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年龄相关的调节性 T 淋巴细胞发育和功能变化:综述

Age-Dependent Changes in Regulatory T Lymphocyte Development and Function: A Mini-Review.

机构信息

CPTP, Université de Toulouse, CNRS, Inserm, UPS, Toulouse, France.

出版信息

Gerontology. 2018;64(1):28-35. doi: 10.1159/000478044. Epub 2017 Jul 14.

Abstract

The generation and function of immuno-suppressive regulatory T lymphocytes (Treg), which can differentiate in the thymus (tTreg) or in the periphery (pTreg), are regulated in an age-dependent manner. tTreg are produced at high levels in the first weeks of age, when they expand and colonize secondary lymphoid organs and peripheral tissues to protect the organism from autoimmune diseases and to promote tissue repair. Once this population of Treg is operational in the periphery, at puberty, thymic output of Treg declines, but self-reactive tTreg generated early on in life are maintained over time and play a major role in preserving homeostasis of the immune system. Extra-thymic pTreg differentiation declines later on in life. pTreg generated throughout life mainly protect the organism from chronic inflammation and the semi-allogeneic fetus from rejection. In this review, age-dependent modulation of the production and function of these two populations of Treg is described.

摘要

免疫抑制调节性 T 淋巴细胞(Treg)的产生和功能受年龄依赖性调节,其可在胸腺(tTreg)或外周分化(pTreg)。tTreg 在出生后的前几周高水平产生,此时它们扩增并定植于次级淋巴器官和外周组织,以防止自身免疫性疾病并促进组织修复。一旦外周存在 Treg 群体,即青春期时,胸腺 Treg 的产生减少,但生命早期产生的自身反应性 tTreg 会随时间推移而被维持,并在维持免疫系统的内稳态方面发挥主要作用。此外,生命后期的非胸腺 pTreg 分化减少。一生中产生的 pTreg 主要保护机体免受慢性炎症和半同种异体胎儿排斥。在本综述中,描述了这两种 Treg 群体的产生和功能的年龄依赖性调节。

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