O'Sullivan Brendan, Thomas Ranjeny
Centre for Immunology and Cancer Research, Princess Alexandra Hospital, University of Queensland, Brisbane, Queensland 4102, Australia.
Crit Rev Immunol. 2003;23(1-2):83-107. doi: 10.1615/critrevimmunol.v23.i12.50.
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.
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。