Immune boosting bridges leaky and polarized vaccination models
Park, S. W.; Li, M.; Metcalf, J.; Grenfell, B.; Dushoff, J.
Show abstract
Two different epidemiological models of vaccination are commonly used in dynamical modeling studies. The leaky vaccination model assumes that all vaccinated individuals experience a reduced force of infection by the same amount. The polarized vaccination model assumes that some fraction of vaccinated individuals are completely protected, while the remaining fraction remains completely susceptible; this seemingly extreme assumption causes the polarized model to always predict lower final epidemic size than the leaky model under the same vaccine efficacy. However, the leaky model also makes an implicit, unrealistic assumption: vaccinated individuals who are exposed to infection but not infected remain just as susceptible as they were prior to exposures (i.e., independent of previous exposures). To resolve the independence assumption, we introduce an immune boosting mechanism, through which vaccinated, yet susceptible, individuals can gain protection without developing a transmissible infection. The boosting model further predicts identical epidemic dynamics as the polarized vaccination model, thereby bridging the differences between two models. We further develop a generalized vaccination model to explore how the assumptions of immunity affect epidemic dynamics and estimates of vaccine effectiveness. Significance statementDifferent assumptions about the long- and medium-term effects of protective vaccination can predict sharply different epidemiological dynamics. However, there has been limited discussion about which assumptions are more realistic and therefore more appropriate for making public health decisions. Here, we show that the differences between the two most common assumptions (the "leaky" and "polarized" vaccination models) are bridged by immune boosting, a mechanism by which individuals who resist infectious challenge due to partial immunity have their immunity increased. We demonstrate that this mechanism has important implications for measuring vaccine effectiveness. Our study challenges fundamental assumptions about commonly used vaccination models and provides a novel framework for understanding the epidemiological impact of vaccination.
Matching journals
The top 7 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Vaccination strategies when vaccines are scarce: On conflicts between reducing the burden and avoiding the evolution of escape mutants 98%
- The Complex Interplay Between Risk Tolerance and the Spread of Infectious Diseases 97%
- A stochastic epidemiological model to estimate the size of an outbreak at the first case identification 97%
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.