T 细胞衰老与系统性红斑狼疮患者的早期动脉粥样硬化有关

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Mirza Zaka Pratama, Cesarius Singgih Wahono, Ahmad Bayhaqi Nasir Aslam, Syahrul Chilmi, Vidia Purnama Sari, Anugrah Abdurrohman, Ike Sulistiyowati, Aldo Aditya, Maxie Felix Johono,  Robert
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引用次数: 0

摘要

目的 探讨系统性红斑狼疮(SLE)患者体内T细胞衰老与动脉粥样硬化标志物之间的相关性。 方法 研究对象为 40 名符合 2019 年 EULAR/ACR 标准的 18-45 岁女性系统性红斑狼疮患者和 40 名健康人。动脉粥样硬化标志物的研究采用多普勒超声检查法测量颈动脉内膜厚度(cIMT)和血流介导的扩张(FMD),血清标志物采用可溶性ICAM-1和VCAM-1。流式细胞术检测 CD4+CD57+、CD8+CD57+、CD4+CD28null 和 CD8+CD28null T 细胞以评估免疫衰老标志物。 结果 与对照组相比,系统性红斑狼疮患者的 cIMT(p <.001)、sICAM-1(p <.001)和 sVCAM-1(p <.001)明显升高,而系统性红斑狼疮患者的 FMD 则明显降低(p <.001)。系统性红斑狼疮患者所有 T 细胞衰老标记物的百分比也明显高于健康人。cIMT与CD4+CD57+(R = .301,p = .005)、CD4+CD28null(R = .448,p <.001)和CD8+CD28null(R = .422,p <.001)之间呈正相关。相反,FMD 与 CD4+CD57+ (R = -.236, p = .023)、CD8+CD57+ (R = -.409, p < .001)、CD4+CD28null (R = -.422, p < .001) 和 CD8+CD28null (R = -.318, p = .003)之间呈负相关。可溶性标记物 sICAM-1 和 sVCAM-1 也与 T 细胞衰老标记物呈正相关。 结论 在这项研究中,系统性红斑狼疮患者出现了动脉粥样硬化的早期症状。T细胞衰老标志物与动脉粥样硬化标志物(包括cIMT、FMD和可溶性粘附分子水平)有显著相关性。了解免疫衰老与动脉粥样硬化之间的联系可能有助于找到一种新的方法来早期检测和治疗系统性红斑狼疮患者的动脉粥样硬化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
T-cell senescence was correlated with early atherosclerosis in patients with systemic lupus erythematosus

Aim

To investigate the correlation between T-cell senescence with the atherosclerosis markers in patients with systemic lupus erythematosus (SLE).

Methods

The study participants were 40 female SLE patients aged 18–45 years who met the 2019 EULAR/ACR criteria and 40 healthy individuals. The atherosclerosis markers were investigated using the Doppler ultrasonography examinations to measure the cIMT (carotid intima-media thickness) and flow-mediated dilation (FMD) and serological markers using soluble ICAM-1 and VCAM-1. Flow cytometry of CD4+CD57+, CD8+CD57+, CD4+CD28null, and CD8+CD28null T cells were used to assess the immunosenescence markers.

Results

The cIMT (p < .001), sICAM-1 (p < .001), and sVCAM-1 (p < .001) were significantly higher in SLE patients compared with control, while FMD was significantly lower in SLE patients (p < .001). The percentages of all T-cell senescence markers are also significantly higher in SLE patients than in healthy individuals. Positive correlations were shown between cIMT with the CD4+CD57+ (R = .301, p = .005), CD4+CD28null (R = .448, p < .001), and CD8+CD28null (R = .422, p < .001). Conversely, negative correlations were demonstrated between the FMD with CD4+CD57+ (R = −.236, p = .023), CD8+CD57+ (R = −.409, p < .001), CD4+CD28null (R = −.422, p < .001), and CD8+CD28null (R = −.318, p = .003). The soluble markers of sICAM-1 and sVCAM-1 were also positively correlated with the T-cell senescence markers.

Conclusion

Early sign of atherosclerosis was demonstrated in patients with SLE in this study. T-cell senescence markers had significant correlations with the atherosclerosis markers, including the cIMT, FMD, and soluble adhesion molecules levels. Understanding the link between immunosenescence and atherosclerosis might help to identify a new method for early detection and treatment of atherosclerosis in SLE.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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