Related Experiment Video
Updated: Jul 12, 2025

Sexual Transmission of American Trypanosomes from Males and Females to Naive Mates
Published on: January 27, 2019
Immunologic changes are detectable in the peripheral blood transcriptome of clinically asymptomatic Chagas
Carolina Duque1, Jaime So2, Yagahira E Castro-Sesquen3
1Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Insights
Early Chagas disease shows reduced immune response gene activity, distinct from other cardiomyopathies. These findings may help identify biomarkers for early intervention in Chagas cardiomyopathy.
Area of Science:
- Immunology
- Cardiology
- Infectious Diseases
Background:
- Chagas disease, caused by *Trypanosoma cruzi*, affects millions globally.
- 20-30% of infected individuals develop chronic Chagas cardiomyopathy (CCC), potentially leading to heart failure.
- The early pathogenesis of CCC remains poorly understood.
Purpose of the Study:
- To investigate the physiological changes in early Chagas cardiomyopathy (CCC).
- To understand the immune response alterations in asymptomatic Chagas patients with early cardiac disease.
- To differentiate the mechanisms of CCC from other cardiomyopathies.
Main Methods:
- Gene expression analysis in peripheral blood.
- Comparison between asymptomatic Chagas patients with early heart disease, asymptomatic Chagas patients, and Chagas-negative controls with/without heart disease.
- Analysis focused on identifying differential gene expression patterns.
Main Results:
- Early CCC was associated with downregulated peripheral immune response genes.
- Gene expression changes indicated reduced antigen presentation and T cell activation in early CCC.
- These immune changes were distinct from those observed in early cardiomyopathy in Chagas-negative individuals.
Conclusions:
- The immune response plays a critical role in the early pathogenesis of Chagas cardiomyopathy (CCC).
- Identified gene expression changes may serve as potential biomarkers for CCC progression.
- Findings suggest unique mechanisms underlying CCC, distinct from other cardiomyopathies, offering targets for early treatment strategies.
Abstract:
Chagas disease, caused by the protozoan parasite Trypanosoma cruzi, is a neglected parasitic disease that affects approximately 6 million individuals worldwide. Of those infected, 20-30% will go on to develop chronic Chagas cardiomyopathy (CCC), and ultimately many of these individuals will progress to advanced heart failure. The mechanism by which this progression occurs is poorly understood, as few studies have focused on early CCC. In this study, we sought to understand the physiologic changes associated with T. cruzi infection and the development of CCC. We analyzed gene expression in the peripheral blood of asymptomatic Chagas patients with early structural heart disease, Chagas patients without any signs or symptoms of disease, and Chagas-negative patients with and without early structural heart disease. Our analysis shows that early CCC was associated with a downregulation of various peripheral immune response genes, with gene expression changes suggestive of reduced antigen presentation and T cell activation. Notably, these genes and processes were distinct from those of early cardiomyopathy in Chagas-negative patients, suggesting that the processes mediating CCC may be unique from those mediating progression to other cardiomyopathies. This work highlights the importance of the immune response in early CCC, providing insight into the early pathogenesis of this disease. The changes we have identified may serve as biomarkers of progression and could inform strategies for the treatment of CCC in its early stages, before significant cardiac damage has occurred.
Related Concept Videos
Myocarditis II: Clinical Features and Diagnostic Tests
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy II: Dilated Cardiomyopathy
Myocarditis I: Introduction
Cardiomyopathy IV: Restrictive Cardiomyopathy
Cardiomyopathy I: Introduction and Classification

