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高血压病理生理学中的免疫机制。

Immune mechanisms in the pathophysiology of hypertension.

机构信息

Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, USA.

Department of Medicine, Division of Clinical Pharmacology, Vanderbilt University Medical Center, Nashville, TN, USA.

出版信息

Nat Rev Nephrol. 2024 Aug;20(8):530-540. doi: 10.1038/s41581-024-00838-w. Epub 2024 Apr 24.

DOI:10.1038/s41581-024-00838-w
PMID:38658669
Abstract

Hypertension is a leading risk factor for morbidity and mortality worldwide. Despite current anti-hypertensive therapies, most individuals with hypertension fail to achieve adequate blood pressure control. Moreover, even with adequate control, a residual risk of cardiovascular events and associated organ damage remains. These findings suggest that current treatment modalities are not addressing a key element of the underlying pathology. Emerging evidence implicates immune cells as key mediators in the development and progression of hypertension. In this Review, we discuss our current understanding of the diverse roles of innate and adaptive immune cells in hypertension, highlighting key findings from human and rodent studies. We explore mechanisms by which these immune cells promote hypertensive pathophysiology, shedding light on their multifaceted involvement. In addition, we highlight advances in our understanding of autoimmunity, HIV and immune checkpoints that provide valuable insight into mechanisms of chronic and dysregulated inflammation in hypertension.

摘要

高血压是全球发病率和死亡率的主要危险因素。尽管有目前的抗高血压治疗方法,但大多数高血压患者仍无法达到足够的血压控制。此外,即使血压得到充分控制,心血管事件和相关器官损害的残余风险仍然存在。这些发现表明,目前的治疗方法并没有解决潜在病理的一个关键因素。新出现的证据表明,免疫细胞是高血压发生和发展的关键介质。在这篇综述中,我们讨论了我们目前对先天和适应性免疫细胞在高血压中的多种作用的理解,重点介绍了来自人类和啮齿动物研究的关键发现。我们探讨了这些免疫细胞促进高血压病理生理学的机制,阐明了它们多方面的参与。此外,我们还强调了我们对自身免疫、HIV 和免疫检查点的理解的进展,这些进展为高血压中慢性和失调炎症的机制提供了有价值的见解。

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本文引用的文献

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CD28 T cells in aging and diseases: From biology to assessment and intervention.衰老和疾病中的 CD28 T 细胞:从生物学到评估和干预。
Int Immunopharmacol. 2024 Apr 20;131:111807. doi: 10.1016/j.intimp.2024.111807. Epub 2024 Mar 12.
2
The Association of Psoriasis, Diabetes Mellitus, and Hypertension: A Meta-Analysis.银屑病、糖尿病和高血压的关联:一项荟萃分析。
Cureus. 2023 Nov 15;15(11):e48855. doi: 10.7759/cureus.48855. eCollection 2023 Nov.
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P2RX7 gene knockout or antagonism reduces angiotensin II-induced hypertension, vascular injury and immune cell activation.
揭示炎性细胞因子与高血压肾病之间的因果关系:孟德尔随机化分析
Int Urol Nephrol. 2025 Jul 23. doi: 10.1007/s11255-025-04674-0.
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The immune system in cardiovascular diseases: from basic mechanisms to therapeutic implications.心血管疾病中的免疫系统:从基本机制到治疗意义
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Immunotherapy for hypertensive end-organ damage: a new therapeutic strategy.高血压性靶器官损害的免疫治疗:一种新的治疗策略。
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GWAS for Defining the Pathogenesis of Hypertension: Have They Delivered?全基因组关联研究在明确高血压发病机制中的作用:它们实现目标了吗?
Hypertension. 2025 Apr;82(4):573-582. doi: 10.1161/HYPERTENSIONAHA.124.23451. Epub 2025 Feb 12.
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Bone Marrow Niche in Cardiometabolic Disease: Mechanisms and Therapeutic Potential.心血管代谢疾病中的骨髓微环境:机制与治疗潜力
Circ Res. 2025 Jan 31;136(3):325-353. doi: 10.1161/CIRCRESAHA.124.323778. Epub 2025 Jan 30.
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Recent advances on immunity and hypertension: the new cells on the kidney block.免疫与高血压的最新进展:肾脏中的新细胞阻滞
Am J Physiol Renal Physiol. 2025 Mar 1;328(3):F301-F315. doi: 10.1152/ajprenal.00309.2024. Epub 2025 Jan 24.
9
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P2RX7 基因敲除或拮抗可降低血管紧张素 II 诱导的高血压、血管损伤和免疫细胞激活。
J Hypertens. 2023 Nov 1;41(11):1701-1712. doi: 10.1097/HJH.0000000000003520. Epub 2023 Jul 27.
4
CRISPR screens decode cancer cell pathways that trigger γδ T cell detection.CRISPR 筛选解码触发 γδ T 细胞检测的癌细胞途径。
Nature. 2023 Sep;621(7977):188-195. doi: 10.1038/s41586-023-06482-x. Epub 2023 Aug 30.
5
Angiotensin II-Induced Memory γδ T Cells Sensitize Mice to a Mild Hypertensive Stimulus.血管紧张素 II 诱导的记忆性γδ T 细胞使小鼠对轻度高血压刺激敏感。
Am J Hypertens. 2023 Oct 13;36(11):619-628. doi: 10.1093/ajh/hpad072.
6
Immune Profiling Reveals Decreases in Circulating Regulatory and Exhausted T Cells in Human Hypertension.免疫谱分析揭示人类高血压患者循环调节性T细胞和耗竭性T细胞减少。
JACC Basic Transl Sci. 2023 Jan 4;8(3):319-336. doi: 10.1016/j.jacbts.2022.09.007. eCollection 2023 Mar.
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