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Giant cell myocarditis: from immune pathogenesis to contemporary management
1Division of Cardiology, Department of Internal Medicine, University Heart Center Graz Medical University Graz, Auenbruggerplatz 15, Graz, 8036, Austria.
Insights
Giant cell myocarditis (GCM) is a rare, aggressive autoimmune heart disease. Prompt immunosuppression and advanced therapies significantly improve survival, though heart transplantation is often needed.
Area of Science:
- Cardiology
- Immunology
- Pathology
Background:
- Giant cell myocarditis (GCM) is a rare, severe inflammatory cardiac condition.
- It presents with rapid hemodynamic decline, arrhythmias, and high mortality without treatment.
- GCM is primarily a T cell-mediated autoimmune disorder.
Purpose of the Study:
- To provide a comprehensive review of giant cell myocarditis.
- To cover its pathogenesis, diagnosis, and current management strategies.
- To identify future research priorities for GCM.
Main Methods:
- Review of existing literature on GCM.
- Analysis of diagnostic criteria and imaging modalities.
- Evaluation of current and emerging treatment protocols.
Main Results:
- GCM diagnosis is challenging due to nonspecific symptoms and overlap with cardiac sarcoidosis.
- Endomyocardial biopsy is the gold standard for diagnosis.
- Combination immunosuppressive therapy, mechanical support, and transplantation improve outcomes.
Conclusions:
- Early diagnosis and prompt immunosuppression are critical for GCM management.
- Further research is needed for noninvasive diagnostics and standardized treatments.
- Mechanical circulatory support and heart transplantation are vital for refractory cases.
Abstract:
Giant cell myocarditis (GCM) is a rare but devastating inflammatory cardiac disease characterized by rapid hemodynamic deterioration, malignant arrhythmias, and high rates of death or heart transplantation. Without immunosuppressive treatment, median transplant-free survival is approximately three months. Current evidence identifies GCM as a predominantly T cell-mediated autoimmune disorder driven by a breakdown of immune tolerance, with contributions from macrophage-derived multinucleated giant cells and neutrophil extracellular trap formation. Viral infections and environmental factors have been implicated as potential triggers. GCM typically affects middle-aged adults, with concomitant non-cardiac autoimmune diseases present in approximately 20% of cases. Early diagnosis remains challenging, as clinical presentation and imaging findings are nonspecific and overlap considerably with cardiac sarcoidosis. Endomyocardial biopsy continues to represent the diagnostic gold standard, with a sensitivity of 85%, while cardiac biomarkers including cardiac troponins and NT-proBNP provide important prognostic information. Cardiac magnetic resonance imaging and FDG-PET contribute to the diagnostic workup but cannot reliably differentiate GCM from cardiac sarcoidosis. Management requires prompt initiation of combination immunosuppressive therapy-typically corticosteroids combined with T cell-targeted agents such as cyclosporine and azathioprine or tacrolimus and mycophenolate mofetil, which has substantially improved survival in contemporary registries. Mechanical circulatory support and heart transplantation are frequently required for refractory cases. Given the high arrhythmic burden, systematic evaluation for implantable cardioverter-defibrillator placement is recommended. This review provides a comprehensive overview of the pathogenesis, diagnosis, and current management of GCM and highlights priorities for future research, including noninvasive diagnostic tools and standardized treatment protocols.
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