• 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

芳香烃受体在宿主-病原体相互作用中的作用。

The role of the AHR in host-pathogen interactions.

作者信息

Barreira-Silva Palmira, Lian Yilong, Kaufmann Stefan H E, Moura-Alves Pedro

机构信息

IBMC, Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.

i3S, Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.

出版信息

Nat Rev Immunol. 2025 Mar;25(3):178-194. doi: 10.1038/s41577-024-01088-4. Epub 2024 Oct 16.

DOI:10.1038/s41577-024-01088-4
PMID:39415055
Abstract

Host-microorganism encounters take place in many different ways and with different types of outcomes. Three major types of microorganisms need to be distinguished: (1) pathogens that cause harm to the host and must be controlled; (2) environmental microorganisms that can be ignored but must be controlled at higher abundance; and (3) symbiotic microbiota that require support by the host. Recent evidence indicates that the aryl hydrocarbon receptor (AHR) senses and initiates signalling and gene expression in response to a plethora of microorganisms and infectious conditions. It was originally identified as a receptor that binds xenobiotics. However, it was subsequently found to have a critical role in numerous biological processes, including immunity and inflammation and was recently classified as a pattern recognition receptor. Here we review the role of the AHR in host-pathogen interactions, focusing on AHR sensing of different microbial classes, the ligands involved, responses elicited and disease outcomes. Moreover, we explore the therapeutic potential of targeting the AHR in the context of infection.

摘要

宿主与微生物的相遇以多种不同方式发生,并产生不同类型的结果。需要区分三种主要类型的微生物:(1)对宿主造成伤害且必须加以控制的病原体;(2)可被忽略但在数量较多时必须加以控制的环境微生物;(3)需要宿主支持的共生微生物群。最近的证据表明,芳烃受体(AHR)可感知并启动信号传导和基因表达,以应对大量微生物和感染情况。它最初被鉴定为一种结合外源性物质的受体。然而,随后发现它在包括免疫和炎症在内的众多生物学过程中起关键作用,最近被归类为一种模式识别受体。在此,我们综述AHR在宿主-病原体相互作用中的作用,重点关注AHR对不同微生物类别的感知、所涉及的配体、引发的反应和疾病结果。此外,我们探讨在感染背景下靶向AHR的治疗潜力。

相似文献

1
The role of the AHR in host-pathogen interactions.芳香烃受体在宿主-病原体相互作用中的作用。
Nat Rev Immunol. 2025 Mar;25(3):178-194. doi: 10.1038/s41577-024-01088-4. Epub 2024 Oct 16.
2
Cross-regulatory Circuit Between AHR and Microbiota.AHR 与微生物群之间的交叉调控回路。
Curr Drug Metab. 2019;20(1):4-8. doi: 10.2174/1389200219666180129151150.
3
Engagement of the Aryl Hydrocarbon Receptor in Mycobacterium tuberculosis-Infected Macrophages Has Pleiotropic Effects on Innate Immune Signaling.芳烃受体在结核分枝杆菌感染的巨噬细胞中的激活对固有免疫信号传导具有多效性作用。
J Immunol. 2015 Nov 1;195(9):4479-91. doi: 10.4049/jimmunol.1501141. Epub 2015 Sep 28.
4
Host/microbiota interactions-derived tryptophan metabolites modulate oxidative stress and inflammation via aryl hydrocarbon receptor signaling.宿主/微生物群相互作用产生的色氨酸代谢产物通过芳烃受体信号传导调节氧化应激和炎症。
Free Radic Biol Med. 2022 May 1;184:30-41. doi: 10.1016/j.freeradbiomed.2022.03.025. Epub 2022 Mar 31.
5
The Aryl Hydrocarbon Receptor as a Modulator of Anti-viral Immunity.芳香烃受体作为抗病毒免疫的调节剂。
Front Immunol. 2021 Mar 5;12:624293. doi: 10.3389/fimmu.2021.624293. eCollection 2021.
6
The role of aryl hydrocarbon receptor in the occurrence and development of periodontitis.芳香烃受体在牙周炎发生发展中的作用。
Front Immunol. 2024 Nov 6;15:1494570. doi: 10.3389/fimmu.2024.1494570. eCollection 2024.
7
Diet-Host-Microbiota Interactions Shape Aryl Hydrocarbon Receptor Ligand Production to Modulate Intestinal Homeostasis.饮食-宿主-微生物群相互作用塑造芳香烃受体配体的产生,以调节肠道内稳态。
Annu Rev Nutr. 2021 Oct 11;41:455-478. doi: 10.1146/annurev-nutr-043020-090050.
8
The Aryl Hydrocarbon Receptor (AHR) as a Potential Target for the Control of Intestinal Inflammation: Insights from an Immune and Bacteria Sensor Receptor.芳香烃受体(AHR)作为控制肠道炎症的潜在靶点:免疫和细菌传感器受体的见解。
Clin Rev Allergy Immunol. 2020 Dec;59(3):382-390. doi: 10.1007/s12016-020-08789-3.
9
Dietary Tryptophan-Mediated Aryl Hydrocarbon Receptor Activation by the Gut Microbiota Alleviates Escherichia coli-Induced Endometritis in Mice.饮食色氨酸通过肠道微生物群激活芳香烃受体可减轻大肠杆菌引起的小鼠子宫内膜炎。
Microbiol Spectr. 2022 Aug 31;10(4):e0081122. doi: 10.1128/spectrum.00811-22. Epub 2022 Jun 21.
10
Benzo(a)pyrene attenuates the pattern-recognition-receptor induced proinflammatory phenotype of murine macrophages by inducing IL-10 expression in an aryl hydrocarbon receptor-dependent manner.苯并(a)芘通过芳烃受体依赖性诱导白细胞介素-10 的表达来减轻模式识别受体诱导的小鼠巨噬细胞的促炎表型。
Toxicology. 2018 Nov 1;409:80-90. doi: 10.1016/j.tox.2018.07.011. Epub 2018 Jul 24.

引用本文的文献

1
Structural Features and In Vitro Antiviral Activities of Fungal Metabolites Sphaeropsidins A and B Against Bovine Coronavirus.真菌代谢产物球壳菌素A和B对牛冠状病毒的结构特征及体外抗病毒活性
Int J Mol Sci. 2025 Jul 22;26(15):7045. doi: 10.3390/ijms26157045.
2
Decoding Blastocystis-Driven Mechanisms in Gut Microbiota and Host Metabolism.解读肠道微生物群和宿主代谢中由芽囊原虫驱动的机制
Adv Sci (Weinh). 2025 May;12(17):e2416325. doi: 10.1002/advs.202416325. Epub 2025 Apr 4.
3
Insight into the Role of the Aryl Hydrocarbon Receptor in Bovine Coronavirus Infection by an Integrated Approach Combining In Vitro and In Silico Methods.

本文引用的文献

1
HIV Immunocapture Reveals Particles Expressed in Semen Under Integrase Strand Transfer Inhibitor-Based Therapy Are Largely Myeloid Cell-Derived and Disparate.HIV 免疫捕获显示,在基于整合酶链转移抑制剂的治疗下,精液中表达的颗粒主要来源于骨髓细胞,且具有多样性。
J Infect Dis. 2024 Jul 25;230(1):78-85. doi: 10.1093/infdis/jiae073.
2
Sustained AhR activity programs memory fate of early effector CD8 T cells.持续的 AhR 活性决定早期效应性 CD8 T 细胞的记忆命运。
Proc Natl Acad Sci U S A. 2024 Mar 12;121(11):e2317658121. doi: 10.1073/pnas.2317658121. Epub 2024 Mar 4.
3
Dietary environmental factors shape the immune defense against Cryptosporidium infection.
通过结合体外和计算机模拟方法的综合方法深入了解芳烃受体在牛冠状病毒感染中的作用
Microorganisms. 2025 Mar 4;13(3):579. doi: 10.3390/microorganisms13030579.
4
In Vitro Evaluation of Aryl Hydrocarbon Receptor Involvement in Feline Coronavirus Infection.芳烃受体参与猫冠状病毒感染的体外评估
Viruses. 2025 Feb 6;17(2):227. doi: 10.3390/v17020227.
5
Canine coronavirus infection is intensified by 2,3,7,8-tetrachlorodibenzo-p-dioxin.犬冠状病毒感染会因2,3,7,8-四氯二苯并对二恶英而加剧。
Arch Toxicol. 2025 May;99(5):2211-2223. doi: 10.1007/s00204-025-03981-w. Epub 2025 Feb 22.
饮食环境因素影响机体对隐孢子虫感染的免疫防御。
Cell Host Microbe. 2023 Dec 13;31(12):2038-2050.e4. doi: 10.1016/j.chom.2023.11.008. Epub 2023 Dec 4.
4
Targeting the aryl hydrocarbon receptor (AhR) with BAY 2416964: a selective small molecule inhibitor for cancer immunotherapy.针对芳基烃受体 (AhR) 的 BAY 2416964:一种用于癌症免疫治疗的选择性小分子抑制剂。
J Immunother Cancer. 2023 Nov;11(11). doi: 10.1136/jitc-2023-007495.
5
Endothelial AHR activity prevents lung barrier disruption in viral infection.内皮细胞 AHR 活性可防止病毒感染引起的肺屏障破坏。
Nature. 2023 Sep;621(7980):813-820. doi: 10.1038/s41586-023-06287-y. Epub 2023 Aug 16.
6
Identification of aryl hydrocarbon receptor as a barrier to HIV-1 infection and outgrowth in CD4 T cells.鉴定芳香烃受体作为 CD4 T 细胞中 HIV-1 感染和生长的屏障。
Cell Rep. 2023 Jun 27;42(6):112634. doi: 10.1016/j.celrep.2023.112634. Epub 2023 Jun 12.
7
isolates from atopic or healthy skin have opposite effect on skin cells: potential implication of the AHR pathway modulation.从特应性或健康皮肤中分离出的物质对皮肤细胞有相反的影响:AHR 通路调节的潜在意义。
Front Immunol. 2023 May 26;14:1098160. doi: 10.3389/fimmu.2023.1098160. eCollection 2023.
8
Aryl hydrocarbon receptor is a proviral host factor and a candidate pan-SARS-CoV-2 therapeutic target.芳香烃受体是一种前病毒宿主因子,也是候选的泛 SARS-CoV-2 治疗靶点。
Sci Adv. 2023 Jun 2;9(22):eadf0211. doi: 10.1126/sciadv.adf0211. Epub 2023 May 31.
9
Targeting the aryl hydrocarbon receptor by gut phenolic metabolites: A strategy towards gut inflammation.靶向肠道酚类代谢物的芳烃受体:一种针对肠道炎症的策略。
Redox Biol. 2023 May;61:102622. doi: 10.1016/j.redox.2023.102622. Epub 2023 Feb 1.
10
Tripartite interactions between filamentous Pf4 bacteriophage, Pseudomonas aeruginosa, and bacterivorous nematodes.丝状 Pf4 噬菌体、铜绿假单胞菌和食细菌线虫之间的三方相互作用。
PLoS Pathog. 2023 Feb 17;19(2):e1010925. doi: 10.1371/journal.ppat.1010925. eCollection 2023 Feb.