Institute of Health Sciences, Federal University of Mato Grosso, Sinop, MT, Brazil.
Department of Pharmacology, Institute of Biological Science, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Br J Pharmacol. 2019 Jun;176(12):2028-2048. doi: 10.1111/bph.14436. Epub 2018 Jul 31.
Arterial hypertension represents a serious public health problem, being a major cause of morbidity and mortality worldwide. The availability of many antihypertensive therapeutic strategies still fails to adequately treat around 20% of hypertensive patients, who are considered resistant to conventional treatment. In the pathogenesis of hypertension, immune system mechanisms are activated and both the innate and adaptive immune responses play a crucial role. However, what, when and how the immune system is triggered during hypertension development is still largely undefined. In this context, this review highlights scientific advances in the manipulation of the immune system in order to attenuate hypertension and end-organ damage. Here, we discuss the potential use of immunosuppressants and immunomodulators as pharmacological tools to control the activation of the immune system, by non-specific and specific mechanisms, to treat hypertension and improve end-organ damage. Nevertheless, more clinical trials should be performed with these drugs to establish their therapeutic efficacy, safety and risk-benefit ratio in hypertensive conditions. LINKED ARTICLES: This article is part of a themed section on Immune Targets in Hypertension. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v176.12/issuetoc.
动脉高血压是一个严重的公共健康问题,也是全世界发病率和死亡率的主要原因。尽管有许多抗高血压的治疗策略,但仍有大约 20%的高血压患者治疗效果不佳,被认为对常规治疗有抵抗。在高血压的发病机制中,免疫系统机制被激活,先天和适应性免疫反应都起着至关重要的作用。然而,免疫系统在高血压发展过程中何时以及如何被触发,在很大程度上仍未得到明确。在这方面,本文重点介绍了操纵免疫系统以减轻高血压和靶器官损伤的科学进展。在这里,我们讨论了免疫抑制剂和免疫调节剂作为药理学工具的潜在用途,通过非特异性和特异性机制来控制免疫系统的激活,以治疗高血压并改善靶器官损伤。然而,仍需要进行更多的临床试验来评估这些药物在高血压情况下的治疗效果、安全性和风险效益比。相关文章:本文是高血压免疫靶点专题的一部分。要查看该专题中的其他文章,请访问:http://onlinelibrary.wiley.com/doi/10.1111/bph.v176.12/issuetoc/。