Skip to content

Bacillus Calmette-guérin Vaccination to Prevent Infections of the Elderly

A Randomized Clinical Trial for Enhanced Trained Immune Responses Through Bacillus Calmette-guérin Vaccination to Prevent Infections of the Elderly

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03296423
Acronym
ACTIVATE
Enrollment
200
Registered
2017-09-28
Start date
2017-09-21
Completion date
2020-11-30
Last updated
2021-01-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hospitalization, Infection, Mortality

Keywords

BCG vaccination

Brief summary

One small recent trial in elderly volunteers showed that BCG vaccination can protect against infectious complications, while several studies have demonstrated an increased capacity of innate immune responses to react against pathogens. This process, also called trained immunity, generates the hypothesis that BCG vaccination can prevent or delay new infections in the elderly patients and is studied in the ACTIVATE trial

Detailed description

In an era of antimicrobial resistance, where the already existing antimicrobials are not sufficient, the development of new strategies for the prevention and treatment of infections is of great interest. This approach becomes more and more mandatory in our current era of the financial crisis where bacterial infections by multidrug-resistant emerge and impose heavily on the financial burden of the disease. These infections occur more frequently among elderly patients leading to prolonged hospitalization where unfavorable outcome is not infrequent1. Vaccination is the traditional approach of infection prevention. A classic example focusing on the need to prevent morbid re-infection is vaccination with pneumococcal vaccine the incidence of pneumococcal pneumonia and bacteremia is enormously increasing among the elderly2. The principle of vaccination is to develop memory B-lymphocytes so that early and adequate antibody titers are produced upon re-exposure to the same antigen. This is called the memory function of the adaptive immune system. Well before adaptive immunity develops proper recognition of a bacterial pathogen is done through binding of well-preserved structures known as pathogen-associated molecular patterns (PAMPs) on pattern-recognition receptors (PRRs) of the innate immune system and mainly of blood monocytes and tissue macrophages. Through a series of experiments in cell systems and animals, it was found that exposure of macrophages to small amounts of PAMPs like the β-glucan of Candida albicans and constituents of Mycobacterium tuberculosis may prevent death upon re-exposure to lethal bacterial challenges like C.albicans and Staphylococcus aureus3-6. Initial exposure to small amounts of PAMPs leads to epigenetic changes that induce the capacity of macrophages and monocytes to produce high amounts of pro-inflammatory cytokines like tumour necrosis factor-alpha (TNFα) and interferon-gamma (IFNγ) that clear efficiently the pathogen3. This enhancement of the immune cells reaction after appropriate priming to stimuli totally different from the initial ones is called trained immunity and it could be a potential pathway of preventing serious infections without having severe adverse effects. The concept has also been tested in healthy volunteers that were vaccinated with placebo or BCG (Baccillus Calmette Guérin) vaccine. These volunteers were injected 14 days latter a tri-valent influenza A vaccine. Volunteers previous vaccinated by BCG developed significantly greater titers against hemagglutinin A of the influenza A virus whereas their circulating monocytes were more potent for the production of IFNγ7. Finally, a small study has recently reported that BCG vaccination of the elderly may protect against infections8, but larger studies are necessary to confirm these findings. This generates hopes that vaccination by BCG may increase immune resistance and/or tolerance of elderly patients upon exposure to bacterial infections. This generates hopes that vaccination by BCG may increase immune tolerance of elderly patients upon exposure to bacterial diseases. The aim of the study is to demonstrate in a double-blind, placebo-controlled approach if vaccination of elderly patients with BCG vaccine may modulate their disease susceptibility for bacterial diseases. This will be validated using both clinical and immunological criteria.

Interventions

BIOLOGICALVaccination

Patients discharged from hospital will be vaccinated with one intradermal injection of 0.1ml of BCG vaccine

BIOLOGICALPlacebo

Patients discharged from hospital will be vaccinated with one intradermal injection of 0.1ml of sodium chloride 0.9%

Sponsors

Radboud University Medical Center
CollaboratorOTHER
Hellenic Institute for the Study of Sepsis
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Intervention model description

Patients vaccinated with placebo or BCG

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male or female * Age more than or equal to 65 years based on the precise date of birth * Discharge from hospital after hospitalization for a medical cause. All medical causes make patients eligible for enrolment with the only exception of medical causes mentioned in the

Design outcomes

Primary

MeasureTime frameDescription
Time to first infection12 monthsThe time interval to the first infection post hospital discharge between the two groups of treatment.

Secondary

MeasureTime frameDescription
Time to first infection or sepsis episodeMonth 12The time to first infection or sepsis episode will be compared between the two groups of treatment
Total number of infectionsMonth 12The total number of infections will be compared between the two groups of treatment
Time to first hospitalizationMonth 12The time to first hospitalization will be compared between the two groups of treatment
Number of antibiotic administrationsMonth 12The number of antibiotic administrations will be compared between the two groups of treatment
HospitalizationMonth 12The rate of hospitalizations will be compared between the two groups of treatment
Cytokine stimulationMonth 3Cytokine stimulation from peripheral blood monuclear cells will be compared between the two groups of treatment
Epigenetic changesMonth 3Epigenetic changes of circulating monocytes will be compared between the two groups of treatment
Cost of treatmentMonth 12The effect of BCG vaccination on cost of treatment for infections will be compared between the two groups of treatment
MortalityMonth 12Mortality will be compared between the two groups of treatment

Countries

Greece

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026