BCG Vaccination-Associated Lower HbA1c and Increased CD25 Expression on CD8+ T Cells in Patients with Type 1 Diabetes in Ghana

Author:

Aniagyei Wilfred12ORCID,Mohayideen Sumaya2,Sarfo-Kantanka Osei34ORCID,Bittner Sarah1,Vivekanandan Monika M.2,Arthur Joseph F.2ORCID,Boateng Agnes O.3,Yeboah Augustine2ORCID,Ahor Hubert S.1ORCID,Asibey Shadrack O.3,Owusu Elizabeth3,Herebian Diran1ORCID,Huttasch Maximilian56ORCID,Burkart Volker56,Wagner Robert567,Roden Michael567,Adankwah Ernest2ORCID,Owusu Dorcas O.2ORCID,Mayatepek Ertan1ORCID,Jacobsen Marc1ORCID,Phillips Richard O.24ORCID,Seyfarth Julia1ORCID

Affiliation:

1. Department of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany

2. Kumasi Centre for Collaborative Research in Tropical Medicine (KCCR), Kumasi 00233, Ghana

3. Komfo Anokye Teaching Hospital, Kumasi 00233, Ghana

4. School of Medicine and Dentistry, College of Health Sciences, Kwame Nkrumah University of Science and Technology (KNUST), Kumasi 00233, Ghana

5. Institute for Clinical Diabetology, German Diabetes Center, Leibniz Center for Diabetes Research at Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany

6. German Center for Diabetes Research, Partner Düsseldorf, 85764 Neuherberg, Germany

7. Department of Endocrinology and Diabetology, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany

Abstract

BCG vaccination affects other diseases beyond tuberculosis by unknown—potentially immunomodulatory—mechanisms. Recent studies have shown that BCG vaccination administered during overt type 1 diabetes (T1D) improved glycemic control and affected immune and metabolic parameters. Here, we comprehensively characterized Ghanaian T1D patients with or without routine neonatal BCG vaccination to identify vaccine-associated alterations. Ghanaian long-term T1D patients (n = 108) and matched healthy controls (n = 214) were evaluated for disease-related clinical, metabolic, and immunophenotypic parameters and compared based on their neonatal BCG vaccination status. The majority of study participants were BCG-vaccinated at birth and no differences in vaccination rates were detected between the study groups. Notably, glycemic control metrics, i.e., HbA1c and IDAA1c, showed significantly lower levels in BCG-vaccinated as compared to unvaccinated patients. Immunophenotype comparisons identified higher expression of the T cell activation marker CD25 on CD8+ T cells from BCG-vaccinated T1D patients. Correlation analysis identified a negative correlation between HbA1c levels and CD25 expression on CD8+ T cells. In addition, we observed fractional increases in glycolysis metabolites (phosphoenolpyruvate and 2/3-phosphoglycerate) in BCG-vaccinated T1D patients. These results suggest that neonatal BCG vaccination is associated with better glycemic control and increased activation of CD8+ T cells in T1D patients.

Funder

Else Kröner-Fresenius-Stiftung

German Federal Ministry of Health and the Ministry of Culture and Science of the state of North Rhine-Westphalia

European Community

German Science Foundation

Publisher

MDPI AG

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