Chagasic patients are able to respond against a viral antigen from influenza virus

BMC Infect Dis. 2012 Aug 24:12:198. doi: 10.1186/1471-2334-12-198.

Abstract

Background: Trypanosoma cruzi, the etiological agent of Chagas' disease, is an obligate intracellular parasite which induces a CD8+ T cell immune response with secretion of cytokines and release of cytotoxic granules. Although an immune-suppressive effect of T. cruzi on the acute phase of the disease has been described, little is known about the capacity of CD8+ T cell from chronic chagasic patients to respond to a non-T. cruzi microbial antigen.

Methods: In the present paper, the frequency, phenotype and the functional activity of the CD8+ T cells specific from Flu-MP*, an influenza virus epitope, were determined in 13 chagasic patients and 5 healthy donors.

Results: The results show that Flu-MP* peptide specific CD8+ T cells were found with similar frequencies in both groups. In addition, Flu-MP* specific CD8+ T cells were distributed in the early or intermediate/late differentiation stages without showing enrichment of a specific sub-population. The mentioned Flu-MP* specific CD8+ T cells from chagasic patients were predominately TEM (CCR7- CD62L-), producing IL-2, IFNγ, CD107a/b and perforin, and did not present significant differences when compared with those from healthy donors.

Conclusions: Our results support the hypothesis that there is no CD8+ T cell nonspecific immune-suppression during chronic Chagas disease infection. Nonetheless, other viral antigens must be studied in order to confirm our findings.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Viral / immunology*
  • CD8-Positive T-Lymphocytes / immunology*
  • Chagas Disease / immunology*
  • Humans
  • Immune Tolerance
  • Interferon-gamma / metabolism
  • Interleukin-2 / metabolism
  • Lysosomal-Associated Membrane Protein 1 / analysis
  • Lysosomal-Associated Membrane Protein 2 / analysis
  • Orthomyxoviridae / immunology*
  • Perforin / metabolism
  • T-Lymphocyte Subsets / immunology*
  • Trypanosoma cruzi / pathogenicity*

Substances

  • Antigens, Viral
  • Interleukin-2
  • Lysosomal-Associated Membrane Protein 1
  • Lysosomal-Associated Membrane Protein 2
  • Perforin
  • Interferon-gamma