• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

特应性皮炎的皮肤微生物组。

Skin microbiome of atopic dermatitis.

机构信息

A∗STAR Skin Research Labs (A∗SRL), Singapore, Singapore.

A∗STAR Skin Research Labs (A∗SRL), Singapore, Singapore.

出版信息

Allergol Int. 2022 Jan;71(1):31-39. doi: 10.1016/j.alit.2021.11.001. Epub 2021 Nov 24.

DOI:10.1016/j.alit.2021.11.001
PMID:34838450
Abstract

The skin microbiome is a key component of pathogenesis in atopic dermatitis (AD). The skin of AD patients is characterized by microbial dysbiosis, with a reduction of microbial diversity and overrepresentation of pathogenic Staphylococcus aureus (S. aureus). Recent exciting studies have elucidated an importance of establishing an appropriate immune response to microbes in early life and uncovered the new mechanisms of microbial community dynamics in modulating our skin microbiome. Several microbes are associated with AD pathogenesis, with proposed pathogenic effects from S. aureus and Malassezia. The complex relationships between microbes within the skin microbiome consortia includes various species, such as Staphylococcal, Roseomonas and Cutibacterium strains, that can inhibit S. aureus and are potential probiotics for AD skin. Numerous microbes are now also reported to modulate host response via communication with keratinocytes, specialized immune cells and adipocytes to improve skin health and barrier function. This increased understanding of skin microbiota bioactives has led to new biotherapeutic approaches that target the skin surface microenvironment for AD treatment.

摘要

皮肤微生物组是特应性皮炎(AD)发病机制的关键组成部分。AD 患者的皮肤表现为微生物失调,微生物多样性减少,致病性金黄色葡萄球菌(S. aureus)过度表达。最近令人兴奋的研究阐明了在生命早期建立对微生物的适当免疫反应的重要性,并揭示了微生物群落动态调节我们皮肤微生物组的新机制。一些微生物与 AD 的发病机制有关,金黄色葡萄球菌和马拉色菌有潜在的致病作用。皮肤微生物组联合体中微生物之间的复杂关系包括各种物种,如葡萄球菌、玫瑰单胞菌和棒状杆菌菌株,它们可以抑制金黄色葡萄球菌,是 AD 皮肤的潜在益生菌。现在也有大量微生物通过与角质形成细胞、特化免疫细胞和脂肪细胞的通讯来调节宿主反应,以改善皮肤健康和屏障功能。对皮肤微生物组生物活性的这种深入了解导致了针对 AD 治疗的皮肤表面微环境的新的生物治疗方法。

相似文献

1
Skin microbiome of atopic dermatitis.特应性皮炎的皮肤微生物组。
Allergol Int. 2022 Jan;71(1):31-39. doi: 10.1016/j.alit.2021.11.001. Epub 2021 Nov 24.
2
Effect of Staphylococcus aureus colonization and immune defects on the pathogenesis of atopic dermatitis.金黄色葡萄球菌定植和免疫缺陷对特应性皮炎发病机制的影响。
Arch Microbiol. 2024 Sep 20;206(10):410. doi: 10.1007/s00203-024-04134-w.
3
Skin dysbiosis in the microbiome in atopic dermatitis is site-specific and involves bacteria, fungus and virus.特应性皮炎的微生物组皮肤微生态失调具有特定部位特征,涉及细菌、真菌和病毒。
BMC Microbiol. 2021 Sep 23;21(1):256. doi: 10.1186/s12866-021-02302-2.
4
Microbiome and pediatric atopic dermatitis.微生物群与儿童特应性皮炎
J Dermatol. 2015 Dec;42(12):1137-42. doi: 10.1111/1346-8138.13072. Epub 2015 Sep 21.
5
Skin Microbiome in Atopic Dermatitis.特应性皮炎的皮肤微生物组。
Acta Derm Venereol. 2020 Jun 9;100(12):adv00164. doi: 10.2340/00015555-3514.
6
The microbiome in patients with atopic dermatitis.特应性皮炎患者的微生物组。
J Allergy Clin Immunol. 2019 Jan;143(1):26-35. doi: 10.1016/j.jaci.2018.11.015. Epub 2018 Nov 23.
7
Biotherapeutic Approaches in Atopic Dermatitis.特应性皮炎的生物治疗方法。
Biotechnol J. 2020 Oct;15(10):e1900322. doi: 10.1002/biot.201900322. Epub 2020 Apr 6.
8
Exploring the skin microbiome in atopic dermatitis pathogenesis and disease modification.探索特应性皮炎发病机制和疾病修饰中的皮肤微生物组。
J Allergy Clin Immunol. 2024 Jul;154(1):31-41. doi: 10.1016/j.jaci.2024.04.029. Epub 2024 May 16.
9
First-in-human topical microbiome transplantation with Roseomonas mucosa for atopic dermatitis.人体首次局部微生物组移植用粘玫瑰单胞菌治疗特应性皮炎。
JCI Insight. 2018 May 3;3(9):120608. doi: 10.1172/jci.insight.120608.
10
The role of the skin microbiome in atopic dermatitis.皮肤微生物群在特应性皮炎中的作用。
Curr Allergy Asthma Rep. 2015 Nov;15(11):65. doi: 10.1007/s11882-015-0567-4.

引用本文的文献

1
A pilot study on the cutaneous effects of ethanol in a moisturizing cream on non-lesional skin of patients with atopic dermatitis.一项关于含乙醇的保湿霜对特应性皮炎患者非皮损皮肤的皮肤影响的初步研究。
Sci Rep. 2025 Sep 15;15(1):32536. doi: 10.1038/s41598-025-18487-9.
2
Skin Microbiome Shifts in Various Dermatological Conditions.不同皮肤病中的皮肤微生物群变化
J Clin Med. 2025 Aug 30;14(17):6137. doi: 10.3390/jcm14176137.
3
Multi-Omics Profiling of the 42-Day Infant Gut as a Pilot Predictor of Atopic Dermatitis at One Year: A Birth Cohort Study in China.
42日龄婴儿肠道多组学分析作为1岁时特应性皮炎的初步预测指标:中国一项出生队列研究
J Inflamm Res. 2025 Aug 19;18:11205-11216. doi: 10.2147/JIR.S534551. eCollection 2025.
4
Comparison of Colony-forming Units of . in Patients with Atopic Dermatitis with and without Response to Systemic Treatment.特应性皮炎患者中对全身治疗有反应和无反应者的[具体对象]菌落形成单位比较。
J Clin Aesthet Dermatol. 2025 Aug;18(8):41-43.
5
Unlocking the molecular pathway of atopic dermatitis: journey so far and roads ahead.揭示特应性皮炎的分子途径:迄今为止的历程与未来之路。
Inflammopharmacology. 2025 Aug 18. doi: 10.1007/s10787-025-01900-0.
6
Organoids/organs-on-chips towards biomimetic human artificial skin.用于仿生人类人造皮肤的类器官/芯片上器官
Burns Trauma. 2025 May 3;13:tkaf029. doi: 10.1093/burnst/tkaf029. eCollection 2025.
7
Comparative Efficacy and Safety of Tralokinumab and Dupilumab in Moderate-to-Severe Atopic Dermatitis: A Narrative Review.曲罗芦单抗与度普利尤单抗治疗中度至重度特应性皮炎的疗效和安全性比较:一项叙述性综述
J Clin Med. 2025 Jul 13;14(14):4960. doi: 10.3390/jcm14144960.
8
Sequential Triple Therapy for Facial Inflammation: Prospective Evaluation of Facial Microneedle, Hydrolifting, and Intense Pulsed Light Therapy.面部炎症的序贯三联疗法:面部微针、水光提升和强脉冲光治疗的前瞻性评估
J Cosmet Dermatol. 2025 Jul;24(7):e70327. doi: 10.1111/jocd.70327.
9
Skin-associated commensal microorganisms and their metabolites.皮肤共生微生物及其代谢产物。
J Appl Microbiol. 2025 May 2;136(5). doi: 10.1093/jambio/lxaf111.
10
Selected traditional Chinese herbal medicines for the treatment of atopic dermatitis - research progress on the effect and mechanism of actions.用于治疗特应性皮炎的精选传统中药——作用效果与机制的研究进展
Front Pharmacol. 2025 Mar 26;16:1553251. doi: 10.3389/fphar.2025.1553251. eCollection 2025.