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Research Article: Aberrant IL-21/STAT3 signaling disrupts regulatory T cell function and CD4 + T cell homeostasis in children with type 1 diabetes

Date Published: 2026-05-18

Abstract:
Type 1 diabetes (T1D) is an autoimmune disease characterized by profound dysregulation of CD4 + T cell subsets, particularly impaired regulatory T cell (Treg) function accompanied by excessive Th17 and T follicular helper (Tfh) cell responses. Interleukin-21 (IL-21) has been implicated in T cell–mediated autoimmunity; however, the immunoregulatory mechanisms linking IL-21 signaling to T cell imbalance in pediatric T1D remain incompletely understood. Single-cell RNA sequencing data from children with T1D were analyzed to characterize IL-21/STAT3 pathway activity across immune cell subsets. Functional assays were performed using primary human CD4 + T cells and Tregs treated with IL-21 and the STAT3 inhibitor Stattic. T cell differentiation, suppressive function, cytokine production, and STAT3 activation were assessed in vitro . The immunological and pathological effects of STAT3 inhibition were further evaluated in a non-obese diabetic (NOD) mouse model. Single-cell transcriptomic analysis revealed enhanced IL-21/STAT3 signaling activity in CD4 + T cell populations from children with T1D. IL-21 stimulation induced STAT3 phosphorylation and nuclear translocation, leading to reduced FoxP3 expression, impaired Treg-associated suppressive function, and a shift in CD4 + T cell differentiation toward Th17 and Tfh phenotypes. Pharmacological inhibition of STAT3 effectively reversed IL-21–mediated Treg dysfunction and restored CD4 + T cell balance in vitro . In NOD mice, STAT3 inhibition ameliorated hyperglycemia, reduced pancreatic inflammation, preserved insulin-positive islets, and corrected systemic T cell subset imbalance. Aberrant activation of the IL-21/STAT3 signaling axis may contribute to impaired Treg function and CD4 + T cell imbalance in pediatric T1D. These findings suggest that IL-21–STAT3–dependent immune dysregulation represents an important mechanism involved in T cell imbalance and autoimmune pathology in T1D.

Introduction:
Type 1 diabetes (T1D) is an autoimmune disease characterized by profound dysregulation of CD4 + T cell subsets, particularly impaired regulatory T cell (Treg) function accompanied by excessive Th17 and T follicular helper (Tfh) cell responses. Interleukin-21 (IL-21) has been implicated in T cell–mediated autoimmunity; however, the immunoregulatory mechanisms linking IL-21 signaling to T cell imbalance in pediatric T1D remain incompletely understood.

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