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Regulatory T Cells and Vitamin D Status in Children with Chronic Autoimmune Thyroiditis
Zeynep Şıklar1, Deniz Karataş, Figen Doğu
1Ankara University Faculty of Medicine, Department of Pediatric Endocrinology, Ankara, Turkey,
Insights
Vitamin D may enhance regulatory T cell (Treg) function in children with chronic autoimmune thyroiditis (CAT). Lower FOXP3 expression in CAT patients was linked to vitamin D deficiency, improving with supplementation.
Area of Science:
- Immunology
- Endocrinology
- Pediatrics
Background:
- Regulatory T cells (Treg) are crucial for immune homeostasis.
- Vitamin D is implicated in modulating immune cell function.
- Pediatric chronic autoimmune thyroiditis (CAT) involves immune dysregulation.
Purpose of the Study:
- To investigate the relationship between Treg cells and vitamin D levels in pediatric CAT patients.
- To assess the impact of vitamin D on Treg cell function, specifically FOXP3 expression.
Main Methods:
- Studied 32 children with CAT and 24 healthy controls.
- Identified Treg cells by CD4+CD25+high Foxp3+ T cell markers.
- Measured 25-hydroxycholecalciferol (25OHD3) and FOXP3 expression before and after vitamin D therapy in deficient patients.
Main Results:
- Treg cell counts did not differ between CAT patients and controls.
- Vitamin D deficiency was more frequent, and FOXP3 expression was lower in CAT patients.
- Vitamin D replacement therapy significantly increased FOXP3 expression in deficient CAT patients.
Conclusions:
- FOXP3 expression is reduced in pediatric CAT patients, associated with lower vitamin D levels.
- Vitamin D appears to play a role in enhancing the function of natural Treg cells.
- These findings suggest a potential therapeutic role for vitamin D in managing pediatric CAT.
Objective:
It is suggested that vitamin D is one of the factors that can regulate the function of Treg cells. In this study, the relationships between Treg cells and vitamin D levels was investigated in pediatric chronic autoimmune thyroiditis (CAT) patients.
Methods:
Thirty-two children with CAT and 24 healthy subjects were studied. FOXP3 expressing CD4+CD25+high Foxp3+T cells were identified as Treg cells. At diagnosis, 25-hydroxycholecalciferol (25OHD3) levels were determined in all patients. FOXP3 expression was measured before and after vitamin D replacement therapy in patients having low levels of 25OHD3.
Results:
In the CAT patients, Treg cell levels did not differ from the control group, while the frequency of vitamin D deficiency was higher and FOXP3 molecule expression was lower. FOXP3 molecule expression significantly increased in CAT patients having vitamin D deficiency who were given vitamin D replacement.
Conclusion:
FOXP3 expression is decreased in pediatric CAT patients. This reduction seems to be associated with vitamin D levels. Vitamin D can play a role in enhancing natural Treg cell functions.
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