[细胞因子面板在诊断眼部慢性移植物抗宿主病中的临床研究]。

Q3 Medicine
X J Cheng, R Ji, R H Huan, S Q Huang, W Fan, Y C Zhao, R D Yuan, X Q Wang, X Zhang
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引用次数: 0

摘要

目的研究细胞因子与眼部慢性移植物抗宿主病(cGVHD)之间的关系,并确定眼部慢性移植物抗宿主病的特异性生物标志物,以加强临床诊断、治疗和评估。方法:建立小鼠 cGVHD 模型,探讨 cGVHD 与血清细胞因子之间的相关性。根据动物实验结果和文献综述,确定了 16 种细胞因子组合。采用酶联免疫吸附试验(ELISA)比较了2017年6月至2022年3月期间在陆军军医大学新桥医院血液病医学中心接受异基因造血干细胞移植的患者血清和泪液样本中的细胞因子浓度。研究结果与对照组相比,cGVHD小鼠血清IL-1β、IL-6、IL-8、IL-17、IFN-γ、CX3CL1、CXCL11、CXCL13、CCL11和CCL19浓度升高(PP均=0.032,曲线下面积(AUC)=0.678];血清 IL-10 降低(P=0.030,AUC=0.701);泪液样本中 IL-8、IFN-γ、CXCL9 和 CCL17 升高;泪液样本中 IL-10 和 CCL19 降低(均为 P0.7)。此外,泪液样本中的细胞因子与眼部 cGVHD 相关的眼表参数存在相关性。结论:泪液具有更高的特异性:与血清生物标志物相比,泪液作为诊断眼部 cGVHD 的生物标志物具有更高的特异性和敏感性。在泪液样本中发现的细胞因子中,IL-8、IL-10、IFN-γ、CXCL9、CCL17 和 CCL19 可作为移植后眼部 cGVHD 的诊断生物标志物,为诊断提供实用参考价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Clinical study of the cytokine panel in the diagnosis of ocular chronic graft-versus-host disease].

Objective: To investigate the association between cytokines and ocular chronic graft-versus-host disease (cGVHD) and identify specific biomarkers for ocular cGVHD to enhance clinical diagnosis, treatment, and evaluation. Methods: A mouse model of cGVHD was established to explore the correlation between cGVHD and serum cytokines. Based on the findings from the animal experiments and literature review, a panel of 16 cytokine combinations was identified. Enzyme-linked immunosorbent assay (ELISA) was used to compare the cytokine concentrations in the serum and tear samples from patients who underwent allogeneic hematopoietic stem cell transplantation from June 2017 to March 2022 at the Medical Center of Hematology, Xinqiao Hospital, Army Medical University. Results: ① Compared with the control group, mice with cGVHD exhibited elevated serum IL-1β, IL-6, IL-8, IL-17, IFN-γ, CX3CL1, CXCL11, CXCL13, CCL11, and CCL19 concentrations (all P<0.05). ② Analysis of the cytokine profiles of the serum and tear samples revealed that compared with patients without ocular cGVHD, those with ocular cGVHD exhibited increased serum IL-8 [P=0.032, area under the curve (AUC) =0.678]; decreased serum IL-10 (P=0.030, AUC=0.701) ; elevated IL-8, IFN-γ, CXCL9, and CCL17 in tear samples; and lower IL-10 and CCL19 in tear samples (all P<0.05, all AUC>0.7). Moreover, cytokines in tear samples showed correlations with ocular surface parameters related to ocular cGVHD. Conclusions: Tear fluid demonstrates greater specificity and sensitivity as a biomarker for diagnosing ocular cGVHD than serum biomarkers. Among the identified cytokines in tear samples, IL-8, IL-10, IFN-γ, CXCL9, CCL17, and CCL19 serve as diagnostic biomarkers for ocular cGVHD post-transplantation, offering practical reference value for diagnosis.

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CiteScore
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