Department of Dermatology, University of California, Davis, Sacramento, CA, United States.
Department of Dermatology, University of California, Davis, Sacramento, CA, United States; University of California, Davis, School of Medicine, Sacramento, CA, United States.
Clin Immunol. 2020 Sep;218:108537. doi: 10.1016/j.clim.2020.108537. Epub 2020 Jul 15.
Psoriasis (PsO) and psoriatic arthritis (PsA) are chronic immune-mediated inflammatory diseases of multifactorial 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.
银屑病(PsO)和银屑病关节炎(PsA)是一种慢性免疫介导的炎症性疾病,其病因具有多因素性。除了遗传和环境因素外,有证据表明,失调的人类微生物组在银屑病发病机制中发挥作用。特别是,微生物组组成的改变,即生态失调,可能导致肠道、皮肤和关节的下游促炎作用。皮肤和肠道微生物群都与银屑病发病机制有关,尽管确切机制尚不清楚。本文综述了人类微生物组与银屑病发病机制的关系。进一步了解微生物组的功能可能有助于更好地理解炎症性疾病过程,并确定更多的治疗靶点。