T1D 患者和进展期患者体内细胞因子、趋化因子和生长因子的性别特异性特征

Khyati Girdhar, Keiichiro Mine, Jeffrey M DaCosta, Mark A Atkinson, Johnny Ludvigsson, Emrah Altindis
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引用次数: 0

摘要

尽管有研究报告称 1 型糖尿病(T1D)患者的细胞因子水平发生了变化,但结果并不一致,这可能是由于各种因素的影响。本研究对 T1D 患者在发病前和发病后细胞因子水平存在性别差异的假设进行了检验。我们使用多重检测法分析了 48 种血液细胞因子、趋化因子和生长因子的水平。我们发现只有 M-CSF 和 IL-6 这两种细胞因子在 T1D 患者(25 人)与对照组(25 人)之间存在显著差异。不过,在比较性别年龄匹配的对照组和 T1D 样本时,我们发现了明显的变化。与女性对照组相比,女性 T1D 患者的炎性细胞因子(TNF-α、IL-6、IL-1a)、Th2 细胞因子(IL-4、IL-13)和趋化因子(MIP-1α、RANTES、MIP-3)较低,但男性患者则不低。与女性对照组相比,T1D 女性患者的 IL-22 较低,而与男性对照组相比,T1D 男性患者的 IL-22 较高。相比之下,男性 T1D 患者的生长因子(EGF、PDGF-AB/BB)高于男性对照组。在T1D进展期患者(样本采集数年后才发病的儿童,人数=16-21)中,男女患者的GROa均低于对照组。我们的发现强调了了解 T1D 发病机制中性别特异性差异的重要性及其对开发个性化治疗方法的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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-α, IL-6, IL-1a), Th2 cytokines (IL-4, IL-13), and chemokines (MIP-1α, 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.
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