Tomoiu Andru, Larbi Anis, Fortin Carl, Dupuis Gilles, Fulop Tamas
Research Center on Aging, Immunology Program, Geriatric Division, Faculty of Medicine, University of Sherbrooke, 1036 rue Belvedere sud, Sherbrooke J1H 4C4, Quebec, Canada.
Ann N Y Acad Sci. 2007 Apr;1100:98-110. doi: 10.1196/annals.1395.008.
Aging is associated with an alteration of the immune response called immunosenescence. It is now well accepted that all parts of the immune system, the adaptive as well as the innate, undergo immunosenescence. However, the adaptive immune response and especially T cell functions are the most affected by aging. Aging is associated with profound changes in lymphocytes subpopulations, however, the functional changes within these subsets are more important to elucidate. Indeed, T cells present functional modifications resulting in a decreased clonal expansion and interleukin-2 (IL-2) production. So there should be an alteration in the activation process of T cells with aging involving the T cell receptor (TCR) and CD28 receptor signaling cascades. The alterations in membrane rafts composition and function can underline this altered activation of T cells with aging and then contribute to human immunosenescence. The experimental data in favor of this hypothesis will be reviewed.
衰老与一种称为免疫衰老的免疫反应改变有关。现在人们普遍认为,免疫系统的所有部分,无论是适应性免疫还是先天性免疫,都会经历免疫衰老。然而,适应性免疫反应,尤其是T细胞功能受衰老影响最大。衰老与淋巴细胞亚群的深刻变化有关,然而,阐明这些亚群内的功能变化更为重要。事实上,T细胞存在功能改变,导致克隆扩增减少和白细胞介素-2(IL-2)产生减少。因此,随着年龄增长,T细胞的激活过程应该会发生改变,涉及T细胞受体(TCR)和CD28受体信号级联反应。膜筏组成和功能的改变可能是衰老导致T细胞激活改变的基础,进而导致人类免疫衰老。支持这一假设的实验数据将进行综述。