The decay of maternally derived antibodies to measles, mumps, and rubella v
iruses in Swiss infants was studied in order to determine the optimal time
for vaccination. A total of 500 serum or plasma samples from infants up to
2 years of age were tested by enzyme-linked immunosorbent assay and fluores
cent-antibody testing. The decline of antibody prevalence was slowest again
st the measles virus. By 9 to 12 months of age, only 5 of 58 (8.6%; 95% CI,
2.9 to 19.0) infants were antibody positive for the measles virus, and onl
y 2 had levels above 200 mIU/ml, Mumps and rubella virus antibody seroposit
ivity was lowest at 9 to 12 months of age with 3 of 58 (5.2%; 95% CI, 1.1 t
o 14.4) infants and at 12 to 15 months with I of 48 (2.1%; 95% CI, 0.1 to 1
1.1) infants, respectively. Concentrations of passively acquired antibodies
decreased rapidly within the first 6 months of life. We observed no signif
icant differences in antibody prevalence or concentration according to gend
er in any age group. In conclusion, MMR vaccination at 12 instead of 15 mon
ths of age could reduce the pool of susceptible subjects in infancy and sup
port the efforts to eliminate these infections, particularly in combination
with a second vaccine dose before school entry.