Z Z Ren, S S Jia, X L Zhong, Y F Zhang, T T Li, F Qiu
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引用次数: 0

摘要

研究目的本研究探讨了阿尔茨海默病(AD)患者外周血 CD45RO⁺ T 细胞中 C-X-C motif 趋化因子受体 3 (CXCR3) 的表达及其与临床特征的关系。研究方法2022年9月至2024年3月期间,从解放军总医院内科神经内科共招募了41名AD患者和30名年龄与性别匹配的健康对照组(HCs)。流式细胞术用于量化外周血中CD45RO⁺ T细胞亚群的CXCR3表达。使用迷你精神状态检查(MMSE)和蒙特利尔认知评估(MoCA)对AD患者的痴呆严重程度进行评估。斯皮尔曼相关分析检验了 CD45RO⁺CXCR3⁺ T 细胞水平与 AD 组认知功能之间的关系。接收者操作特征(ROC)曲线分析确定了CD45RO⁺CXCR3⁺T细胞对AD的预测效用,以曲线下面积(AUC)进行量化。结果显示与健康对照组相比,AD患者的CD8⁺CD45RO⁺CXCR3⁺T细胞水平明显升高[17.8% (7.2%, 40.3%) vs. 8.2% (5.1%, 12.3%), Z=-2.59, PP>0.05]。斯皮尔曼相关分析显示,CD8⁺CD45RO⁺CXCR3⁺T细胞水平与认知评分之间存在负相关(MMSE:r=-0.72,Pr=-0.70,PC结论:AD患者CD8⁺CD45RO⁺T细胞上的CXCR3表达明显上调,其水平与认知障碍的严重程度相关。这些发现表明,CD8⁺CD45RO⁺CXCR3⁺T细胞可作为诊断和监测AD进展的潜在生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Expression and clinical significance of CXCR3 on effector T cells in the peripheral blood of patients with Alzheimer's disease].

Objective: This study investigated the expression of C-X-C motif chemokine receptor 3 (CXCR3) on CD45RO⁺ T cells in the peripheral blood of patients with Alzheimer's disease (AD) and its association with clinical features. Methods: A total of 41 AD patients and 30 age-and sex-matched healthy controls (HCs) were recruited from the Department of Neurology at the Medical Division of PLA General Hospital between September 2022 and March 2024. Flow cytometry was used to quantify CXCR3 expression on CD45RO⁺ T cell subsets in peripheral blood. Dementia severity in AD patients was assessed using the Mini-Mental State Examination (MMSE) and Montreal Cognitive Assessment (MoCA). Spearman correlation analysis examined the relationship between CD45RO⁺CXCR3⁺ T cell levels and cognitive function in the AD group. Receiver operating characteristic (ROC) curve analysis determined the predictive utility of CD45RO⁺CXCR3⁺ T cells for AD, quantified by the area under the curve (AUC). Results: Compared to healthy controls, AD patients exhibited significantly elevated levels of CD8⁺CD45RO⁺CXCR3⁺ T cells [17.8% (7.2%, 40.3%) vs. 8.2% (5.1%, 12.3%), Z=-2.59, P<0.05]. However, no significant differences were observed for CD4⁺CD45RO⁺CXCR3⁺ T cells, CD4⁺CD45RO⁻CXCR3⁺ T cells, or CD8⁺CD45RO⁻CXCR3⁺ T cells (P>0.05). Spearman correlation analysis revealed a negative correlation between CD8⁺CD45RO⁺CXCR3⁺ T cell levels and cognitive scores (MMSE: r=-0.72, P<0.05; MoCA: r=-0.70, P<0.05). ROC analysis demonstrated an AUC of 0.81 for CD8⁺CD45RO⁺CXCR3⁺ T cells in predicting AD, with a sensitivity of 59.0% and specificity of 93.3%. Conclusions: CXCR3 expression is significantly upregulated on CD8⁺CD45RO⁺ T cells in AD patients, and its levels correlate with cognitive impairment severity. These findings suggest that CD8⁺CD45RO⁺CXCR3⁺ T cells may serve as a potential biomarker for AD diagnosis and progression monitoring.

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