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治疗特应性皮炎的新型治疗靶点

Novel Therapeutic Targets for the Treatment of Atopic Dermatitis.

作者信息

Tsuji Gaku, Yamamura Kazuhiko, Kawamura Koji, Kido-Nakahara Makiko, Ito Takamichi, Nakahara Takeshi

机构信息

Research and Clinical Center for Yusho and Dioxin, Kyushu University Hospital, Fukuoka 812-8582, Japan.

Department of Dermatology, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan.

出版信息

Biomedicines. 2023 Apr 27;11(5):1303. doi: 10.3390/biomedicines11051303.

Abstract

Atopic dermatitis (AD) is a chronic inflammatory skin disease that significantly impacts quality of life. The pathogenesis of AD is a complex combination of skin barrier dysfunction, type II immune response, and pruritus. Progress in the understanding of the immunological mechanisms of AD has led to the recognition of multiple novel therapeutic targets. For systemic therapy, new biologic agents that target IL-13, IL-22, IL-33, the IL-23/IL-17 axis, and OX40-OX40L are being developed. Binding of type II cytokines to their receptors activates Janus kinase (JAK) and its downstream signal, namely signal transduction and activator of transcription (STAT). JAK inhibitors block the activation of the JAK-STAT pathway, thereby blocking the signaling pathways mediated by type II cytokines. In addition to oral JAK inhibitors, histamine H4 receptor antagonists are under investigation as small-molecule compounds. For topical therapy, JAK inhibitors, aryl hydrocarbon receptor modulators, and phosphodiesterase-4 inhibitors are being approved. Microbiome modulation is also being examined for the treatment of AD. This review outlines current and future directions for novel therapies of AD that are currently being investigated in clinical trials, focusing on their mechanisms of action and efficacy. This supports the accumulation of data on advanced treatments for AD in the new era of precision medicine.

摘要

特应性皮炎(AD)是一种严重影响生活质量的慢性炎症性皮肤病。AD的发病机制是皮肤屏障功能障碍、II型免疫反应和瘙痒的复杂组合。对AD免疫机制认识的进展已导致识别出多个新的治疗靶点。对于全身治疗,正在研发靶向IL-13、IL-22、IL-33、IL-23/IL-17轴和OX40-OX40L的新型生物制剂。II型细胞因子与其受体的结合激活Janus激酶(JAK)及其下游信号,即信号转导和转录激活因子(STAT)。JAK抑制剂阻断JAK-STAT途径的激活,从而阻断由II型细胞因子介导的信号通路。除口服JAK抑制剂外,组胺H4受体拮抗剂作为小分子化合物正在研究中。对于局部治疗,JAK抑制剂、芳烃受体调节剂和磷酸二酯酶-4抑制剂正在获批。微生物群调节也正在研究用于AD的治疗。本综述概述了目前正在临床试验中研究的AD新型疗法的当前和未来方向,重点关注其作用机制和疗效。这支持了在精准医学新时代积累AD先进治疗的数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fc6/10215969/64e598e4c03c/biomedicines-11-01303-g001.jpg

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