Ej. Mcfarland et al., Human immunodeficiency virus type 1 (HIV-1) gp120-specific antibodies in neonates receiving an HIV-1 recombinant gp120 vaccine, J INFEC DIS, 184(10), 2001, pp. 1331-1335
Infants born to human immunodeficiency virus type 1 (HIV-1)-infected mother
s were immunized at birth and at ages 4, 12, and 20 weeks with low-, medium
-, or high-dose recombinant gp120 vaccine with MF59 adjuvant (HIV-1(SF-2);
n = 52) or with MF59 alone as a placebo (n = 9). An accelerated schedule (b
irth and ages 2, 8, and 20 weeks) was used for an additional 10 infants rec
eiving the defined optimal dose and for 3 infants receiving placebo. At 24
weeks, anti-gp120 ELISA titers were greater for vaccine-immunized than for
placebo-immunized infants on both schedules, and 87% of vaccinees had a vac
cine-induced antibody response. At 12 weeks, antibody titers of infants on
the accelerated vaccine schedule exceeded those of infants receiving placeb
o (4949 vs. 551; P = .01), and 63% of the vaccinees met the response criter
ia. Thus, an accelerated schedule of gp120 vaccinations generated an antibo
dy response to HIV-1 envelope distinct from transplacental maternal antibod
y by age 12 weeks. These results provide support for further studies of vac
cine strategies to prevent mother-to-infant HIV-1 transmission.