The cutaneous and intestinal microbiome in psoriatic disease

被引:17
|
作者
Le, Stephanie T. [1 ]
Toussi, Atrin [1 ,2 ]
Maverakis, Natalia [3 ]
Marusina, Alina, I [1 ]
Barton, Virgina R. [1 ]
Merleev, Alexander A. [1 ]
Luxardi, Guillaume [1 ]
Raychaudhuri, Siba P. [1 ,4 ,5 ]
Maverakis, Emanual [1 ]
机构
[1] Univ Calif Davis, Dept Dermatol, Sacramento, CA 95816 USA
[2] Univ Calif Davis, Sch Med, Sacramento, CA 95816 USA
[3] NYU, New York, NY USA
[4] VA Med Ctr, Dept Med, Mather, CA USA
[5] Univ Calif Davis, Div Rheumatol Allergy & Clin Immunol, Sacramento, CA 95816 USA
关键词
Microbiome; Psoriatic arthritis; Autoimmunity; Psoriasis; Inflammatory bowel disease; GUT MICROBIOTA; ARTHRITIS; PATHOGENESIS; SKIN; TRANSPLANTATION; INTERLEUKIN-9; ETIOLOGY; AXIS;
D O I
10.1016/j.clim.2020.108537
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Psoriasis (PsO) and psoriatic arthritis (PsA) are chronic immune-mediated inflammatory diseases of multi-factorial etiology. In addition to genetic and environmental factors, evidence supports involvement of a dysregulated human microbiome in the pathogenesis of psoriatic disease. In particular, alterations in the composition of the microbiome, termed dysbiosis, can result in downstream proinflammatory effects in the gut, skin, and joints. Both the cutaneous and intestinal microbial populations are implicated in the pathogenesis of psoriatic disease, although exact mechanisms are unclear. Herein, we review the relationship between the human microbiome and psoriatic disease. Further insight into the functions of the microbiome may allow for greater understanding of inflammatory disease processes and identification of additional therapeutic targets.
引用
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页数:5
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