Serum antibodies to the capsular polysaccharide of Haemophilus influenzae t
ype b (Hib) are effective in pl eventing or ameliorating invasive disease c
aused by this human pathogen. Polysaccharide and conjugate (saccharide cova
lently linked to protein carrier) vaccines have been developed which stimul
ate the production of such antibodies. The polysaccharide-specific antibody
concentrations in the sera of vaccine-naive adults and toddlers on days 1,
3, 7, 14 and 28 following immunisation with one dose of the Hib polysaccha
ride vaccine (PRP, polyribosylribitol phosphate) or an oligosaccharide-CRM1
97 conjugate vaccine (HbOC, HibTITER(R)) were determined. Antibody response
s occurred within 7 days of immunisation with the maximum response usually
occurring 14 days post-immunisation, irrespective of vaccine or subject age
. In this small study, a significant transient decline in pre-existing anti
bodies was observed only in the groups receiving the polysaccharide vaccine
and not in the groups receiving HbOC vaccine. Because of the small magnitu
de of antigen-specific antibody decline and its transient nature, it is unl
ikely that this observation has clinical significance.