protection against a lethal influenza B virus infection was examined in BAL
B/c mice immunized with plasmid DNAs encoding hemagglutinin (HA), neuramini
dase (NA and NE) and nucleoprotein (NP) from the B/Ibaraki/2/85 virus. Each
DNA vaccine was administered twice, 3 weeks apart, at a dose of 1 mug per
mouse by particle-mediated DNA transfer to the epidermis (gene gun) or at a
dose of 30 mug per mouse by electroporation into the muscle. Three weeks a
fter the second vaccination, the mice were challenged with a lethal dose of
homologous virus. HA and NA DNAs conferred complete protection against the
lethal viral challenge, whereas NE and NP DNAs failed to provide protectio
n against infection. Furthermore, protection in different strains of mice,
BALB/c, B10 and C3H. immunized with HA and NA DNAs was compared. Both HA an
d NA DNAs conferred complete protection against the lethal challenge in all
the tested mouse strains. These results suggest that both the HA and NA mo
lecules can be used as vaccine components to provide effective protection a
gainst influenza B virus infection. (C) 2001 Elsevier Science Ltd. All righ
ts reserved.