Suppr超能文献

天然免疫中的 Toll 样受体 (TLRs)、NOD 样受体 (NLRs) 和 RIG-I 样受体 (RLRs)。TLRs、NLRs 和 RLRs 配体作为造血疾病的免疫治疗药物。

Toll-Like Receptors (TLRs), NOD-Like Receptors (NLRs), and RIG-I-Like Receptors (RLRs) in Innate Immunity. TLRs, NLRs, and RLRs Ligands as Immunotherapeutic Agents for Hematopoietic Diseases.

机构信息

Department and Clinic of Hematology, Blood Neoplasms and Bone Marrow Transplantation, Wroclaw Medical University, 50-367 Wroclaw, Poland.

出版信息

Int J Mol Sci. 2021 Dec 13;22(24):13397. doi: 10.3390/ijms222413397.

Abstract

The innate immune system plays a pivotal role in the first line of host defense against infections and is equipped with patterns recognition receptors (PRRs) that recognize pathogen-associated molecular patterns (PAMPs) and damage-associated molecular patterns (DAMPs). Several classes of PRRS, including Toll-like receptors (TLRs), NOD-like receptors (NLRs), and RIG-I-like receptors (RLRs) recognize distinct microbial components and directly activate immune cells. TLRs are transmembrane receptors, while NLRs and RLRs are intracellular molecules. Exposure of immune cells to the ligands of these receptors activates intracellular signaling cascades that rapidly induce the expression of a variety of overlapping and unique genes involved in the inflammatory and immune responses. The innate immune system also influences pathways involved in cancer immunosurveillance. Natural and synthetic agonists of TLRs, NLRs, or RLRs can trigger cell death in malignant cells, recruit immune cells, such as DCs, CD8+ T cells, and NK cells, into the tumor microenvironment, and are being explored as promising adjuvants in cancer immunotherapies. In this review, we provide a concise overview of TLRs, NLRs, and RLRs: their structure, functions, signaling pathways, and regulation. We also describe various ligands for these receptors and their possible application in treatment of hematopoietic diseases.

摘要

固有免疫系统在宿主抗感染的第一道防线中起着至关重要的作用,它配备了模式识别受体 (PRRs),可以识别病原体相关分子模式 (PAMPs) 和损伤相关分子模式 (DAMPs)。几类 PRRs,包括 Toll 样受体 (TLRs)、NOD 样受体 (NLRs) 和 RIG-I 样受体 (RLRs),识别不同的微生物成分,并直接激活免疫细胞。TLRs 是跨膜受体,而 NLRs 和 RLRs 是细胞内分子。免疫细胞暴露于这些受体的配体激活细胞内信号级联反应,迅速诱导参与炎症和免疫反应的多种重叠和独特基因的表达。固有免疫系统还影响参与癌症免疫监视的途径。TLRs、NLRs 或 RLRs 的天然和合成激动剂可以触发恶性细胞死亡,招募免疫细胞,如 DCs、CD8+T 细胞和 NK 细胞,进入肿瘤微环境,并被探索作为癌症免疫疗法的有前途的佐剂。在这篇综述中,我们提供了 TLRs、NLRs 和 RLRs 的简要概述:它们的结构、功能、信号通路和调节。我们还描述了这些受体的各种配体及其在治疗造血疾病中的可能应用。

相似文献

2
Pattern-recognition receptors in endometriosis: A narrative review.
Front Immunol. 2023 Mar 23;14:1161606. doi: 10.3389/fimmu.2023.1161606. eCollection 2023.
3
Progresses on three pattern recognition receptor families (TLRs, RLRs and NLRs) in teleost.
Dev Comp Immunol. 2021 Sep;122:104131. doi: 10.1016/j.dci.2021.104131. Epub 2021 May 19.
4
The molecular mechanisms of signaling by cooperative assembly formation in innate immunity pathways.
Mol Immunol. 2017 Jun;86:23-37. doi: 10.1016/j.molimm.2017.02.012. Epub 2017 Feb 27.
5
The hepatocyte in the innate immunity.
Virology. 2022 Nov;576:111-116. doi: 10.1016/j.virol.2022.09.011. Epub 2022 Oct 6.
7
TLRs/NLRs: Shaping the landscape of host immunity.
Int Rev Immunol. 2018 Jan 2;37(1):3-19. doi: 10.1080/08830185.2017.1397656. Epub 2017 Dec 1.
8
Pathogen recognition in the innate immune response.
Biochem J. 2009 Apr 28;420(1):1-16. doi: 10.1042/BJ20090272.
9
Mechanisms and pathways of innate immune activation and regulation in health and cancer.
Hum Vaccin Immunother. 2014;10(11):3270-85. doi: 10.4161/21645515.2014.979640.
10
Recognition of bacterial infection by innate immune sensors.
Crit Rev Microbiol. 2013 Aug;39(3):229-46. doi: 10.3109/1040841X.2012.706249. Epub 2012 Aug 6.

引用本文的文献

2
Damage-associated molecular patterns (DAMPs) in diseases: implications for therapy.
Mol Biomed. 2025 Aug 29;6(1):60. doi: 10.1186/s43556-025-00305-3.
3
Fabry Disease Beyond Storage: The Role of Inflammation in Disease Progression.
Int J Mol Sci. 2025 Jul 22;26(15):7054. doi: 10.3390/ijms26157054.
4
Biological Function of Medium-Chain Fatty Acids and Their Application in Aquatic Animals: A Review.
Animals (Basel). 2025 Aug 6;15(15):2294. doi: 10.3390/ani15152294.
6
Intestinal ischemia-reperfusion and blood-brain barrier compromise: pathways to cognitive dysfunction.
Front Neurosci. 2025 Jul 15;19:1597170. doi: 10.3389/fnins.2025.1597170. eCollection 2025.
7
Emerging highly pathogenic H5N1 influenza triggers fibrotic remodeling in human airway organoids.
Emerg Microbes Infect. 2025 Dec;14(1):2532684. doi: 10.1080/22221751.2025.2532684. Epub 2025 Jul 25.
8
Innate immune mechanisms of infection: what we know and potential conserved mechanisms affecting sleep during infection.
Neurobiol Sleep Circadian Rhythms. 2025 Apr 21;18(Suppl):100121. doi: 10.1016/j.nbscr.2025.100121. eCollection 2025 May.
9
Cell surface Toll-like receptor polymorphisms influence and ectoparasite infections in striped hamsters.
iScience. 2025 Jun 13;28(7):112883. doi: 10.1016/j.isci.2025.112883. eCollection 2025 Jul 18.
10
Interferon in Liver Diseases: Recent Advances.
Adv Ther. 2025 Jul 17. doi: 10.1007/s12325-025-03291-8.

本文引用的文献

1
TIRAP in the Mechanism of Inflammation.
Front Immunol. 2021 Jul 8;12:697588. doi: 10.3389/fimmu.2021.697588. eCollection 2021.
2
Role of Immunomodulation of BCG Therapy on AML Remission.
Int Med Case Rep J. 2021 Feb 25;14:115-119. doi: 10.2147/IMCRJ.S296387. eCollection 2021.
3
Ferroptosis, necroptosis, and pyroptosis in anticancer immunity.
J Hematol Oncol. 2020 Aug 10;13(1):110. doi: 10.1186/s13045-020-00946-7.
4
RIG-I-like receptors: their regulation and roles in RNA sensing.
Nat Rev Immunol. 2020 Sep;20(9):537-551. doi: 10.1038/s41577-020-0288-3. Epub 2020 Mar 13.
5
Toll-like Receptors and the Control of Immunity.
Cell. 2020 Mar 19;180(6):1044-1066. doi: 10.1016/j.cell.2020.02.041. Epub 2020 Mar 11.
6
Targeting innate sensing in the tumor microenvironment to improve immunotherapy.
Cell Mol Immunol. 2020 Jan;17(1):13-26. doi: 10.1038/s41423-019-0341-y. Epub 2019 Dec 16.
7
Pyroptosis: A new frontier in cancer.
Biomed Pharmacother. 2020 Jan;121:109595. doi: 10.1016/j.biopha.2019.109595. Epub 2019 Nov 9.
8
DAMP-sensing receptors in sterile inflammation and inflammatory diseases.
Nat Rev Immunol. 2020 Feb;20(2):95-112. doi: 10.1038/s41577-019-0215-7. Epub 2019 Sep 26.
9
RNA Helicase LGP2 Negatively Regulates RIG-I Signaling by Preventing TRIM25-Mediated Caspase Activation and Recruitment Domain Ubiquitination.
J Interferon Cytokine Res. 2019 Nov;39(11):669-683. doi: 10.1089/jir.2019.0059. Epub 2019 Jun 25.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验