Protective immunity against influenza A virus induced by immunization with DNA plasmid containing influenza M gene

被引:118
作者
Okuda, K
Ihata, A
Watabe, S
Okada, E
Yamakawa, T
Hamajima, K
Yang, J
Ishii, N
Nakazawa, M
Okuda, K
Ohnari, K
Nakajima, K
Xin, KQ
机构
[1] Yokohama City Univ, Sch Med, Dept Bacteriol, Kanazawa Ku, Yokohama, Kanagawa 2360004, Japan
[2] Yokohama City Univ, Sch Med, Dept Internal Med, Kanazawa Ku, Yokohama, Kanagawa 2360004, Japan
[3] Yokohama City Univ, Sch Med, Dept Dermatol, Kanazawa Ku, Yokohama, Kanagawa 2360004, Japan
[4] Yokohama City Univ, Sch Med, Dept Parasitol, Kanazawa Ku, Yokohama, Kanagawa 2360004, Japan
[5] Tokyo Dent Coll, Dept Microbiol, Chiba 2618502, Japan
[6] Yokohama Minami Kyosai Hosp, Dept Orthopaed Surg, Yokohama, Kanagawa 2360032, Japan
[7] Nagoya City Univ, Sch Med, Dept Virol, Nagoya, Aichi 4678601, Japan
关键词
influenza A virus; influenza M gene; DNA plasmid;
D O I
10.1016/S0264-410X(01)00078-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
DNA vaccination is characterized by its preferential induction of the cytotoxic T cell lymphocyte (CTL) response and is expected to be a useful means of protection against viral infection. We examined the protective effect of an expression plasmid (pME18S-M) containing M1 and M2 genes of influenza A/PR/8/34. We detected the CTL activity by introducing these plasmids into BALB/c mice by either the intramuscular or the intranasal route. The influenza-specific antibody response was also induced, although its neutralizing effect against influenza virus was not observed. From 70 to 80% protection was observed in the mice immunized with the pME18S-M plasmid followed by lethal infection with influenza viruses of the A/WSN/33 and A/PR/8/34 strains, whereas all mice without the plasmid vaccination failed to survive. This protective activity was significantly weakened when the CD8(+) cells of these immunized mice were eliminated by several injections of anti-CD8 antibody. The protective activity was also weakened when anti-CD4 antibody was injected in the early phase of DNA vaccination. These data suggest that the pME18S-M plasmid is useful as a DNA vaccine for overcoming highly mutational influenza viruses. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:3681 / 3691
页数:11
相关论文
共 36 条
[31]   FUNCTIONAL-ROLE OF RESPIRATORY-TRACT HEMAGGLUTININ-SPECIFIC IGA ANTIBODIES IN PROTECTION AGAINST INFLUENZA [J].
TAMURA, S ;
FUNATO, H ;
HIRABAYASHI, Y ;
KIKUTA, K ;
SUZUKI, Y ;
NAGAMINE, T ;
AIZAWA, C ;
NAKAGAWA, M ;
KURATA, T .
VACCINE, 1990, 8 (05) :479-485
[32]  
Tamura S, 1996, J IMMUNOL, V156, P3892
[33]   BETA(2)-MICROGLOBULIN-DEFICIENT MICE DEMONSTRATE CLASS-II MHC RESTRICTED ANTIVIRAL CD4(+) BUT NOT CD8(+) CTL AGAINST INFLUENZA-SENSITIZED AUTOLOGOUS SPLENOCYTES [J].
TAYLOR, SF ;
BENDER, BS .
IMMUNOLOGY LETTERS, 1995, 46 (1-2) :67-73
[34]   PROTECTIVE IMMUNITY BY INTRAMUSCULAR INJECTION OF LOW-DOSES OF INFLUENZA-VIRUS DNA VACCINES [J].
ULMER, JB ;
DECK, RR ;
DEWITT, CM ;
FRIEDMAN, A ;
DONNELLY, JJ ;
LIU, MA .
VACCINE, 1994, 12 (16) :1541-1544
[35]   HETEROLOGOUS PROTECTION AGAINST INFLUENZA BY INJECTION OF DNA ENCODING A VIRAL PROTEIN [J].
ULMER, JB ;
DONNELLY, JJ ;
PARKER, SE ;
RHODES, GH ;
FELGNER, PL ;
DWARKI, VJ ;
GROMKOWSKI, SH ;
DECK, RR ;
DEWITT, CM ;
FRIEDMAN, A ;
HAWE, LA ;
LEANDER, KR ;
MARTINEZ, D ;
PERRY, HC ;
SHIVER, JW ;
MONTGOMERY, DL ;
LIU, MA .
SCIENCE, 1993, 259 (5102) :1745-1749
[36]   Protective CD4+ and CD8+ T cells against influenza virus induced by vaccination with nucleoprotein DNA [J].
Ulmer, JB ;
Fu, TM ;
Deck, RR ;
Friedman, A ;
Guan, LM ;
DeWitt, C ;
Liu, X ;
Wang, S ;
Liu, MA ;
Donnelly, JJ ;
Caulfield, MJ .
JOURNAL OF VIROLOGY, 1998, 72 (07) :5648-5653