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Parasite Induced Genetically Driven Autoimmune Chagas Heart Disease in the Chicken Model
Published on: July 29, 2012
Heart transplants for patients with Chagas' heart disease
1Heart Institute, Hospital das Clínicas, Faculdade de Medicina de Universidade de São Paulo, Brazil.
Insights
Heart transplantation for Chagas' heart disease can lead to Trypanosoma cruzi infection resurgence. Early treatment with benzonidazole is effective, and lower immunosuppression improves patient survival.
Area of Science:
- Cardiology
- Infectious Diseases
- Transplantation Immunology
Background:
- Chagas' heart disease poses challenges for heart transplantation due to potential Trypanosoma cruzi (T. cruzi) reactivation.
- Immunosuppression post-transplant may increase the risk of T. cruzi infection and allograft damage.
- Limited data exists on managing T. cruzi resurgence after heart transplantation.
Purpose of the Study:
- To evaluate the outcomes of orthotopic heart transplantation in patients with Chagas' heart disease.
- To assess the incidence and management of T. cruzi infection resurgence post-transplant.
- To analyze factors influencing survival rates in this patient population.
Main Methods:
- Retrospective analysis of 18 patients with Chagas' heart disease undergoing heart transplantation (1985-1993).
- Standard immunosuppression (cyclosporin, azathioprine, corticosteroid) and intensive T. cruzi monitoring (blood tests, biopsies).
- Treatment of T. cruzi parasitemia and disease resurgence with benzonidazole.
Main Results:
- T. cruzi parasitemia detected in 13 patients; Chagas' disease resurgence in 5 patients, presenting with fever, nodules, and myocarditis.
- All parasitemia and resurgence episodes were successfully treated with benzonidazole.
- Improved survival rates observed with lower-dose cyclosporin regimens, correlating with fewer disease resurgences.
- Neoplasias, including lymphoproliferative disease and skin cancer, were noted in 3 patients.
Conclusions:
- Heart transplantation is a viable option for advanced Chagas' heart disease, but carries a risk of T. cruzi reactivation.
- Proactive monitoring and prompt treatment with benzonidazole are crucial for managing T. cruzi resurgence.
- Optimizing immunosuppression, particularly reducing cyclosporin dosage, can mitigate T. cruzi reactivation and improve long-term survival.
Abstract:
The role of heart transplants for treating Chagas' heart disease is not quite clear. Immunosuppression could lead to resurgence of T. cruzi infection with acute or chronic damage to the allograft. There are few publications regarding this issue. Thus we reported the follow-up of 18-patients with Chagas' heart disease submitted to orthotopic heart transplants from 1985 to 1993 at The Heart Institute. The patients were in functional class IV or II, with sustained ventricular tachycardia episodes. The mean left ventricular ejection fraction was 25 +/- 9% and the mean right ventricular ejection was 22 +/- 5% (MUGA). Immunosuppression was based on cyclosporin, azathioprine and corticosteroid. For specific post-transplant monitoring of T. cruzi infection, blood tests were performed (examination of blood or leukocyte concentrate, Giemsa-stained blood smears, blood culture, xenodiagnosis, mouse inoculation) and tissue biopsy (skin or myocardium). In addition, complement fixation hemagglutination and immunofluorescence assays were performed. T. cruzi parasitemias were detected in 18 circumstances in 13 patients. Resurgence of Chagas' disease was diagnosed in 11 circumstances in 5 patients. Fever, subcutaneous nodules and myocarditis predominated in these episodes. All episodes of parasitemia and Chagas' disease resurgence were successfully treated with benzonidazole. Al surviving patients had normal cardia function despite left ventricular function worsening during some myocarditis episodes. Neoplasias were important findings and 3 patients developed lymphoproliferative disease, 2 developed Karposi's sarcoma and 1 patient developed skin cancer. The survival rates of 4 and 12 months were 83% and 49% respectively. The survival of patients who underwent heart transplants from August 1991 to April 1993 was 100% at 4 months and 75% at 12 months. Heart transplants for Chagas' heart disease may be associated with episodes of parasitemia and a reoccurrence of episodes of Chaga's disease. The survival of heart transplanted patients has improved when associated with lower doses of cyclosporins and thus, fewer resurgences of the disease.
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