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COVID-19 vaccine effectiveness in children by age groups. A population-based study in Galicia, Spain
Narmeen Mallah1,2,3,4, Jacobo Pardo-Seco1,2,3, Sonia Ares-Gómez1,2,3
1Genetics, Vaccines and Pediatric Infectious Diseases Research Group (GENVIP), Instituto de Investigación Sanitaria de Santiago (IDIS), Santiago de Compostela, Galicia, Spain.
Insights
mRNA vaccines offer moderate COVID-19 protection for children aged 5-11 but high protection for older children. Vaccine effectiveness declined over time, indicating a need for booster doses.
Area of Science:
- Immunology
- Public Health
- Pediatrics
Background:
- Ongoing studies are evaluating COVID-19 vaccine effectiveness (VE) in pediatric populations.
- Research is crucial to understand protection levels in different age groups and against various SARS-CoV-2 variants.
Purpose of the Study:
- To quantify VE against SARS-CoV-2 in children aged 5-11 and 12-17 years.
- To analyze VE based on vaccine type, SARS-CoV-2 variant, and duration of protection.
Main Methods:
- A population-based test-negative control study was conducted in Galicia, Spain.
- VE was calculated using logistic regression models, with participants categorized by vaccination status (unvaccinated, partially vaccinated, fully vaccinated).
Main Results:
- Fully vaccinated 5-11 year olds showed 44.1% VE against Omicron.
- Fully vaccinated 12-17 year olds had 83.4% VE against Delta and 74.8% VE against Omicron.
- Both Comirnaty® and SpikeVax® demonstrated similar VE against Delta; Comirnaty® showed slightly higher VE against Omicron, though confidence intervals overlapped. VE declined over time.
Conclusions:
- mRNA vaccine effectiveness against SARS-CoV-2 is moderate in 5-11 year olds and high in 12-17 year olds.
- Declining VE over time suggests a potential need for booster vaccinations in pediatric populations.
- Findings support ongoing vaccination strategies and highlight the importance of monitoring long-term protection.
Background:
Studies on vaccine effectiveness (VE) against COVID-19 in the pediatric population are outgoing. We aimed to quantify VE against SARS-CoV-2 in two pediatric age groups, 5-11 and 12-17-year-old, while considering vaccine type, SARS-CoV-2 variant, and duration of protection.
Methods:
A population-based test-negative control study was undertaken in Galicia, Spain. Children 5-11-year-old received the Comirnaty® (Pfizer, US) vaccine, while those aged 12-17-year-old received the Comirnaty® (Pfizer, US) or SpikeVax® (ModernaTX, Inc) vaccine. Participants were categorized into unvaccinated (0 doses or one dose with <14 days since vaccination), partially vaccinated (only one dose with ≥14 days, or two doses with <14 days after the second dose administration), and fully vaccinated (two doses with ≥14 days after the second injection). Adjusted odds ratios (OR) and their 95% confidence intervals (CI) were estimated using multiple logistic regression models. VE was calculated as (1-OR) * 100. Stratified and sensitivity analyses were performed.
Results:
In the fully vaccinated 5-11-year-old children, VE against the Omicron variant was 44.1% (95% CI: 38.2%-49.4%). In the fully vaccinated 12-17-year-old individuals, VE was 83.4% (95% CI: 81.2%-85.3%) against Delta and 74.8% (95% CI: 58.5%-84.9%) against Omicron. Comirnaty® and SpikeVax® vaccines showed a similar magnitude of VE against Delta [Comirnaty® VE: 81.9% (95% CI: 79.3%-84.1%) and SpikeVax® VE: 85.3% (95% CI: 81.9%-88.1%)]. Comirnaty® (Pfizer, US; VE: 79.7%; 95% CI: 50.7%-92.4%) showed a slightly higher magnitude of protection against Omicron than SpikeVax® (ModernaTX, Inc), yet with an overlapping CI (VE: 74.3%; 95% CI: 56.6%-84.9%). VE was maintained in all age subgroups in both pediatric populations, but it declined over time.
Conclusions:
In Galicia, mRNA VE was moderate against SARS-CoV-2 infections in the 5-11-year-old populations, but high in older children. VE declined over time, suggesting a potential need for booster dose schedules.
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