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本文引用的文献

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Effect of interleukin-1β inhibition with canakinumab on incident lung cancer in patients with atherosclerosis: exploratory results from a randomised, double-blind, placebo-controlled trial.卡那单抗抑制白细胞介素-1β对动脉粥样硬化患者肺癌发病的影响:一项随机、双盲、安慰剂对照试验的探索性结果。
Lancet. 2017 Oct 21;390(10105):1833-1842. doi: 10.1016/S0140-6736(17)32247-X. Epub 2017 Aug 27.
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Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease.卡那奴单抗治疗动脉粥样硬化疾病的抗炎疗法。
N Engl J Med. 2017 Sep 21;377(12):1119-1131. doi: 10.1056/NEJMoa1707914. Epub 2017 Aug 27.
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Targeting Inflammation in Coronary Artery Disease.针对冠状动脉疾病中的炎症
N Engl J Med. 2017 Sep 21;377(12):1197-1198. doi: 10.1056/NEJMe1709904. Epub 2017 Aug 27.
4
Flow Perturbation Mediates Neutrophil Recruitment and Potentiates Endothelial Injury via TLR2 in Mice: Implications for Superficial Erosion.血流扰动通过Toll样受体2介导小鼠中性粒细胞募集并增强内皮损伤:对浅表糜烂的意义
Circ Res. 2017 Jun 23;121(1):31-42. doi: 10.1161/CIRCRESAHA.117.310694. Epub 2017 Apr 20.
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How Common Is Residual Inflammatory Risk?残余炎症风险有多常见?
Circ Res. 2017 Feb 17;120(4):617-619. doi: 10.1161/CIRCRESAHA.116.310527.
6
Clonal hematopoiesis associated with TET2 deficiency accelerates atherosclerosis development in mice.与TET2缺陷相关的克隆性造血加速小鼠动脉粥样硬化发展。
Science. 2017 Feb 24;355(6327):842-847. doi: 10.1126/science.aag1381. Epub 2017 Jan 19.
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Temporal shifts in clinical presentation and underlying mechanisms of atherosclerotic disease.动脉粥样硬化疾病的临床表现和潜在机制的时间变化。
Nat Rev Cardiol. 2017 Jan;14(1):21-29. doi: 10.1038/nrcardio.2016.166. Epub 2016 Oct 20.
8
Arterial Effects of Canakinumab in Patients With Atherosclerosis and Type 2 Diabetes or Glucose Intolerance.卡那单抗对动脉粥样硬化合并2型糖尿病或糖耐量异常患者的动脉影响
J Am Coll Cardiol. 2016 Oct 18;68(16):1769-1780. doi: 10.1016/j.jacc.2016.07.768.
9
Activation of the pluripotency factor OCT4 in smooth muscle cells is atheroprotective.平滑肌细胞中多能性因子OCT4的激活具有抗动脉粥样硬化作用。
Nat Med. 2016 Jun;22(6):657-65. doi: 10.1038/nm.4109. Epub 2016 May 16.
10
Acute coronary syndromes without coronary plaque rupture.无冠状动脉斑块破裂的急性冠状动脉综合征。
Nat Rev Cardiol. 2016 May;13(5):257-65. doi: 10.1038/nrcardio.2016.19. Epub 2016 Feb 25.

CANTOS 试验:临床心脏病学的重要一步,但也是血管生物学的巨大飞跃。

The CANTOS Trial: One Important Step for Clinical Cardiology but a Giant Leap for Vascular Biology.

机构信息

From the Robert M. Berne Cardiovascular Research Center (R.A.B., G.K.O.), Department of Biochemistry and Molecular Genetics (R.A.B.), and Department of Molecular Physiology and Biological Physics (G.K.O.), University of Virginia, Charlottesville; Pittsburgh Heart, Lung, Blood and Vascular Medicine Institute (D.G.), Division of Cardiology, University of Pittsburgh School of Medicine, PA (D.G.); Division of Cardiovascular Medicine, University of Cambridge, United Kingdom (Z.M.); Institut National de la Santé et de la Recherche Médicale, Paris Cardiovascular Research Center, France (Z.M.); and Laboratory of Clinical Chemistry, University Medical Centre Utrecht, The Netherlands (G.P.).

出版信息

Arterioscler Thromb Vasc Biol. 2017 Nov;37(11):e174-e177. doi: 10.1161/ATVBAHA.117.310097. Epub 2017 Sep 28.

DOI:10.1161/ATVBAHA.117.310097
PMID:28970294
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5685554/
Abstract

The results of the CANTOS trial provide exciting evidence in support of the inflammatory hypothesis of atherosclerosis in humans, and is the first phase III clinical trial to show clinical benefit of a targeted anti-inflammatory therapy. However, the modest overall clinical benefit and safety concerns with increased susceptibility to fatal infections indicate that we need much more work in this critical area.

摘要

CANTOS 试验的结果为支持人类动脉粥样硬化炎症假说提供了令人兴奋的证据,也是首个显示靶向抗炎治疗临床获益的 III 期临床试验。然而,整体临床获益有限,以及增加致命感染易感性的安全性担忧表明,我们在这一关键领域还需要做更多的工作。