[1]刘君宇 张敏 彭建强.白介素-37在心血管疾病中的研究进展[J].心血管病学进展,2022,(2):120.[doi:10.16806/j.cnki,issn.1004-3934.2022.02.007]
 LIU Junyu,ZHANG Min,PENG Jianqiang.Interleukin-37 in Cardiovascular Disease[J].Advances in Cardiovascular Diseases,2022,(2):120.[doi:10.16806/j.cnki,issn.1004-3934.2022.02.007]
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白介素-37在心血管疾病中的研究进展()
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《心血管病学进展》[ISSN:51-1187/R/CN:1004-3934]

卷:
期数:
2022年2期
页码:
120
栏目:
综述
出版日期:
2022-02-25

文章信息/Info

Title:
Interleukin-37 in Cardiovascular Disease
作者:
刘君宇1 张敏1 彭建强2
(1.湖南师范大学附属第一医院(湖南省人民医院)
Author(s):
LIU Junyu1 ZHANG Min1 PENG Jianqiang2
(1.The First Affiliated Hospital of Hunan Normal University(Hunan Provincial Peoples Hospital),Clinical Medical Research Center for Heart Failure of Hunan Province,Changsha 410005,Hunan,China; 2.Department of Cardiology,Hunan Provincial Peoples Hospital,The First Affiliated Hospital of Hunan Normal University,Clinical Medical Research Center for Heart Failure of Hunan Province,Changsha 410005,Hunan,China)
关键词:
白介素-37炎症心血管疾病
Keywords:
Interleukin-37InflammatoryCardiovascular diseases
DOI:
10.16806/j.cnki,issn.1004-3934.2022.02.007
摘要:
越来越多的证据表明,炎症与心血管疾病的发病机制和预后密切相关,炎症标志物是心血管疾病不良临床结局的预测因子。过度的炎症会导致不利的左心室重塑、心力衰竭和心血管不良事件的发生,而适当、及时的炎症反应被认为是改善心血管疾病预后的关键因素之一。白介素-37是一种经典的抗炎因子,其参与心血管疾病炎症反应的多个环节,现总结相关研究,旨在阐明白介素-37和心血管疾病的关系,并展望白介素-37在心血管疾病中的治疗价值。
Abstract:
More and more evidence shows that inflammation is closely related to the pathogenesis and prognosis of cardiovascular diseases,and inflammatory markers are predictors of adverse clinical outcomes in cardiovascular diseases. Excessive inflammation can lead to adverse left ventricular remodeling,heart failure and cardiovascular adverse events. At present,appropriate and timely regulation of inflammatory response is considered to be one of the key factors to improve the prognosis of cardiovascular diseases. Interleukin-37 is a classical inflammatory factor,which is involved in many links of inflammatory response in cardiovascular disease. This paper aims to clarify the relationship between interleukin-37 and cardiovascular disease,summarize relevant studies,and look into the therapeutic value of interleukin-37 in cardiovascular disease

参考文献/References:


[1] 胡盛寿,高润霖,刘力生,等. 《中国心血管病报告2018》概要[J]. 中国循环杂志,2019,34(3):209-220.

[2] Golia E,Limongelli G,Natale F,et al. Inflammation and cardiovascular disease:from pathogenesis to therapeutic target[J]. Curr Atheroscler Rep,2014,16(9):435.

[3] Zhuang X,Wu B,Li J,et al. The emerging role of interleukin-37 in cardiovascular diseases[J]. Immun Inflamm Dis,2017,5(3):373-379.

[4] Dunn E,Sims JE,Nicklin MJ,et al. Annotating genes with potential roles in the immune system:six new members of the IL-1 family[J]. Trends Immunol,2001,22(10):533-536.

[5] Lunding L,Webering S,Vock C,et al. IL-37 requires IL-18Rα and SIGIRR/IL-1R8 to diminish allergic airway inflammation in mice[J]. Allergy,2015,70(4):366-373.

[6] Taylor SL,Renshaw BR,Garka KE,et al. Genomic organization of the interleukin-1 locus[J]. Genomics,2002,79(5):726-733.

[7] Kumar S,Hanning CR,Brigham-Burke MR,et al. Interleukin-1F7B (IL-1H4/IL-1F7) is processed by caspase-1 and mature IL-1F7B binds to the IL-18 receptor but does not induce IFN-gamma production[J]. Cytokine,2002,18(2):61-71.

[8] Nold MF,Nold-Petry CA,Zepp JA,et al. IL-37 is a fundamental inhibitor of innate immunity[J]. Nat Immunol,2010,11(11):1014-1022.

[9] Cavalli G,DInarello CA. Suppression of inflammation and acquired immunity by IL-37[J]. Immunol Rev,2018,281(1):179-190.

[10] Rafieian-Kopaei M,Setorki M,Doudi M,et al. Atherosclerosis:process,indicators,risk factors and new hopes[J]. Int J Prev Med,2014,5(8):927-946.

[11] Xie Y,Li Y,Cai X,et al. Interleukin-37 suppresses ICAM-1 expression in parallel with NF-κB down-regulation following TLR2 activation of human coronary artery endothelial cells[J]. Int Immunopharmacol,2016,38:26-30.

[12] Hong YJ,Jeong MH,Ahn Y,et al. Relationship between peripheral monocytosis and nonrecovery of left ventricular function in patients with left ventricular dysfunction complicated with acute myocardial infarction[J]. Circ J,2007,71(8):1219-1224.

[13] Wu BW,Zeng QT,Meng K,et al. The potential role of IL-37 in atherosclerosis[J]. Pharmazie,2013,68(11):857-860.

[14] Zhou P,Li Q,Su S,et al. Interleukin 37 Suppresses M1 Macrophage Polarization Through Inhibition of the Notch1 and Nuclear Factor Kappa B Pathways[J]. Front Cell Dev Biol,2020,8:56.

[15] McCurdy S,Baumer Y,Toulmin E,et al. Macrophage-specific expression of il-37 in hyperlipidemic mice attenuates atherosclerosis[J]. J Immunol,2017,199(10):3604-3613.

[16] Ji Q,Meng K,Yu K,et al. Exogenous interleukin 37 ameliorates atherosclerosis via inducing the Treg response in ApoE-deficient mice[J]. Sci Rep,2017,7(1):3310.

[17] Yu K,Min X,Lin Y,et al. Increased IL-37 concentrations in patients with arterial calcification[J]. Clin Chim Acta,2016,461:19-24.

[18] Liu J,Lin J,He S,et al. Transgenic overexpression of IL-37 protects against atherosclerosis and strengthens plaque stability[J]. Cell Physiol Biochem,2018,45(3):1034-1050.

[19] Huang J,Hou FL,Zhang AY,et al. Protective effect of the polarity of macrophages regulated by IL-37 on atherosclerosis[J]. Genet Mol Res,2016,15(2):gmr7616.

[20] Chai M,Ji Q,Zhang H,et al. The protective effect of interleukin-37 on vascular calcification and atherosclerosis in apolipoprotein e-deficient mice with diabetes[J]. J Interferon Cytokine Res,2015,35(7):530-539.

[21] Fang L,Moore XL,Dart AM,et al. Systemic inflammatory response following acute myocardial infarction[J]. J Geriatr Cardiol,2015,12(3):305-312.

[22] Ji Q,Zeng Q,Huang Y,et al. Elevated plasma IL-37,IL-18,and IL-18BP concentrations in patients with acute coronary syndrome[J]. Mediators Inflamm,2014,2014:165742.

[23] Li J,Zhang W,Yao H,et al. Therapeutic effects of interleukin-37 and induced cardiosphere on treating myocardial ischemia-reperfusion injury[J]. Int Immunopharmacol,2020,88:106719.

[24] Wu B,Meng K,Ji Q,et al. Interleukin-37 ameliorates myocardial ischaemia/reperfusion injury in mice[J]. Clin Exp Immunol,2014,176(3):438-451.

[25] Yang T,Fang F,Chen Y,et al. Elevated plasma interleukin-37 playing an important role in acute coronary syndrome through suppression of ROCK activation[J]. Oncotarget,2017,8(6):9686-9695.

[26] Mao X,Zhu R,Zhang F,et al. IL-37 plays a beneficial role in patients with acute coronary syndrome[J]. Mediators Inflamm,2019,2019:9515346.

[27] Xu D,Wang A,Jiang F,et al. Effects of interleukin-37 on cardiac function after myocardial infarction in mice[J]. Int J Clin Exp Pathol,2015,8(5):5247-5251.

[28] Zhu R,Sun H,Yu K,et al. Interleukin-37 and dendritic cells treated with interleukin-37 plus troponin I ameliorate cardiac remodeling after myocardial infarction[J]. J Am Heart Assoc,2016,5(12):e004406.

[29] Chugh SS,Havmoeller R,Narayanan K,et al. Worldwide epidemiology of atrial fibrillation:a Global Burden of Disease 2010 Study[J]. Circulation,2014,129(8):837-847.

[30] Aviles RJ,Martin DO,Apperson-Hansen C,et al. Inflammation as a risk factor for atrial fibrillation[J]. Circulation,2003,108(24):3006-3010.

[31] Li W,Li S,Li X,et al. Interleukin-37 elevation in patients with atrial fibrillation[J]. Clin Cardiol,2017,40(2):66-72.

[32] Shirazi LF,Bissett J,Romeo F,et al. Role of inflammation in heart failure[J]. Curr Atheroscler Rep,2017,19(6):27.

[33] Pasqui AL,di Renzo M,Bova G,et al. Pro-inflammatory/anti-inflammatory cytokine imbalance in acute coronary syndromes[J]. Clin Exp Med,2006,6(1):38-44.

[34] Kang SH,Park JJ,Choi DJ,et al. Prognostic value of NT-proBNP in heart failure with preserved versus reduced EF[J]. Heart,2015,101(23):1881-1888.

[35] Shou X,Lin J,Xie C,et al. Plasma IL-37 elevated in patients with chronic heart failure and predicted major adverse cardiac events:a 1-year follow-up study[J]. Dis Markers,2017,2017:9134079.

[36] Sagar S,Liu PP,Cooper LT Jr. Myocarditis[J]. Lancet,2012,379(9817):738-747.

[37] An B,Liu X,Li G,et al. Interleukin-37 ameliorates coxsackievirus B3-induced viral myocarditis by modulating the Th17/regulatory T cell immune response[J]. J Cardiovasc Pharmacol,2017,69(5):305-313.

[38] Guzik TJ,Touyz RM. Oxidative stress,inflammation,and vascular aging in hypertension[J]. Hypertension,2017,70(4):660-667.

[39] Ye J,Wang Y,Wang Z,et al. Circulating IL-37 levels are elevated in patients with hypertension[J]. Exp Ther Med,2021,21(6):558.

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更新日期/Last Update: 2022-08-19