Related Experiment Video
Updated: Jun 19, 2026

Accelerated Type 1 Diabetes Induction in Mice by Adoptive Transfer of Diabetogenic CD4+ T Cells
Published on: May 6, 2013
CD40 expression and its association with low-grade inflammation in a Greek population of type 1 diabetic juveniles:
A E Chatzigeorgiou1, P E Lembessis, C F Mylona-Karagianni
1Department of Experimental Physiology, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Insights
CD40 signalling is implicated in type 1 diabetes (T1DM) pathogenesis. Elevated CD40 markers in T1DM patients, particularly those with poor glycemic control, correlate with increased inflammation, suggesting a key role in disease progression.
Area of Science:
- Immunology
- Endocrinology
- Molecular Biology
Background:
- CD40 signalling is linked to autoimmune diseases and chronic inflammation.
- Understanding CD40's role in early-stage type 1 diabetes (T1DM) is crucial.
Purpose of the Study:
- To examine CD40 system component expression in T1DM patients.
- To correlate plasma and urine CD40 levels with inflammatory markers in T1DM.
Main Methods:
- Analyzed plasma, urine, and PBMCs from 70 T1DM patients and 40 healthy controls.
- Utilized ELISA, western-blot, RT-PCR, and DNA sequencing.
Main Results:
- T1DM patients showed higher plasma soluble CD40 (sCD40) linked to elevated IL-6, MMP-9, and CRP.
- Elevated urinary sCD40 suggested increased CD40 production, not reduced excretion.
- PBMCs in T1DM patients exhibited CD40 upregulation, correlating with inflammatory markers.
Conclusions:
- CD40 dysregulation is associated with inflammation in T1DM.
- Poor glycemic control in T1DM exacerbates CD40 upregulation and inflammation.
- CD40 plays a pathophysiological role in the low-grade inflammation of T1DM.
Background:
CD40 signalling has been associated with the pathogenesis of autoimmune diseases and diseases with low-grade chronic inflammation.
Objective:
To investigate, early in the course of type 1 diabetes (T1DM) patients, the expression of CD40 system components, as well as to explore the association of plasma and urine concentrations of CD40 with known inflammatory markers in T1DM.
Methods:
Plasma, urine and peripheral blood mononuclear cells (PBMCs) from 70 T1DM patients without clinically detected chronic complications and 40 healthy controls (HCs) were examined using ELISA, western-blot, semi-quantitative RT-PCR and DNA-sequencing.
Results:
Patients had significantly higher plasma soluble CD40 (sCD40) levels associated with higher Interleukin-6 (IL-6), matrix metalloproteinase-9 (MMP-9) and CRP levels compared with healthy controls. This difference was also evident between poorly and well-controlled diabetic patients. The elevated plasma sCD40 levels do not appear to be due to diminished renal excretion since sCD40 concentrations in the urine were also elevated, suggesting an increased CD40 production. An upregulation of PBMCs' CD40 was evident in T1DM patients associated with higher sCD40, IL-6 and CRP levels. Furthermore, the main CD40 isoform (isoform-I) was solely expressed in poorly controlled diabetics' PBMCs, who also demonstrated cellular CD40 upregulation, higher plasma CD40, CRP, IL-6 and MMP-9 levels compared with the well-controlled diabetics and the control group, who co-expressed type I and II isoforms.
Conclusions:
Homeostatic dysregulation of CD40 and its association with inflammatory markers in T1DM patients, especially in those with poor glycaemic control, implies a pathophysiological role of CD40 in the low-grade inflammatory process in T1DM.
Related Concept Videos
Type I Diabetes I: Introduction
Type I Diabetes II: Pathophysiology
Type II Diabetes I: Introduction
Type II Diabetes II: Pathophysiology
Inflammatory Bowel Disease III: Crohn's Disease
Type I Diabetes III: Clinical Manifestations
