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Updated: Nov 2, 2025

Accelerated Type 1 Diabetes Induction in Mice by Adoptive Transfer of Diabetogenic CD4+ T Cells
Published on: May 6, 2013
CD5-expressing CD8+ T-cell subsets differ between children with type 1 diabetes and controls
Josefine Wadenpohl1, Julia Seyfarth1, Paul Hehenkamp1
1Department of General Pediatrics, Neonatology and Pediatric Cardiology, University Children's Hospital, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University Düsseldorf, Duesseldorf, Germany.
Children with type 1 diabetes (T1D) show reduced CD8+ T cells with lower CD5 expression. These findings suggest altered T-cell regulation in T1D pathogenesis, impacting immune responses.
Area of Science:
- Immunology
- Endocrinology
- Autoimmunity
Background:
- Type 1 diabetes (T1D) pathogenesis involves various lymphocyte subsets.
- Previous research indicated a role for CD5-expressing T and B cells, including dual-expressing (DE) cells.
Purpose of the Study:
- To investigate immune cell subsets and DE cells in children with T1D compared to controls.
- To analyze CD5 expression on T and B cells in T1D patients.
Main Methods:
- Algorithm-supported multiparameter flow cytometry and quantitative PCR were used.
- Self-organizing maps (FlowSOM) and t-distributed stochastic neighbor embedding (tSNE) analyses were applied.
- In vitro experiments assessed CD5 expression stability after T-cell activation and stimulation.
Main Results:
- Increased CD3+ T cells were observed in T1D patients, while CD19+ B-cell proportions were similar to controls.
- No significant differences in CD5-expressing B-cell subsets or DE cells were found between groups.
- Significantly reduced CD8+ T-cell proportions with moderate or low CD5 expression were identified in T1D patients.
- In vitro studies confirmed stable CD5 expression differences in CD8+ T cells post-activation.
Conclusions:
- T1D patients exhibit distinct CD8+ T-cell populations characterized by reduced CD5 expression.
- Altered CD5 expression on CD8+ T cells may play a role in T1D immune regulation and pathogenesis.
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