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Seroconversion of a trivalent measles, mumps, and rubella vaccine in children aged 9 and 15 months
E Forleo-Neto1, E S Carvalho, I C Fuentes
1Departamento de Pediatria, Universidade Federal de São Paulo/Escola Paulista de Medicina, Brazil.
Insights
The measles, mumps, and rubella (MMR) vaccine is safe and effective for infants as young as 9 months. High seroconversion rates were observed, supporting a two-dose schedule for robust immunity.
Area of Science:
- Pediatrics
- Immunology
- Vaccinology
Background:
- Maternal antibodies to measles, mumps, and rubella wane by 9 months of age.
- Understanding serological responses to the MMR vaccine in infants is crucial for optimizing vaccination schedules.
Purpose of the Study:
- To evaluate the serological response to the combined measles, mumps, and rubella (MMR) vaccine in 9-month-old infants.
- To compare the response in 9-month-olds to that of 15-month-old children previously vaccinated with monocomponent measles vaccine.
- To assess the safety and efficacy of the MMR vaccine administered at 9 months of age.
Main Methods:
- Serological evaluation of 109 9-month-old infants and 98 15-month-old children.
- Administration of a combined MMR vaccine containing Schwarz, Urabe Am9, and Wistar RA 27/3 live attenuated virus strains.
- Measurement of pre- and post-immunisation antibody levels for measles, mumps, and rubella.
Main Results:
- Pre-immunisation antibody levels were low in 9-month-olds, indicating minimal persistence of maternal antibodies.
- Post-immunisation rubella antibody titres were significantly higher in the 15-month-old group compared to the 9-month-old group.
- High seroconversion rates for all three components were observed in both age groups, with no serious adverse events.
Conclusions:
- The MMR vaccine can be safely administered to infants at 9 months of age.
- The findings support the efficacy of a two-dose MMR vaccination schedule (at 9 and 15 months) for achieving adequate immunity.
- Early infant vaccination with MMR is a viable strategy, with potential for enhanced rubella antibody responses in older infants.
Abstract:
The serological response to MMR vaccine was evaluated in 109 9-month-old infants having no history of measles vaccination, and in 98 15-month-old children who had received monocomponent measles immunisation at 9 months. The combined vaccine contained Schwarz, Urabe Am9, and Wistar RA 27/3 live attenuated virus strains. Preimmunisation antibody levels were extremely low for the 9-month-old children, indicating that maternally-transmitted antibodies do not persist at this age. In the case of mumps, preimmunisation antibody levels were significantly higher in the 15-month-old than in the 9-month-old group. A difference between groups in terms of postimmunisation antibody titres was observed only for rubella, with titres being significantly higher in the older group. Seroconversion rates were high in both groups and no serious events attributable to vaccination were observed. The MMR vaccine can thus be administered to children as young as 9 months of age. Evidence for the efficacy of a two-dose schedule, i.e. at 9 and 15 months, is presented.
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