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深入探讨:用于改善过敏性接触性皮炎管理的生物标志物和神经生物标志物

Scratching the surface: biomarkers and neurobiomarkers for improved allergic contact dermatitis management.

作者信息

Sasaki Akimi, Sargen Manuel, Maskey Anish R, Li Xiu-Min

机构信息

Department of Pathology, Microbiology, & Immunology, New York Medical College, Valhalla, NY, United States.

Department of Otolaryngology, New York Medical College, Valhalla, NY, United States.

出版信息

Front Allergy. 2025 Mar 13;6:1564528. doi: 10.3389/falgy.2025.1564528. eCollection 2025.

Abstract

Allergic contact dermatitis (ACD), also known as allergic eczema, is a common inflammatory skin disorder that affects millions of Americans and imposes significant physical, psychological, and economic burdens. Differentiating ACD from other forms of dermatitis remains a challenge, with patch testing as the gold standard. Despite its utility, patch testing can lack diagnostic accuracy, highlighting the importance of molecular biomarkers to refine diagnosis and treatment. Advances in transcriptomics and machine-learning have enabled the identification of biomarkers involved in ACD, such as loricrin (LOR), ADAM8, CD47, BATF, SELE, and IL-37. Moreover, biomarkers such as LOR, NMF, and TEWL, may have prognostic value in evaluating therapeutic response. Emerging neurological biomarkers (neurobiomarkers), including IL-31 and TRPV1, target pathways involved in the pruritic and inflammatory responses, offering novel therapeutic targets as well. This mini review summarizes current ACD treatments, biomarkers for targeted therapies, and emphasizes the role of neurobiomarkers in ACD treatment. Additional research on the validity of the therapeutic potential of these biomarkers is necessary to improve ACD treatment and outcomes.

摘要

过敏性接触性皮炎(ACD),也称为过敏性湿疹,是一种常见的炎症性皮肤病,影响着数百万美国人,并带来了巨大的身体、心理和经济负担。将ACD与其他形式的皮炎区分开来仍然是一项挑战,斑贴试验是金标准。尽管其有用性,但斑贴试验可能缺乏诊断准确性,这凸显了分子生物标志物对完善诊断和治疗的重要性。转录组学和机器学习的进展使得能够识别参与ACD的生物标志物,如兜甲蛋白(LOR)、ADAM8、CD47、BATF、SELE和白细胞介素-37(IL-37)。此外,诸如LOR、天然保湿因子(NMF)和经皮水分流失(TEWL)等生物标志物在评估治疗反应方面可能具有预后价值。新兴的神经生物标志物,包括白细胞介素-31(IL-31)和瞬时受体电位香草酸亚型1(TRPV1),靶向参与瘙痒和炎症反应的途径,也提供了新的治疗靶点。本综述总结了当前ACD的治疗方法、靶向治疗的生物标志物,并强调了神经生物标志物在ACD治疗中的作用。有必要对这些生物标志物治疗潜力的有效性进行更多研究,以改善ACD的治疗和预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45bd/11966390/a76bf3efe391/falgy-06-1564528-g001.jpg

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