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Immune Pathways in Atopic Dermatitis, and Definition of Biomarkers through Broad and Targeted Therapeutics

期刊

JOURNAL OF CLINICAL MEDICINE
卷 4, 期 5, 页码 858-873

出版社

MDPI AG
DOI: 10.3390/jcm4050858

关键词

atopic dermatitis; eczema; biomarker; translational revolution; T-cells; intrinsic; extrinsic; immune phenotype

资金

  1. Geoffrey Dowling Fellowship, a grant from the British Association of Dermatologists (United Kingdom)

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Atopic dermatitis (AD) is the most common inflammatory skin disease. Recent research findings have provided an insight into the complex pathogenic mechanisms involved in this disease. Despite a rising prevalence, effective and safe therapeutics for patients with moderate-to-severe AD are still lacking. Biomarkers of lesional, nonlesional skin, and blood have been developed for baseline as well as after treatment with broad and specific treatments (i.e., cyclosporine A and dupilumab). These biomarkers will help with the development of novel targeted therapeutics and assessment of disease reversal, with the promise of a more personalized treatment approach. Since AD involves more than one subtype (i.e., intrinsic/extrinsic, pediatric/adult, etc.), these molecular fingerprints needs to be validated in all subpopulations with AD.

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