J Transl Autoimmun. 2026 Sep 1;13:100400. doi: 10.1016/j.jtauto.2026.100400. eCollection 2026 Dec.
ABSTRACT
Type 1 diabetes (T1D) in sub-Saharan Africa exhibits heterogeneity, characterised by alternative phenotypes that retain C-peptide levels. The T-cell pathology linked to these atypical phenotypes remains largely unexplored. CD25, the interleukin-2 receptor alpha chain, and IL2RA genetic variants are key T-cell factors implicated in T1D immunopathology and may contribute to the heterogeneity of T1D in an African context. This study examined IL2RA genotypes and T-cell phenotypes, both ex vivo and following in vitro stimulation, in Ghanaian individuals diagnosed with T1D and classified into groups of low, mid and high C-peptide levels, alongside healthy controls. Immunophenotyping showed increased CD25 expression on CD4 and CD8 T cells in the diabetes cohorts, correlating with age, C-peptide and HbA1c. IL2RA genotyping revealed limited variability and no link to CD25 expression. An expansion of CD25/CD127 double-positive conventional T cells, mainly in naïve and central memory subsets, was observed in T1D with mid and high C-peptide. Following age-matching, the low C-peptide group also demonstrated an increase in CD25/CD127 double-positive T cells, both ex vivo and after in vitro stimulation. The findings indicate a common pattern of immune dysregulation characterized by the expansion of activated conventional T cells in T1D with varying C-peptide levels in Ghana.
PMID:42740916 | PMC:PMC13572010 | DOI:10.1016/j.jtauto.2026.100400
