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树突状细胞与衰老:对自身免疫的影响。

Dendritic cells and aging: consequences for autoimmunity.

机构信息

Division of Basic and Clinical Immunology, Department of Medicine, University of California, Irvine, CA 92697, USA.

出版信息

Expert Rev Clin Immunol. 2012 Jan;8(1):73-80. doi: 10.1586/eci.11.77.

Abstract

The immune system has evolved to mount immune responses against foreign pathogens and to remain silent against self-antigens. A balance between immunity and tolerance is required as any disturbance may result in chronic inflammation or autoimmunity. Dendritic cells (DCs) actively participate in maintaining this balance. Under steady-state conditions, DCs remain in an immature state and do not mount an immune response against circulating self-antigens in the periphery, which maintains a state of tolerance. By contrast, foreign antigens result in DC maturation and DC-induced T-cell activation. Inappropriate maturation of DCs due to infections or tissue injury may cause alterations in the balance between the tolerogenic and immunogenic functions of DCs and instigate the development of autoimmune diseases. This article provides an overview of the effects of advancing age on DC functions and their implications in autoimmunity.

摘要

免疫系统的进化目的是针对外来病原体产生免疫反应,同时对自身抗原保持沉默。免疫和耐受之间需要达到平衡,因为任何干扰都可能导致慢性炎症或自身免疫。树突状细胞(DC)积极参与维持这种平衡。在稳态条件下,DC 处于未成熟状态,不会对循环中的外周自身抗原产生免疫反应,从而维持耐受状态。相比之下,外来抗原导致 DC 成熟和 DC 诱导的 T 细胞激活。感染或组织损伤引起的 DC 异常成熟可能导致 DC 耐受和免疫功能之间的平衡发生改变,并引发自身免疫性疾病的发展。本文概述了年龄增长对 DC 功能的影响及其在自身免疫中的意义。

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