Multiplex serology reveals age-specific immunodynamics of respiratory pathogens in the wake of the COVID-19 pandemic.
Summary
Using a quantitative multiplex serology platform, the study shows children under five mount larger but faster-waning antibody responses across multiple respiratory viruses compared to older individuals. Validation in a separate pre-pandemic cohort and model calibration suggest age-specific immunodynamics are critical to forecasting post-pandemic epidemic patterns and guiding vaccination strategy.
Key Findings
- Children <5 years exhibited larger antibody boosts but faster waning across influenza, RSV, seasonal coronaviruses, and SARS-CoV-2.
- Findings were validated using pre-pandemic influenza serology from South Africa (n=1028).
- An influenza transmission model incorporating age-specific immunodynamics improved forecasts of post-pandemic epidemic patterns.
Clinical Implications
Age-specific waning should inform vaccine schedules (timing/boosters) and surveillance thresholds, especially in young children who exhibit rapid decline after strong boosts.
Why It Matters
This work provides high-resolution, age-specific immune profiles across pathogens and translates them into forecasting models with direct policy relevance for vaccination and NPIs.
Limitations
- Serology reflects humoral immunity; cellular responses were not directly measured
- Generalizability beyond studied geographies requires further validation
Future Directions
Extend to cellular immunity, link antibody kinetics to clinical protection, and test optimized age-stratified vaccination schedules in prospective studies.
Study Information
- Study Type
- Cohort
- Research Domain
- Prevention/Pathophysiology
- Evidence Level
- III - Prospective/retrospective observational serology analyses with modeling and external validation
- Study Design
- OTHER