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Aging and immunity - Impact of behavioral intervention

机译:衰老和免疫力-行为干预的影响

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Immune responses to pathogens to which they were not previously exposed are commonly less effective in elderly people than in young adults, whereas those to agents previously encountered and overcome in earlier life may be amplified. This is reflected in the robust finding in many studies that the proportions and numbers of naive B and T cells are lower and memory cells higher in the elderly. In addition to the "extrinsic" effects of pathogen exposure, "intrinsic" events such as age-associated differences in hae-matopoeitic stem cells and their niches in the bone marrow associated with differences in cell maturation and output to the periphery are also observed. In the case of T cells, the "intrinsic" process of thymic involution, beginning before puberty, further contributes to reducing the production of naive T cells. Like memory T cell populations, innate immune cells may be increased in number but decreased in efficacy on a per-cell basis. Thus, superimposed on chronological age alone, remodelling of immunity as a result of interactions with the environment over the life course is instrumental in shaping immune status in later life. In addition to interactions with pathogens, host microbiome and nutrition, exercise and stress, and many other extrinsic factors are crucial modulators of this "immunosenescence" process. In this review, we briefly outline the observed immune differences between younger and older people, and discuss the possible impacts of behavioral variations thereon.
机译:对于老年人而言,对以前未接触过病原体的免疫反应通常不如在年轻人中有效,而对先前在生命中遇到和克服的病原体的免疫反应则可能会放大。这在许多研究中强有力的发现中得到了反映,即老年人中幼稚的B和T细胞的比例和数量较低,而记忆细胞较高。除了病原体暴露的“外在”效应外,还观察到“内在”事件,例如与血液成熟的造血干细胞及其在骨髓中的壁ni的年龄相关的差异,这些差异与细胞成熟度和​​向外周输出的差异有关。对于T细胞,胸腺退化的“内在”过程始于青春期之前,进一步有助于减少幼稚T细胞的产生。像记忆T细胞群体一样,先天免疫细胞的数量可能会增加,但每个细胞的功效却会下降。因此,仅按时间顺序叠加,由于在整个生命过程中与环境的相互作用而导致的免疫重塑有助于塑造以后的免疫状态。除了与病原体的相互作用之外,宿主微生物组和营养,运动和压力以及许多其他外在因素也是这种“免疫衰老”过程的关键调节剂。在这篇综述中,我们简要概述了观察到的年轻人和老年人之间的免疫差异,并讨论了行为变化对其可能产生的影响。

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