CXCL10型
趋化因子
心肌炎
细胞毒性T细胞
CCR2型
CXCL9型
医学
CD8型
免疫学
免疫系统
人口
T细胞
生物
趋化因子受体
内科学
体外
环境卫生
生物化学
作者
Pan Ma,Jing Liu,Juan Qin,Lulu Lai,Gyu Seong Heo,Hannah Luehmann,Deborah Sultan,Andrea L. Bredemeyer,Geetika Bajapa,Guoshuai Feng,Jesús Jiménez,Ruijun He,Antanisha Parks,Junedh M. Amrute,Ana Villanueva,Yongjian Liu,Chieh‐Yu Lin,Matthias Mack,Kaushik Amancherla,Javid J. Moslehi
出处
期刊:Circulation
[Lippincott Williams & Wilkins]
日期:2023-09-25
卷期号:149 (1): 48-66
被引量:56
标识
DOI:10.1161/circulationaha.122.062551
摘要
Immune checkpoint inhibitors (ICIs), antibodies targeting PD-1 (programmed cell death protein 1)/PD-L1 (programmed death-ligand 1) or CTLA4 (cytotoxic T-lymphocyte-associated protein 4), have revolutionized cancer management but are associated with devastating immune-related adverse events including myocarditis. The main risk factor for ICI myocarditis is the use of combination PD-1 and CTLA4 inhibition. ICI myocarditis is often fulminant and is pathologically characterized by myocardial infiltration of T lymphocytes and macrophages. Although much has been learned about the role of T-cells in ICI myocarditis, little is understood about the identity, transcriptional diversity, and functions of infiltrating macrophages.
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