Tapinarof Validates the Aryl Hydrocarbon Receptor as a Therapeutic Target: A Clinical Review.

Aryl hydrocarbon receptor atopic dermatitis inflammatory disorders psoriasis tapinarof cream

Journal

The Journal of allergy and clinical immunology
ISSN: 1097-6825
Titre abrégé: J Allergy Clin Immunol
Pays: United States
ID NLM: 1275002

Informations de publication

Date de publication:
26 Dec 2023
Historique:
received: 10 08 2023
revised: 09 11 2023
accepted: 08 12 2023
medline: 29 12 2023
pubmed: 29 12 2023
entrez: 28 12 2023
Statut: aheadofprint

Résumé

The aryl hydrocarbon receptor (AhR) is a ligand-dependent transcription factor that has wide-ranging roles, including regulation of inflammation and homeostasis. AhR is not a cell-surface receptor but exists in a cytoplasmic complex that responds to a wide variety of structurally dissimilar endogenous, microbial, and environmental ligands. The ubiquitous expression of AhR, its ability to be activated by a wide range of ligands, and its capacity to act as a master regulator for gene expression and homeostasis make it a promising new therapeutic target. Clinical trials of tapinarof cream have now validated AhR agonism as a therapeutic approach that can deliver significant efficacy for treating inflammatory skin diseases, including psoriasis and atopic dermatitis (AD). Tapinarof cream 1%, is a first-in-class, non-steroidal, topical, AhR agonist with a pharmacokinetic profile that results in localized exposure at sites of disease, avoiding systemic safety concerns, drug interactions, or off-target effects. Psoriasis and AD both involve epidermal inflammation, cellular immune responses, dysregulation of skin barrier protein expression and oxidative stress. Based on the clinical effectiveness of tapinarof cream for treating inflammatory skin diseases, we review how targeting AhR may offer a significant opportunity in other conditions that share key aspects of pathogenesis, including asthma, inflammatory bowel disease, eosinophilic esophagitis, ophthalmic, and nervous system diseases.

Identifiants

pubmed: 38154665
pii: S0091-6749(23)02547-2
doi: 10.1016/j.jaci.2023.12.013
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023. Published by Elsevier Inc.

Auteurs

Jonathan I Silverberg (JI)

Department of Dermatology, George Washington University, Washington, DC, USA. Electronic address: kimberly.mchale@dermavant.com.

Mark Boguniewicz (M)

Division of Allergy-Immunology, Department of Pediatrics, National Jewish Health and University of Colorado School of Medicine, Denver, CO, USA.

Francisco J Quintana (FJ)

Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Rachael A Clark (RA)

Brigham and Women's Hospital, Boston, MA, USA.

Lara Gross (L)

Dallas Allergy and Asthma Center, Dallas, TX, USA; Allergy and Immunology Division, Baylor University Medical Center, Dallas, TX, USA.

Ikuo Hirano (I)

Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

Anna M Tallman (AM)

Dermavant Sciences, Inc., Morrisville, NC, USA.

Philip M Brown (PM)

Dermavant Sciences, Inc., Morrisville, NC, USA.

Doral Fredericks (D)

Dermavant Sciences, Inc., Morrisville, NC, USA.

David S Rubenstein (DS)

Dermavant Sciences, Inc., Morrisville, NC, USA.

Kimberly A McHale (KA)

Dermavant Sciences, Inc., Morrisville, NC, USA. Electronic address: kimberly.mchale@dermavant.com.

Classifications MeSH