Monocyte and macrophage subsets along the continuum to heart failure: Misguided heroes or targetable villains?

Nadezhda Glezeva1, Stephen Horgan2, John A Baugh1

  • 1Conway Institute of Biomolecular and Biomedical Research, School of Medicine and Medical Science, University College Dublin, Belfield, Dublin 4, Ireland.

Insights

Monocytes and macrophages are key players in heart disease and heart failure. Understanding their subsets and functions offers potential for new diagnostic biomarkers and therapies for heart conditions.

Area of Science:

  • Cardiovascular Science
  • Immunology
  • Pathophysiology

Background:

  • Monocytes and macrophages significantly contribute to cardiovascular disease and heart failure.
  • These immune cells, particularly subsets, are involved in initiating and worsening conditions like atherosclerosis, myocardial infarction, and cardiac fibrosis.

Purpose of the Study:

  • To review the role of monocytes and macrophages in the progression to heart failure.
  • To examine the influence of different monocyte and macrophage subsets on cardiac injury and repair.

Main Methods:

  • Review of pre-clinical and clinical studies.
  • Analysis of monocyte/macrophage phenotypic plasticity, inflammatory, and fibrotic functions.
  • Evaluation of therapeutic strategies targeting monocyte and macrophage manipulation.

Main Results:

  • Monocyte/macrophage system critically regulates cardiac inflammation and extracellular matrix remodeling in heart disease.
  • Phenotypic plasticity of these cells influences their pro- or anti-cardiac injury roles.
  • Evidence supports monocyte subset regulation's significance in cardiovascular disease and heart failure development.

Conclusions:

  • Monocyte and macrophage manipulation presents a promising therapeutic avenue for cardiovascular disease and heart failure.
  • Further research can identify novel diagnostic biomarkers and treatments for chronic heart failure.

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