Mt. Jelonek et al., COMPARISON OF NATURALLY ACQUIRED AND VACCINE-INDUCED ANTIBODIES TO HAEMOPHILUS-INFLUENZAE TYPE-B CAPSULAR POLYSACCHARIDE, Infection and immunity, 61(12), 1993, pp. 5345-5350
The objective of this study was to assess qualitative differences in t
he types of Haemophilus influenzae type B (Hib) capsular polysaccharid
e (polyribosylribitol phosphate [PRP]) antibodies induced in children
15 to 27 months of age by (i) natural exposure, (ii) PRP vaccine, and
by (iii) PRP-diphtheria toroid conjugate vaccine, (iv) PRP-group B Nei
sseria meningitidis outer membrane vesicle conjugate vaccine, and (v)
Haemophilus type B oligosaccharide conjugate vaccine (HbOC). The highe
st levels of total Hib-PRP antibody measured by radioimmunoassay and i
mmunoglobulin G (IgG) measured by enzyme-linked immunosorbent assay we
re seen after HbOC immunization. IgG1 Hib-PRP antibodies predominated
in all groups, and there were no differences between the groups in the
proportion of IgG and IgA Hib-PRP antibodies. However, the proportion
s of IgM differed significantly by group. The highest proportions of I
gM occurred in naturally acquired antibody and after PRP vaccine, and
the lowest proportion occurred after HbOC vaccine. IgG light-chain V k
appa II type alpha PRP antibody was present in all groups, and the lev
el correlated with the total IgG Hib-PRP antibody level. Therefore, Hb
OC induced the highest concentrations of V kappa II type alpha PRP ant
ibody, and the naturally acquired antibody group had the lowest levels
. IgG light-chain V kappa III antibody levels were also highest in the
HbOC group, but there was no correlation between V kappa III antibody
levels and total amount of IgG Hib-PRP antibody. These data demonstra
te qualitative differences in the antibody repertoires induced by natu
ral exposure, the Hib-PRP vaccine, and each of the different Hib conju
gate vaccines. We doubt that there are major differences in the protec
tion afforded by these different antibody repertoires, because these d
ifferences do not appear to correlate with differences in protective e
fficacy in older children.