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衰老过程中的胸腺退化。

Thymic involution in aging.

作者信息

Aspinall R, Andrew D

机构信息

Department of Immunology, ICSTM at Chelsea and Westminster Hospital, London, England.

出版信息

J Clin Immunol. 2000 Jul;20(4):250-6. doi: 10.1023/a:1006611518223.

Abstract

The size of the naive T-cell pool is governed by output from the thymus and not by replication. This pool contributes cells to the activated/memory T-cell pool whose size can be increased through cell multiplication; both pools together constitute the peripheral T-cell pool. Aging is associated with involution of the thymus leading to a reduction in its contribution to the naive T-cell pool; however, despite this diminished thymic output, there is no significant decline in the total number of T cells in the peripheral T-cell pool. There are, however, considerable shifts in the ratios of both pools of cells, with an increase in the number of activated/memory T cells and the accumulation in older individuals of cells that fail to respond to stimuli as efficiently as T cells from younger individuals. Aging is also associated with a greater susceptibility to some infections and some cancers. An understanding of the causal mechanism of thymic involution could lead to the design of a rational therapy to reverse the loss of thymic tissue, renew thymic function, increase thymic output, and potentially improve immune function in aged individuals.

摘要

初始T细胞库的大小由胸腺输出决定,而非细胞增殖。该细胞库为活化/记忆T细胞库提供细胞,后者的大小可通过细胞增殖增加;这两个细胞库共同构成外周T细胞库。衰老与胸腺退化相关,导致其对初始T细胞库的贡献减少;然而,尽管胸腺输出减少,外周T细胞库中T细胞的总数并无显著下降。不过,这两个细胞库的细胞比例发生了相当大的变化,活化/记忆T细胞数量增加,且在老年个体中积累了一些对刺激反应不如年轻个体的T细胞有效的细胞。衰老还与对某些感染和某些癌症的易感性增加有关。了解胸腺退化的因果机制可能会促成一种合理疗法的设计,以逆转胸腺组织的丧失、恢复胸腺功能、增加胸腺输出,并有可能改善老年个体的免疫功能。

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