Abstract

BackgroundVaccines may cause non-specific effects (NSEs) on morbidity and mortality through immune-mediated mechanisms that are not explained by the prevention of the targeted disease. Much of the evidence for NSEs comes from observational studies with a high risk of bias, and there is a clear need for new data from randomized controlled trials. Recently, it was proposed that rabies vaccine has protective NSEs in people and in animals. The aim of the proposed study is to determine whether rabies vaccine reduces the incidence rate of episodes of common infectious disease syndromes in a population of veterinary students on the island of St. Kitts.MethodsThe trial design is a single-site, two-arm, parallel-group, participant-blinded, randomized, placebo-controlled, two-sided comparative study, with an internal pilot study for blinded sample size re-estimation. Allocation to study arm is by block randomization stratified by sex within cohort with a 1:1 allocation ratio. The primary study outcome is the number of new weekly episodes of common infectious diseases including respiratory, diarrheal and febrile illnesses. A vaccine immunogenicity ancillary study is planned.DiscussionDemonstration of a non-specific protective effect of rabies vaccine against unrelated respiratory, gastrointestinal and febrile illnesses would provide supportive evidence for the design of similar studies in children in populations with a high burden of these illnesses.Trial registrationClinicalTrials.gov, ID: NCT03656198. Registered on 24 August 2018.

Highlights

  • Background and rationale {6a} Non-specific effects (NSEs) of vaccines – known as heterologous effects [1] – are those immunemediated effects of vaccines on morbidity and mortality that are not explained by the prevention of the targeted disease [2]

  • A participant cannot experience more than two common infectious disease (CID) episodes within a week, as occurrence of Upper respiratory illness (URI) together with Influenza-like illness (ILI) is considered an episode of ILI only, and occurrence of URI, ILI and/or DIA precludes the occurrence of undifferentiated febrile illness (UFI)

  • This paper describes the protocol for a Randomized controlled trial (RCT) of the nonspecific effect of rabies vaccine on the incidence of common infectious disease episodes in a population of veterinary students

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Summary

Methods

The trial design is a single-site, two-arm, parallel-group, participant-blinded, randomized, placebo-controlled, two-sided comparative study, with an internal pilot study for blinded sample size re-estimation. Allocation to study arm is by block randomization stratified by sex within cohort with a 1:1 allocation ratio. The primary study outcome is the number of new weekly episodes of common infectious diseases including respiratory, diarrheal and febrile illnesses. A vaccine immunogenicity ancillary study is planned

Discussion
Introduction
Incidence rate of self-reported new weekly episodes of DIA
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Statistical methods
Findings
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