• 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

高血压免疫机制的最新研究进展。

Update on Immune Mechanisms in Hypertension.

机构信息

Department of Medical Physiology, Texas A&M College of Medicine, Bryan, Texas, USA.

出版信息

Am J Hypertens. 2022 Oct 3;35(10):842-851. doi: 10.1093/ajh/hpac077.

DOI:10.1093/ajh/hpac077
PMID:35704473
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9527774/
Abstract

The contribution of immune cells in the initiation and maintenance of hypertension is undeniable. Several studies have established the association between hypertension, inflammation, and immune cells from the innate and adaptive immune systems. Here, we provide an update to our 2017 American Journal of Hypertension review on the overview of the cellular immune responses involved in hypertension. Further, we discuss the activation of immune cells and their contribution to the pathogenesis of hypertension in different in vivo models. We also highlight existing gaps in the field of hypertension that need attention. The main goal of this review is to provide a knowledge base for translational research to develop therapeutic strategies that can improve cardiovascular health in humans.

摘要

免疫细胞在高血压的发生和维持中的作用是不可否认的。有几项研究已经确立了高血压、炎症和先天及适应性免疫系统中的免疫细胞之间的关联。在这里,我们对 2017 年发表在《美国高血压杂志》上的综述进行了更新,概述了参与高血压的细胞免疫反应。此外,我们还讨论了免疫细胞的激活及其在不同体内模型中对高血压发病机制的贡献。我们还强调了高血压领域中需要关注的现有空白。本篇综述的主要目的是为转化研究提供一个知识库,以开发能够改善人类心血管健康的治疗策略。

相似文献

1
Update on Immune Mechanisms in Hypertension.高血压免疫机制的最新研究进展。
Am J Hypertens. 2022 Oct 3;35(10):842-851. doi: 10.1093/ajh/hpac077.
2
Innate immunity in hypertension.高血压的固有免疫。
Curr Hypertens Rep. 2014 Feb;16(2):413. doi: 10.1007/s11906-013-0413-9.
3
The interplay between Angiotensin II, TLR4 and hypertension.血管紧张素II、Toll样受体4与高血压之间的相互作用。
Pharmacol Res. 2017 Jun;120:88-96. doi: 10.1016/j.phrs.2017.03.017. Epub 2017 Mar 19.
4
Recent Advances in Immunity and Hypertension.免疫与高血压的最新进展
Am J Hypertens. 2017 Jul 1;30(7):643-652. doi: 10.1093/ajh/hpx011.
5
Are the innate and adaptive immune systems setting hypertension on fire?先天性和适应性免疫系统会引发高血压吗?
Pharmacol Res. 2017 Mar;117:377-393. doi: 10.1016/j.phrs.2017.01.010. Epub 2017 Jan 16.
6
Role of Inflammation and Immunity in Hypertension: Recent Epidemiological, Laboratory, and Clinical Evidence.炎症与免疫在高血压中的作用:近期的流行病学、实验室及临床证据
Curr Hypertens Rep. 2016 Mar;18(3):21. doi: 10.1007/s11906-016-0628-7.
7
Immune mechanisms in hypertension.高血压中的免疫机制。
High Blood Press Cardiovasc Prev. 2014 Dec;21(4):227-34. doi: 10.1007/s40292-014-0040-9. Epub 2014 Jan 21.
8
Novel adaptive and innate immunity targets in hypertension.高血压中的新型适应性免疫和固有免疫靶点。
Pharmacol Res. 2017 Jun;120:109-115. doi: 10.1016/j.phrs.2017.03.015. Epub 2017 Mar 20.
9
Innate immunity as the orchestrator of allergic airway inflammation and resolution in asthma.先天性免疫作为哮喘中过敏性气道炎症及缓解的协调者。
Int Immunopharmacol. 2017 Jul;48:43-54. doi: 10.1016/j.intimp.2017.04.027. Epub 2017 May 3.
10
Innate and Innate-Like Immune System in Hypertension and Vascular Injury.固有和固有样免疫系统在高血压和血管损伤中的作用。
Curr Hypertens Rep. 2019 Jan 18;21(1):4. doi: 10.1007/s11906-019-0907-1.

引用本文的文献

1
Relationship Between Dietary Inflammatory Index, Diets, and Cardiovascular Medication.饮食炎症指数、饮食与心血管药物之间的关系
Nutrients. 2025 May 2;17(9):1570. doi: 10.3390/nu17091570.
2
Prevention of hypertension-induced renal vascular dysfunction through a p66Shc-targeted mechanism.通过靶向p66Shc的机制预防高血压诱导的肾血管功能障碍。
Am J Physiol Renal Physiol. 2025 May 1;328(5):F693-F701. doi: 10.1152/ajprenal.00331.2024. Epub 2025 Apr 2.
3
Immunotherapy for hypertensive end-organ damage: a new therapeutic strategy.

本文引用的文献

1
Time restricted feeding decreases renal innate immune cells and blood pressure in hypertensive mice.限时喂养可减少高血压小鼠的肾脏固有免疫细胞和血压。
J Hypertens. 2022 Oct 1;40(10):1960-1968. doi: 10.1097/HJH.0000000000003200. Epub 2022 Jul 11.
2
Sex differences in TLR4 expression in SHR do not contribute to sex differences in blood pressure or the renal T cell profile.TLR4 在 SHR 中的表达存在性别差异,但不会导致血压或肾脏 T 细胞谱存在性别差异。
Am J Physiol Regul Integr Comp Physiol. 2022 Apr 1;322(4):R319-R325. doi: 10.1152/ajpregu.00237.2021. Epub 2022 Feb 2.
3
Manipulating CD4+ T Cell Pathways to Prevent Preeclampsia.
高血压性靶器官损害的免疫治疗:一种新的治疗策略。
Essays Biochem. 2025 Mar 25;0(0):EBC20243000. doi: 10.1042/EBC20243000.
4
The clinical significance of T-cell regulation in hypertension treatment.T细胞调节在高血压治疗中的临床意义。
Front Immunol. 2025 Feb 26;16:1550206. doi: 10.3389/fimmu.2025.1550206. eCollection 2025.
5
A comprehensive review on cardiovascular disorders development due to salt intake: an emphasis on policy implementation.关于盐摄入导致心血管疾病发展的综合综述:强调政策实施。
Health Res Policy Syst. 2025 Mar 11;23(1):32. doi: 10.1186/s12961-025-01305-z.
6
Salt sensitivity of blood pressure: mechanisms and sex-specific differences.血压的盐敏感性:机制及性别特异性差异
Nat Rev Cardiol. 2025 Feb 21. doi: 10.1038/s41569-025-01135-0.
7
Hypertension: A Continuing Public Healthcare Issue.高血压:一个持续存在的公共卫生问题。
Int J Mol Sci. 2024 Dec 26;26(1):123. doi: 10.3390/ijms26010123.
8
Improvement of the Immunity System Through Sports: Novel Regulatory Mechanisms for Hypertension.通过运动改善免疫系统:高血压的新型调节机制
Rev Cardiovasc Med. 2024 Oct 25;25(10):385. doi: 10.31083/j.rcm2510385. eCollection 2024 Oct.
9
Inflammatory Alterations to Renal Lymphatic Endothelial Cell Gene Expression in Mouse Models of Hypertension.高血压小鼠模型中肾脏淋巴内皮细胞基因表达的炎症改变。
Kidney Blood Press Res. 2024;49(1):588-604. doi: 10.1159/000539721. Epub 2024 Jul 22.
10
A new immune disease: systemic hypertension.一种新的免疫性疾病:系统性高血压。
Clin Kidney J. 2023 Mar 23;16(9):1403-1419. doi: 10.1093/ckj/sfad059. eCollection 2023 Sep.
调控CD4+ T细胞通路以预防子痫前期。
Front Bioeng Biotechnol. 2022 Jan 12;9:811417. doi: 10.3389/fbioe.2021.811417. eCollection 2021.
4
A Kidney-Targeted Nanoparticle to Augment Renal Lymphatic Density Decreases Blood Pressure in Hypertensive Mice.一种靶向肾脏的纳米颗粒可增加肾淋巴管密度,从而降低高血压小鼠的血压。
Pharmaceutics. 2021 Dec 30;14(1):84. doi: 10.3390/pharmaceutics14010084.
5
Splenocyte transfer from hypertensive donors eliminates premenopausal female protection from ANG II-induced hypertension.高血压供体的脾细胞转移消除了绝经前女性对 ANG II 诱导的高血压的保护作用。
Am J Physiol Renal Physiol. 2022 Mar 1;322(3):F245-F257. doi: 10.1152/ajprenal.00369.2021. Epub 2022 Jan 10.
6
DAMPs are able to skew CD4 T cell subsets and increase the inflammatory profile in pregnant women with preeclampsia.DAMPs 能够使 CD4 T 细胞亚群发生倾斜,并增加子痫前期孕妇的炎症特征。
J Reprod Immunol. 2022 Feb;149:103470. doi: 10.1016/j.jri.2021.103470. Epub 2021 Dec 26.
7
A newly intervention strategy in preeclampsia: Targeting PD-1/Tim-3 signaling pathways to modulate the polarization of decidual macrophages.子痫前期的新干预策略:靶向 PD-1/Tim-3 信号通路调节胎盘巨噬细胞的极化。
FASEB J. 2022 Jan;36(1):e22073. doi: 10.1096/fj.202101306R.
8
Macrophage 12(S)-HETE Enhances Angiotensin II-Induced Contraction by a BLT2 (Leukotriene B Type-2 Receptor) and TP (Thromboxane Receptor)-Mediated Mechanism in Murine Arteries.巨噬细胞 12(S)-HETE 通过 BLT2(白三烯 B 型-2 受体)和 TP(血栓素受体)介导的机制增强血管紧张素 II 诱导的小鼠动脉收缩。
Hypertension. 2022 Jan;79(1):104-114. doi: 10.1161/HYPERTENSIONAHA.121.17824. Epub 2021 Nov 17.
9
Altering Early Life Gut Microbiota Has Long-Term Effect on Immune System and Hypertension in Spontaneously Hypertensive Rats.改变早期生命阶段的肠道微生物群对自发性高血压大鼠的免疫系统和高血压具有长期影响。
Front Physiol. 2021 Oct 29;12:752924. doi: 10.3389/fphys.2021.752924. eCollection 2021.
10
Systemic administration of choline acetyltransferase decreases blood pressure in murine hypertension.胆碱乙酰转移酶全身给药可降低高血压小鼠的血压。
Mol Med. 2021 Oct 21;27(1):133. doi: 10.1186/s10020-021-00380-6.