Swine-origin pandemic H1N1 influenza virus-like particles produced in insect cells induce hemagglutination inhibiting antibodies in BALB/c mice

被引:32
作者
Krammer, Florian
Nakowitsch, Sabine [2 ]
Messner, Paul [3 ]
Palmberger, Dieter
Ferko, Boris [2 ]
Grabherr, Reingard [1 ]
机构
[1] Univ Nat Resources & Appl Life Sci, Vienna Inst BioTechnol, Dept Biotechnol, A-1190 Vienna, Austria
[2] Avir Green Hills Biotechnol AG, Vienna, Austria
[3] Univ Nat Resources & Appl Life Sci, Vienna Inst BioTechnol, Dept Nanobiotechnol, A-1190 Vienna, Austria
基金
奥地利科学基金会;
关键词
H1N1; Influenza vaccine; Insect cells; Pandemic influenza; Virus-like particle; PROTECTIVE IMMUNE-RESPONSES; HIGHLY PATHOGENIC H5N1; STRUCTURAL PROTEINS; GENE-DELIVERY; VACCINE; EXPRESSION; CHALLENGE; BACULOVIRUS; VECTORS; FERRETS;
D O I
10.1002/biot.200900267
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recent outbreaks of influenza A highlight the importance of rapid and sufficient supply for pandemic and inter-pandemic vaccines. Classical manufacturing methods for influenza vaccines fail to satisfy this demand. Alternatively, cell culture-based production systems and virus-like particle (VLP)-based technologies have been established. We developed swine-origin pandemic H1N1 influenza VLPs consisting of hemagglutinin (A/California/04/2009) and matrix protein. Hemagglutinin and matrix protein were co-expressed in insect cells by the baculovirus expression system. VLPs were harvested from infection supernatants, purified and used for intraperitoneal immunization of BALB/c mice. Immunization induced high serum antibody titers against A/California/04/2009 as well as hemagglutination inhibiting antibodies. Additionally, we compared VLP production in two different insect cell lines, Sf9 and BTI-TN5B1-4 (High Five (TM)). Taken together VLPs represent a potential strategy for the fight against new pandemic influenza viruses.
引用
收藏
页码:17 / 23
页数:7
相关论文
共 27 条
[1]   Insect cells as hosts for the expression of recombinant glycoproteins [J].
Altmann, F ;
Staudacher, E ;
Wilson, IBH ;
März, L .
GLYCOCONJUGATE JOURNAL, 1999, 16 (02) :109-123
[2]   Influenza virus-like particles elicit broader immune responses than whole virion inactivated influenza virus or recombinant hemagglutinin [J].
Bright, Rick A. ;
Carter, Donald M. ;
Daniluk, Shannon ;
Toapanta, Franklin R. ;
Ahmad, Attiya ;
Gavrilov, Victor ;
Massare, Mike ;
Pushko, Peter ;
Mytle, Nutan ;
Rowe, Thomas ;
Smith, Gale ;
Ross, Ted M. .
VACCINE, 2007, 25 (19) :3871-3878
[3]  
Cox MMJ, 2008, CURR OPIN MOL THER, V10, P56
[4]   Influenza virus-like particles produced by transient expression in Nicotiana benthamiana induce a protective immune response against a lethal viral challenge in mice [J].
D'Aoust, Marc-Andre ;
Lavoie, Pierre-Olivier ;
Couture, Manon M.-J. ;
Trepanier, Sonia ;
Guay, Jean-Martin ;
Dargis, Michele ;
Mongrand, Sebastien ;
Landry, Nathalie ;
Ward, Brian J. ;
Vezina, Louis-P. .
PLANT BIOTECHNOLOGY JOURNAL, 2008, 6 (09) :930-940
[5]   Virus-like particle (VLP) vaccine conferred complete protection against a lethal influenza virus challenge [J].
Galarza, JM ;
Latham, T ;
Cupo, A .
VIRAL IMMUNOLOGY, 2005, 18 (01) :244-251
[6]   Influenza-pseudotyped Gag virus-like particle vaccines provide broad protection against highly pathogenic avian influenza challenge [J].
Haynes, Joel R. ;
Dokken, Leslie ;
Wiley, James A. ;
Cawthon, Andrew G. ;
Bigger, John ;
Harmsen, Allen G. ;
Richardson, Charles .
VACCINE, 2009, 27 (04) :530-541
[7]   Baculoviral vectors for gene delivery: A review [J].
Hu, Yu-Chen .
CURRENT GENE THERAPY, 2008, 8 (01) :54-65
[8]   Influenza vaccines based on virus-like particles [J].
Kang, Sang-Moo ;
Song, Jae-Min ;
Quan, Fu-Shi ;
Compans, Richard W. .
VIRUS RESEARCH, 2009, 143 (02) :140-146
[9]  
King Linda A., 2007, V388, P77
[10]   Baculovirus as versatile vectors for protein expression in insect and mammalian cells [J].
Kost, TA ;
Condreay, JP ;
Jarvis, DL .
NATURE BIOTECHNOLOGY, 2005, 23 (05) :567-575