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通过重新表达 CD45RA 定义的终末期人 T 细胞的特性。

Properties of end-stage human T cells defined by CD45RA re-expression.

机构信息

Division of Infection and Immunity, University College London, 5 University Street, London, WC1E 6JF, UK.

出版信息

Curr Opin Immunol. 2012 Aug;24(4):476-81. doi: 10.1016/j.coi.2012.04.001. Epub 2012 May 1.

Abstract

Persistent viral infections, inflammatory syndromes and ageing all induce the accumulation of highly differentiated CD45RA re-expressing memory T cells. These cells increase during ageing, especially in individuals who are infected with cytomegalovirus (CMV). These cells have decreased proliferative capacity, increased activation of senescence signalling pathways and greater susceptibility to apoptosis in vitro. However these cells are capable of multiple effector functions and thus bear all the hallmarks of short-lived effector T cells. This indicates that senescence signalling may govern the unique characteristics of effector T cells. In this article, we address the functional and migratory properties of these T cells and mechanisms that are involved in their generation. Finally we assess the potential for manipulation of their activity and whether this may improve immune function during ageing.

摘要

持续的病毒感染、炎症综合征和衰老都会导致高度分化的 CD45RA 再表达记忆 T 细胞的积累。这些细胞在衰老过程中会增加,特别是在感染巨细胞病毒 (CMV) 的个体中。这些细胞的增殖能力下降,衰老信号通路的激活增加,体外凋亡的易感性增加。然而,这些细胞能够发挥多种效应功能,因此具有短暂效应 T 细胞的所有特征。这表明衰老信号可能控制效应 T 细胞的独特特征。在本文中,我们探讨了这些 T 细胞的功能和迁移特性以及它们产生的机制。最后,我们评估了其活性的可操作性以及这是否可能改善衰老过程中的免疫功能。

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