricia [3 ]
Fiers, Walter [1 ,2 ]
Saelens, Xavier [1 ,2 ]
机构
[1] Univ Ghent, Dept Mol Biomed Res, VIB, B-9025 Ghent, Zwijnaarde, Belgium
[2] Univ Ghent, Dept Mol Biol, B-9025 Ghent, Zwijnaarde, Belgium
[3] Acambis Inc, Cambridge, MA 02139 USA
关键词
Virus-like particle; Influenza A; M2e; Hepatitis B Virus core; Anti-carrier immunity;
D O I
10.1016/j.vaccine.2008.09.038
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The extracellular domain of influenza A virus matrix protein 2 (M2e) is Strongly conserved. Therefore, vaccines based on M2e can induce broad-spectrum immunity against influenza. We have mainly used recombinant virus-like particles derived from Hepatitis B virus core (HBc) as carrier for efficacious presentation of the M2e antigen. Here, we address whether pre-existing HBc-specific immunity interferes with the protective immune response obtained by M2e-HBc vaccination. Anti-HBc antibodies were induced by immunizing mice with unsubstituted HBc virus-like particles in the presence of two different adjuvants. We demonstrate that pre-existing HBc-specific antibodies affect neither the induction of M2e-specific antibody responses to vaccination with M2e-HBc particles, nor the protective efficacy of the resulting response. These results suggest that vaccination with M2e-Hbc can induce protective anti-M2e antibodies even in anti-HBc positive individuals. The implications of these findings are discussed in the context of the clinical development of an M2e-based universal influenze vaccine, which recently successfully completed a Phase I trial. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6503 / 6507
页数:5
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