Targeting the immune system to treat hypertension: where are we?
- PMID: 25036747
- DOI: 10.1097/MNH.0000000000000052
Targeting the immune system to treat hypertension: where are we?
Abstract
Purpose of review: Research over the past decade has significantly deepened our understanding of mechanisms that drive the development of hypertension. In particular, a novel paradigm of inflammation as a common mediator of cardiovascular and kidney disease has emerged. This review will summarize the role of the immune system in cardiovascular disease, explore some of the most promising new therapeutic directions and consider their potential as new treatments for hypertension.
Recent findings: Recent data continue to demonstrate that targeting the immune system can prevent hypertension in a variety of experimental models. Tempering the enthusiasm for a long-awaited new approach to treating hypertension is decades of clinical data, showing that classic immunosuppression regimens are associated with significant side-effects - including cardiovascular disease - that effectively preclude their use in the setting of chronic hypertension. New, more specific therapies are being developed that target cytokines including IL-17, IL-6 and TNFα.
Summary: Preclinical data convincingly demonstrate a key role for the immune system and specific cytokine mediators. Several biotherapeutics targeting these pathways are on the market and more are in development. Side-effects, however, continue to resemble those of classic immunosuppressants, highlighting the challenge of translating these research advances into new therapies for hypertension.
Video abstract: http://links.lww.com/CONH/A9.
Similar articles
-
Relevance of Immune-Sympathetic Nervous System Interplay for the Development of Hypertension.Adv Exp Med Biol. 2016;884:37-43. doi: 10.1007/5584_2015_169. Adv Exp Med Biol. 2016. PMID: 26453069 Review.
-
The immune system in hypertension.Trans Am Clin Climatol Assoc. 2014;125:130-38; discussion 138-40. Trans Am Clin Climatol Assoc. 2014. PMID: 25125726 Free PMC article. Review.
-
Novel Pathophysiological Mechanisms in Hypertension.Adv Exp Med Biol. 2017;956:21-35. doi: 10.1007/5584_2016_96. Adv Exp Med Biol. 2017. PMID: 27981434 Review.
-
Cytokine networking of innate immunity cells: a potential target of therapy.Clin Sci (Lond). 2014 May;126(9):593-612. doi: 10.1042/CS20130497. Clin Sci (Lond). 2014. PMID: 24450743 Review.
-
Role of the immune system in hypertensive target organ damage.Trends Cardiovasc Med. 2009 Oct;19(7):242-6. doi: 10.1016/j.tcm.2010.02.004. Trends Cardiovasc Med. 2009. PMID: 20382349 Review.
Cited by
-
Antiglycation Activities and Common Mechanisms Mediating Vasculoprotective Effect of Quercetin and Chrysin in Metabolic Syndrome.Evid Based Complement Alternat Med. 2020 Jul 27;2020:3439624. doi: 10.1155/2020/3439624. eCollection 2020. Evid Based Complement Alternat Med. 2020. PMID: 32802123 Free PMC article.
-
Hydrogen Sulfide Attenuates Hypertensive Inflammation via Regulating Connexin Expression in Spontaneously Hypertensive Rats.Med Sci Monit. 2018 Feb 27;24:1205-1218. doi: 10.12659/msm.908761. Med Sci Monit. 2018. PMID: 29485979 Free PMC article.
-
Novel adaptive and innate immunity targets in hypertension.Pharmacol Res. 2017 Jun;120:109-115. doi: 10.1016/j.phrs.2017.03.015. Epub 2017 Mar 20. Pharmacol Res. 2017. PMID: 28336371 Free PMC article. Review.
-
Prediction of marker genes associated with hypertension by bioinformatics analyses.Int J Mol Med. 2017 Jul;40(1):137-145. doi: 10.3892/ijmm.2017.3000. Epub 2017 May 25. Int J Mol Med. 2017. PMID: 28560446 Free PMC article.
-
Review Article on Molecular Mechanism of Regulation of Hypertension by Macro-elements (Na, K, Ca and Mg), Micro-elements/Trace Metals (Zn and Cu) and Toxic Elements (Pb and As).Biol Trace Elem Res. 2024 Apr;202(4):1477-1502. doi: 10.1007/s12011-023-03784-z. Epub 2023 Jul 31. Biol Trace Elem Res. 2024. PMID: 37523058 Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous