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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
  • Pontificia Universidad Javeriana
  • Universidad de los Andes Colombia
  • Núcleo de Biotecnología Curauma, Pontificia Universidad Católica Valparaíso
  • Instituto Nacional de Salud
  • Fundación Clínica Abood Shaio
  • Consejo Sup. de Investigacions Cie.

Producción: Contribución a una revistaArtículorevisión exhaustiva

8 Citas (Scopus)

Resumen

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.

Idioma originalInglés
Número de artículo198
PublicaciónBMC Infectious Diseases
Volumen12
DOI
EstadoPublicada - 24 ago. 2012

ODS de las Naciones Unidas

Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

  1. ODS 3: Salud y bienestar
    ODS 3: Salud y bienestar

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