CD8(+) T-Cells Expressing Interferon Gamma or Perforin Play Antagonistic Roles in Heart Injury in Experimental Trypanosoma Cruzi-Elicited Cardiomyopathy

• Autor(a) principal: Silverio, Jaline Coutinho
• Data de Publicação: 2012
• Outros Autores: Pereira, Isabela Resende, Cipitelli, Marcio da Costa, Vinagre, Nathalia Ferreira, Rodrigues, Mauricio Martins [UNIFESP], Gazzinelli, Ricardo Tostes, Lannes-Vieira, Joseli
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UNIFESP
• Texto Completo: http://dx.doi.org/10.1371/journal.ppat.1002645; http://repositorio.unifesp.br/handle/11600/34735

In Chagas disease, CD8(+) T-cells are critical for the control of Trypanosoma cruzi during acute infection. Conversely, CD8(+) T-cell accumulation in the myocardium during chronic infection may cause tissue injury leading to chronic chagasic cardiomyopathy (CCC). Here we explored the role of CD8(+) T-cells in T. cruzi-elicited heart injury in C57BL/6 mice infected with the Colombian strain. Cardiomyocyte lesion evaluated by creatine kinase-MB isoenzyme activity levels in the serum and electrical abnormalities revealed by electrocardiogram were not associated with the intensity of heart parasitism and myocarditis in the chronic infection. Further, there was no association between heart injury and systemic anti-T. cruzi CD8(+) T-cell capacity to produce interferon-gamma (IFN gamma) and to perform specific cytotoxicity. Heart injury, however, paralleled accumulation of anti-T. cruzi cells in the cardiac tissue. in T. cruzi infection, most of the CD8(+) T-cells segregated into IFN gamma(+) perforin (Pfn)(neg) or IFN gamma(neg)Pfn(+) cell populations. Colonization of the cardiac tissue by anti-T. cruzi CD8(+)Pfn(+) cells paralleled the worsening of CCC. the adoptive cell transfer to T. cruzi-infected cd8(-/-) recipients showed that the CD8(+) cells from infected ifn gamma(-/-) pfn(+/+) donors migrate towards the cardiac tissue to a greater extent and caused a more severe cardiomyocyte lesion than CD8(+) cells from ifn gamma(+/+) pfn(-/-) donors. Moreover, the reconstitution of naive cd8(-/-) mice with CD8(+) cells from naive ifn gamma(+/+) pfn(-/-) donors ameliorated T. cruzi-elicited heart injury paralleled IFN gamma(+) cells accumulation, whereas reconstitution with CD8(+) cells from naive ifn gamma(-/-) pfn(+/+) donors led to an aggravation of the cardiomyocyte lesion, which was associated with the accumulation of Pfn(+) cells in the cardiac tissue. Our data support a possible antagonist effect of CD8(+) Pfn(+) and CD8(+)IFN gamma(+) cells during CCC. CD8(+)IFN gamma(+) cells may exert a beneficial role, whereas CD8(+)Pfn(+) may play a detrimental role in T. cruzi-elicited heart injury.