血清TSLP是寻常型银屑病活性的潜在生物标志物

M. El-Ghareeb, Afaf Helmy, Sally Al Kazzaz, H. Samir
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引用次数: 11

摘要

原过敏细胞因子胸腺基质淋巴生成素(TSLP)可能与T细胞衍生的CD40配体(CD40L)协同作用,使银屑病患者产生IL-23。IL-23是介导银屑病患者不适当免疫反应的中枢细胞因子。目的探讨血清TSLP水平与银屑病严重程度的相关性。方法对53例银屑病患者进行临床研究。根据PASI评分分为轻度、中度和重度。患者年龄从10岁到62岁不等。其中男性29例,女性24例。53名年龄、性别相匹配的健康受试者作为对照组。分别采集患者和对照组静脉血,分离血清。血清样品立即在-20°C冷冻。采用夹心酶联免疫吸附试验(ELISA)测定血清TSLP。结果病例组血清TSLP水平(1042.7±812.93)高于对照组(314.21±220.78),差异有统计学意义(p<0.001)。血清TSLP水平随着PASI评分估计的银屑病严重程度的增加也有统计学上非常显著的增加(p<0.001)。结论本研究发现银屑病患者血清TSLP升高,且与病情严重程度相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum TSLP is a potential biomarker of psoriasis vulgaris activity
Background The proallergic cytokine, thymic stromal lymphopoietin (TSLP) may synergize with T cell–derived CD40 ligand (CD40L) to allow IL-23 production in patients with psoriasis. IL-23 is a central cytokine that mediates the inappropriate immune reaction in patients with psoriasis. Objective The aim of the study was to correlate serum level of TSLP with psoriasis severity. Methods The study was carried out on 53 patients with psoriasis. They were divided into mild, moderate, and severe according to PASI score. The patients’ ages ranged from 10 to 62 years. The patients included 29 males and 24 females. A total of 53 healthy subjects with matched age and sex served as control group. Blood samples were collected from the venous blood of the patients and control subjects then the serum was separated. The serum samples were immediately frozen at -20°C. Serum TSLP was measured by Sandwich Enzyme–linked Immunosorbant Assay (ELISA). Results There was a statistically very highly significant increase (p<0.001) in serum TSLP levels among the case group (1042.7±812.93) compared to the control group (314.21±220.78). There was also a statistically very highly significant increase (p<0.001) in serum TSLP levels with increased psoriasis severity estimated by PASI score. Conclusion In this study, we found that serum TSLP is elevated in psoriasis patients and is correlated with disease severity.
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