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白细胞介素-18作为急性心肌梗死和心力衰竭的治疗靶点。

Interleukin-18 as a therapeutic target in acute myocardial infarction and heart failure.

作者信息

O'Brien Laura C, Mezzaroma Eleonora, Van Tassell Benjamin W, Marchetti Carlo, Carbone Salvatore, Abbate Antonio, Toldo Stefano

机构信息

Department of Physiology and Biophysics, Virginia Commonwealth University, Richmond, Virginia, United States of America.

Victoria Johnson Research Laboratories, Virginia Commonwealth University, Richmond, Virginia, United States of America Virginia Commonwealth University Pauley Heart Center, School of Medicine, Virginia Commonwealth University, Richmond, Virginia, United States of America Pharmacotherapy and Outcome Sciences, School of Pharmacy, Virginia Commonwealth University, Richmond, Virginia, United States of America.

出版信息

Mol Med. 2014 Jun 12;20(1):221-9. doi: 10.2119/molmed.2014.00034.

Abstract

Interleukin 18 (IL-18) is a proinflammatory cytokine in the IL-1 family that has been implicated in a number of disease states. In animal models of acute myocardial infarction (AMI), pressure overload, and LPS-induced dysfunction, IL-18 regulates cardiomyocyte hypertrophy and induces cardiac contractile dysfunction and extracellular matrix remodeling. In patients, high IL-18 levels correlate with increased risk of developing cardiovascular disease (CVD) and with a worse prognosis in patients with established CVD. Two strategies have been used to counter the effects of IL-18:IL-18 binding protein (IL-18BP), a naturally occurring protein, and a neutralizing IL-18 antibody. Recombinant human IL-18BP (r-hIL-18BP) has been investigated in animal studies and in phase I/II clinical trials for psoriasis and rheumatoid arthritis. A phase II clinical trial using a humanized monoclonal IL-18 antibody for type 2 diabetes is ongoing. Here we review the literature regarding the role of IL-18 in AMI and heart failure and the evidence and challenges of using IL-18BP and blocking IL-18 antibodies as a therapeutic strategy in patients with heart disease.

摘要

白细胞介素18(IL-18)是IL-1家族中的一种促炎细胞因子,与多种疾病状态有关。在急性心肌梗死(AMI)、压力超负荷和脂多糖诱导的功能障碍的动物模型中,IL-18调节心肌细胞肥大,并诱导心脏收缩功能障碍和细胞外基质重塑。在患者中,高IL-18水平与患心血管疾病(CVD)风险增加以及已患CVD患者的不良预后相关。已经采用两种策略来对抗IL-18的作用:IL-18结合蛋白(IL-18BP),一种天然存在的蛋白质,以及一种中和性IL-18抗体。重组人IL-18BP(r-hIL-18BP)已在动物研究以及针对银屑病和类风湿性关节炎的I/II期临床试验中进行了研究。一项使用人源化单克隆IL-18抗体治疗2型糖尿病的II期临床试验正在进行。在此,我们综述了关于IL-18在AMI和心力衰竭中的作用以及使用IL-18BP和阻断IL-18抗体作为心脏病患者治疗策略的证据和挑战的文献。

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本文引用的文献

1
NLRP3 inflammasome as a novel player in myocardial infarction.
Int Heart J. 2014;55(2):101-5. doi: 10.1536/ihj.13-388. Epub 2014 Mar 14.
2
Interleukin-18 mediates interleukin-1-induced cardiac dysfunction.
Am J Physiol Heart Circ Physiol. 2014 Apr 1;306(7):H1025-31. doi: 10.1152/ajpheart.00795.2013. Epub 2014 Feb 14.
3
Anti-inflammatory strategies for ventricular remodeling following ST-segment elevation acute myocardial infarction.
J Am Coll Cardiol. 2014 Apr 29;63(16):1593-603. doi: 10.1016/j.jacc.2014.01.014. Epub 2014 Feb 13.
4
Formation of the inflammasome in acute myocarditis.
Int J Cardiol. 2014 Feb 15;171(3):e119-21. doi: 10.1016/j.ijcard.2013.12.137. Epub 2014 Jan 4.
5
A novel pharmacologic inhibitor of the NLRP3 inflammasome limits myocardial injury after ischemia-reperfusion in the mouse.
J Cardiovasc Pharmacol. 2014 Apr;63(4):316-322. doi: 10.1097/FJC.0000000000000053.
8
Targeting interleukin-1 in heart disease.
Circulation. 2013 Oct 22;128(17):1910-23. doi: 10.1161/CIRCULATIONAHA.113.003199.
9
10
IL-1 induces proinflammatory leukocyte infiltration and regulates fibroblast phenotype in the infarcted myocardium.
J Immunol. 2013 Nov 1;191(9):4838-48. doi: 10.4049/jimmunol.1300725. Epub 2013 Sep 27.

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