Key result
Immune modifying therapies hold promise for treating cardiac injury and HF by targeting immune-driven fibrosis.
Why the study?
The mechanisms underlying incomplete cardiac recovery and progression to heart failure after acute injury remain poorly understood, and no existing medical therapies reliably halt or reverse heart failure progression.
This review highlights the emerging role of the immune system in cardiac injury and repair, suggesting immune-modifying therapies as potential new treatments for heart failure.
Should not yet alter HF management; leaves open whether immune-modifying therapies improve outcomes in trials.
Cardiac injury remains a major cause of morbidity and mortality worldwide. Despite significant advances, a full understanding of why the heart fails to fully recover function after acute injury, and why progressive heart failure frequently ensues, remains elusive. No therapeutics, short of heart transplantation, have emerged to reliably halt or reverse the inexorable progression of heart failure in the majority of patients once it has become clinically evident. To date, most pharmacological interventions have focused on modifying hemodynamics (reducing afterload, controlling blood pressure and blood volume) or on modifying cardiac myocyte function. However, important contributions of the immune system to normal cardiac function and the response to injury have recently emerged as exciting areas of investigation. Therapeutic interventions aimed at harnessing the power of immune cells hold promise for new treatment avenues for cardiac disease. Here, we review the immune response to heart injury, its contribution to cardiac fibrosis, and the potential of immune modifying therapies to affect cardiac repair.
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Rurik et al. (2021) conducted a review in Cardiac injury and heart failure. Immune modifying therapies was evaluated. Immune modifying therapies hold promise for treating cardiac injury and heart failure by targeting the immune response and its contribution to cardiac fibrosis.
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