TY - JOUR
T1 - Manipulating Microbiota to Treat Atopic Dermatitis
T2 - Functions and Therapies
AU - Alam, Md Jahangir
AU - Xie, Liang
AU - Yap, Yu-Anne
AU - Marques, Francine Z.
AU - Robert, Remy
N1 - Funding Information:
This research received no external funding. F.Z.M. is supported by a National Heart Foundation Future Leader Fellowship (105663) and a Senior Medical Research Fellowship from the Sylvia and Charles Viertel Charitable Foundation. M.J.A and L.X. are supported by Monash Graduate Scholarship from Monash University, Australia.
Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/6
Y1 - 2022/6
N2 - Atopic dermatitis (AD) is a globally prevalent skin inflammation with a particular impact on children. Current therapies for AD are challenged by the limited armamentarium and the high heterogeneity of the disease. A novel promising therapeutic target for AD is the microbiota. Numerous studies have highlighted the involvement of the skin and gut microbiota in the pathogenesis of AD. The resident microbiota at these two epithelial tissues can modulate skin barrier functions and host immune responses, thus regulating AD progression. For example, the pathogenic roles of Staphylococcus aureus in the skin are well-established, making this bacterium an attractive target for AD treatment. Targeting the gut microbiota is another therapeutic strategy for AD. Multiple oral supplements with prebiotics, probiotics, postbiotics, and synbiotics have demonstrated promising efficacy in both AD prevention and treatment. In this review, we summarize the association of microbiota dysbiosis in both the skin and gut with AD, and the current knowledge of the functions of commensal microbiota in AD pathogenesis. Furthermore, we discuss the existing therapies in manipulating both the skin and gut commensal microbiota to prevent or treat AD. We also propose potential novel therapies based on the cutting-edge progress in this area.
AB - Atopic dermatitis (AD) is a globally prevalent skin inflammation with a particular impact on children. Current therapies for AD are challenged by the limited armamentarium and the high heterogeneity of the disease. A novel promising therapeutic target for AD is the microbiota. Numerous studies have highlighted the involvement of the skin and gut microbiota in the pathogenesis of AD. The resident microbiota at these two epithelial tissues can modulate skin barrier functions and host immune responses, thus regulating AD progression. For example, the pathogenic roles of Staphylococcus aureus in the skin are well-established, making this bacterium an attractive target for AD treatment. Targeting the gut microbiota is another therapeutic strategy for AD. Multiple oral supplements with prebiotics, probiotics, postbiotics, and synbiotics have demonstrated promising efficacy in both AD prevention and treatment. In this review, we summarize the association of microbiota dysbiosis in both the skin and gut with AD, and the current knowledge of the functions of commensal microbiota in AD pathogenesis. Furthermore, we discuss the existing therapies in manipulating both the skin and gut commensal microbiota to prevent or treat AD. We also propose potential novel therapies based on the cutting-edge progress in this area.
KW - aryl hydrocarbon receptors
KW - atopic dermatitis
KW - fecal microbiota transplantation
KW - G-protein-coupled receptors
KW - gut microbiota
KW - histone deacetylases
KW - metabolites
KW - short-chain fatty acids
KW - skin microbiota
KW - toll-like receptors
UR - http://www.scopus.com/inward/record.url?scp=85131712125&partnerID=8YFLogxK
U2 - 10.3390/pathogens11060642
DO - 10.3390/pathogens11060642
M3 - Review Article
C2 - 35745496
AN - SCOPUS:85131712125
SN - 2076-0817
VL - 11
JO - Pathogens
JF - Pathogens
IS - 6
M1 - 642
ER -