Sibilano Riccardo, Pucillo Carlo E, Gri Giorgia
Department of Pathology, CCSR 3255, 269 Campus Drive, Stanford, CA 94305, USA.
Department of Medical and Biological Sciences, University of Udine, P.le M. Kolbe 4, 33100 Udine, Italy.
Mol Immunol. 2015 Jan;63(1):69-73. doi: 10.1016/j.molimm.2014.02.015. Epub 2014 Mar 18.
The activation of the transcription factor aryl hydrocarbon receptor (AhR) is modulated by a wide variety of xenobiotics and ligands deriving from products of metabolism. The study of the contribution of AhR to allergic diseases has gained much interest in recent years. Here we discuss the role that environmental factors and metabolic products, particularly acting on AhR-expressing mast cells (MCs), could have in the development of local allergic/atopic response. Thus, this review will cover: a brief overview of the AhR mechanism of action in the immune system; a description of different AhR ligands and their effects to IgE-mediated MC activation in the allergic response, with particular attention to the role of IL-17; a discussion about the potential involvement of AhR in immune tolerance; and a conclusion on human diseases in which direct AhR activation of MC might have a major impact.
转录因子芳烃受体(AhR)的激活受多种外源性物质和代谢产物衍生配体的调节。近年来,AhR对过敏性疾病影响的研究备受关注。在此,我们讨论环境因素和代谢产物,特别是作用于表达AhR的肥大细胞(MCs),在局部过敏/特应性反应发展中可能发挥的作用。因此,本综述将涵盖:AhR在免疫系统中作用机制的简要概述;不同AhR配体及其在过敏反应中对IgE介导的MC激活作用的描述,尤其关注IL-17的作用;关于AhR在免疫耐受中潜在作用的讨论;以及关于MC的直接AhR激活可能产生重大影响的人类疾病的结论。