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Review
. 2021 Jun;102(3):142-157.
doi: 10.1016/j.jdermsci.2021.04.007. Epub 2021 May 2.

Atopic dermatitis: Role of the skin barrier, environment, microbiome, and therapeutic agents

Affiliations
Review

Atopic dermatitis: Role of the skin barrier, environment, microbiome, and therapeutic agents

Thomas Luger et al. J Dermatol Sci. 2021 Jun.

Abstract

Atopic dermatitis (AD) is a chronic, inflammatory skin disorder characterized by eczematous and pruritic skin lesions. In recent decades, the prevalence of AD has increased worldwide, most notably in developing countries. The enormous progress in our understanding of the complex composition and functions of the epidermal barrier allows for a deeper appreciation of the active role that the skin barrier plays in the initiation and maintenance of skin inflammation. The epidermis forms a physical, chemical, immunological, neuro-sensory, and microbial barrier between the internal and external environment. Not only lesional, but also non-lesional areas of AD skin display many morphological, biochemical and functional differences compared with healthy skin. Supporting this notion, genetic defects affecting structural proteins of the skin barrier, including filaggrin, contribute to an increased risk of AD. There is evidence to suggest that natural environmental allergens and man-made pollutants are associated with an increased likelihood of developing AD. A compromised epidermal barrier predisposes the skin to increased permeability of these compounds. Numerous topical and systemic therapies for AD are currently available or in development; while anti-inflammatory therapy is central to the treatment of AD, some existing and novel therapies also appear to exert beneficial effects on skin barrier function. Further research on the skin barrier, particularly addressing epidermal differentiation and inflammation, lipid metabolism, and the role of bacterial communities for skin barrier function, will likely expand our understanding of the complex etiology of AD and lead to identification of novel targets and the development of new therapies.

Keywords: Atopic dermatitis; Filaggrin; Inflammation; Microbiota; Skin barrier; Treatment.

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Conflict of interest statement

Declaration of Competing Interest T. Luger has participated as Principal Investigator in clinical trials, advisory boards and has given lectures, sponsored by Novartis, Lilly, La Roche Posay, Pfizer, Janssen, and Sanofi. He has received consultancy/speaker honoraria from Novartis, Abbvie, Galderma, La Roche Posay, Meda Pharma S.p.A. (a Viatris company), Janssen, and Sanofi, and has acted as a scientific Advisory Board member for Abbvie, Celgene, La Roche Posay, Janssen, Pfizer, Menlo, Meda Pharma S.p.A. (a Viatris company), Galderma, Symrise, and Lilly. He has received research grants from: Celgene, Janssen-Cilag, Leo, Meda Pharma S.p.A. (a Viatris company), and Pfizer. M. Amagai has received research grants from Maruho, Kose, and JSR. B. Dreno has no relevant conflict of interest to declare. M.A. Dagnelie has no relevant conflict of interest to declare. W. Liao has received research grant funding from Abbvie, Amgen, Janssen, Leo Pharma, Novartis, Pfizer, Regeneron, Sanofi, and TRex Bio. K. Kabashima has received consulting fees or advisory board honoraria from Japan tobacco Inc., Chugai Pharmaceutical, Maruho, and Pola Pharma, and has received research grants from LEO Pharma, Japan tobacco Inc., P&G Japan, Eli Lilly Japan, Tanabe Mitsubishi, Ono Pharmaceutical, Kyowa Hakko Kirin, Pola Pharma, AbbVie, Sanofi, and Kyorin Pharmaceutical. T. Schikowski: No conflict of interest to declare. E. Proksch has received funding from Bayer Consumer Care and Dr. August Wolff, Arzneimittel. P.M. Elias: No conflict of interest to declare. M. Simon has received funding from Pierre Fabre Dermo-Cosmétique, L’Oréal and BASF Beauty Care Solutions France. He is co-author of patent #WO2012140095A1. E. Simpson reports grants and personal fees from AbbVie, Eli Lilly, Incyte, Leo Pharmaceutical, Pfizer and Regeneron. He reports grants and fees from Novartis. He reports grants from Kyowa Hakko Kirin and Merck and he reports personal fees from Dermira, Forte Bio Rx, Menlo Therapeutics, Ortho Dermatologics and Sanofi-Genzyme. E.Grinich: No conflict of interest to declare. M. Schmuth has received research grants from ExpanScience, has participated as Principal Investigator in trials sponsored by Roche, Amgen, MSD, GSK, Eli Lilly, Abbvie, Scenesse, Orfagen and has received travel funds from Nogra Pharma. He has not accepted any honoraria from industry for advisory boards or speakers’ bureau participation and does not own pharma stocks, equity or patent licenses.

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