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Formyl peptide receptor 2 and heart disease. | LitMetric

Formyl peptide receptor 2 and heart disease.

Semin Immunol

Department of Cardiovascular and Fibrosis Drug Discovery, Bristol Myers Squibb, Princeton, NJ, USA; Department of Medicine, University of California San Diego, San Diego, CA, USA. Electronic address:

Published: January 2022

AI Article Synopsis

  • FPR2 plays a crucial role in managing inflammation during heart injuries, affecting both the start and end phases of the inflammatory response.
  • Uncontrolled inflammation can worsen heart conditions, leading to poor healing and increased risk of heart failure.
  • The review highlights new findings about FPR2 in heart disease, discusses the potential benefits of using FPR2 agonists in treatment, and mentions ongoing clinical evaluations of these drugs.

Article Abstract

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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Source
http://dx.doi.org/10.1016/j.smim.2022.101602DOI Listing

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