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In Chagas disease, transforming growth factor beta neutralization reduces Trypanosoma cruzi infection and improves
Roberto Rodrigues Ferreira1,2, Elen Mello de Souza3, Glaucia Vilar-Pereira4
1Laboratório de Genômica Funcional e Bioinformática, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (Fiocruz), Rio de Janeiro, Brazil.
Insights
Neutralizing transforming growth factor-beta (TGF-β) with the 1D11 antibody reduced Trypanosoma cruzi infection in cardiac cells and experimental models. This approach shows promise for treating cardiac fibrosis in chronic Chagas heart disease.
Area of Science:
- Cardiovascular Research
- Infectious Diseases
- Immunology
Background:
- Chronic Chagasic cardiomyopathy (CCC) is a severe complication of Chagas disease, caused by Trypanosoma cruzi infection, characterized by inflammation and fibrosis.
- Transforming growth factor-beta (TGF-β) plays a critical role in the pathogenesis of CCC by promoting extracellular matrix synthesis and cardiac fibrosis.
- Previous studies suggest that inhibiting TGF-β signaling can attenuate T. cruzi infection and prevent cardiac damage in acute models.
Purpose of the Study:
- To investigate the efficacy of TGF-β neutralization using the 1D11 monoclonal antibody in both in vitro and in vivo preclinical models of T. cruzi infection.
- To assess the impact of TGF-β inhibition on parasite invasion, cardiac fibrosis, and electrical conduction abnormalities in experimental models of Chagas disease.
Main Methods:
- In vitro studies involved infecting primary cardiac cell cultures with T. cruzi and treating them with the 1D11 antibody.
- In vivo studies utilized Swiss mice (acute model) and C57BL/6 mice (chronic model) infected with different strains of T. cruzi, with 1D11 administered at various time points.
- Cardiac function and fibrosis were assessed, along with parasite load and electrical conduction parameters (heart rate, PR interval, P wave duration).
Main Results:
- The 1D11 antibody significantly reduced T. cruzi invasion into cardiac cells and the number of parasites per infected cell in vitro.
- In both acute and chronic experimental models, T. cruzi infection led to altered electrical conduction and decreased cardiac performance.
- Treatment with 1D11 effectively reduced cardiac fibrosis and reversed electrical abnormalities, thereby improving cardiac function.
Conclusions:
- TGF-β signaling is a key mediator of T. cruzi infection and its detrimental effects on cardiac tissue.
- Therapeutic neutralization of TGF-β with the 1D11 antibody demonstrates significant potential for treating cardiac fibrosis and improving cardiac performance in Chagas heart disease.
- These findings support TGF-β neutralization as a promising therapeutic strategy for managing the chronic phase of Chagas heart disease.
Abstract:
Chronic Chagasic cardiomyopathy (CCC), a progressive inflammatory and fibrosing disease, is the most prominent clinical form of Chagas disease, a neglected tropical disease caused by Trypanosoma cruzi infection. During CCC, the parasite remains inside the cardiac cells, leading to tissue damage, involving extensive inflammatory response and irregular fibrosis. Among the fibrogenic factors is transforming growth factor-β (TGF-β), a key cytokine controlling extracellular matrix synthesis and degradation. TGF-β is involved in CCC onset and progression, with increased serum levels and activation of its signaling pathways in the cardiac tissue, which crucially contributes to fibrosis. Inhibition of the TGF-β signaling pathway attenuates T. cruzi infection and prevents cardiac damage in an experimental model of acute Chagas disease. The aim of this study was to investigate the effect of TGF-β neutralization on T. cruzi infection in both in vitro and in vivo pre-clinical models, using the 1D11 monoclonal antibody. To this end, primary cultures of cardiac cells were infected with T. cruzi trypomastigote forms and treated with 1D11. For in vivo studies, 1D11 was administered in different schemes for acute and chronic phase models (Swiss mice infected with 104 parasites from the Y strain and C57BL/6 mice infected with 102 parasites from the Colombian strain, respectively). Here we show that the addition of 1D11 to cardiac cells greatly reduces cardiomyocyte invasion by T. cruzi and the number of parasites per infected cell. In both acute and chronic experimental models, T. cruzi infection altered the electrical conduction, decreasing the heart rate, increasing the PR interval and the P wave duration. The treatment with 1D11 reduced cardiac fibrosis and reversed electrical abnormalities improving cardiac performance. Taken together, these data further support the major role of the TGF-β signaling pathways in T. cruzi-infection and their biological consequences on parasite/host interactions. The therapeutic effects of the 1D11 antibody are promising and suggest a new possibility to treat cardiac fibrosis in the chronic phase of Chagas' heart disease by TGF-β neutralization.
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