Department of Immunobiology and the Arizona Center on Aging, University of Arizona College of Medicine, Tucson, AZ 85724, United States.
Department of Immunobiology and the Arizona Center on Aging, University of Arizona College of Medicine, Tucson, AZ 85724, United States.
Exp Gerontol. 2018 May;105:140-145. doi: 10.1016/j.exger.2018.01.011. Epub 2018 Jan 11.
Aging has a profound effect on the immune system, and both innate and adaptive arms of the immune system show functional decline with age. In response to infection with intracellular microorganisms, old animals mobilize decreased numbers of antigen-specific CD8+ T cells with reduced production of effector molecules and impaired cytolytic activity. However, the CD8+ T cell-intrinsic contribution to, and molecular mechanisms behind, these defects remain unclear. In this review we will discuss the mechanistic contributions of age related changes in the CD8+ T cell pool and the relative roles of intrinsic functional defects in aged CD8+ T cells vs. defects in the aged environment initiating the CD8+ T cell response.
衰老是免疫系统的一个重要影响因素,固有免疫和适应性免疫系统都随着年龄的增长而出现功能下降。在应对细胞内微生物感染时,老年动物动员的抗原特异性 CD8+T 细胞数量减少,效应分子生成减少,细胞毒性活性受损。然而,CD8+T 细胞内在因素对这些缺陷的贡献以及背后的分子机制尚不清楚。在这篇综述中,我们将讨论 CD8+T 细胞池中与年龄相关的变化的机制贡献,以及固有功能缺陷在老年 CD8+T 细胞中与启动 CD8+T 细胞反应的老年环境中的相对作用。