Arya Preeti, Kaur Manpreet, Chosyang Stanzin, Kushwaha Neelam, Singh Balvinder
Bioinformatics Centre, CSIR-Institute of Microbial Technology, Chandigarh, India.
Department of Paramedical Sciences, Faculty of Allied Health Sciences, Shree Guru Gobind Singh Tricentenary University, Gurugram, Haryana, India.
J Psoriasis Psoriatic Arthritis. 2023 Oct;8(4):166-178. doi: 10.1177/24755303231194293. Epub 2023 Aug 11.
Psoriasis is an autoimmune, chronic, inflammatory skin condition of multifactorial etiology. Recent studies in human skin microbiome research have revealed the dysbiosis in lesional skin of psoriatic patients, as well as have established the association of dysbiosis in the elicitation of inflammatory response of psoriatic skin.
The present review aimed to recapitulate the insights of psoriasis lesional skin microbiome studies published in the last 2 decades, and to determine the most important bacterial genera that can be deployed as psoriatic skin microbial signature for therapeutic intervention.
To achieve the stated objectives, full-text analysis of literature selected through systematic search of digital literature databases has been carried out following PRISMA guidelines.
Literature analysis suggests differential abundance of specific bacterial genera in the lesional psoriatic skin (LPS) compared to normal skin (NS) of psoriasis patients and skin from healthy subjects. These bacterial genera collectively can be utilized as potential biomarker for constructing lesional psoriatic skin specific microbial signature, and to explore the role of bacterial species in maintaining the skin homeostasis. The analysis further revealed that multiple bacterial species instead of a single bacterial species is important for understanding the psoriasis etiogenesis. Furthermore, decreased microbiome stability and increased diversity might have role in the exacerbation of lesions on skin of psoriatic patients.
Considering the importance of human skin microbiome dysbiosis in psoriasis, research efforts should be carried out to develop new therapeutic measures in addition to current therapies by exploiting the human and host-skin-associated microbial genomic and metabolomic knowledge.
银屑病是一种病因多因素的自身免疫性慢性炎症性皮肤病。近期人类皮肤微生物组研究表明,银屑病患者皮损部位存在微生物群落失调,且已证实这种失调与银屑病皮肤炎症反应的诱发有关。
本综述旨在总结过去20年发表的关于银屑病皮损部位皮肤微生物组研究的见解,并确定可作为银屑病皮肤微生物特征用于治疗干预的最重要细菌属。
为实现上述目标,按照PRISMA指南对通过系统检索数字文献数据库筛选出的文献进行了全文分析。
文献分析表明,与银屑病患者的正常皮肤(NS)及健康受试者的皮肤相比,银屑病皮损部位皮肤(LPS)中特定细菌属的丰度存在差异。这些细菌属可共同用作构建银屑病皮损部位皮肤特异性微生物特征的潜在生物标志物,并探索细菌种类在维持皮肤稳态中的作用。分析还显示,对于理解银屑病的病因,多种细菌而非单一细菌种类具有重要意义。此外,微生物组稳定性降低和多样性增加可能在银屑病患者皮肤病变的加重中起作用。
鉴于人类皮肤微生物群失调在银屑病中的重要性,除现有疗法外,应利用人类及宿主皮肤相关微生物的基因组和代谢组学知识开展研究,以开发新的治疗措施。