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Published on: May 26, 2021
Bone marrow cell transplantation in Chagas' disease heart failure: report of the first human experience
Fábio Vilas-Boas1, Gilson Soares Feitosa, Milena B P Soares
1Hospital Santa Izabel, Santa Casa de Misericórdia da Bahia, Brazil. fabiovboas@cardiol.br
Insights
Bone marrow mononuclear cell transplantation (BMCT) shows promise for treating Chagas
Area of Science:
- Cardiology
- Regenerative Medicine
- Infectious Diseases
Background:
- Chagas' disease causes heart failure, a progressive inflammatory cardiomyopathy affecting millions globally.
- Studies in animal models suggest bone marrow mononuclear cell transplantation (BMCT) can reduce inflammation and fibrosis, improving heart function.
Purpose of the Study:
- To assess the safety and efficacy of myocardial BMCT in human patients with heart failure due to Chagas' disease (HFCD).
- This is the first human trial evaluating BMCT for HFCD.
Main Methods:
- Twenty-eight patients with NYHA class III-IV HFCD underwent intracoronary injection of BMCT.
- Evaluated outcomes included left ventricle ejection fraction (LVEF), functional capacity, quality of life, arrhythmias, and biomarkers.
Main Results:
- The BMCT procedure was safe, with no procedure-related complications.
- Significant improvements were observed in LVEF, NYHA class, quality of life, and six-minute walking test at 180 days post-procedure.
- No significant changes were noted in immune or neurohormonal markers.
Conclusions:
- Intracoronary BMCT appears safe and potentially effective for treating HFCD patients.
- The observed benefits were modest, necessitating confirmation in larger, randomized, double-blind, placebo-controlled trials.
Background:
Heart failure due to Chagas' disease (HFCD) is a progressive inflammatory cardiomyopathy that affects millions of individuals in Latin America. Studies using mice models of HFCD indicate that bone marrow mononuclear cell transplantation (BMCT) may reduce inflammation, fibrosis, and improve myocardial function.
Objective:
The purpose of this study was to evaluate, for the first time in humans, the safety and efficacy of BMCT to the myocardium of patients with HFCD.
Methods:
A total of 28 HFCD patients (mean age 52.2 ± 9.9 years) with NYHA class III and IV were submitted to BMCT through intracoronary injection. Effects on the left ventricle ejection fraction (LVEF), functional capacity, quality-of-life, arrhythmias, biochemical, immunological, and neuro-humoral parameters, were evaluated.
Results:
There were no complications directly related to the procedure. LVEF was 20.1 ± 6.8% and 28.3 ± 7.9%, p < 0.03 at baseline and 180 days after the procedure, respectively. In the same period, significant improvements were observed in the NYHA class (3.1 ± 0.3 to 1.8 ± 0.5; p < 0.001), quality-of-life (50.9 ± 11.7 to 25.1 ± 15.9; p < 0.001), and in the six-minute walking test (355 ± 136 m to 437 ± 94 m; p < 0,01). There were no changes in markers of immune or neurohormonal activation. No complications were registered.
Conclusion:
Our data suggest that the intracoronary injection of BMCT is safe and potentially effective in patients with HFCD. The extent of the benefit, however, appears to be small and needs to be confirmed in a larger randomized, double blind, placebo controlled clinical trial.
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