Characteristics of T cell premature senescence in maintenance hemodialysis patients.

IF 4.8 3区 医学 Q2 CELL BIOLOGY Inflammation Research Pub Date : 2024-08-01 Epub Date: 2024-06-08 DOI:10.1007/s00011-024-01897-2
Wangshu Wu, Ahui Song, Kewei Xie, Jiayue Lu, Bingru Zhao, Cheng Qian, Minzhou Wang, Lulin Min, Wenkai Hong, Huihua Pang, Renhua Lu, Leyi Gu
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Abstract

Background: Uremia-associated immunodeficiency, mainly characterized by T cell dysfunction, exists in patients on maintenance hemodialysis (MHD) and promotes systemic inflammation. However, T cell senescence, one of the causes of T cell dysfunction, has not been clearly revealed yet. In this cross-sectional research, we aimed to study the manifestation of T cell premature senescence in MHD patients and further investigate the associated clinical factors.

Methods: 76 MHD patients including 33 patients with cardiovascular diseases (CVD) and 28 patients with arteriovenous fistula (AVF) event history were enrolled in this study. Complementarity determining region 3 (CDR3) of T cell receptor (TCR) was analyzed by immune repertoire sequencing (IR-Seq). CD28- T cell subsets and expression of senescence marker p16 and p21 genes were detected by multicolor flow cytometry and RT-qPCR, respectively.

Results: MHD patients had significantly decreased TCR diversity (P < 0.001), increased CDR3 clone proliferation (P = 0.001) and a left-skewed CDR3 length distribution. The proportion of CD4 + CD28- T cells increased in MHD patients (P = 0.014) and showed a negative correlation with TCR diversity (P = 0.001). p16 but not p21 expression in T cells was up-regulated in MHD patients (P = 0.039). Patients with CVD exhibited increased expression of p16 and p21 genes (P = 0.010 and 0.004, respectively), and patients with AVF events showed further TCR diversity and evenness reduction (P = 0.002 and 0.017, respectively) compared to patients without the comorbidities. Moreover, age, average convection volume, total cholesterol, high-density lipoprotein cholesterol and transferrin saturation were associated with TCR diversity or CD4 + CD28- T cell proportion (P < 0.05).

Conclusions: MHD patients undergo T cell premature senescence characterized by significant TCR diversity reduction and repertoire skew, as well as accumulation of the CD4 + CD28- subset and up-regulation of p16 gene. Patients with CVD or AVF events show higher level of immunosenescence. Furthermore, T cell senescence in MHD patients is associated with blood cholesterol and uremic toxin retention, suggesting potential intervention strategies in the future.

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维持性血液透析患者 T 细胞早衰的特征。
背景:维持性血液透析(MHD)患者中存在以 T 细胞功能障碍为主要特征的尿毒症相关免疫缺陷,并导致全身性炎症。然而,T 细胞衰老是导致 T 细胞功能障碍的原因之一,目前尚未明确揭示。在这项横断面研究中,我们旨在研究 MHD 患者中 T 细胞早衰的表现,并进一步调查相关的临床因素。通过免疫组群测序(IR-Seq)分析了T细胞受体(TCR)的互补决定区3(CDR3)。多色流式细胞术和 RT-qPCR 分别检测了 CD28- T 细胞亚群以及衰老标志物 p16 和 p21 基因的表达:结果表明:MHD 患者的 TCR 多样性明显降低(P<0.05):MHD患者的T细胞早衰表现为TCR多样性明显降低、TCR库偏斜、CD4 + CD28-亚群聚集和p16基因上调。心血管疾病或房室纤维化事件患者的免疫衰老程度更高。此外,MHD患者的T细胞衰老与血液中胆固醇和尿毒症毒素的滞留有关,这表明未来可能采取干预策略。
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来源期刊
Inflammation Research
Inflammation Research 医学-免疫学
CiteScore
9.90
自引率
1.50%
发文量
134
审稿时长
3-8 weeks
期刊介绍: Inflammation Research (IR) publishes peer-reviewed papers on all aspects of inflammation and related fields including histopathology, immunological mechanisms, gene expression, mediators, experimental models, clinical investigations and the effect of drugs. Related fields are broadly defined and include for instance, allergy and asthma, shock, pain, joint damage, skin disease as well as clinical trials of relevant drugs.
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