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CD40与树突状细胞功能

CD40 and dendritic cell function.

作者信息

O'Sullivan Brendan, Thomas Ranjeny

机构信息

Centre for Immunology and Cancer Research, Princess Alexandra Hospital, University of Queensland, Brisbane, Queensland 4102, Australia.

出版信息

Crit Rev Immunol. 2003;23(1-2):83-107. doi: 10.1615/critrevimmunol.v23.i12.50.

Abstract

CD40 has emerged as a key signaling pathway for the function of B cells, monocytes, and dendritic cells (DC) in the immune system, and plays a major role in inflammatory pathways of nonhemopoietic cells. CD40 is expressed by monocytes and DC and is up-regulated when DC migrate from the periphery to draining lymph nodes (DLN) in response to microbial challenge. CD154 signaling by MHC-restricted, activated CD4+ T cells induces differentiation of DC, as defined by an increased surface expression of MHC, costimulatory, and adhesion molecules. Thus, CD40 functions in the adaptive immune response as a trigger for the expression of costimulatory molecules for efficient T-cell activation. CD40 ligation of DC also has the capacity to induce high levels of the cytokine IL-12, which polarizes CD4+ T cells toward a T helper 1 (Th1) type, enhances proliferation of CD8+ T cells, and activates NK cells. CD40 may also play an important role in the decision between tolerance and immunity and the generation of regulatory CD4+ T cells that are thought to maintain peripheral self-tolerance in vivo.

摘要

CD40已成为免疫系统中B细胞、单核细胞和树突状细胞(DC)功能的关键信号通路,并在非造血细胞的炎症通路中发挥主要作用。CD40由单核细胞和DC表达,当DC响应微生物刺激从外周迁移至引流淋巴结(DLN)时,其表达上调。MHC限制的活化CD4 + T细胞发出的CD154信号可诱导DC分化,表现为MHC、共刺激分子和黏附分子的表面表达增加。因此,CD40在适应性免疫反应中作为有效激活T细胞的共刺激分子表达的触发因素发挥作用。DC的CD40连接还能够诱导高水平的细胞因子IL - 12,使CD4 + T细胞向辅助性T细胞1(Th1)型极化,增强CD8 + T细胞的增殖,并激活NK细胞。CD40在耐受与免疫的抉择以及调节性CD4 + T细胞的产生中可能也起重要作用,这些调节性CD4 + T细胞被认为可在体内维持外周自身耐受。

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