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
{"title":"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","authors":"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","doi":"10.1111/1756-185X.15339","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Aim</h3>\n \n <p>To investigate the correlation between T-cell senescence with the atherosclerosis markers in patients with systemic lupus erythematosus (SLE).</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>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<sup>+</sup>CD57<sup>+</sup>, CD8<sup>+</sup>CD57<sup>+</sup>, CD4<sup>+</sup>CD28<sup>null</sup>, and CD8<sup>+</sup>CD28<sup>null</sup> T cells were used to assess the immunosenescence markers.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>The cIMT (<i>p</i> < .001), sICAM-1 (<i>p</i> < .001), and sVCAM-1 (<i>p</i> < .001) were significantly higher in SLE patients compared with control, while FMD was significantly lower in SLE patients (<i>p</i> < .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<sup>+</sup>CD57<sup>+</sup> (<i>R</i> = .301, <i>p</i> = .005), CD4<sup>+</sup>CD28<sup>null</sup> (<i>R</i> = .448, <i>p</i> < .001), and CD8<sup>+</sup>CD28<sup>null</sup> (<i>R</i> = .422, <i>p</i> < .001). Conversely, negative correlations were demonstrated between the FMD with CD4<sup>+</sup>CD57<sup>+</sup> (<i>R</i> = −.236, <i>p</i> = .023), CD8<sup>+</sup>CD57<sup>+</sup> (<i>R</i> = −.409, <i>p</i> < .001), CD4<sup>+</sup>CD28<sup>null</sup> (<i>R</i> = −.422, <i>p</i> < .001), and CD8<sup>+</sup>CD28<sup>null</sup> (<i>R</i> = −.318, <i>p</i> = .003). The soluble markers of sICAM-1 and sVCAM-1 were also positively correlated with the T-cell senescence markers.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>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.</p>\n </section>\n </div>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"T-cell senescence was correlated with early atherosclerosis in patients with systemic lupus erythematosus\",\"authors\":\"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\",\"doi\":\"10.1111/1756-185X.15339\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Aim</h3>\\n \\n <p>To investigate the correlation between T-cell senescence with the atherosclerosis markers in patients with systemic lupus erythematosus (SLE).</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>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<sup>+</sup>CD57<sup>+</sup>, CD8<sup>+</sup>CD57<sup>+</sup>, CD4<sup>+</sup>CD28<sup>null</sup>, and CD8<sup>+</sup>CD28<sup>null</sup> T cells were used to assess the immunosenescence markers.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>The cIMT (<i>p</i> < .001), sICAM-1 (<i>p</i> < .001), and sVCAM-1 (<i>p</i> < .001) were significantly higher in SLE patients compared with control, while FMD was significantly lower in SLE patients (<i>p</i> < .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<sup>+</sup>CD57<sup>+</sup> (<i>R</i> = .301, <i>p</i> = .005), CD4<sup>+</sup>CD28<sup>null</sup> (<i>R</i> = .448, <i>p</i> < .001), and CD8<sup>+</sup>CD28<sup>null</sup> (<i>R</i> = .422, <i>p</i> < .001). Conversely, negative correlations were demonstrated between the FMD with CD4<sup>+</sup>CD57<sup>+</sup> (<i>R</i> = −.236, <i>p</i> = .023), CD8<sup>+</sup>CD57<sup>+</sup> (<i>R</i> = −.409, <i>p</i> < .001), CD4<sup>+</sup>CD28<sup>null</sup> (<i>R</i> = −.422, <i>p</i> < .001), and CD8<sup>+</sup>CD28<sup>null</sup> (<i>R</i> = −.318, <i>p</i> = .003). The soluble markers of sICAM-1 and sVCAM-1 were also positively correlated with the T-cell senescence markers.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>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.</p>\\n </section>\\n </div>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-09-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/1756-185X.15339\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/1756-185X.15339","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
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.