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Published on: August 14, 2019
Age-specific mortality risk from pandemic influenza
Junling Ma1, Jonathan Dushoff, David J D Earn
1Department of Mathematics and Statistics, University of Victoria, Victoria, BC, Canada.
Insights
Influenza pandemics disproportionately affect younger age groups. This study suggests that "antigenic imprinting," influenced by early infections, significantly impacts age-specific influenza mortality patterns during pandemics.
Area of Science:
- Immunology
- Epidemiology
- Virology
Background:
- Younger populations experience higher mortality during influenza pandemics compared to seasonal epidemics.
- Potential mechanisms include over-reactive immune responses (cytokine storm) in the young, cross-immunity from prior infections in the old (antigenic history), and the lifelong impact of the first influenza A infection (antigenic imprinting).
Purpose of the Study:
- To investigate whether proposed immunological mechanisms can explain the observed age-specific mortality patterns in influenza pandemics.
- To analyze the role of antigenic imprinting in shaping age-specific virulence during pandemics.
Main Methods:
- Utilized a comprehensive database of individual deaths in Canada spanning from 1951 to 1999.
- Analyzed mortality patterns, specifically focusing on the 1957 influenza pandemic, to assess the influence of antigenic imprinting.
Main Results:
- The mortality patterns observed during the 1957 pandemic provide evidence that antigenic imprinting is a crucial factor in determining age-specific influenza virulence.
- Both major antigenic shift and drift years significantly contribute to the formation of these antigenic imprints.
Conclusions:
- Antigenic imprinting, shaped by initial influenza A infections, plays a significant role in age-specific mortality during influenza pandemics.
- Understanding these imprinting effects can aid pandemic preparedness by identifying age groups likely to exhibit differential responses to novel influenza strains.
Abstract:
Younger age groups account for proportionally more mortality in influenza pandemics than in seasonal influenza epidemics. Mechanisms that might explain this include young people suffering from an over-reactive immune system ("cytokine storm"), older people benefiting from cross-immunity from a wider variety of previous influenza infections ("antigenic history"), and lifetime immune responses in all people being shaped by their first influenza A infection ("antigenic imprinting" or "original antigenic sin"). We examined whether these mechanisms can explain age-specific influenza mortality patterns, using the complete database of individual deaths in Canada from 1951 to 1999. The mortality pattern during the 1957 pandemic indicates that antigenic imprinting plays an important role in determining age-specific influenza virulence and that both shift years and major drift years contribute significantly to antigenic imprints. This information should help pandemic planners to identify age groups that might respond differently to novel influenza strains.
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