• 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

辅助性 T 细胞 17 细胞的双重性质。

The dichotomous nature of T helper 17 cells.

机构信息

The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.

出版信息

Nat Rev Immunol. 2017 Sep;17(9):535-544. doi: 10.1038/nri.2017.50. Epub 2017 May 30.

DOI:10.1038/nri.2017.50
PMID:28555673
Abstract

T helper 17 (T17) cells have been extensively studied since their discovery 10 years ago, primarily because of their known pathogenic role in many inflammatory diseases. Substantial progress has been made in understanding their development, regulation and functional activities, and genome-wide transcriptomic analysis has identified regulatory networks, nodes and interactions that provide vital clues for further studies. In this Review, we describe recent studies that have revealed the dichotomous nature of T17 cells, which on the one hand allows these cells to be pathogenic drivers of inflammatory disorders and on the other hand allows them to support the integrity of the intestinal barrier in a non-inflammatory manner.

摘要

辅助性 T 细胞 17(T17)细胞自 10 年前被发现以来,得到了广泛的研究,主要是因为它们在许多炎症性疾病中具有已知的致病作用。人们在理解它们的发育、调节和功能活动方面取得了重大进展,全基因组转录组分析确定了调节网络、节点和相互作用,为进一步的研究提供了重要线索。在这篇综述中,我们描述了最近的研究揭示了 T17 细胞的二分性,一方面使这些细胞成为炎症性疾病的致病驱动因素,另一方面使它们以非炎症的方式支持肠道屏障的完整性。

相似文献

1
The dichotomous nature of T helper 17 cells.辅助性 T 细胞 17 细胞的双重性质。
Nat Rev Immunol. 2017 Sep;17(9):535-544. doi: 10.1038/nri.2017.50. Epub 2017 May 30.
2
Th17 plasticity and its relevance to inflammatory bowel disease.辅助性 T 细胞 17 可塑性及其与炎症性肠病的关系。
J Autoimmun. 2018 Feb;87:38-49. doi: 10.1016/j.jaut.2017.12.004. Epub 2017 Dec 28.
3
The Intestine Harbors Functionally Distinct Homeostatic Tissue-Resident and Inflammatory Th17 Cells.肠道中存在具有不同功能的稳态组织驻留和炎症性 Th17 细胞。
Immunity. 2019 Jul 16;51(1):77-89.e6. doi: 10.1016/j.immuni.2019.05.004. Epub 2019 Jun 19.
4
IL-33 and the intestine: The good, the bad, and the inflammatory.白细胞介素 33 与肠道:好、坏与炎症。
Cytokine. 2017 Dec;100:1-10. doi: 10.1016/j.cyto.2017.06.017. Epub 2017 Jul 4.
5
Microbiota-specific Th17 Cells: Yin and Yang in Regulation of Inflammatory Bowel Disease.微生物群特异性Th17细胞:炎症性肠病调节中的阴阳平衡
Inflamm Bowel Dis. 2016 Jun;22(6):1473-82. doi: 10.1097/MIB.0000000000000775.
6
The balance of intestinal Foxp3+ regulatory T cells and Th17 cells and its biological significance.肠道 Foxp3+ 调节性 T 细胞和 Th17 细胞的平衡及其生物学意义。
Expert Rev Clin Immunol. 2014 Mar;10(3):353-62. doi: 10.1586/1744666X.2014.882232. Epub 2014 Feb 3.
7
Microbiome Dependent Regulation of T and Th17 Cells in Mucosa.黏膜中微生物组依赖的 T 和 Th17 细胞调控。
Front Immunol. 2019 Mar 8;10:426. doi: 10.3389/fimmu.2019.00426. eCollection 2019.
8
Functions of innate immune cells and commensal bacteria in gut homeostasis.固有免疫细胞和共生细菌在肠道稳态中的作用。
J Biochem. 2016 Feb;159(2):141-9. doi: 10.1093/jb/mvv119. Epub 2015 Nov 27.
9
Th17 Cell Plasticity and Functions in Cancer Immunity.Th17细胞的可塑性及其在癌症免疫中的作用
Biomed Res Int. 2015;2015:314620. doi: 10.1155/2015/314620. Epub 2015 Oct 25.
10
Integrated Analysis of Biopsies from Inflammatory Bowel Disease Patients Identifies SAA1 as a Link Between Mucosal Microbes with TH17 and TH22 Cells.炎症性肠病患者活检组织的综合分析鉴定 SAA1 为黏膜微生物与 TH17 和 TH22 细胞之间的联系。
Inflamm Bowel Dis. 2017 Sep;23(9):1544-1554. doi: 10.1097/MIB.0000000000001208.

引用本文的文献

1
Emerging therapies for the treatment of systemic sclerosis.系统性硬化症的新兴治疗方法。
Nat Rev Rheumatol. 2025 Sep 8. doi: 10.1038/s41584-025-01294-x.
2
Beneath the surface in autoimmune hemolytic anemia: pathogenetic networks, therapeutic advancements and open questions.自身免疫性溶血性贫血的潜在机制:发病机制网络、治疗进展与待解决问题
Front Immunol. 2025 Jul 31;16:1624667. doi: 10.3389/fimmu.2025.1624667. eCollection 2025.
3
A Comparative Analysis of Feeding Practices and Oral Immunity in Infants.婴儿喂养方式与口腔免疫的比较分析

本文引用的文献

1
Ustekinumab as Induction and Maintenance Therapy for Crohn's Disease.乌司奴单抗诱导和维持治疗克罗恩病。
N Engl J Med. 2016 Nov 17;375(20):1946-1960. doi: 10.1056/NEJMoa1602773.
2
Trans-presentation of IL-6 by dendritic cells is required for the priming of pathogenic T17 cells.树突状细胞对白细胞介素-6的反式呈递是致病性T17细胞启动所必需的。
Nat Immunol. 2017 Jan;18(1):74-85. doi: 10.1038/ni.3632. Epub 2016 Nov 28.
3
Autoimmune Renal Disease Is Exacerbated by S1P-Receptor-1-Dependent Intestinal Th17 Cell Migration to the Kidney.
Medicina (Kaunas). 2025 Jun 19;61(6):1114. doi: 10.3390/medicina61061114.
4
Multiple sclerosis: etiology in the context of neurovascular unit and immune system involvement and advancements with blood-brain barrier models.多发性硬化症:神经血管单元和免疫系统参与背景下的病因学以及血脑屏障模型的进展
Front Immunol. 2025 Jun 10;16:1595276. doi: 10.3389/fimmu.2025.1595276. eCollection 2025.
5
Variable innate lymphoid cells predominancy in oral lichen planus latently led to diverse clinical outcomes: a proof-of-concept study.口腔扁平苔藓中可变固有淋巴细胞优势潜伏导致多种临床结局:一项概念验证研究。
Front Immunol. 2025 Apr 28;16:1551311. doi: 10.3389/fimmu.2025.1551311. eCollection 2025.
6
Mast Cells Promote Inflammatory Th17 Cells and Impair Treg Cells Through an IL-1β and PGE Axis.肥大细胞通过白细胞介素-1β和前列腺素E轴促进炎症性辅助性T细胞17(Th17)的生成并损害调节性T细胞(Treg细胞)。
J Inflamm Res. 2025 Apr 30;18:5851-5865. doi: 10.2147/JIR.S509931. eCollection 2025.
7
Beneficial Effects of Omega-3 Fatty Acids on Obesity and Related Metabolic and Chronic Inflammatory Diseases.ω-3脂肪酸对肥胖及相关代谢和慢性炎症性疾病的有益作用。
Nutrients. 2025 Apr 3;17(7):1253. doi: 10.3390/nu17071253.
8
Lipid metabolism analysis reveals that DGAT1 regulates Th17 survival by controlling lipid peroxidation in uveitis.脂质代谢分析表明,二酰甘油酰基转移酶1(DGAT1)通过控制葡萄膜炎中的脂质过氧化来调节辅助性T细胞17(Th17)的存活。
JCI Insight. 2025 Apr 8;10(7):e184072. doi: 10.1172/jci.insight.184072.
9
The integrated stress response pathway controls cytokine production in tissue-resident memory CD4 T cells.整合应激反应途径控制组织驻留记忆性CD4 T细胞中的细胞因子产生。
Nat Immunol. 2025 Apr;26(4):557-566. doi: 10.1038/s41590-025-02105-x. Epub 2025 Mar 6.
10
in Inflammation and Pain: Update on Pathologic Mechanisms.《炎症与疼痛:病理机制的最新进展》
Pathogens. 2025 Feb 12;14(2):185. doi: 10.3390/pathogens14020185.
S1P受体1依赖性肠道Th17细胞向肾脏的迁移会加剧自身免疫性肾病。
Immunity. 2016 Nov 15;45(5):1078-1092. doi: 10.1016/j.immuni.2016.10.020.
4
Protein C receptor (PROCR) is a negative regulator of Th17 pathogenicity.蛋白C受体(PROCR)是Th17致病性的负调节因子。
J Exp Med. 2016 Oct 17;213(11):2489-2501. doi: 10.1084/jem.20151118. Epub 2016 Sep 26.
5
Hypoxia and inflammatory bowel disease.缺氧与炎症性肠病。
Microbes Infect. 2017 Mar;19(3):210-221. doi: 10.1016/j.micinf.2016.09.004. Epub 2016 Sep 20.
6
Oxygen metabolism and barrier regulation in the intestinal mucosa.肠道黏膜中的氧代谢与屏障调节
J Clin Invest. 2016 Oct 3;126(10):3680-3688. doi: 10.1172/JCI84429. Epub 2016 Aug 8.
7
RBPJ Controls Development of Pathogenic Th17 Cells by Regulating IL-23 Receptor Expression.RBPJ通过调控白细胞介素-23受体表达来控制致病性辅助性T细胞17的发育。
Cell Rep. 2016 Jul 12;16(2):392-404. doi: 10.1016/j.celrep.2016.05.088. Epub 2016 Jun 23.
8
The MicroRNA-183-96-182 Cluster Promotes T Helper 17 Cell Pathogenicity by Negatively Regulating Transcription Factor Foxo1 Expression.微小RNA-183-96-182簇通过负向调控转录因子Foxo1的表达促进辅助性T细胞17的致病性。
Immunity. 2016 Jun 21;44(6):1284-98. doi: 10.1016/j.immuni.2016.05.015.
9
Plasticity of Th17 Cells in Autoimmune Kidney Diseases.自身免疫性肾脏疾病中Th17细胞的可塑性
J Immunol. 2016 Jul 15;197(2):449-57. doi: 10.4049/jimmunol.1501831. Epub 2016 Jun 6.
10
T-bet is a key modulator of IL-23-driven pathogenic CD4(+) T cell responses in the intestine.T 细胞激活蛋白(T-bet)是肠道中白细胞介素-23(IL-23)驱动致病性 CD4+T 细胞应答的关键调节因子。
Nat Commun. 2016 May 19;7:11627. doi: 10.1038/ncomms11627.