Unité de Différenciation Epithéliale et Autoimmunité Rhumatoïde, UMR 1056, INSERM, Université de Toulouse, Toulouse, France.
Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
Nat Immunol. 2019 Nov;20(11):1435-1443. doi: 10.1038/s41590-019-0493-z. Epub 2019 Oct 7.
Allergic skin diseases, such as atopic dermatitis, are clinically characterized by severe itching and type 2 immunity-associated hypersensitivity to widely distributed allergens, including those derived from house dust mites (HDMs). Here we found that HDMs with cysteine protease activity directly activated peptidergic nociceptors, which are neuropeptide-producing nociceptive sensory neurons that express the ion channel TRPV1 and Tac1, the gene encoding the precursor for the neuropeptide substance P. Intravital imaging and genetic approaches indicated that HDM-activated nociceptors drive the development of allergic skin inflammation by inducing the degranulation of mast cells contiguous to such nociceptors, through the release of substance P and the activation of the cationic molecule receptor MRGPRB2 on mast cells. These data indicate that, after exposure to HDM allergens, activation of TRPV1Tac1 nociceptor-MRGPRB2 mast cell sensory clusters represents a key early event in the development of allergic skin reactions.
变应性皮肤疾病(如特应性皮炎)的临床特征为剧烈瘙痒和 2 型免疫相关的过敏反应,其广泛的过敏原包括屋尘螨(HDM)来源的过敏原。在这里,我们发现具有半胱氨酸蛋白酶活性的 HDM 可直接激活肽能伤害感受器,即表达离子通道 TRPV1 和 Tac1 的产生神经肽的伤害感受感觉神经元,Tac1 基因编码神经肽物质 P 的前体。活体成像和遗传方法表明,HDM 激活的伤害感受器通过释放物质 P 和激活肥大细胞上的阳离子分子受体 MRGPRB2,诱导与伤害感受器相邻的肥大细胞脱颗粒,从而驱动过敏性皮肤炎症的发展。这些数据表明,在接触 HDM 过敏原后,TRPV1Tac1 伤害感受器-MRGPRB2 肥大细胞感觉簇的激活代表过敏性皮肤反应发展的关键早期事件。