首页> 外文期刊>The journals of gerontology.Series A. Biological sciences and medical sciences >IFN gamma-TNF alpha(-)IL2(-)MIP1 alpha(-)CD107a(+)PRF1(+) CD8 pp65-Specific T-Cell Response Is Independently Associated With Time to Death in Elderly Humans
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IFN gamma-TNF alpha(-)IL2(-)MIP1 alpha(-)CD107a(+)PRF1(+) CD8 pp65-Specific T-Cell Response Is Independently Associated With Time to Death in Elderly Humans

机译:IFN gamma-TNF alpha(-)IL2(-)MIP1 alpha(-)CD107a(+)PRF1(+)CD8 pp65-特定的T细胞反应与老年人的死亡时间独立相关

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Persistent cytomegalovirus (CMV) infection has been suggested to be a major driving force in the immune deterioration and an underlying source of age-related diseases in the elderly. CMV antibody titers are associated with lower responses to vaccination, cardiovascular diseases, frailty, and mortality. CMV infection is also associated with shorter T-cell telomeres and replicative senescence. Although an age-related deregulation of CMV-specific T-cell responses could be an underlying cause of the relationship between CMV and immune defects, strong and polyfunctional responses are observed in elderly individuals, casting uncertainty on their direct role in age-related immune frailty. In this study, we longitudinally followed a cohort of healthy donors aged over 50 years, assessing their mortality rates and time to death during a 2-year period. Specific T-cell responses to the immunodominant antigen pp65 (IFN gamma, TNF alpha, IL2, MIP1 alpha, CD107a, and perforin production) were analyzed at the beginning of the 2-year observation period. A cytotoxic CD8 pp65-specific T-cell response, without cytokine or chemokine coexpression, was independently associated with all-cause mortality in these elderly individuals. This pp65-specific CD8 T-cell response could be a useful tool to identify individuals with depressed immune function and a higher risk of death.
机译:持久性巨细胞病毒(CMV)感染已被认为是老年人免疫功能下降的主要驱动力,也是与年龄相关疾病的潜在来源。 CMV抗体滴度与疫苗接种,心血管疾病,虚弱和死亡率较低的反应有关。 CMV感染还与较短的T细胞端粒和复制性衰老有关。尽管与年龄有关的CMV特异性T细胞反应的失调可能是CMV与免疫缺陷之间关系的根本原因,但在老年患者中观察到了强烈且多功能的反应,不确定了它们在与年龄有关的免疫脆弱中的直接作用。在这项研究中,我们纵向追踪了一群年龄超过50岁的健康捐献者,评估了他们在两年内的死亡率和死亡时间。在2年观察期开始时,分析了对免疫优势抗原pp65(IFNγ,TNFα,IL2,MIP1α,CD107a和穿孔素产生)的特定T细胞应答。没有细胞因子或趋化因子共表达的细胞毒性CD8 pp65特异性T细胞应答与这些老年人的全因死亡率独立相关。这种pp65特异性CD8 T细胞应答可能是一种有用的工具,可用于识别免疫功能低下和较高死亡风险的个体。

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