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皮肤微生物群:在特应性皮炎中的致病作用及影响

Skin microbiota: pathogenic roles and implications in atopic dermatitis.

作者信息

Huang Cong, Zhuo Fan, Guo Yang, Wang Siyu, Zhang Kaoyuan, Li Xiahong, Dai Wenkui, Dou Xia, Yu Bo

机构信息

Department of Dermatology, Skin Research Institute of Peking University Shenzhen Hospital, Peking University Shenzhen Hospital, Shenzhen, China.

Shenzhen Key Laboratory for Translational Medicine of Dermatology, Shenzhen Peking University - the Hong Kong University of Science and Technology Medical Center, Shenzhen, China.

出版信息

Front Cell Infect Microbiol. 2025 Jan 14;14:1518811. doi: 10.3389/fcimb.2024.1518811. eCollection 2024.

DOI:10.3389/fcimb.2024.1518811
PMID:39877655
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11772334/
Abstract

Atopic dermatitis (AD) is a chronic and inflammatory skin disorder characterized by impaired barrier function and imbalanced immunity. Recent advances have revealed that dysbiosis of skin microbiota plays important roles in the pathogenesis and development of AD. Meanwhile, endogenous and external factors contribute to the dysbiosis of skin microbiota in AD. Additionally, various treatments, including topical treatments, phototherapy, and systemic biologics, have demonstrated positive impacts on the clinical outcomes, alongside with the modulations of cutaneous microbiota in AD patients. Importantly, therapeutics or products regulating skin microbiota homeostasis have demonstrated potential for AD treatment in early clinical studies. In this review, we underline changes of the skin microbiota correlated with AD. Meanwhile, we provide an overview of the skin microbiota regarding its roles in the pathogenesis and development of AD. Finally, we summarize therapeutic strategies restoring the skin microbial homeostasis in AD management.

摘要

特应性皮炎(AD)是一种慢性炎症性皮肤病,其特征是屏障功能受损和免疫失衡。最近的研究进展表明,皮肤微生物群的失调在AD的发病机制和发展中起重要作用。同时,内源性和外源性因素导致了AD患者皮肤微生物群的失调。此外,包括局部治疗、光疗和全身性生物制剂在内的各种治疗方法,已证明对临床结果有积极影响,同时也对AD患者的皮肤微生物群产生了调节作用。重要的是,在早期临床研究中,调节皮肤微生物群稳态的治疗方法或产品已显示出治疗AD的潜力。在这篇综述中,我们强调了与AD相关的皮肤微生物群的变化。同时,我们概述了皮肤微生物群在AD发病机制和发展中的作用。最后,我们总结了在AD管理中恢复皮肤微生物稳态的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6d6/11772334/6601bb1cb4b9/fcimb-14-1518811-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6d6/11772334/8505d9378e6d/fcimb-14-1518811-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6d6/11772334/6601bb1cb4b9/fcimb-14-1518811-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6d6/11772334/8505d9378e6d/fcimb-14-1518811-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6d6/11772334/6601bb1cb4b9/fcimb-14-1518811-g002.jpg

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本文引用的文献

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Unraveling the gut-skin axis in atopic dermatitis: exploiting insights for therapeutic strategies.揭开特应性皮炎的肠-皮轴:利用研究进展制定治疗策略。
Gut Microbes. 2024 Jan-Dec;16(1):2430420. doi: 10.1080/19490976.2024.2430420. Epub 2024 Nov 27.
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Association of breast milk-derived arachidonic acid-induced infant gut dysbiosis with the onset of atopic dermatitis.母乳源性花生四烯酸诱导的婴儿肠道菌群失调与特应性皮炎发病的关联。
Gut. 2024 Dec 10;74(1):45-57. doi: 10.1136/gutjnl-2024-332407.
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The Role of the Microbiota in the Pathogenesis and Treatment of Atopic Dermatitis-A Literature Review.
肠道菌群在特应性皮炎发病机制和治疗中的作用——文献综述。
Int J Mol Sci. 2024 Jun 13;25(12):6539. doi: 10.3390/ijms25126539.
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Antibiotics taken within the first year of life are linked to infant gut microbiome disruption and elevated atopic dermatitis risk.婴儿时期使用抗生素与肠道微生物组紊乱和特应性皮炎风险升高有关。
J Allergy Clin Immunol. 2024 Jul;154(1):131-142. doi: 10.1016/j.jaci.2024.03.025. Epub 2024 Apr 24.
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The skin microbiome in pediatric atopic dermatitis and food allergy.儿童特应性皮炎和食物过敏的皮肤微生物组。
Allergy. 2024 Jun;79(6):1470-1484. doi: 10.1111/all.16044. Epub 2024 Feb 3.
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The Skin Microbiome and its Significance for Dermatologists.皮肤微生物组及其对皮肤科医生的意义。
Am J Clin Dermatol. 2024 Mar;25(2):169-177. doi: 10.1007/s40257-023-00842-z. Epub 2024 Jan 22.
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Staphylococcus epidermidis activates keratinocyte cytokine expression and promotes skin inflammation through the production of phenol-soluble modulins.表皮葡萄球菌通过产生酚可溶性调节素激活角质形成细胞细胞因子表达并促进皮肤炎症。
Cell Rep. 2023 Sep 26;42(9):113024. doi: 10.1016/j.celrep.2023.113024. Epub 2023 Aug 22.
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IL-4 receptor alpha blockade dampens allergic inflammation and upregulates IL-17A expression to promote Saureus clearance in antigen sensitized mouse skin.白细胞介素-4 受体 α 阻断可抑制过敏炎症反应并上调白细胞介素-17A 的表达,从而促进抗原致敏小鼠皮肤中金黄色葡萄球菌的清除。
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