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.