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一项关于白癜风中趋化因子的荟萃分析:将免疫细胞招募到黑色素细胞中。

A meta-analysis of chemokines in vitiligo: Recruiting immune cells towards melanocytes.

机构信息

Department of Dermatology, Ghent University Hospital, Gent, Belgium.

Department of Nephrology, Ghent University Hospital, Gent, Belgium.

出版信息

Front Immunol. 2023 Feb 24;14:1112811. doi: 10.3389/fimmu.2023.1112811. eCollection 2023.

Abstract

Chemokine research offers insightful information on the pathogenesis of cutaneous immune disorders, such as vitiligo. Compared to cytokines, the higher detectable levels of chemokines display promising potential as future disease biomarkers. Nonetheless, some published study results are contradictory, which can be attributed to patient characteristics and methodological differences. In this study, a meta-analysis was performed to compare chemokine expression in blood and skin samples from vitiligo patients versus healthy controls. Furthermore, the relationship between chemokine expression and disease activity was evaluated. Chemokine levels were investigated in 15 articles in the circulation and in 9 articles in vitiligo skin. Overall, some clear trends were observed. CXCR3 signaling by CXCL10 and CXCL9 has been confirmed by several reports, although CXCL10 showed more robust findings in blood samples. In this meta-analysis, CCL5, CXCL8, CXCL12, and CXCL16 levels were also significantly elevated. This indicates a complex immune pathway activation in vitiligo that overall supports a Th1-dominant response. Chemokines linked to the Th2 and Th17 pathways were less prevalent. Despite these findings, study protocols that examine a broader range of chemokines are encouraged, because current research is mostly focused on a small number of chemokines that were differentially expressed in previous studies.

摘要

趋化因子研究为皮肤免疫紊乱(如白癜风)的发病机制提供了有价值的信息。与细胞因子相比,趋化因子的可检测水平更高,显示出作为未来疾病生物标志物的巨大潜力。然而,一些已发表的研究结果存在矛盾,这可能归因于患者特征和方法学差异。在这项研究中,进行了荟萃分析以比较白癜风患者与健康对照组的血液和皮肤样本中的趋化因子表达。此外,还评估了趋化因子表达与疾病活动之间的关系。在循环系统的 15 篇文章和白癜风皮肤的 9 篇文章中研究了趋化因子水平。总的来说,观察到了一些明显的趋势。尽管 CXCL10 在血液样本中表现出更稳健的发现,但几项报告已经证实了 CXCR3 信号由 CXCL10 和 CXCL9 介导。在这项荟萃分析中,CCL5、CXCL8、CXCL12 和 CXCL16 水平也显著升高。这表明白癜风中存在复杂的免疫途径激活,总体上支持 Th1 优势反应。与 Th2 和 Th17 途径相关的趋化因子则不太常见。尽管有这些发现,但仍鼓励采用更广泛的趋化因子研究方案,因为目前的研究主要集中在少数在以前的研究中差异表达的趋化因子上。

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