Kay M M
Fed Proc. 1978 Apr;37(5):1241-4.
A brief overview of the area of T cell aging is presented by first discussing the age-related changes in T cell activities, and then by focusing attention on the possible mechanisms that may be responsible for the decline. Present evidence indicates that thymic involution precedes and therefore may be responsible for the age-dependent decline in the ability of the immune system to generate functional T cells. At this time, it appears that the primary effect of thymic involution is on a T cell differentiation pathway affecting the more mature T cells first with time, and then the less mature T cells. Thus, the thymus may be the aging clock for the immune system. Further studies should be centered around processes regulating growth and atrophy of the thymus.
本文首先讨论T细胞活性的年龄相关变化,然后关注可能导致这种下降的潜在机制,从而对T细胞衰老领域进行简要概述。目前的证据表明,胸腺退化先于免疫系统产生功能性T细胞能力的年龄依赖性下降,因此可能是其原因。此时,胸腺退化的主要影响似乎是作用于T细胞分化途径,随着时间的推移,首先影响更成熟的T细胞,然后是不太成熟的T细胞。因此,胸腺可能是免疫系统的老化时钟。进一步的研究应围绕调节胸腺生长和萎缩的过程展开。