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Mine, K.

Publications and source records attributed to Mine, K..

2 recordsLinked to original sources

Sex-Specific Cytokine, Chemokine, and Growth Factor Signatures in T1D Patients and Progressors

While studies have reported altered levels of cytokines in type 1 diabetes (T1D) patients, the results are inconsistent, likely because of variable factors. This study tests the hypothesis that there are sex-based differences in cytokine levels in T1D, prior to and after disease onset. We analyzed 48 blood cytokine, chemokine, and growth factor levels using a multiplex assay. We found only two cytokines, M-CSF and IL-6, with significant differences between T1D patients (n=25) versus controls overall (n=25). However, we identified notable alterations when comparing sex-age-matched controls and T1D samples. Inflammatory cytokines (TNF-, IL-6, IL-1a), Th2 cytokines (IL-4, IL-13), and chemokines (MIP-1, RANTES, MIP-3) were lower in female T1D patients compared to female controls, but not in males. IL-22 was lower in female T1D patients compared to female controls, while it was higher in male T1D patients compared to male controls. In contrast, growth factors (EGF, PDGF-AB/BB) were higher in male T1D patients compared to male controls. In T1D progressors (children who developed the disease years after the sample collection, n=16-21), GROa was lower compared to controls in both sexes. Our findings underscore the importance of understanding sex-specific differences in T1D pathogenesis and their implications for developing personalized treatments.

immunology↗

Tyk2-mediated signaling promotes the development of autoreactive CD8+ CTLs and autoimmune type 1 diabetes

Tyrosine kinase 2 (TYK2), a member of the JAK family, might be a susceptibility gene for type 1 diabetes (T1D), whereas its precise role in autoimmune T1D remains unknown. We showed Tyk2 deficiency and inhibition suppressed autoimmune T1D development in non-obese diabetic (NOD) mice. Defective IL-12 signaling due to Tyk2 deficiency in islet-autoreactive CD8+ CTLs during their priming reduced T-bet expression, leading to impaired Cxcr3 expression and effector functions against {beta}-cells. Tyk2 deficient CD8+ resident dendritic cells (rDC) exhibited reduced MHC I expression and impaired cross-priming of CTLs. In {beta}-cells, increased expressions of Fas, MHC I, and chemokines with age were attenuated by Tyk2 deficiency. We demonstrated that treatment with BMS-986165, a Tyk2 inhibitor, inhibited the development of CTLs and inflammation in {beta}-cells in vitro. BMS-986165 reduced the incidence of diabetes in NOD mice. Thus, we demonstrated that Tyk2-mediated signaling has a critical role in the development of autoreactive CD8+ CTLs, inflammation in {beta}-cells, and the pathogenesis of autoimmune T1D. SummaryWe demonstrated that Tyk2-mediated signaling plays a critical role in the development of autoreactive CD8+ CTLs, inflammation in {beta}-cells, and the pathogenesis of autoimmune T1D. These findings will lead to the development of safety and effective prevention strategies for T1D.

immunology↗