Please use this identifier to cite or link to this item: https://doi.org/10.1002/biot.201900322
Title: Biotherapeutic Approaches in Atopic Dermatitis
Authors: Tham E.H. 
Koh E. 
Common J.E.A.
Hwang I.Y. 
Keywords: atopic dermatitis
biotherapeutics
medical biotechnology
microbiome
synthetic biology
Issue Date: 16-Mar-2020
Publisher: Wiley-VCH Verlag
Citation: Tham E.H., Koh E., Common J.E.A., Hwang I.Y. (2020-03-16). Biotherapeutic Approaches in Atopic Dermatitis. Biotechnology Journal 15 (10). ScholarBank@NUS Repository. https://doi.org/10.1002/biot.201900322
Abstract: The skin microbiome plays a central role in inflammatory skin disorders such as atopic dermatitis (AD). In AD patients, an imbalance between pathogenic Staphylococcus aureus (S. aureus) and resident skin symbionts creates a state of dysbiosis which induces immune dysregulation and impairs skin barrier function. There are now exciting new prospects for microbiome-based interventions for AD prevention. In the hopes of achieving sustained control and management of disease in AD patients, current emerging biotherapeutic strategies aim to harness the skin microbiome associated with health by restoring a more diverse symbiotic skin microbiome, while selectively removing pathogenic S. aureus. Examples of such strategies are demonstrated in skin microbiome transplants, phage-derived anti-S. aureus endolysins, monoclonal antibodies, and quorum sensing (QS) inhibitors. However, further understanding of the skin microbiome and its role in AD pathogenesis is still needed to understand how these biotherapeutics alter the dynamics of the microbiome community; to optimize patient selection, drug delivery, and treatment duration; overcome rapid recolonization upon treatment cessation; and improve efficacy to allow these therapeutic options to eventually reach routine clinical practice. © 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Source Title: Biotechnology Journal
URI: https://scholarbank.nus.edu.sg/handle/10635/184722
ISSN: 18606768
DOI: 10.1002/biot.201900322
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