Mt. Jelonek et al., HIV HYPERIMMUNE GLOBULIN OR INTRAVENOUS IMMUNE GLOBULIN INHIBITS RESPONSE TO AN HIV VACCINE, Biotechnology and applied biochemistry, 27, 1998, pp. 89-95
The murine model was developed to assess the effects of maternally tra
nsferred HIV hyperimmune globulin or human intravenous immune globulin
on the immunization of the offspring at 18-21 days of age with rgp120
(SF2)-complete Freund's adjuvant, Either HIV hyperimmune globulin or i
ntravenous immune globulin was administered intraperitoneally to post-
partum BALB/c mice and was transferred via milk to the offspring, Both
HIV hyperimmune globulin and intravenous immune globulin inhibited th
e offspring anti-rgp120(SF2) IgG response to the vaccine. The HIV hype
rimmune globulin inhibition persisted for 28 days after immunization w
hile the intravenous immune globulin inhibition was still present at 6
3 days after immunization, In addition, the intravenous immune globuli
n had a more generalized immunosuppressive effect, inhibiting the IgG
response to both rpg120(SF2) and an additional protein antigen, hen eg
g-white lysozyme, Effects of maternal or exogenously administered pre-
existing antibody, including control antibodies (intravenous immune gl
obulin), on the newborn response to HIV and other vaccines must be car
efully evaluated when vaccine studies proceed in newborns.