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树突状细胞、T细胞耐受性与不良免疫反应的治疗

Dendritic cells, T cell tolerance and therapy of adverse immune reactions.

作者信息

Morel P A, Feili-Hariri M, Coates P T, Thomson A W

机构信息

Department of Immunology, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.

出版信息

Clin Exp Immunol. 2003 Jul;133(1):1-10. doi: 10.1046/j.1365-2249.2003.02161.x.

Abstract

Dendritic cells (DC) are uniquely able to either induce immune responses or to maintain the state of self tolerance. Recent evidence has shown that the ability of DC to induce tolerance in the steady state is critical to the prevention of the autoimmune response. Likewise, DC have been shown to induce several type of regulatory T cells including Th2, Tr1, Ts and NKT cells, depending on the maturation state of the DC and the local microenvironment. DC have been shown to have therapeutic value in models of allograft rejection and autoimmunity, although no success has been reported in allergy. Several strategies, including the use of specific DC subsets, genetic modification of DC and the use of DC at various maturation stages for the treatment of allograft rejection and autoimmune disease are discussed. The challenge for the future use of DC therapy in human disease is to identify the appropriate DC for the proposed therapy; a task made more daunting by the extreme plasticity of DC that has recently been demonstrated. However, the progress achieved to date suggests that these are not insurmountable obstacles and that DC may become a useful therapeutic tool in transplantation and autoimmune disease.

摘要

树突状细胞(DC)具有独特的能力,既能诱导免疫反应,又能维持自身耐受状态。最近的证据表明,DC在稳态下诱导耐受的能力对于预防自身免疫反应至关重要。同样,根据DC的成熟状态和局部微环境,DC已被证明可诱导多种类型的调节性T细胞,包括Th2、Tr1、Ts和NKT细胞。DC在同种异体移植排斥和自身免疫模型中已显示出治疗价值,尽管在过敏方面尚未有成功报道。本文讨论了几种策略,包括使用特定的DC亚群、对DC进行基因改造以及使用处于不同成熟阶段的DC来治疗同种异体移植排斥和自身免疫性疾病。DC疗法未来在人类疾病中的应用面临的挑战是为所提议的治疗确定合适的DC;最近已证明DC具有极强的可塑性,这使得这项任务更加艰巨。然而,迄今为止取得的进展表明,这些并非不可逾越的障碍,DC可能会成为移植和自身免疫性疾病中一种有用的治疗工具。

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