• 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

皮肤和口生殖器微生物群在保护性免疫和慢性免疫介导炎症性疾病中的作用

The Role of Skin and Orogenital Microbiota in Protective Immunity and Chronic Immune-Mediated Inflammatory Disease.

作者信息

Park Young Joon, Lee Heung Kyu

机构信息

Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, South Korea.

KAIST Institute for Health Science and Technology, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, South Korea.

出版信息

Front Immunol. 2018 Jan 10;8:1955. doi: 10.3389/fimmu.2017.01955. eCollection 2017.

DOI:10.3389/fimmu.2017.01955
PMID:29375574
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5767596/
Abstract

The skin and orogenital mucosae, which constitute complex protective barriers against infection and injuries, are not only the first to come into contact with pathogens but are also colonized by a set of microorganisms that are essential to maintain a healthy physiological environment. Using 16S ribosomal RNA metagenomic sequencing, scientists recognized that the microorganism colonization has greater diversity and variability than previously assumed. These microorganisms, such as commensal bacteria, affect the host's immune response against pathogens and modulate chronic inflammatory responses. Previously, a single pathogen was thought to cause a single disease, but current evidence suggests that dysbiosis of the tissue microbiota may underlie the disease status. Dysbiosis results in aberrant immune responses at the surface and furthermore, affects the systemic immune response. Hence, understanding the initial interaction between the barrier surface immune system and local microorganisms is important for understanding the overall systemic effects of the immune response. In this review, we describe current evidence for the basis of the interactions between pathogens, microbiota, and immune cells on surface barriers and offer explanations for how these interactions may lead to chronic inflammatory disorders.

摘要

皮肤和口腔生殖器黏膜构成了抵御感染和损伤的复杂保护屏障,它们不仅最先接触病原体,还被一组对维持健康生理环境至关重要的微生物所定植。通过16S核糖体RNA宏基因组测序,科学家认识到微生物定植的多样性和变异性比之前设想的更大。这些微生物,如共生细菌,会影响宿主对病原体的免疫反应并调节慢性炎症反应。以前,人们认为单一病原体导致单一疾病,但目前的证据表明,组织微生物群的失调可能是疾病状态的基础。失调会导致表面异常的免疫反应,进而影响全身免疫反应。因此,了解屏障表面免疫系统与局部微生物之间的初始相互作用对于理解免疫反应的整体全身效应很重要。在这篇综述中,我们描述了目前关于病原体、微生物群和免疫细胞在表面屏障上相互作用基础的证据,并解释了这些相互作用如何可能导致慢性炎症性疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/906e/5767596/c5ba375404ee/fimmu-08-01955-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/906e/5767596/372630add7e9/fimmu-08-01955-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/906e/5767596/43ed8489a9de/fimmu-08-01955-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/906e/5767596/c5ba375404ee/fimmu-08-01955-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/906e/5767596/372630add7e9/fimmu-08-01955-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/906e/5767596/43ed8489a9de/fimmu-08-01955-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/906e/5767596/c5ba375404ee/fimmu-08-01955-g003.jpg

相似文献

1
The Role of Skin and Orogenital Microbiota in Protective Immunity and Chronic Immune-Mediated Inflammatory Disease.皮肤和口生殖器微生物群在保护性免疫和慢性免疫介导炎症性疾病中的作用
Front Immunol. 2018 Jan 10;8:1955. doi: 10.3389/fimmu.2017.01955. eCollection 2017.
2
Commensal bacteria (normal microflora), mucosal immunity and chronic inflammatory and autoimmune diseases.共生菌(正常微生物群)、黏膜免疫与慢性炎症及自身免疫性疾病。
Immunol Lett. 2004 May 15;93(2-3):97-108. doi: 10.1016/j.imlet.2004.02.005.
3
Dismicrobism in inflammatory bowel disease and colorectal cancer: changes in response of colocytes.炎症性肠病和结直肠癌中的微生物群变化:结肠细胞反应的改变
World J Gastroenterol. 2014 Dec 28;20(48):18121-30. doi: 10.3748/wjg.v20.i48.18121.
4
Interactions between intestinal microbiota and innate immune system in pediatric inflammatory bowel disease.小儿炎症性肠病中肠道微生物群与固有免疫系统的相互作用。
J Clin Gastroenterol. 2012 Oct;46 Suppl:S64-6. doi: 10.1097/MCG.0b013e31826a857f.
5
The role of innate immune signaling in the pathogenesis of atopic dermatitis and consequences for treatments.天然免疫信号在特应性皮炎发病机制中的作用及对治疗的影响。
Semin Immunopathol. 2016 Jan;38(1):29-43. doi: 10.1007/s00281-015-0544-y. Epub 2015 Nov 16.
6
The influence of skin microorganisms on cutaneous immunity.皮肤微生物对皮肤免疫的影响。
Nat Rev Immunol. 2016 May 27;16(6):353-66. doi: 10.1038/nri.2016.48.
7
[Diversity of cutaneous bacteria decreases inflammation].皮肤细菌的多样性可减轻炎症
Ann Dermatol Venereol. 2015 Jan;142 Suppl 1:S13-7. doi: 10.1016/S0151-9638(15)30002-8.
8
Richness and diversity of mammalian fungal communities shape innate and adaptive immunity in health and disease.哺乳动物真菌群落的丰富度和多样性塑造了健康和疾病中的先天和适应性免疫。
Eur J Immunol. 2014 Nov;44(11):3166-81. doi: 10.1002/eji.201344403. Epub 2014 Oct 30.
9
Skin Immune Landscape: Inside and Outside the Organism.皮肤免疫全景:机体内外
Mediators Inflamm. 2017;2017:5095293. doi: 10.1155/2017/5095293. Epub 2017 Oct 18.
10
Bridging the gap between host immune response and intestinal dysbiosis in inflammatory bowel disease: does immunoglobulin A mark the spot?在炎症性肠病中弥合宿主免疫反应和肠道菌群失调之间的差距:免疫球蛋白 A 能指明方向吗?
Clin Gastroenterol Hepatol. 2015 May;13(5):842-6. doi: 10.1016/j.cgh.2015.02.028. Epub 2015 Feb 25.

引用本文的文献

1
SIRT1 in acute lung injury: unraveling its pleiotropic functions and therapeutic development prospects.SIRT1在急性肺损伤中的作用:揭示其多效性功能及治疗发展前景
Mol Cell Biochem. 2025 Mar;480(3):1449-1464. doi: 10.1007/s11010-024-05111-z. Epub 2024 Sep 13.
2
A Comprehensive Analysis of Liposomal-Based Nanocarriers for Treating Skin and Soft Tissue Infection.用于治疗皮肤和软组织感染的脂质体纳米载体综合分析
Curr Drug Deliv. 2025;22(5):552-573. doi: 10.2174/0115672018328954240801110200.
3
Phenylalanine Butyramide: A Butyrate Derivative as a Novel Inhibitor of Tyrosinase.

本文引用的文献

1
Staphylococcus aureus Virulent PSMα Peptides Induce Keratinocyte Alarmin Release to Orchestrate IL-17-Dependent Skin Inflammation.金黄色葡萄球菌毒力 PSMα 肽诱导角质形成细胞警报素释放以协调白细胞介素 17 依赖的皮肤炎症。
Cell Host Microbe. 2017 Nov 8;22(5):667-677.e5. doi: 10.1016/j.chom.2017.10.008.
2
Staphylococcus aureus Epicutaneous Exposure Drives Skin Inflammation via IL-36-Mediated T Cell Responses.金黄色葡萄球菌经皮暴露通过 IL-36 介导的 T 细胞反应引发皮肤炎症。
Cell Host Microbe. 2017 Nov 8;22(5):653-666.e5. doi: 10.1016/j.chom.2017.10.006.
3
Ectopic colonization of oral bacteria in the intestine drives T1 cell induction and inflammation.
苯丙氨酸丁酰胺:一种新型酪氨酸酶抑制剂的丁酸盐衍生物。
Int J Mol Sci. 2024 Jul 3;25(13):7310. doi: 10.3390/ijms25137310.
4
[Research progress on the mechanisms of probiotics promoting wound healing].[益生菌促进伤口愈合机制的研究进展]
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2024 Jun 25;41(3):635-640. doi: 10.7507/1001-5515.202208003.
5
Exploring the Microbial Landscape of Neonatal Skin Flora: A Comprehensive Review.探索新生儿皮肤菌群的微生物景观:综述
Cureus. 2024 Jan 26;16(1):e52972. doi: 10.7759/cureus.52972. eCollection 2024 Jan.
6
Enhancement of Wound Healing Efficacy by Chitosan-based Hydrocolloid on Sprague Dawley Rats.壳聚糖水胶体促进 Sprague Dawley 大鼠伤口愈合的效果。
In Vivo. 2023 May-Jun;37(3):1052-1064. doi: 10.21873/invivo.13180.
7
Role of the skin microbiota and intestinal microbiome in rosacea.皮肤微生物群和肠道微生物组在玫瑰痤疮中的作用。
Front Microbiol. 2023 Feb 10;14:1108661. doi: 10.3389/fmicb.2023.1108661. eCollection 2023.
8
Modeling an Optimal 3D Skin-on-Chip within Microfluidic Devices for Pharmacological Studies.在微流控设备中构建用于药理学研究的最优三维芯片皮肤模型。
Pharmaceutics. 2022 Jul 6;14(7):1417. doi: 10.3390/pharmaceutics14071417.
9
Advances in Microbiome-Derived Solutions and Methodologies Are Founding a New Era in Skin Health and Care.微生物群衍生解决方案和方法的进展正在开创皮肤健康与护理的新纪元。
Pathogens. 2022 Jan 20;11(2):121. doi: 10.3390/pathogens11020121.
10
Effect of treatments on skin microbiota in patients with atopic dermatitis: a protocol for systematic review.治疗对特应性皮炎患者皮肤微生物群的影响:系统评价方案。
BMJ Open. 2022 Jan 7;12(1):e053488. doi: 10.1136/bmjopen-2021-053488.
口腔细菌在肠道中的异位定植驱动T1细胞诱导和炎症反应。
Science. 2017 Oct 20;358(6361):359-365. doi: 10.1126/science.aan4526.
4
Advanced glycation end-products and Porphyromonas gingivalis lipopolysaccharide increase calprotectin expression in human gingival epithelial cells.晚期糖基化终产物和牙龈卟啉单胞菌脂多糖增加人牙龈上皮细胞钙卫蛋白的表达。
J Cell Biochem. 2018 Feb;119(2):1591-1603. doi: 10.1002/jcb.26319. Epub 2017 Sep 7.
5
The periodontal war: microbes and immunity.牙周炎之战:微生物与免疫
Periodontol 2000. 2017 Oct;75(1):52-115. doi: 10.1111/prd.12222.
6
Cutaneous Leishmaniasis Induces a Transmissible Dysbiotic Skin Microbiota that Promotes Skin Inflammation.皮肤利什曼病诱导出一种可传播的失调皮肤微生物群,该微生物群会促进皮肤炎症。
Cell Host Microbe. 2017 Jul 12;22(1):13-24.e4. doi: 10.1016/j.chom.2017.06.006. Epub 2017 Jun 29.
7
Inter-personal diversity and temporal dynamics of dental, tongue, and salivary microbiota in the healthy oral cavity.健康口腔中牙齿、舌头和唾液微生物群的人际多样性和时间动态变化。
NPJ Biofilms Microbiomes. 2017 Jan 26;3:2. doi: 10.1038/s41522-016-0011-0. eCollection 2017.
8
Cutaneous Nod2 Expression Regulates the Skin Microbiome and Wound Healing in a Murine Model.皮肤Nod2表达调节小鼠模型中的皮肤微生物群和伤口愈合。
J Invest Dermatol. 2017 Nov;137(11):2427-2436. doi: 10.1016/j.jid.2017.05.029. Epub 2017 Jun 22.
9
Porphyromonas gingivalis-induced IL-33 down-regulates hCAP-18/LL-37 production in human gingival epithelial cells.牙龈卟啉单胞菌诱导的白细胞介素-33下调人牙龈上皮细胞中hCAP-18/LL-37的产生。
Biomed Res. 2017;38(3):167-173. doi: 10.2220/biomedres.38.167.
10
Vaginal Inhibits HIV-1 Replication in Human Tissues .阴道分泌物可抑制HIV-1在人体组织中的复制。
Front Microbiol. 2017 May 19;8:906. doi: 10.3389/fmicb.2017.00906. eCollection 2017.