Mackey M F, Barth R J, Noelle R J
Department of Microbiology, Dartmouth Medical School and the Norris Cotton Cancer Center, Lebanon, New Hampshire 03756, USA.
J Leukoc Biol. 1998 Apr;63(4):418-28. doi: 10.1002/jlb.63.4.418.
This review focuses on the emerging body of literature suggesting a critical role for CD40/CD154 interactions in antigen-presenting cell (APC) activation, CD4+ and CD8+ T cell priming, and effector T cell maturation. In this context effective antigen presentation involves not only T cell expansion and long-term survival but also the ability of the APC to guide the T cell response toward the Th1 (interferon-gamma producing) or the Th2 (interleukin-4 producing) phenotype. We suggest a model to explain why CD40/CD154 interactions are critical for some helper and cytotoxic T cell responses, whereas others occur independently of this receptor/ligand pair. In addition, we will discuss the potential role for CD40/CD154 interactions in effector T cell maturation and cytokine production.
本综述聚焦于新兴的文献体系,这些文献表明CD40/CD154相互作用在抗原呈递细胞(APC)激活、CD4⁺和CD8⁺T细胞致敏以及效应T细胞成熟过程中发挥关键作用。在这种情况下,有效的抗原呈递不仅涉及T细胞扩增和长期存活,还涉及APC引导T细胞反应向Th1(产生干扰素-γ)或Th2(产生白细胞介素-4)表型发展的能力。我们提出一个模型来解释为什么CD40/CD154相互作用对某些辅助性和细胞毒性T细胞反应至关重要,而其他反应则独立于该受体/配体对发生。此外,我们将讨论CD40/CD154相互作用在效应T细胞成熟和细胞因子产生中的潜在作用。