Schaenman Joanna M, Rossetti Maura, Lum Erik, Abdalla Basmah, Bunnapradist Suphamai, Pham Thu-Phuong, Danovitch Gabriel, Reed Elaine F, Cole Steve
Division of Infectious Diseases, Department of Medicine, UCLA Immunogenetics Center, Los Angeles, CA.
Department of Pathology and Laboratory Medicine, UCLA Immunogenetics Center, Los Angeles, CA.
Transplant Direct. 2019 Mar 4;5(4):e436. doi: 10.1097/TXD.0000000000000870. eCollection 2019 Apr.
For the growing numbers of older transplant patients, increased incidence of infection and death compared with younger patients may limit the many benefits provided by transplantation. However, little is known about age-associated immune dysfunction in the older transplant recipient.
A cohort of 60 kidney transplant recipients, 23 older (≥ 60y) and 37 younger (30-59y), matched on antithymocyte induction and donor type (living vs deceased) was evaluated. Gene expression in peripheral blood mononuclear cells 3 months after kidney transplantation was analyzed to compare differences between older and younger patients.
Proinflammatory genes were upregulated in older kidney transplant patients, including cytokines IL1-β and IL-6. Downregulated genes were associated with B-cell and T-cell function, including CCR7 and CD27. Analysis of predicted transcription factor binding suggested an increase in proinflammatory transcription factor CCAAT/enhancer binding protein β-binding sites in older patients, whereas interferon regulatory factor 2 transcription factor binding sites were less prevalent.
Older kidney transplant recipients exhibited multiple differences in gene expression compared with younger patients, with upregulation of proinflammatory genes and downregulation of adaptive immune response genes. These findings may explain the mechanism of increased vulnerability to infection and malignancy observed in older transplant patients.
对于越来越多的老年移植患者而言,与年轻患者相比,感染和死亡发生率的增加可能会限制移植所带来的诸多益处。然而,关于老年移植受者中与年龄相关的免疫功能障碍,我们知之甚少。
评估了一组60例肾移植受者,其中23例为老年患者(≥60岁),37例为年轻患者(30 - 59岁),两组在抗胸腺细胞诱导和供体类型(活体供体与尸体供体)方面进行了匹配。分析肾移植3个月后外周血单个核细胞中的基因表达,以比较老年患者和年轻患者之间的差异。
老年肾移植患者中促炎基因上调,包括细胞因子IL1-β和IL-6。下调的基因与B细胞和T细胞功能相关,包括CCR7和CD27。对预测的转录因子结合的分析表明,老年患者中促炎转录因子CCAAT/增强子结合蛋白β结合位点增加,而干扰素调节因子2转录因子结合位点则较少见。
与年轻患者相比,老年肾移植受者在基因表达方面存在多种差异,促炎基因上调,适应性免疫反应基因下调。这些发现可能解释了老年移植患者中观察到的感染和恶性肿瘤易感性增加的机制。