Healthy aging and latent infection with CMV lead to distinct changes in CD8+ and CD4+ T-cell subsets in the elderly

Healthy aging and latent infection with CMV lead to distinct changes in CD8+ and CD4+ T-cell subsets in the elderly
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DOI:
10.1016/j.humimm.2006.10.019
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发表时间:
2007-02-01
期刊:
影响因子:
2.7
通讯作者:
Grubeck-Loebenstein, Beatrix
Grubeck-Loebenstein, Beatrix
中科院分区:
医学4区
文献类型:
--
作者:
Weinberger, Birgit;Lazuardi, Lutfan;Grubeck-Loebenstein, Beatrix

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尽管普遍认为免疫学变化与衰老和巨细胞病毒(CMV)潜伏感染有关,但迄今为止,严格的年龄相关性变化和CMV诱导的变化之间没有明确的区别。因此,我们比较了CMV阳性(n = 164)和CMV阴性(n = 87)老年人中的CD 4(+)和CD 8(+)幼稚(CD 45 RA + CD 28+)、记忆(CD 45 RA-CD 28+)和效应(CD 28(-))T细胞,并将CD 8(+)和CD 4(+)效应T细胞与其他T细胞亚群相关联。与CMV阴性老年人相比,CMV阳性老年人中CD 8(+)和CD 4(+)效应T细胞的百分比较高,但幼稚和记忆细胞的百分比较低。发现在CMV阳性和CMV阴性的老年个体中,CD 8(+)T细胞亚群之间存在负相关。相反,CD 4(+)T细胞亚群内的相关性和CD 8(+)和CD 4(+)效应T细胞之间的正相关性仅在CMV阳性个体中发现。我们的研究结果表明:(a)在老年人中,不同的T细胞亚群在CD 8(+)T细胞群中竞争空间,但不是在CD 4(+)T细胞群中竞争空间;(B)CMV诱导的CD 4(+)区室的变化不同于在CMV阴性老年人中观察到的仅与年龄相关的变化;以及(c)在得出关于衰老对T细胞库组成的影响的结论之前,必须考虑群体的CMV状态。
Despite general acceptance that immunologic changes are associated with aging and latent infection with Cytomegalovirus (CMV), no clear-cut distinction has so far been made between strictly age-related and CMV-induced changes. We therefore compared CD4(+) and CD8(+) naive (CD45RA+CD28+), memory (CD45RA-CD28+), and effector (CD28(-)) T cells in CMV-positive (n = 164) and CMV-negative (n = 87) elderly persons and correlated CD8(+) and CD4(+) effector T cells with other T-cell subpopulations. Percentages of CD8(+) as well as CD4(+) effector T cells were higher, but percentages of naive and memory cells were lower in CMV-positive compared to CMV-negative elderly persons. Negative correlations within CD8(+) T-cell subsets were found to be present: in both CMV-positive and CMV-negative elderly individuals. In contrast, correlations within CD4(+) T-cell subpopulations and a positive correlation between CD8(+) and CD4(+) effector T cells were found in CMV-positive individuals only. Our results demonstrate that (a) in the elderly different T-cell subsets compete for space within the CD8(+), but not the CD4(+) T-cell population; (b) CMV induces changes in the CD4(+) compartment that differ from the solely age-related changes seen in CMV-negative elderly population; and (c) the CMV-status of a population has to be taken into account before a conclusion on the effect of aging on the composition of the T-cell pool can be reached.