Therapeutic Implications of a Barrier-based Pathogenesis of Atopic Dermatitis
- PMID: 20711259
- PMCID: PMC2917676
- DOI: 10.5021/ad.2010.22.3.245
Therapeutic Implications of a Barrier-based Pathogenesis of Atopic Dermatitis
Abstract
In this review, I first provide relevant background information about normal epidermal barrier structure and function. I then update recent information about how inherited defects in either filaggrin and/or in the serine protease inhibitor, lymphoepithelial Kazal-type inhibitor 1, converge to stimulate the development of atopic dermatitis (AD). Next I explain the multiple mechanisms whereby a primary barrier abnormality in AD can lead to inflammation. Furthermore, I explore how certain acquired stressors, such as a reduced external humidity, high pH soaps/surfactants, psychological stress, as well as secondary Staphylococcus aureus infections initiate or further aggravate AD. Finally, and most importantly, I compare various therapeutic paradigms for AD, highlighting the risks and benefits of glucocorticoids and immunomodulators vs. corrective, lipid replacement therapy.
Keywords: Antimicrobial peptides; Atopic dermatitis; Barrier function; Barrier repair.
Conflict of interest statement
Dr. Elias is a co-inventor of the optimal ratio, ceramide-dominant, triple-lipid therapy for atopic dermatitis. He also is a consultant for Promius Pharma, LLC and Pediapharm, Inc., which market EpiCeram® in the United States and Canada, respectively.
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