Section for Transplantation Immunology, 2nd Dept of Internal Medicine, University of Tübingen Center for Medical Research, Tübingen Ageing and Tumour Immunology Group, Waldhörnlestr 22, D-72072 Tübingen, Germany.
Virus Res. 2011 May;157(2):175-9. doi: 10.1016/j.virusres.2010.09.010. Epub 2010 Oct 1.
"Immune senescence" is a descriptive term for the deleterious age-associated changes to immunity observed in all mammals studied so far. While all components of innate and adaptive immunity are changed with age, the clinical impact of these changes is not clear, and mechanisms of and markers for immunosenescence are controversial. In humans, several cross-sectional studies have demonstrated that the major accepted age-associated changes to parameters used to assess adaptive immune status are markedly influenced by infection with cytomegalovirus (CMV). In the very limited longitudinal studies thus far carried out, a cluster of immune parameters associating with 2-, 4- and 6-year survival of the very elderly has been identified and termed the "immune risk profile" (IRP). This cluster includes seropositivity for CMV and is characterised by accumulations of clonal expansions of late-differentiated CD8+ T cells, many of which are specific for CMV antigens. Here we review the impact of CMV on "immune senescence" in humans.
“免疫衰老”是一个描述性术语,用于描述迄今为止在所有研究的哺乳动物中观察到的与年龄相关的免疫有害变化。虽然先天免疫和适应性免疫的所有成分都随年龄而变化,但这些变化的临床影响尚不清楚,免疫衰老的机制和标志物也存在争议。在人类中,几项横断面研究表明,用于评估适应性免疫状态的参数的主要公认的与年龄相关的变化受到巨细胞病毒 (CMV) 感染的显著影响。在迄今为止进行的非常有限的纵向研究中,已经确定了一组与非常年长的人的 2 年、4 年和 6 年生存率相关的免疫参数簇,并将其命名为“免疫风险特征”(IRP)。这个簇包括对 CMV 的血清阳性反应,其特征是晚期分化的 CD8+T 细胞的克隆性扩张的积累,其中许多细胞针对 CMV 抗原。在这里,我们回顾了 CMV 对人类“免疫衰老”的影响。