Immunological equivalence between mouse brain-derived and Vero cell-derived Japanese encephalitis vaccines

被引:12
作者
Abe, Motoharu [1 ]
Shiosaki, Kouichi
Hammar, Lena
Sonoda, Kengo
Xing, Li
Kuzuhara, Syoji
Kino, Yoichiro
Cheng, R. Holland
机构
[1] Kikuchi Res Ctr, Chemo Sero Therapeut Res Inst, Kumamoto 8691298, Japan
[2] Karolinska Inst, Dept Biosci, SE-14157 Huddinge, Sweden
[3] Univ Calif Davis, Davis, CA 95616 USA
关键词
Japanese encephalitis; neutralizing antibodies; cell system derived whole virus vaccine; fusion protein refolding;
D O I
10.1016/j.virusres.2006.05.004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The persistent spread via animal reservoirs urges expanding vaccination programs against pathogens like the Japanese encephalitis virus, JEV The JEV is spreads to new areas by domestic as well as by wild animals. Although there is a safe and efficient vaccine on the market, this is derived from infected mouse brains, why today's situation requires overcoming the potential risk caused by using animal tissues. To meet this demand we have developed a Vero cell-derived JEV vaccine, using the same virus strain as in the established one. A phase III clinical study of the new vaccine has recently been completed with positive outcome. Like the established mouse brain-derived vaccine, the Vero cell-derived one is a formialin inactivated whole virus vaccine. We here demonstrate the very good agreement in immunological tests between the two antigens. The study includes analyses with two neutralizing monoclonal antibodies that blocks cell entry at a late stage in infection, assumedly interfering with fusion-related refolding in the virus fusion protein. It is obvious that the formalin inactivation treatment, with both virus preparations, retains these essential vaccine epitopes. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:152 / 160
页数:9
相关论文
共 42 条
[1]   Establishment of an analyzing method for a Japanese encephalitis virus neutralization test in Vero cells [J].
Abe, M ;
Kuzuhara, S ;
Kino, Y .
VACCINE, 2003, 21 (17-18) :1989-1994
[2]   Antigenic and genetic variations among Japanese encephalitis virus strains belonging to genotype 1 [J].
Ali, A ;
Igarashi, A .
MICROBIOLOGY AND IMMUNOLOGY, 1997, 41 (03) :241-252
[3]   Structure of a flavivirus envelope glycoprotein in its low-pH-induced membrane fusion conformation [J].
Bressanelli, S ;
Stiasny, K ;
Allison, SL ;
Stura, EA ;
Duquerroy, S ;
Lescar, J ;
Heinz, FX ;
Rey, FA .
EMBO JOURNAL, 2004, 23 (04) :728-738
[4]   Neutralizing mechanism of a monoclonal antibody against Japanese encephalitis virus glycoprotein E [J].
Butrapet, S ;
Kimura-Kuroda, J ;
Zhou, DS ;
Yasui, K .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1998, 58 (04) :389-398
[5]   Vaccine development against dengue and Japanese encephalitis: report of a World Health Organization meeting [J].
Chambers, TJ ;
Tsai, TF ;
Pervikov, Y ;
Monath, TP .
VACCINE, 1997, 15 (14) :1494-1502
[6]   Purification and crystallization reveal two types of interactions of the fusion protein homotrimer of Semliki Forest Virus [J].
Gibbons, DL ;
Reilly, B ;
Ahn, A ;
Vaney, MC ;
Vigouroux, A ;
Rey, FA ;
Kielian, M .
JOURNAL OF VIROLOGY, 2004, 78 (07) :3514-3523
[7]  
HOMBACH J, 2004, P M JOINTL ORG WHO T, V23, P2689
[8]   IMMOBILIZATION OF PROTEINS TO A CARBOXYMETHYLDEXTRAN-MODIFIED GOLD SURFACE FOR BIOSPECIFIC INTERACTION ANALYSIS IN SURFACE-PLASMON RESONANCE SENSORS [J].
JOHNSSON, B ;
LOFAS, S ;
LINDQUIST, G .
ANALYTICAL BIOCHEMISTRY, 1991, 198 (02) :268-277
[9]   Japanese encephalitis in India: An overview [J].
Kabilan L. ;
Rajendran R. ;
Arunachalam N. ;
Ramesh S. ;
Srinivasan S. ;
Samuel P.P. ;
Dash A.P. .
The Indian Journal of Pediatrics, 2004, 71 (7) :609-615
[10]  
KIMURAKURODA J, 1988, J IMMUNOL, V141, P3606