• 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

黏膜相关恒定 T 细胞与持续性根尖周炎的口腔微生物组。

Mucosal-associated invariant T cells and oral microbiome in persistent apical periodontitis.

机构信息

Department of Dental Medicine, Karolinska Institutet, Huddinge, Sweden.

Department of Microbiology, Tumor and Cell Biology and Science for Life Laboratory, Karolinska Institutet, Stockholm, Sweden.

出版信息

Int J Oral Sci. 2019 May 9;11(2):16. doi: 10.1038/s41368-019-0049-y.

DOI:10.1038/s41368-019-0049-y
PMID:31068577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6506549/
Abstract

Opportunistic bacteria in apical periodontitis (AP) may pose a risk for systemic dissemination. Mucosal-associated invariant T (MAIT) cells are innate-like T cells with a broad and potent antimicrobial activity important for gut mucosal integrity. It was recently shown that MAIT cells are present in the oral mucosal tissue, but the involvement of MAIT cells in AP is unknown. Here, comparison of surgically resected AP and gingival tissues demonstrated that AP tissues express significantly higher levels of Vα7.2-Jα33, Vα7.2-Jα20, Vα7.2-Jα12, Cα and tumour necrosis factor (TNF), interferon (IFN)-γ and interleukin (IL)-17A transcripts, resembling a MAIT cell signature. Moreover, in AP tissues the MR1-restricted MAIT cells positive for MR1-5-OP-RU tetramer staining appeared to be of similar levels as in peripheral blood but consisted mainly of CD4 subset. Unlike gingival tissues, the AP microbiome was quantitatively impacted by factors like fistula and high patient age and had a prominent riboflavin-expressing bacterial feature. When merged in an integrated view, the examined immune and microbiome data in the sparse partial least squares discriminant analysis could identify bacterial relative abundances that negatively correlated with Vα7.2-Jα33, Cα, and IL-17A transcript expressions in AP, implying that MAIT cells could play a role in the local defence at the oral tissue barrier. In conclusion, we describe the presence of MAIT cells at the oral site where translocation of oral microbiota could take place. These findings have implications for understanding the immune sensing of polymicrobial-related oral diseases.

摘要

根尖周炎(AP)中的机会性细菌可能会对全身传播构成威胁。黏膜相关不变 T(MAIT)细胞是具有广谱和强大抗菌活性的固有样 T 细胞,对肠道黏膜完整性很重要。最近的研究表明,MAIT 细胞存在于口腔黏膜组织中,但 MAIT 细胞在 AP 中的参与情况尚不清楚。在这里,对手术切除的 AP 和牙龈组织进行比较,结果表明 AP 组织表达的 Vα7.2-Jα33、Vα7.2-Jα20、Vα7.2-Jα12、Cα 和肿瘤坏死因子(TNF)、干扰素(IFN)-γ 和白细胞介素(IL)-17A 转录本水平显著升高,类似于 MAIT 细胞特征。此外,在 AP 组织中,MR1 限制性 MAIT 细胞对 MR1-5-OP-RU 四聚体染色呈阳性,其水平似乎与外周血相似,但主要由 CD4 亚群组成。与牙龈组织不同,AP 微生物组受瘘管和患者年龄等因素的定量影响,并且具有突出的核黄素表达细菌特征。当将检查的免疫和微生物组数据合并到稀疏偏最小二乘判别分析的综合视图中时,可以识别与 AP 中 Vα7.2-Jα33、Cα 和 IL-17A 转录物表达呈负相关的细菌相对丰度,这意味着 MAIT 细胞可能在口腔组织屏障的局部防御中发挥作用。总之,我们描述了 MAIT 细胞在口腔部位的存在,口腔微生物群可能在此处发生易位。这些发现对理解多微生物相关口腔疾病的免疫感应具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/9f4541978a5e/41368_2019_49_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/972f0e86d9e7/41368_2019_49_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/7b88d0af22e3/41368_2019_49_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/4e04084ff90d/41368_2019_49_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/77ebd6eae93c/41368_2019_49_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/ac8298de86cb/41368_2019_49_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/9a278ba9da7f/41368_2019_49_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/d1b1ceb89fc0/41368_2019_49_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/5b79a2fcb1d6/41368_2019_49_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/ddab73b8fdd8/41368_2019_49_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/234c8477d775/41368_2019_49_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/9f4541978a5e/41368_2019_49_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/972f0e86d9e7/41368_2019_49_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/7b88d0af22e3/41368_2019_49_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/4e04084ff90d/41368_2019_49_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/77ebd6eae93c/41368_2019_49_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/ac8298de86cb/41368_2019_49_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/9a278ba9da7f/41368_2019_49_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/d1b1ceb89fc0/41368_2019_49_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/5b79a2fcb1d6/41368_2019_49_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/ddab73b8fdd8/41368_2019_49_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/234c8477d775/41368_2019_49_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf69/6506549/9f4541978a5e/41368_2019_49_Fig11_HTML.jpg

相似文献

1
Mucosal-associated invariant T cells and oral microbiome in persistent apical periodontitis.黏膜相关恒定 T 细胞与持续性根尖周炎的口腔微生物组。
Int J Oral Sci. 2019 May 9;11(2):16. doi: 10.1038/s41368-019-0049-y.
2
Invariant Valpha7.2-Jalpha33 TCR is expressed in human kidney and brain tumors indicating infiltration by mucosal-associated invariant T (MAIT) cells.恒定链Vα7.2-Jα33 TCR在人类肾脏和脑肿瘤中表达,表明存在黏膜相关恒定T(MAIT)细胞浸润。
Int Immunol. 2008 Dec;20(12):1517-25. doi: 10.1093/intimm/dxn111. Epub 2008 Oct 16.
3
MAIT cells are critical for optimal mucosal immune responses during in vivo pulmonary bacterial infection.MAIT 细胞对于体内肺部细菌感染期间的最佳黏膜免疫反应至关重要。
Proc Natl Acad Sci U S A. 2013 Aug 13;110(33):E3119-28. doi: 10.1073/pnas.1302799110. Epub 2013 Jul 29.
4
Ontogeny of human mucosal-associated invariant T cells and related T cell subsets.人类黏膜相关恒定 T 细胞及其相关 T 细胞亚群的个体发生。
J Exp Med. 2018 Feb 5;215(2):459-479. doi: 10.1084/jem.20171739. Epub 2018 Jan 16.
5
Shared and Distinct Phenotypes and Functions of Human CD161++ Vα7.2+ T Cell Subsets.人类CD161++Vα7.2+T细胞亚群的共享和独特表型与功能
Front Immunol. 2017 Aug 30;8:1031. doi: 10.3389/fimmu.2017.01031. eCollection 2017.
6
Mucosal-associated invariant T cells for cancer immunotherapy.黏膜相关恒定 T 细胞用于癌症免疫治疗。
Mol Ther. 2023 Mar 1;31(3):631-646. doi: 10.1016/j.ymthe.2022.11.019. Epub 2022 Dec 5.
7
Pathophysiological Roles of Mucosal-Associated Invariant T Cells in the Context of Gut Microbiota-Liver Axis.肠道微生物群-肝脏轴背景下黏膜相关恒定T细胞的病理生理作用
Microorganisms. 2021 Feb 1;9(2):296. doi: 10.3390/microorganisms9020296.
8
Mucosal-associated invariant T cell alterations during the development of human type 1 diabetes.黏膜相关不变 T 细胞在人类 1 型糖尿病发病过程中的改变。
Diabetologia. 2020 Nov;63(11):2396-2409. doi: 10.1007/s00125-020-05257-7. Epub 2020 Sep 3.
9
Mucosal-associated invariant T cells regulate Th1 response in multiple sclerosis.黏膜相关恒定 T 细胞调节多发性硬化症中的 Th1 反应。
Int Immunol. 2011 Sep;23(9):529-35. doi: 10.1093/intimm/dxr047. Epub 2011 Jun 28.
10
Detection, Expansion, and Isolation of Human MAIT Cells.人 MAIT 细胞的检测、扩增和分离。
Methods Mol Biol. 2020;2111:285-293. doi: 10.1007/978-1-0716-0266-9_22.

引用本文的文献

1
MAIT cells modulating the oral lichen planus immune microenvironment: a cellular crosstalk perspective.调节口腔扁平苔藓免疫微环境的黏膜相关恒定T细胞:细胞间相互作用视角
Inflamm Res. 2025 Jan 7;74(1):10. doi: 10.1007/s00011-024-01990-6.
2
Correlation between PD-1/PD-L1 and RANKL/OPG in chronic apical periodontitis model of Sprague-Dawley rats.PD-1/PD-L1 与 RANKL/OPG 在 Sprague-Dawley 大鼠慢性根尖周炎模型中的相关性。
Odontology. 2024 Oct;112(4):1113-1122. doi: 10.1007/s10266-024-00911-7. Epub 2024 Mar 25.
3
Signals that control MAIT cell function in healthy and inflamed human tissues.

本文引用的文献

1
Tissue-resident MAIT cell populations in human oral mucosa exhibit an activated profile and produce IL-17.人类口腔黏膜组织驻留的 MAIT 细胞群体表现出激活状态,并产生 IL-17。
Eur J Immunol. 2019 Jan;49(1):133-143. doi: 10.1002/eji.201847759. Epub 2018 Nov 14.
2
Genes Critical for Developing Periodontitis: Lessons from Mouse Models.对牙周炎发展至关重要的基因:来自小鼠模型的经验教训。
Front Immunol. 2017 Oct 27;8:1395. doi: 10.3389/fimmu.2017.01395. eCollection 2017.
3
mixOmics: An R package for 'omics feature selection and multiple data integration.
调控健康和炎症组织中 MAIT 细胞功能的信号。
Immunol Rev. 2024 May;323(1):138-149. doi: 10.1111/imr.13325. Epub 2024 Mar 22.
4
Cross-Talk between Mucosal-Associated Invariant T, Natural Killer, and Natural Killer T Cell Populations is Implicated in the Pathogenesis of Placenta Accreta Spectrum.黏膜相关恒定 T 细胞、自然杀伤细胞和自然杀伤 T 细胞群体之间的串扰与胎盘植入谱系疾病的发病机制有关。
Inflammation. 2023 Aug;46(4):1192-1208. doi: 10.1007/s10753-023-01799-1. Epub 2023 Mar 31.
5
MAIT cells and the microbiome.MAIT 细胞与微生物组。
Front Immunol. 2023 Feb 23;14:1127588. doi: 10.3389/fimmu.2023.1127588. eCollection 2023.
6
Relevant mechanisms of MAIT cells involved in the pathogenesis of periodontitis.MAIT 细胞参与牙周炎发病机制的相关机制。
Front Cell Infect Microbiol. 2023 Feb 21;13:1104932. doi: 10.3389/fcimb.2023.1104932. eCollection 2023.
7
Poor dental health and risk of pancreatic cancer: a nationwide registry-based cohort study in Sweden, 2009-2016.口腔健康状况不佳与胰腺癌风险:2009-2016 年瑞典全国注册队列研究。
Br J Cancer. 2022 Dec;127(12):2133-2140. doi: 10.1038/s41416-022-02018-8. Epub 2022 Oct 22.
8
Effect of Enterococcus faecalis OG1RF on human calvarial osteoblast apoptosis.屎肠球菌 OG1RF 对人颅骨成骨细胞凋亡的影响。
BMC Oral Health. 2022 Jul 8;22(1):279. doi: 10.1186/s12903-022-02295-y.
9
MAIT cells and their implication in human oral diseases.MAIT 细胞及其在人类口腔疾病中的作用。
Inflamm Res. 2022 Sep;71(9):1041-1054. doi: 10.1007/s00011-022-01600-3. Epub 2022 Jul 4.
10
Preserved Mucosal-Associated Invariant T Cells in the Cervical Mucosa of HIV-Infected Women with Dominant Expression of the TRAV1-2-TRAJ20 T Cell Receptor α-Chain.HIV 感染女性宫颈黏膜中表达优势的 TRAV1-2-TRAJ20 T 细胞受体 α 链的保留黏膜相关不变 T 细胞。
J Infect Dis. 2022 Oct 17;226(8):1428-1440. doi: 10.1093/infdis/jiac171.
mixOmics:一个用于“组学”特征选择和多数据整合的R包。
PLoS Comput Biol. 2017 Nov 3;13(11):e1005752. doi: 10.1371/journal.pcbi.1005752. eCollection 2017 Nov.
4
Unique Tailoring of Th17 at the Gingival Oral Mucosal Barrier.Th17 在牙龈口腔黏膜屏障中的独特定制。
J Dent Res. 2018 Feb;97(2):128-131. doi: 10.1177/0022034517736030. Epub 2017 Oct 13.
5
The MAIT conundrum - how human MAIT cells distinguish bacterial colonization from infection in mucosal barrier tissues.MAIT 细胞的难题——人类 MAIT 细胞如何区分黏膜屏障组织中的细菌定植与感染。
Immunol Lett. 2017 Dec;192:7-11. doi: 10.1016/j.imlet.2017.09.013. Epub 2017 Oct 5.
6
MAIT cells in infectious diseases.固有淋巴细胞在感染性疾病中的作用。
Curr Opin Immunol. 2017 Oct;48:7-14. doi: 10.1016/j.coi.2017.07.009. Epub 2017 Jul 24.
7
Multiple layers of heterogeneity and subset diversity in human MAIT cell responses to distinct microorganisms and to innate cytokines.人类 MAIT 细胞对不同微生物和先天细胞因子反应的异质性和亚群多样性的多层次。
Proc Natl Acad Sci U S A. 2017 Jul 3;114(27):E5434-E5443. doi: 10.1073/pnas.1705759114. Epub 2017 Jun 19.
8
Overlapping riboflavin supply pathways in bacteria.细菌中重叠的核黄素供应途径。
Crit Rev Microbiol. 2017 Mar;43(2):196-209. doi: 10.1080/1040841X.2016.1192578. Epub 2016 Nov 8.
9
Microbiome in the Apical Root Canal System of Teeth with Post-Treatment Apical Periodontitis.根管治疗后根尖周炎患牙根尖根管系统中的微生物群
PLoS One. 2016 Sep 30;11(9):e0162887. doi: 10.1371/journal.pone.0162887. eCollection 2016.
10
MAIT, MR1, microbes and riboflavin: a paradigm for the co-evolution of invariant TCRs and restricting MHCI-like molecules?黏膜相关恒定T细胞、MR1、微生物与核黄素:恒定T细胞受体与限制性MHC I类样分子共同进化的范例?
Immunogenetics. 2016 Aug;68(8):537-48. doi: 10.1007/s00251-016-0927-9. Epub 2016 Jul 8.