TY - JOUR
T1 - Biomarkers in atopic dermatitis—a review on behalf of the International Eczema Council
AU - Renert-Yuval, Yael
AU - Thyssen, Jacob P.
AU - Bissonnette, Robert
AU - Bieber, Thomas
AU - Kabashima, Kenji
AU - Hijnen, Dirk Jan
AU - Guttman-Yassky, Emma
N1 - Funding Information:
Y.R.-Y. was supported in part by the National Center for Advancing Translational Sciences , National Institutes of Health , through Rockefeller University (grant no. UL1TR001866 ).
Funding Information:
Y.R.-Y. was supported in part by the National Center for Advancing Translational Sciences, National Institutes of Health, through Rockefeller University (grant no. UL1TR001866). Disclosure of potential conflict of interest: E. Guttman-Yassky is an employee of Mount Sinai and has received research funds (grants paid to the institution) from AbbVie, Celgene, Eli Lilly, Janssen, Medimmune/Astra Zeneca, Novartis, Pfizer, Regeneron, Vitae, Glenmark, Galderma, Asana, Innovaderm, Dermira, and UCB and is also a consultant for Sanofi Aventis, Regeneron, Stiefel/GlaxoSmithKline, MedImmune, Celgene, Anacor, AnaptysBio, Dermira, Galderma, Glenmark, Novartis, Pfizer, Vitae, LEO Pharma, AbbVie, Eli Lilly, Kyowa, Mitsubishi Tanabe, Asana Biosciences, and Promius. J. P. Thyssen has been an investigator/speaker or advisor for Sanofi-Genzyme, Regeneron, Eli Lilly & Co, Pfizer, AbbVie, and LEO Pharma. The rest of the authors declare that they have no relevant conflicts of interest.
Publisher Copyright:
© 2021 The Authors
PY - 2021/4
Y1 - 2021/4
N2 - Atopic dermatitis (AD) is a common yet complex skin disease, posing a therapeutic challenge with increasingly recognized different phenotypes among variable patient populations. Because therapeutic response may vary on the basis of heterogeneous clinical and molecular phenotypes, a shift toward precision medicine approaches may improve AD management. Herein, we will consider biomarkers as potential instruments in the toolbox of precision medicine in AD and will review the process of biomarker development and validation, the opinion of AD experts on the use of biomarkers, types of biomarkers, encompassing biomarkers that may improve AD diagnosis, biomarkers reflecting disease severity, and those potentially predicting AD development, concomitant atopic diseases, or therapeutic response, and current practice of biomarkers in AD. We found that chemokine C-C motif ligand 17/thymus and activation-regulated chemokine, a chemoattractant of TH2 cells, has currently the greatest evidence for robust correlation with AD clinical severity, at both baseline and during therapy, by using the recommendations, assessment, development, and evaluation approach. Although the potential of biomarkers in AD is yet to be fully elucidated, due to the complexity of the disease, a comprehensive approach taking into account both clinical and reliable, AD-specific biomarker evaluations would further facilitate AD research and improve patient management.
AB - Atopic dermatitis (AD) is a common yet complex skin disease, posing a therapeutic challenge with increasingly recognized different phenotypes among variable patient populations. Because therapeutic response may vary on the basis of heterogeneous clinical and molecular phenotypes, a shift toward precision medicine approaches may improve AD management. Herein, we will consider biomarkers as potential instruments in the toolbox of precision medicine in AD and will review the process of biomarker development and validation, the opinion of AD experts on the use of biomarkers, types of biomarkers, encompassing biomarkers that may improve AD diagnosis, biomarkers reflecting disease severity, and those potentially predicting AD development, concomitant atopic diseases, or therapeutic response, and current practice of biomarkers in AD. We found that chemokine C-C motif ligand 17/thymus and activation-regulated chemokine, a chemoattractant of TH2 cells, has currently the greatest evidence for robust correlation with AD clinical severity, at both baseline and during therapy, by using the recommendations, assessment, development, and evaluation approach. Although the potential of biomarkers in AD is yet to be fully elucidated, due to the complexity of the disease, a comprehensive approach taking into account both clinical and reliable, AD-specific biomarker evaluations would further facilitate AD research and improve patient management.
KW - Atopic dermatitis
KW - CCL17/TARC
KW - CCL18/pulmonary and activation-regulated chemokine
KW - CCL22/MDC
KW - CCL26/eotaxin-3
KW - CCL27/CTACK
KW - IL-13
KW - IL-22
KW - IgE
KW - International Eczema Council
KW - biomarker
KW - eosinophils
UR - http://www.scopus.com/inward/record.url?scp=85101681103&partnerID=8YFLogxK
U2 - 10.1016/j.jaci.2021.01.013
DO - 10.1016/j.jaci.2021.01.013
M3 - Article
C2 - 33516871
AN - SCOPUS:85101681103
SN - 0091-6749
VL - 147
SP - 1174-1190.e1
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 4
ER -