J. Bennett et al., Seroconversions in unvaccinated infants: further evidence for subclinical measles from vaccine trials in Niakhar, Senegal, INT J EPID, 28(1), 1999, pp. 147-151
Citations number
15
Categorie Soggetti
Envirnomentale Medicine & Public Health","Medical Research General Topics
Background Increases in measles antibodies without rash-illnesses have been
documented in previously vaccinated children exposed to measles cases. The
phenomenon has been incompletely evaluated in young unvaccinated infants w
ith immunity of maternal origin.
Methods Monthly cohorts of newborns were prospectively randomized to vaccin
e and placebo control groups during a trial of high-titre vaccines in Niakh
ar, Senegal. Measles antibodies were assayed in blood samples of enrolled c
hildren collected at 5 months old, when controls received a placebo injecti
on, and at 10 months, when the placebo group was given measles vaccine. Int
ensive prospective surveillance for measles was conducted throughout the tr
ial.
Results One-fifth (n =53) of the placebo controls seroconverted, with known
exposure to a measles case in only three of them. None of the seroconverte
rs developed a measles-like rash. Sixteen-fold or greater increases in titr
es were noted in about one-quarter of them. Compared with placebo controls
who did not seroconvert, seroconverters were more likely to have had exposu
re to a measles case and to travel, more likely to be boys than girls, and
had significantly lower baseline antibody titres. Measles was endemic in th
e study area throughout the trial. Seroconversions did not adversely effect
subsequent nutritional indices or mortality.
Conclusions Although laboratory errors and inadvertent injection of vaccine
rather than placebo may have played some role, they do not fully explain t
he above observations, which are consistent with subclinical measles in the
seroconverters. The possible role of subclinical measles in occult transmi
ssion, its potential effect on the type and duration of subsequent immunity
, and its impact on response to primary vaccination need to be determined.