Effects of BCG on Influenza Induced Immune Response

NCT ID: NCT02114255

Last Updated: 2015-11-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2/PHASE3

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-05-31

Study Completion Date

2014-09-30

Brief Summary

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In the present study, the investigators want to investigate whether prior BCG-vaccination improves the efficacy of influenza ("the flu") vaccination in young and/or old healthy volunteers and consequently could protect against influenza virus infection.

Detailed Description

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Influenza virus infection leads to millions of cases of severe illnesses worldwide and up to an estimated 500.000 deaths annually. The potential for the sudden emergence of pandemic influenza strains represents an incessant threat on even a larger scale. seasonal influenza vaccination is the backbone of influenza management. However, antibodies generated by vaccination, most often do not effectively neutralize emergent strains due to the high mutation rate of the influenza viral genome. In addition, although vaccination is effective in up to 85% of healthy adults, only 40-60% of the elderly are able to mount an protective antibody response due to an agerelated decline in immune function (so-called immunoscenescence). As a result, the protective effects of influenza vaccination are limited, and strategies to improve host immune defenses against influenza virus infection per se, and following influenza vaccination, are highly warranted.

It is suggested that prior vaccination with Bacille Calmette-Guérin (BCG) could enhance resistance to other infectious diseases in addition to protection to tuberculosis (TBC) and, in mice, protection of prior BCGvaccination against influenza infection was demonstrated long ago. However, only recently substantial evidence for these nonspecific beneficial effects of BCG-vaccination in humans has been provided by several randomized clinical trials. Considering these potentiating effects of BCG-vaccination, it could be a viable strategy to improve efficacy of influenza vaccination, and/or enhance immune defenses against influenza virus infection per se. If so, this would have an enormous impact on clinical practice.

Conditions

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Influenza Virus Infection Trained Immunity

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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BCG vaccination

BCG vaccination

Group Type EXPERIMENTAL

BCG

Intervention Type BIOLOGICAL

Vaccination with the live attenuated BCG vaccine.

NaCl 0.9%

administration of NaCl 0.9%.

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type OTHER

Administration of 0.9% NaCl.

Interventions

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Placebo

Administration of 0.9% NaCl.

Intervention Type OTHER

BCG

Vaccination with the live attenuated BCG vaccine.

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

* Age ≥18 and ≤35 yrs
* Male
* Healthy

Exclusion Criteria

* History of influenza vaccination within the year prior to study entry
* History of BCG vaccination within 5 years prior to study entry
* History of Mantoux testing within the year prior to study entry
* Vaccination other than BCG or influenza, within 3 months prior to study or within study period
* Medical history of any disease associated with immune deficiency
* Clinically significant acute illness, including infections, within 4 weeks before vaccination
* Participation in a drug trial or donation of blood 3 months prior to study entry
* Use of recreational drugs within 21 days prior to experiment day
* Recent hospital admission or surgery with general anaesthesia (\<3 months)
* Known chronic kidney or liver disease
* Latent or active tuberculosis infection
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

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Radboud University Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Mihai Netea, PhD

Role: PRINCIPAL_INVESTIGATOR

Radboud University Nijmegen Medical Centre, The Netherlands

Locations

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Radboud University Nijmegen Medical Centre

Nijmegen, Gelderland, Netherlands

Site Status

Countries

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Netherlands

Other Identifiers

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BCG_influenza

Identifier Type: -

Identifier Source: org_study_id

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