Abstract
Introduction
Bacille Calmette–Guérin (BCG) vaccination has shown promising therapeutic effects for type 1 diabetes (T1D). According to recent studies, immunometabolism modification and regulation of T lymphocytes constitute the proposed mechanisms by which BCG vaccination may delay T1D onset. Clinical trial evidence from Turkey supports that two to three doses of the BCG vaccine in childhood, with the first dose administered in the first year of life, may prevent T1D. In the same study, one or zero vaccinations appeared to have no effect in T1D onset prevention. In Greece, the BCG vaccine was administered in a single dose at the age of 9 years in elementary school. BCG vaccination was not performed on a mandatory basis, creating one BCG vaccinated and one non-vaccinated population. The aim of our study was to investigate the possible effect of a single dose of BCG vaccine, at the age of 9 years, on the time of T1D onset, in a population of BCG vaccinated and non-vaccinated patients with diagnosed T1D.
Methods
To test this hypothesis, a survey through the Pan-Hellenic Federation of People with Diabetes (PFPD) was performed. In this observational, retrospective study, participating patients provided information regarding age, gender, time of diagnosis, and BCG vaccination status. Patients diagnosed with T1D before the age of 9 years were excluded from the analysis.
Results
The final sample included 196 patients (73 male and 123 female) with a mean age of 42.2 ± 14.3 years and a mean duration of diabetes of 16.8 ± 12.9 years. Mean age of T1D diagnosis in the BCG vaccinated group was 24.0 ± 19.0 years, while the mean age of T1D diagnosis in the BCG non-vaccinated group was 21.5 ± 14.3 years (p = 0.03). No interaction was found between gender and the age of diagnosis for BCG vaccinated and unvaccinated patients (p = 0.86).
Conclusion
The results of our study suggest that a single dose of BCG vaccine, performed at the age of 9 years, may delay the onset of T1D by 2.5 years. Additional studies of children receiving multiple doses of BCG should be conducted to possibly prove prolongation of the disease-free interval.
Keywords: Diabetes, Type 1 diabetes, BCG vaccine, Immunometabolism, Hygiene hypothesis
Key Summary Points
| Why carry out this study? |
| Approximately 463 million people are living with diabetes worldwide. |
| Clinical trials support that bacille Calmette–Guérin (BCG) vaccination possibly delays type 1 diabetes (T1D) onset via modification of immunometabolism and inflammation. |
| In Greece BCG vaccination was not performed on a mandatory basis, creating one BCG vaccinated and one non-vaccinated population. |
| What was learned from the study? |
| Differences between the age of diagnosis and BCG vaccination status group were tested by the Mann–Whitney U test. |
| The difference between the two groups was statistically significant (p = 0.03). The BCG non-vaccination group of patients tends to have the initial diagnosis earlier than vaccinated patients. |
| The current trial showed that BCG vaccination, with a single dose at the age of 9 years, probably causes a delay in T1D onset. |
Introduction
The global estimate of adults living with diabetes is 463 million, while a further 1.1 million children and adolescents living with type 1 diabetes (T1D) [1]. Two decades of research have indicated the beneficial effect of bacille Calmette–Guérin (BCG) vaccination for T1D. BCG is one of the commonest vaccines worldwide, and it is has been used for over 100 years with limited side effects. Clinical trials support that BCG vaccination can delay or even prevent the onset of T1D via modification of the immune system response and immunometabolism [2].
According to the immunometabolism mechanism, after BCG vaccination, immune system cells shift their metabolic function from overactive oxidative phosphorylation to aerobic glycolysis. Oxidative phosphorylation depends on small amounts of glucose to produce energy via the Krebs cycle. On the contrary, aerobic glycolysis demands great amounts of extracellular glucose to obtain energy and synthesize purines, which are DNA and RNA building blocks [2]. In addition, BCG vaccination enhances tumor necrosis factor (TNF) production, which activates T regulatory cells (Tregs) and eliminates T cytotoxic lymphocytes (CTL). As a result, the autoimmune response of CTLs against insulin-produced islet of the pancreas is reduced due to the CTLs limited number and the suppressive action of Tregs [3–5].
Clinical trial evidence from Turkey supports that two to three doses of the BCG vaccine in childhood, with the first dose administered in the first year of life, may prevent T1D [6]. In Greece, the BCG vaccine was administered in a single dose at the age of 9 years in elementary school as a part of the national vaccination program. BCG vaccination was not performed on a mandatory basis, creating one BCG vaccinated and one non-vaccinated population. The aim of our study was to investigate the possible effect of a single dose of BCG vaccine, at the age of 9 years, on the time of T1D onset, in a population of BCG vaccinated and non-vaccinated patients with diagnosed T1D.
Methods
To test this hypothesis, a retrospective observational study, through the Pan-Hellenic Federation of People with Diabetes (PFPD), was performed. Participating patients with diagnosed T1D provided information regarding age, gender, time of diagnosis, and BCG vaccination status. Patients diagnosed with T1D before the age of 9 years were excluded from the analysis. The study was conducted from January 2019 to June 2019.
Differences between the age of diagnosis and BCG vaccination status group were tested by the Mann–Whitney U test. Two-way analysis of variance (ANOVA) after logarithmic transformation of the data was used to explore the interaction with gender. Statistical analysis was conducted with SPSS software version 25 for Windows (IBM Corp. Released 2017. IBM SPSS Statistics for Windows, Version 25.0. Armonk, NY: IBM Corp.).
The study protocol was conducted according to the Declaration of Helsinki and approved by the ethics committee of the Salamis Naval and Veterans Hospital, Salamis, Greece.
Results
The final sample included 196 patients diagnosed with T1D (73 male and 123 female) with a mean age (± standard deviation) of 42.2 ± 14.3 years and a mean (± standard deviation) duration of diabetes 16.8 ± 12.9 years.
The median (± interquartile range) age of diagnosis in the BCG vaccinated group of patients was 24.0 ± 19.0 years, while the median (± interquartile range) age of the BCG non-vaccinated group of patients was 21.5 ± 14.3 years (p = 0.03) (Fig. 1). The difference between the two groups was statistically significant. The BCG non-vaccinated group of patients tended to have the initial diagnosis earlier than vaccinated patients.
Fig. 1.
Boxplot of age of diagnosis in bacille Calmette–Guérin (BCG) vaccination groups
No interaction was found between gender and the age of diagnosis for BCG vaccinated and non-vaccinated patients (p = 0.86) (Fig. 2). For male patients, the median (± interquartile range) age of diagnosis in the BCG vaccinated group was 25.0 ± 15.5 years, while the median (± interquartile range) age of the BCG non-vaccinated group was 20.5 ± 14.5 years. For female patients, the median (± interquartile range) age of diagnosis in the BCG vaccinated group was 24.0 ± 21.3 years, while the median (± interquartile range) age of the BCG non-vaccinated group was 21.0 ± 17.0 years.
Fig. 2.
Line chart of interaction between gender and age of diagnosis for bacille Calmette–Guérin (BCG) vaccination groups
Discussion
The aim of this study was to investigate the effect of BCG vaccination on the time of onset of T1D. We found that there is a difference related to the age of diagnosis in favor of BCG vaccinated patients. Previously published studies indicate possible mechanisms to explain the vaccine’s effect on glucose metabolism and the function of pancreatic islets.
In the autoimmune environment, there is an imbalance between Tregs and CTLs. This imbalance leads to increased destruction of pancreatic islet cells, giving a smaller number of Tregs that stabilize the immune response. Several studies have shown that not only BCG vaccination but also tuberculosis infection restore this imbalance of autoimmunity via the production of TNF. TNF activates Tregs and reduces the number of CTLs. This activation occurs via epigenetic changes in the signature genes of the Tregs. Results from trials in diabetic mice have indicated the efficacy of BCG vaccine on the regeneration of the pancreatic islet cells. On the contrary, residual C peptide levels in humans with a long duration of T1D after vaccination were undetectable. In case the vaccination occurs before the onset of diabetes, islets of the pancreas may be protected from autoimmunity. In our study, BCG vaccination was performed approximately at the age of 9 years. According to the aforementioned proposed mechanism, BCG vaccination may presented a protective effect in pancreatic cells from CTLs and autoimmunity. As a result, vaccinated subjects experiences a delay in developing T1D compared to the unvaccinated [4–11].
The hygiene hypothesis contends that in modern societies, there is a rise of autoimmune diseases because of the reduced exposure of the immune system to pathogens. In general, microorganisms shift host cells’ metabolism to aerobic glycolysis. Recent data have indicated the relationship between glucose levels and immunometabolism. In patients with diabetes, immune cells like lymphocytes and macrophages are in an overactive state of oxidative phosphorylation for energy production. Oxidative phosphorylation uses Krebs cycle, producing ketones, and consequently, there is minimal need for glucose uptake. As a result, a greater amount of glucose remains extracellularly. In contrast, after BCG vaccination in patients with diabetes, aerobic glycolysis becomes the predominant metabolic pathway for energy production. Pentose phosphate shunt is activated, and membrane transportation of glucose is also accelerated. Glucose becomes the main fuel of immunometabolism, and fewer metabolites are funneled through the Krebs cycle. Trials have shown that purines which are metabolic products of pentose phosphate shunt are augmented, and as a result, levels of serum glucose tend to be lower. BCG vaccination regulates the imbalance between oxidative phosphorylation and aerobic glycolysis in lymphocytes. Our data suggest that this physiologic mechanism not only delays the onset of diabetes but also ameliorates serum glucose and HbA1c in diabetic patients [12–14].
Several studies in diabetic mice and humans suggest that not one but multiple BCG doses are necessary to prevent T1D. In a randomized, 8-year, prospective trial, two doses of BCG vaccine were performed. After 3 years of clinical observation, HbA1c values had been reduced to near-normal levels and maintained for the next 5 years. mRNA sequencing and metabolomics demonstrated that a shift had occurred from oxidative phosphorylation to aerobic glycolysis during the trial. In our observational study, only a single dose of BCG vaccine had been performed at the age of 9 years old. Nevertheless, we have noticed a significant increase in the age of T1D diagnosis [9, 15].
Limitations
The main limitation of our study is the small sample size. Therefore, larger, high-quality trials with long follow-up periods are required to verify our findings.
Conclusion
The current trial showed that BCG vaccination, with a single dose at the age of 9 years old, probably delays T1D onset. Additional studies of children receiving multiple doses of BCG should be conducted to possibly prove prolongation of the disease-free interval.
Acknowledgements
We would like to express our special thanks of gratitude to the board of the Pan-Hellenic Federation of People with Diabetes, for their continuous help and support throughout the study.
Funding
No funding or sponsorship was received for this study. No funding or sponsorship was received for medical writing services for this manuscript.
Authorship
All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published.
Authors’ Contributions
John Doupis developed the concept and the design of the study also having the overall supervision of the project. Konstantinos Kolokathis conducted the literature review and wrote the manuscript. Markopoulou Eftychia, Festas George, Papandreopoulou Vasiliki, Kallinikou Chrysoula, Antikidou Despina, Gemistou Golfo and Angelopoulos Theodoros contributed equally in data collection and management and Efthymiou Vasiliki performed the statistical analysis of the data.
Prior Presentation
The results of this study were partly disseminated at the 55th European Diabetes Epidemiology Group EDEG Annual Meeting as a virtual conference from 26 to 27th of April 2021.
Disclosures
John Doupis, Konstantinos Kolokathis, Eftychia Markopoulou, Vasiliki Efthymiou, George Festas, Vasiliki Papandreopoulou, Chrysoula Kallinikou, Despina Antikidou, Golfo Gemistou and Theodoros Angelopoulos have nothing to disclose.
Compliance with Ethics Guidelines
The study protocol was conducted according to the Declaration of Helsinki and approved by the ethics committee of the Salamis Naval and Veterans Hospital, Salamis, Greece.
Data Availability
Participating patients with diagnosed T1D diabetes, provided information regarding age, gender, time of diagnosis and BCG vaccination status.
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Associated Data
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Data Availability Statement
Participating patients with diagnosed T1D diabetes, provided information regarding age, gender, time of diagnosis and BCG vaccination status.