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首页|期刊导航|中国临床药理学与治疗学|靶向OX40和OX40L单克隆抗体治疗特应性皮炎的研究进展

靶向OX40和OX40L单克隆抗体治疗特应性皮炎的研究进展

黄帆 丁紫嫣 周茜 胡丁元 聂小燕 丁锐 方翼

中国临床药理学与治疗学2026,Vol.31Issue(5):649-657,9.
中国临床药理学与治疗学2026,Vol.31Issue(5):649-657,9.DOI:10.12092/j.issn.1009-2501.2026.05.009

靶向OX40和OX40L单克隆抗体治疗特应性皮炎的研究进展

Research advances in targeting OX40/OX40L monoclonal antibodies for the treatment of atopic dermatitis

黄帆 1丁紫嫣 1周茜 2胡丁元 1聂小燕 3丁锐 4方翼4

作者信息

  • 1. 北京大学人民医院 临床试验机构,北京 100044||北京大学医学部药学院 药事管理与临床药学系,北京 100191
  • 2. 北京大学人民医院 临床试验机构,北京 100044||徐州医科大学药学院,徐州 221004,江苏
  • 3. 北京大学医学部药学院 药事管理与临床药学系,北京 100191
  • 4. 北京大学人民医院 临床试验机构,北京 100044
  • 折叠

摘要

Abstract

Atopic dermatitis(AD)is a chronic in-flammatory skin disease characterized by a T helper cells(th)2-dominant immune response coupled with multifactorial immune dysregulation involving Th1,Th17,and Th22 pathways.Current therapeutic approaches confront significant clinical challenges,including suboptimal treatment responses in sub-sets of patients,safety risks associated with pro-longed pharmacotherapy,and compromised pa-tient adherence.Emerging evidence demonstrates that the OX40-OX40L signaling pathway orches-trates sustained immunoinflammatory responses through its regulatory role in antigen-presenting cell-T cell interactions.Monoclonal antibodies tar-geting this pathway effectively inhibit pathological immune activation,demonstrating dual clinical ben-efits of ameliorating cutaneous lesions and main-taining durable remission after treatment cessation.This review systematically elucidates the mechanis-tic involvement of the OX40-OX40L axis in AD pathogenesis and provides a comprehensive analy-sis of clinical trial advancements in anti-OX40/OX40L monoclonal antibody therapeutics.

关键词

抗 OX40单克隆抗体/抗 OX40L 单克隆抗体/特应性皮炎/靶向治疗

Key words

anti-OX40 monoclonal antibody/anti-OX40L monoclonal antibody/atopic dermatitis/tar-geted therapy

分类

医药卫生

引用本文复制引用

黄帆,丁紫嫣,周茜,胡丁元,聂小燕,丁锐,方翼..靶向OX40和OX40L单克隆抗体治疗特应性皮炎的研究进展[J].中国临床药理学与治疗学,2026,31(5):649-657,9.

基金项目

北京市通州区科技计划项目(KJ2024CX058) (KJ2024CX058)

河北省创新能力提升计划项目(235A2601D) (235A2601D)

北京国际医药临床研发平台(2107000043) (2107000043)

中国临床药理学与治疗学

1009-2501

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