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衰老过程中T细胞库的年龄依赖性改变及T细胞的功能多样性。

Age-dependent alterations of the T cell repertoire and functional diversity of T cells of the aged.

作者信息

Vallejo Abbe N

机构信息

Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.

出版信息

Immunol Res. 2006;36(1-3):221-8. doi: 10.1385/IR:36:1:221.

DOI:10.1385/IR:36:1:221
PMID:17337782
Abstract

The aging immune system is characterized by the contraction of T cell receptor (TCR) diversity and the de novo expression of NKrelated receptors (NKR) on oligoclonal T cells. NKR+ T cells likely represent a secondary immune diversification as a biological adaptation of aging to ensure host defense despite shrinkage of the TCR repertoire. NKRs are expressed in various combinations even among TCR-identical cells, and are capable of triggering effector pathways in either TCR-independent or TCR-dependent fashion. Understanding the biology of NKR+ T cells will be pivotal to the development of strategies to enhance immunity in the elderly.

摘要

衰老的免疫系统的特征是T细胞受体(TCR)多样性的收缩以及寡克隆T细胞上自然杀伤相关受体(NKR)的从头表达。NKR+ T细胞可能代表一种继发性免疫多样化,作为衰老的一种生物学适应,以确保尽管TCR库缩小但宿主仍能防御。即使在TCR相同的细胞之间,NKR也以各种组合表达,并且能够以TCR非依赖性或TCR依赖性方式触发效应途径。了解NKR+ T细胞的生物学特性对于制定增强老年人免疫力的策略至关重要。

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