BSc, Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Reina Sofia University Hospital, University of Cordoba, Cordoba, Spain.
J Gerontol A Biol Sci Med Sci. 2013 Jan;68(1):1-5. doi: 10.1093/gerona/gls130. Epub 2012 May 2.
The increasing number of elderly people eligible for solid organ transplants has made it necessary to reevaluate how the decline in immune function associated to ageing (immunosenescence) affects solid organ transplants. Some immunosenescence biomarkers, such as the expansion of CD28(-)CD8+ T lymphocytes, have been associated to cytomegalovirus infection and are related to a form of accelerated immune senescence in transplant recipients. However, the impact of cytomegalovirus replication on downregulation of CD28 on total CD8+ T cells is independent of patients' age, whereas downregulation on cytomegalovirus-specific CD8+ T cells depends on patients' age, inducing early immunosenescence of cytomegalovirus-specific CD8+ T cells in young but not elderly solid organ transplants recipients. Although immunosenescence in transplant recipients should be considered a two-edged sword as it is a risk factor for the development of tumors after transplantation, it has a beneficial effect in attenuating acute allograft rejection and correlates with better clinical outcomes.
随着适合接受实体器官移植的老年人数量不断增加,有必要重新评估与衰老相关的免疫功能下降(免疫衰老)如何影响实体器官移植。一些免疫衰老生物标志物,如 CD28(-)CD8+T 淋巴细胞的扩增,与巨细胞病毒感染有关,与移植受者的一种加速免疫衰老形式有关。然而,巨细胞病毒复制对总 CD8+T 细胞上 CD28 下调的影响与患者的年龄无关,而对巨细胞病毒特异性 CD8+T 细胞的下调则取决于患者的年龄,导致年轻但不是老年实体器官移植受者的巨细胞病毒特异性 CD8+T 细胞的早期免疫衰老。尽管移植受者的免疫衰老应被视为一把双刃剑,因为它是移植后肿瘤发展的一个危险因素,但它对减轻急性同种异体移植排斥反应有有益的影响,并与更好的临床结果相关。