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Updated: Jun 10, 2026

A High-Throughput Multiplexed Screening for Type 1 Diabetes, Celiac Diseases, and COVID-19
Published on: July 5, 2022
Enterovirus markers and serum CXCL10 in children with type 1 diabetes
Anna-Karin Berg1, Torsten Tuvemo, Gun Frisk
1Department of Oncology, Radiology and Clinical Immunology, Uppsala University, 751 85 Uppsala, Sweden.
Insights
Serum levels of CXCL10 were not elevated in children with type 1 diabetes or enterovirus infections, suggesting limited clinical use for this chemokine marker in type 1 diabetes diagnosis. This finding contrasts with elevated levels in other viral infections.
Area of Science:
- Immunology
- Virology
- Endocrinology
Background:
- Type 1 diabetes is an autoimmune disease involving T-cells.
- Chemokine CXCL10 attracts activated T-cells and is induced by viral infections.
- Enteroviruses are implicated in type 1 diabetes pathogenesis.
Purpose of the Study:
- To investigate elevated serum CXCL10 levels in children with type 1 diabetes.
- To determine if CXCL10 levels correlate with enterovirus markers.
- To assess CXCL10 as a potential biomarker for type 1 diabetes and enterovirus infection.
Main Methods:
- Measured serum CXCL10, enterovirus antibody titers, and GAD65 antibodies in type 1 diabetes patients, siblings, and controls.
- Performed enterovirus PCR on whole blood.
- Compared CXCL10 levels in patients with proven enterovirus or other virus infections.
Main Results:
- Serum CXCL10 levels were not elevated in children with type 1 diabetes or their siblings compared to controls.
- No significant difference in CXCL10 levels was found between type 1 diabetes patients and those with enterovirus infections.
- CXCL10 levels were significantly elevated in patients with other proven virus infections.
Conclusions:
- Elevated serum CXCL10 levels are not indicative of type 1 diabetes or enterovirus infection.
- The lack of correlation suggests local CXCL10 production is not reflected in serum.
- CXCL10's clinical utility as a biomarker for type 1 diabetes is limited.
Abstract:
Most patients with type 1 diabetes are considered to have a T-cell mediated autoimmune disease. The chemokine CXCL10 promotes the migration of activated T-cells. Virus infections might contribute to the pathogenesis of type 1 diabetes and enterovirus protein and/or genome have been detected in beta-cells from a majority of tested newly diagnosed children with type 1 diabetes. The chemokine CXCL10 is induced in human islet cells by enterovirus infections in vivo and in vitro, but is not expressed in islets from normal organ donors. Since CXCL10 is a chemokine known to be induced by virus infections and/or cellular damage, our aim was to study if levels of CXCL10 are elevated in serum from children with type 1 diabetes and whether it correlates to the presence of enterovirus markers. CXCL10, neutralizing antibody titer rises against certain enterovirus, and antibodies against GAD65 were measured in serum, and enterovirus PCR was performed on whole blood from 83 type 1 diabetes patients at onset, 48 siblings and 69 controls. CXCL10 was also measured in serum from 46 patients with proven enterovirus infection and in serum from 46 patients with other proven virus infections. The CXCL10 serum levels were not elevated in children at onset of type 1 diabetes and there was a considerable overlap between the groups with 99 (8-498) pg/ml in serum from children with type 1 diabetes, 120 (17-538) pg/ml in serum from controls, and 117 (7-448) pg/ml in siblings of the children with type 1 diabetes. The CXCL10 serum levels in patients with proven enterovirus infection were slightly increased compared to the levels in the other groups, 172 (0-585) pg/ml but there was no statistically significant difference. In contrast, CXCL10 serum levels in patients with other proven virus infections were clearly elevated 418 (34-611) pg/ml. Despite that elevated CXCL10 levels have been demonstrated in some groups of patients with type 1 diabetes, in this study the mean CXCL10 serum levels were not elevated in patients with type 1 diabetes neither in patients with proven enterovirus infection. In contrast, in patients with other virus infections the CXCL10 levels were elevated, presumably reflecting the severity or the site of infection. This suggests that local production of CXCL10 in the affected organ cannot be measured reproducible in serum and that its potential use in clinical practice is limited.
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