Baugh J A, Donnelly S C
Department of Medicine and Therapeutics, The Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Belfield, Dublin 4, Ireland.
J Endocrinol. 2003 Oct;179(1):15-23. doi: 10.1677/joe.0.1790015.
The diverse actions of macrophage migration inhibitory factor (MIF) within the immuno-neuroendocrine system are yet to be fully understood, but it is clear that MIF plays a pivotal role in the regulation of both the innate and adaptive immune response. An emerging body of data presently indicates that MIF's position within the cytokine cascade is to act in concert with glucocorticoids to control the 'set point' and magnitude of the immune and inflammatory response. In this article we will review the actions of MIF within the immune system and discuss the overlapping and contrasting aspects of MIF and glucocorticoid biology. In particular we will focus on the role of MIF within the immuno-neuroendocrine interface and suggest molecular mechanisms by which MIF may counter-regulate glucocorticoid function. Finally we will discuss emerging evidence that functional MIF gene-promoter polymorphisms render one susceptible to elevated MIF expression, and the development of an exaggerated immune/inflammatory response that potentiates the progression to chronic inflammatory disease.
巨噬细胞移动抑制因子(MIF)在免疫神经内分泌系统中的多种作用尚未完全明确,但很明显,MIF在先天性和适应性免疫反应的调节中起着关键作用。目前,越来越多的数据表明,MIF在细胞因子级联反应中的作用是与糖皮质激素协同作用,以控制免疫和炎症反应的“设定点”和强度。在本文中,我们将综述MIF在免疫系统中的作用,并讨论MIF与糖皮质激素生物学的重叠和对比方面。特别是,我们将重点关注MIF在免疫神经内分泌界面中的作用,并提出MIF可能对抗糖皮质激素功能的分子机制。最后,我们将讨论新出现的证据,即功能性MIF基因启动子多态性使个体易患MIF表达升高以及过度免疫/炎症反应的发生,而这种反应会加剧慢性炎症疾病的进展。