ANTIBODY-RESPONSES IN VOLUNTEERS INDUCED BY NASAL INFLUENZA VACCINE COMBINED WITH ESCHERICHIA-COLI HEAT-LABILE ENTEROTOXIN-B SUBUNIT CONTAINING A TRACE AMOUNT OF THE HOLOTOXIN
K. Hashigucci et al., ANTIBODY-RESPONSES IN VOLUNTEERS INDUCED BY NASAL INFLUENZA VACCINE COMBINED WITH ESCHERICHIA-COLI HEAT-LABILE ENTEROTOXIN-B SUBUNIT CONTAINING A TRACE AMOUNT OF THE HOLOTOXIN, Vaccine, 14(2), 1996, pp. 113-119
Evaluation of the efficacy of nasal influenza vaccine combined with Es
cherichia coli heat-labile enterotoxin B subunit (LTB) containing a tr
ace amount of the holotoxin (LT) in inducing antibody responses among
volunteers, which was conducted during the winter season of 1993-1994,
is reported. A trivalent inactivated vaccine, composed of A/Yamagata/
32/89 (H1N1), A/Kitakyusyu/159/93 (H3N2) and B/Bangkok/163/90 influenz
a virus strains, was used alone or together with the adjuvant, recombi
nant LTB supplemented with 0.5% recombinant LT (LTB). The volunteers
were divided into two groups: 73 volunteers (mean age 35.0 +/- 12.0 ye
ars) inoculated intranasally (in.) with LTB-combined vaccine and 49 v
olunteers (37.9 +/- 11.3) inoculated in. with the vaccine alone, Vacci
nation was done twice 4 weeks apart. Salivary secretory IgA and serum
hemagglutination-inhibiting (HI) antibodies were measured before and 8
weeks after the primary vaccination. For the sake of convenience, mor
e than a 1.4-fold rise in IgA antibody response (units of specific IgA
antibody per mu g of total IgA) and a fourfold or enter rise in HI an
tibody titer after vaccination were regarded as a positive antibody re
sponse. Thirty-seven (50.3%) and 36 (49.3%) of the 73 vaccinees, respe
ctively, given the nasal LTB-combined vaccine showed positive IgA and
HI antibody responses to one or move of the three vaccine strains. In
comparison, positive antibody responses in the group given vaccine al
one were 32.7% for IgA and 30.6% for HI antibody. There was a signific
ant difference between these two groups. These results suggest that th
e nasal LTB-combined vaccine could enhance the production of higher l
evels not only of serum HI antibody but IgA antibodies in the respirat
ory tract than do the nasal vaccine alone.