Department of Psychology, College of Arts and Sciences, University of Kentucky, Lexington, KY, United States; Department of Pathology and Laboratory Medicine, College of Medicine, University of Kentucky, Lexington, KY, United States.
Department of Pathology and Laboratory Medicine, College of Medicine, University of Kentucky, Lexington, KY, United States.
Brain Behav Immun. 2019 Aug;80:266-274. doi: 10.1016/j.bbi.2019.03.018. Epub 2019 Mar 15.
Cytomegalovirus (CMV) and psychological stress are implicated as drivers of immunological aging. It is unknown, however, whether associations among CMV titers, stress, and immune aging are more stable or dynamic over time. The present investigation tested the between-person (stable differences) and within-person (dynamic fluctuations) associations of CMV titers and perceived stress on late-differentiated T and natural killer (NK) peripheral blood cells in a longitudinal study of older adults aged 64-92 years (N = 149). Participants reported stress levels and provided blood biannually for 2.5 years (up to 5 waves per person) to assess CMV IgG titers and composites of late-differentiated CD8 T cells (CD28- and CD57 + subsets) and CD56 NK cells (CD57+, NKG2C+, and FcεRIγ- subsets). In multilevel models that controlled for demographic variables, higher CMV titers were associated with higher proportions and counts of aged T and NK cells between people and lower counts of aged T cells within people. Perceived stress was associated with higher counts of aged T cells between people, but was not associated with aged NK cells. A significant interaction between stress and CMV titers on T cells between people indicated that older adults with lower stress levels and lower CMV titers had the lowest proportions of late-differentiated T cells, whereas those with higher stress levels had high proportions, regardless of CMV control. Our results provide evidence for longer-term, between-person associations among CMV titers, stress, and immunological aging, rather than dynamic within-person associations. We propose that targeting factors that promote low, stable perceived stress in older adults may retard T cell differentiation and ultimately support healthy aging.
巨细胞病毒 (CMV) 和心理压力被认为是免疫衰老的驱动因素。然而,目前尚不清楚 CMV 滴度、压力和免疫衰老之间的关联是随着时间的推移更加稳定还是动态变化。本研究通过对 64-92 岁的老年人进行纵向研究,测试了 CMV 滴度和感知压力与晚期分化 T 和自然杀伤 (NK) 外周血细胞之间的个体间(稳定差异)和个体内(动态波动)关联(N=149)。参与者报告了压力水平,并在 2.5 年内每两年提供一次血液样本(每人最多 5 次),以评估 CMV IgG 滴度和晚期分化 CD8 T 细胞(CD28-和 CD57+亚群)和 CD56 NK 细胞(CD57+、NKG2C+和 FcεRIγ-亚群)的复合指标。在控制人口统计学变量的多层次模型中,较高的 CMV 滴度与个体之间较高的衰老 T 和 NK 细胞比例和数量以及个体内较低的衰老 T 细胞数量相关。感知压力与个体之间衰老 T 细胞的数量增加相关,但与衰老 NK 细胞无关。压力和 CMV 滴度对个体之间 T 细胞的显著交互作用表明,低压力水平和低 CMV 滴度的老年人具有最低比例的晚期分化 T 细胞,而高压力水平的老年人则具有较高的比例,而与 CMV 控制无关。我们的研究结果提供了更长时间、个体间的 CMV 滴度、压力和免疫衰老之间的关联证据,而不是个体内的动态关联。我们提出,针对促进老年人低水平、稳定感知压力的因素可能会延缓 T 细胞分化,最终支持健康衰老。