Astier Anne L
Institute of Immunology and Infection Research, University of Edinburgh, Edinburgh, UK.
Immunology. 2008 Jun;124(2):149-54. doi: 10.1111/j.1365-2567.2008.02821.x. Epub 2008 Apr 2.
CD46 is a complement regulatory molecule expressed on every cell type, except for erythrocytes. While initially described as a regulator of complement activity, it later became a 'magnet for pathogens', binding to several viruses and bacteria. More recently, an alternative role for such complement molecules has emerged: they do regulate T-cell immunity, affecting T-cell proliferation and differentiation. In particular, CD46 stimulation induces Tr1 cells, regulatory T cells characterized by massive production of interleukin-10 (IL-10), a potent anti-inflammatory cytokine. Hence, CD46 is likely to control inflammation. Indeed, data from CD46 transgenic mice highlight a role for CD46 in inflammation, with antagonist roles depending on the cytoplasmic tail being expressed. Furthermore, recent data have shown that CD46 is defective in multiple sclerosis, IL-10 production being severely impaired in these patients. This lack of IL-10 production probably participates in the inflammation observed in patients with multiple sclerosis. This review will summarize the data on CD46 and T cells, and how CD46 is likely involved in multiple sclerosis.
CD46是一种在除红细胞外的所有细胞类型上均有表达的补体调节分子。虽然最初被描述为补体活性的调节剂,但后来它成为了“病原体的磁石”,可与多种病毒和细菌结合。最近,这类补体分子又出现了另一种作用:它们确实调节T细胞免疫,影响T细胞的增殖和分化。特别是,CD46刺激可诱导Tr1细胞,即一种以大量产生白细胞介素-10(IL-10,一种强效抗炎细胞因子)为特征的调节性T细胞。因此,CD46可能控制炎症。事实上,来自CD46转基因小鼠的数据突出了CD46在炎症中的作用,其拮抗作用取决于所表达的细胞质尾巴。此外,最近的数据表明,CD46在多发性硬化症中存在缺陷,这些患者的IL-10产生严重受损。IL-10产生的缺乏可能参与了多发性硬化症患者中观察到的炎症反应。本综述将总结关于CD46与T细胞的相关数据,以及CD46可能如何参与多发性硬化症。