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Published on: May 8, 2020
Case report of heart transplantation for giant cell myocarditis in a patient with common variable immunodeficiency
Thomas A Franzon1, Anna Kovalszki2, Raja Rabah3
1Cardiovascular Medicine, University of Michigan, 2381 CVC SPC 5853, 1500 E. Medical Center Drive, Ann Arbor, MI 48109-5853, USA.
Insights
Heart transplantation for patients with common variable immunodeficiency (CVID) is feasible. A CVID patient with giant cell myocarditis (GCM) successfully received a heart transplant and remained complication-free for two years.
Area of Science:
- Immunology
- Cardiology
- Transplantation
Background:
- Solid-organ transplantation in common variable immunodeficiency (CVID) patients is controversial due to infection risks and potential recurrence of non-infectious complications.
- Limited data exist on solid-organ transplantation outcomes in CVID patients, especially for heart transplantation.
Observation:
- A 32-year-old female with CVID presented with severe heart failure due to giant cell myocarditis (GCM).
- She underwent orthotopic heart transplantation due to progressive cardiogenic shock despite medical management.
Findings:
- The patient experienced an uncomplicated heart transplant and remained free of major infectious complications for two years post-transplant.
- Graft function remained normal, with no recurrence of GCM observed during the follow-up period.
Implications:
- This case suggests that CVID should not be an absolute contraindication for heart transplantation.
- Successful heart transplantation in CVID patients with GCM is possible, challenging previous concerns about transplant candidacy.
Background:
Solid-organ transplantation in patients with common variable immunodeficiency (CVID) is controversial due to the risk for severe and recurrent infections. Determining transplantation candidacy in CVID patients is further complicated by the presence of CVID-related non-infectious complications that can reduce overall survival and also recur in the transplanted organ. Data regarding solid organ transplantation in patients with CVID are limited, particularly in heart transplantation.
Case Summary:
A 32-year-old female with CVID presented with new heart failure after 3 months of dyspnoea on exertion. Her echocardiogram showed severe global systolic dysfunction with an ejection fraction of approximately 10%, and her right heart catheterization revealed severe biventricular pressure overload and severely reduced cardiac output. Endomyocardial biopsy revealed giant cells and mononuclear infiltrate consistent with giant cell myocarditis (GCM). Despite medical management, she developed progressive cardiogenic shock and underwent uncomplicated orthotopic heart transplantation on hospital Day 38. After 2 years of follow-up, she has had no major infectious complications and continues to have normal graft function with no recurrence of GCM.
Conclusion:
We report a case of successful heart transplantation for GCM in a patient with CVID, with no major infectious complications after 2 years of follow-up. CVID should not be considered an absolute contraindication for heart transplantation.
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