Abstract

Objectives Transmission of polio poses a threat to military forces when deploying to regions where such viruses are endemic. US-born soldiers generally enter service with immunity resulting from childhood immunization against polio; moreover, new recruits are routinely vaccinated with inactivated poliovirus vaccine (IPV), supplemented based upon deployment circumstances. Given residual protection from childhood vaccination, risk-based vaccination may sufficiently protect troops from polio transmission. Methods This analysis employed a mathematical system for polio transmission within military populations interacting with locals in a polio-endemic region to evaluate changes in vaccination policy. Results Removal of blanket immunization had no effect on simulated polio incidence among deployed military populations when risk-based immunization was employed; however, when these individuals reintegrated with their base populations, risk of transmission to nondeployed personnel increased by 19%. In the absence of both blanket- and risk-based immunization, transmission to nondeployed populations increased by 25%. The overall number of new infections among nondeployed populations was negligible for both scenarios due to high childhood immunization rates, partial protection against transmission conferred by IPV, and low global disease incidence levels. Conclusion Risk-based immunization driven by deployment to polio-endemic regions is sufficient to prevent transmission among both deployed and nondeployed US military populations.

Highlights

  • Polio is a viral disease that invades the nervous system and can cause paralysis in a matter of hours, though most poliovirus infections are asymptomatic [1]

  • To determine residual adult protection resulting from childhood immunization, we developed a waning curve based on data provided by Lapinleimu and Stenvik [35], which describe the change in detectable polio antibodies over time in individuals in Finland where inactivated poliovirus vaccine (IPV) is the only implemented vaccination

  • Results from model simulations described the potential benefits of protecting these troops via routine blanket immunization, predeployment booster immunization, and residual protection resulting from childhood vaccination

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Summary

Introduction

Polio is a viral disease that invades the nervous system and can cause paralysis in a matter of hours, though most poliovirus infections are asymptomatic [1]. Polio infection in immunocompetent individuals leads to immunity, immunity induced by one serotype does not protect against the other two [3]. Successful vaccination with either formulation provides at least partial protection from infection and full disease immunity in approximately 7 days [4]. After IPV immunization, antibodies are produced in the blood in response to the inactivated virus, protecting the individual from disease; viral replication in the gut is still possible, with the potential for asymptomatic transmission to the community [5]. IPV-induced antibodies decrease over time, and some adults vaccinated as children may lack a detectable antibody

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