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

  • Paola Lasso
  • , Diana Mesa
  • , Natalia Bolaños
  • , Adriana Cuéllar
  • , Fanny Guzmán
  • , Zulma Cucunuba
  • , Fernando Rosas
  • , Víctor Velasco
  • , Maria C. Thomas
  • , Manuel C. López
  • , John M. González
  • , Concepción J. Puerta

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

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.

Original languageEnglish
Article number198
JournalBMC Infectious Diseases
Volume12
DOIs
StatePublished - 24 Aug 2012

Keywords

  • CD8+ T cells
  • Chagas disease
  • Non-T. cruzi microbial antigen
  • Nonspecific immune-suppression

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