Effros R B, Walford R L
Immunology. 1983 Jun;49(2):387-92.
Declining immunity in aged individuals has been repeatedly verified. However, many of the studies have focused on functions not directly relevant to the antigens normally encountered in vivo. For example, although infectious agents represent a significant cause of morbidity and mortality in the elderly, age-related immune responses in such diseases have received very little experimental attention. The present study was, therefore, initiated to examine T cell-mediated immunity to influenza virus in aged mice. We observed that the primary cytotoxic T lymphocyte (CTL) response to influenza, which peaks at day 5 in young adult mice, is almost completely absent at that timepoint in aged mice. Our experiments indicate that the kinetics of the response are shifted, so that the maximum activity appears at days 7-9. Furthermore, a comparison of the peak responses of both age groups reveals a significantly lower magnitude in the aged mice. The diminished response was also observed for most of the old mice when antigenic stimulation occurred in vitro. Although the overall response was diminished, the characteristic T cell cross-reactivity for all A strain viruses was similar to that observed in young mice. The possible causes and consequences of the age-related decline in influenza-specific CTL activity are discussed.
老年人免疫力下降已被反复证实。然而,许多研究关注的功能与体内正常遇到的抗原并无直接关联。例如,尽管感染因子是老年人发病和死亡的重要原因,但针对此类疾病的年龄相关免疫反应很少受到实验关注。因此,本研究旨在检测老年小鼠对流感病毒的T细胞介导免疫。我们观察到,对流感的主要细胞毒性T淋巴细胞(CTL)反应在年轻成年小鼠中于第5天达到峰值,而在老年小鼠的该时间点几乎完全缺失。我们的实验表明,反应动力学发生了变化,以至于最大活性出现在第7 - 9天。此外,对两个年龄组峰值反应的比较显示,老年小鼠的反应强度明显较低。当在体外进行抗原刺激时,大多数老年小鼠也观察到反应减弱。尽管总体反应减弱,但所有甲型流感病毒株的特征性T细胞交叉反应性与年轻小鼠中观察到的相似。本文讨论了流感特异性CTL活性随年龄下降的可能原因和后果。