医学
封锁
急性冠脉综合征
心肌炎
炎症
癌症
内科学
心脏毒性
PD-L1
心脏病学
心肌梗塞
免疫疗法
化疗
受体
作者
Mei Dong,Ting Yu,Gary Tse,Zerun Lin,Lin Chen,Nan Zhang,Rujian Wang,Tong Liu,Lin Zou
标识
DOI:10.1016/j.cpcardiol.2022.101527
摘要
PD-1(programed death-1)/PD-L1(programed death-1 ligand) blockade represents a major breakthrough of anti-cancer therapies, however, it may come with increased risk of cardiovascular morbidity, such as myocarditis, acute coronary syndrome, arrhythmias, etc. Although the PD-1/PD-L1-blockade-related acute coronary syndrome (ACS) is rare, it can be fatal. Previous studies have implicated a role of the PD-1/PD-L1 axis in the development of atherosclerosis. This review explores a hypothesis that PD-1/PD-L1 blockade accelerates the progression of atherosclerosis and promotes plaque rupture, by synthesizing the evidence of vascular inflammation, as well as plaque progression, destabilization and rupture via T-cell activation and effector function. In order to improve the prognosis of cancer patients and decrease the cardiotoxicity of PD-1/PD-L1 blockade therapy, early recognition of PD-1/PD-L1-blockade-related ACS is important.
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