Formyl peptide receptor 2 and heart disease

被引:19
作者
Lupisella, John A. [1 ]
Shirude, Pravin S. [2 ]
Wurtz, Nicholas R. [1 ]
Garcia, Ricardo A. [1 ,3 ,4 ]
机构
[1] Bristol Myers Squibb, Dept Cardiovasc & Fibrosis Drug Discovery, Princeton, NJ USA
[2] Biocon Bristol Myers Squibb Res Ctr, Bangalore, India
[3] Univ Calif San Diego, Dept Med, San Diego, CA USA
[4] Bristol Myers Squibb, 1000 Sierra Point Pkwy, Brisbane, CA 94005 USA
关键词
FPR2; Formyl peptide receptor 2; Resolution; MI; Myocardial infarction; HF; Heart failure; MYOCARDIAL ISCHEMIA-REPERFUSION; RESIDENT CARDIAC MACROPHAGES; MANNOSE RECEPTOR; FPR2/ALX RECEPTOR; DOWN-REGULATION; IDENTIFICATION; INFARCTION; AGONIST; FAILURE; ATL;
D O I
10.1016/j.smim.2022.101602
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Formyl peptide receptor type 2 (FPR2) regulates the initiation and resolution phases of the inflammatory response. In the setting of heart injury and disease, dysregulated inflammation can potentiate maladaptive healing and pathological remodeling of the heart leading to cardiac dysfunction and failure. The potential to regulate and resolve adverse inflammation is postulated to improve outcome in the setting of heart disease. This review covers emerging concepts on the role of FPR2 in heart disease and strategies to activate pro-resolution processes to limit disease progression. We summarize key preclinical studies that support use of FPR2 agonists in heart disease. Finally, we briefly discuss the status of FPR2 agonists under evaluation in the clinic.
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页数:7
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