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2019 - 2020年特应性皮炎研究进展:基于皮肤屏障、种族、抗原特性、细胞因子谱、微生物群以及免疫细胞相互作用的内型分类

Advances in atopic dermatitis in 2019-2020: Endotypes from skin barrier, ethnicity, properties of antigen, cytokine profiles, microbiome, and engagement of immune cells.

作者信息

Nomura Takashi, Kabashima Kenji

机构信息

Department of Dermatology, Faculty of Medicine, Kyoto University, Kyoto, Japan.

Department of Dermatology, Faculty of Medicine, Kyoto University, Kyoto, Japan.

出版信息

J Allergy Clin Immunol. 2021 Dec;148(6):1451-1462. doi: 10.1016/j.jaci.2021.10.022. Epub 2021 Oct 29.

DOI:10.1016/j.jaci.2021.10.022
PMID:34756922
Abstract

Key research advances in atopic dermatitis (AD) suggest the complexity of its endotypes. A comprehensive serum biomarker panel revealed at least 4 types of AD. Some represent classic T2-dominant AD with filaggrin mutations commonly reported in Europeans, a simultaneously activated multipolar axis of cytokines often reported in Asian individuals, and an intrinsic type characterized by T2 inferiority. Innate lymphoid cells, including natural killer cells, natural killer T cells, and fibroblasts, play a role in AD development and heterogeneity. Here, we discuss the endotypes of AD from the perspective of antigen types (hapten vs protein antigens), barrier function, and a novel set of immune cells. Endotypic stratification of AD may lead to the development of customized therapeutic strategies in the future.

摘要

特应性皮炎(AD)的关键研究进展表明其内在类型具有复杂性。一个综合的血清生物标志物组揭示了至少4种AD类型。一些代表经典的T2主导型AD,其具有在欧洲人中常见的丝聚蛋白突变;一种在亚洲个体中常报道的同时激活的多极细胞因子轴;以及一种以T2劣势为特征的内在类型。固有淋巴细胞,包括自然杀伤细胞、自然杀伤T细胞和成纤维细胞,在AD的发展和异质性中发挥作用。在此,我们从抗原类型(半抗原与蛋白质抗原)、屏障功能和一组新的免疫细胞的角度讨论AD的内在类型。AD的内型分层可能会在未来导致定制化治疗策略的发展。

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