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Parasite Induced Genetically Driven Autoimmune Chagas Heart Disease in the Chicken Model
Published on: July 29, 2012
Plasma cytokine expression is associated with cardiac morbidity in chagas disease
Giovane Rodrigo Sousa1, Juliana Assis Silva Gomes2, Rafaelle Christine Gomes Fares3
1Programa de Pós-graduação em Ciências da Saúde: Infectologia e Medicina Tropical, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Insights
In Chagas disease, higher interleukin 10 (IL-10) indicates better cardiac function, while increased inflammatory cytokines like interferon gamma (IFN-γ) correlate with cardiac morbidity. This highlights the crucial role of cytokine balance in disease progression.
Area of Science:
- Immunology
- Infectious Diseases
- Cardiology
Background:
- Immune response is linked to Chagas disease morbidity.
- Previous studies had small sample sizes and limited statistical analysis for cytokine production variability.
Purpose of the Study:
- To evaluate plasma cytokine levels in well-defined clinical groups of Chagas disease patients.
- To correlate cytokine profiles with disease morbidity, particularly cardiac function.
Main Methods:
- Plasma cytokine levels were measured in indeterminate (IND) and cardiac (CARD) forms of Chagas disease patients and healthy controls (NI).
- Patients were categorized based on clinical presentation and T. cruzi infection status.
- Statistical analyses included correlation of cytokine levels with cardiac function parameters.
Main Results:
- Indeterminate Chagas disease patients showed higher interleukin 10 (IL-10) expression compared to other groups.
- Cardiac Chagas disease patients exhibited elevated levels of inflammatory cytokines: interferon gamma (IFN-γ), tumor necrosis factor alpha (TNF-α), interleukin 6 (IL-6), and interleukin 1 beta (IL-1β).
- Higher IL-10 expression correlated with better cardiac function (left ventricular ejection fraction, left ventricular diastolic diameter).
Conclusions:
- A balanced interplay between regulatory (IL-10) and inflammatory cytokines is critical in determining Chagas disease clinical manifestations.
- Cytokine profiles can distinguish between different clinical forms of chronic Chagas disease.
- Understanding these cytokine dynamics offers insights into Chagas disease pathogenesis and potential therapeutic targets.
Abstract:
The expression of immune response appears to be associated with morbidity in Chagas disease. However, the studies in this field have usually employed small samples of patients and statistical analyses that do not consider the wide dispersion of cytokine production observed in these patients. The aim of this study was to evaluate the plasma cytokine levels in well-defined clinical polar groups of chagasic patients divided into categories that better reflect the wide cytokine profile and its relationship with morbidity. Patients infected with Trypanosoma cruzi (T. cruzi) were grouped as indeterminate (IND) and cardiac (CARD) forms ranging from 23 to 69 years of age (mean of 45.6±11.25). The IND group included 82 individuals, ranging from 24 to 66 years of age (mean of 39.6±10.3). The CARD group included 94 patients ranging from 23 to 69 years of age (mean of 48±12.52) presenting dilated cardiomyopathy. None of the patients have undergone chemotherapeutic treatment, nor had been previously treated for T. cruzi infection. Healthy non-chagasic individuals, ranging from 29 to 55 years of age (mean of 42.6±8.8) were included as a control group (NI). IND patients have a higher intensity of interleukin 10 (IL-10) expression when compared with individuals in the other groups. By contrast, inflammatory cytokine expression, such as interferon gamma (IFN-γ), tumor necrosis factor alpha (TNF-α), interleukin 6 (IL-6), and interleukin 1 beta (IL-1β), proved to be the highest in the CARD group. Correlation analysis showed that higher IL-10 expression was associated with better cardiac function, as determined by left ventricular ejection fraction and left ventricular diastolic diameter values. Altogether, these findings reinforce the concept that a fine balance between regulatory and inflammatory cytokines represents a key element in the establishment of distinct forms of chronic Chagas disease.
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