Manipulating Microbiota to Treat Atopic Dermatitis: Functions and Therapies

被引:38
作者
Alam, Md Jahangir [1 ]
Xie, Liang [1 ,2 ]
Yap, Yu-Anne [3 ]
Marques, Francine Z. [2 ,4 ]
Robert, Remy [3 ]
机构
[1] Monash Univ, Biomed Discovery Inst, Dept Microbiol, Clayton, Vic 3800, Australia
[2] Monash Univ, Sch Biol Sci, Hypertens Res Lab, Clayton, Vic 3800, Australia
[3] Monash Univ, Biomed Discovery Inst, Dept Physiol, Clayton, Vic 3800, Australia
[4] Baker Heart & Diabet Inst, Heart Failure Res Lab, Melbourne, Vic 3004, Australia
关键词
atopic dermatitis; skin microbiota; gut microbiota; metabolites; short-chain fatty acids; G-protein-coupled receptors; aryl hydrocarbon receptors; histone deacetylases; toll-like receptors; fecal microbiota transplantation; ARYL-HYDROCARBON RECEPTOR; CHAIN FATTY-ACIDS; TOLL-LIKE RECEPTOR; 1ST; 6; MONTHS; INTERNATIONAL SCIENTIFIC ASSOCIATION; STAPHYLOCOCCUS-AUREUS COLONIZATION; LACTOBACILLUS-ACIDOPHILUS L-92; RANDOMIZED CONTROLLED-TRIAL; PLACEBO-CONTROLLED TRIAL; PHENOL-SOLUBLE MODULINS;
D O I
10.3390/pathogens11060642
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页数:34
相关论文
共 359 条
[11]   Host-bacterial mutualism in the human intestine [J].
Bäckhed, F ;
Ley, RE ;
Sonnenburg, JL ;
Peterson, DA ;
Gordon, JI .
SCIENCE, 2005, 307 (5717) :1915-1920
[12]  
Bäckhed F, 2015, CELL HOST MICROBE, V17, P690, DOI [10.1016/j.chom.2015.04.004, 10.1016/j.chom.2015.05.012]
[13]   Interventions to reduce Staphylococcus aureus in the management of atopic eczema: an updated Cochrane review [J].
Bath-Hextall, F. J. ;
Birnie, A. J. ;
Ravenscroft, J. C. ;
Williams, H. C. .
BRITISH JOURNAL OF DERMATOLOGY, 2010, 163 (01) :12-26
[14]   Epidermal lipid composition, barrier integrity, and eczematous inflammation are associated with skin microbiome configuration [J].
Baurecht, Hansjorg ;
Ruhlemann, Malte C. ;
Rodriguez, Elke ;
Thielking, Frederieke ;
Harder, Inken ;
Erkens, Anna-Sophie ;
Stolzl, Dora ;
Ellinghaus, Eva ;
Hotze, Melanie ;
Lieb, Wolfgang ;
Wang, Sheng ;
Heinsen-Groth, Femke-Anouska ;
Franke, Andre ;
Weidinger, Stephan .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2018, 141 (05) :1668-+
[15]   Fatal Aspiration Pneumonia as a Complication of Fecal Microbiota Transplant [J].
Baxter, Melissa ;
Ahmad, Tariq ;
Colville, Alaric ;
Sheridan, Ray .
CLINICAL INFECTIOUS DISEASES, 2015, 61 (01) :140-141
[16]   Staphylococcus aureus protein A triggers T cell-independent B cell proliferation by sensitizing B cells for TLR2 ligands [J].
Bekeredjian-Ding, Isabelle ;
Inamura, Seiichi ;
Giese, Thomas ;
Moll, Hermann ;
Endres, Stefan ;
Sing, Andreas ;
Zaehringer, Ulrich ;
Hartmann, Gunther .
JOURNAL OF IMMUNOLOGY, 2007, 178 (05) :2803-2812
[17]   Low neonatal Toll-like receptor 4-mediated interleukin-10 production is associated with subsequent atopic dermatitis [J].
Belderbos, M. E. ;
Knol, E. F. ;
Houben, M. L. ;
van Bleek, G. M. ;
Wilbrink, B. ;
Kimpen, J. L. L. ;
Rovers, M. ;
Bont, L. .
CLINICAL AND EXPERIMENTAL ALLERGY, 2012, 42 (01) :66-75
[18]   Staphylococcus aureus α-Toxin: Nearly a Century of Intrigue [J].
Berube, Bryan J. ;
Wardenburg, Juliane Bubeck .
TOXINS, 2013, 5 (06) :1140-1166
[19]   DENDRITIC CELLS ARE POTENT ANTIGEN-PRESENTING CELLS FOR MICROBIAL SUPERANTIGENS [J].
BHARDWAJ, N ;
FRIEDMAN, SM ;
COLE, BC ;
NISANIAN, AJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (01) :267-273
[20]   Atopic dermatitis: an expanding therapeutic pipeline for a complex disease [J].
Bieber, Thomas .
NATURE REVIEWS DRUG DISCOVERY, 2022, 21 (01) :21-40