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Frequency of specific CD8+ T cells for a promiscuous epitope derived from Trypanosoma cruzi KMP-11 protein in chagasic patients

  • P. Lasso
  • , D. Mesa
  • , A. Cuéllar
  • , F. Guzmán
  • , N. Bolaños
  • , F. Rosas
  • , V. Velasco
  • , M. Del Carmen Thomas
  • , M. C. Lopez
  • , J. M. Gonzalez
  • , C. J. Puerta
  • Pontificia Universidad Javeriana
  • Núcleo de Biotecnología Curauma, Pontificia Universidad Católica Valparaíso
  • Universidad de los Andes Colombia
  • Fundación Abood A Shaio
  • Consejo Sup. de Investigacions Cie.

Producción: Contribución a una revistaArtículorevisión exhaustiva

30 Citas (Scopus)

Resumen

The K1 peptide is a CD8+T cell HLA-A*0201-restricted epitope derived from the Trypanosoma cruzi KMP-11 protein. We have previously shown that this peptide induces IFN-γ secretion by CD8+T cells. The aim of this study was to characterize the frequency of K1-specific CD8 +T cells in chagasic patients. Nineteen HLA-A2+individuals were selected from 50 T. cruzi infected patients using flow cytometry and SSP-PCR assays. Twelve HLA-A*0201+noninfected donors were included as controls. Peripheral blood mononuclear cells were stained with HLA-A2-K1 tetramer, showing that 15 of 19 infected patients have K1-specific CD8+T cells (0·09-0·34% frequency) without differences in disease stages or severity. Of note, five of these responders were A*0205, A*0222, A*0226, A*0259 and A*0287 after molecular typing. Thus, a phenotypic and functional comparison of K1-specific CD8+T cells from non-HLA-A*0201 and HLA-A*0201 +infected patients was performed. The results showed that both non-HLA-A*0201 and HLA-A*0201+individuals have a predominant effector memory CD8+T cell phenotype (CCR7-, CD62L-). Moreover, CD8+T cells from non-HLA-A*0201 and HLA-A*0201+individuals expressed IL-2, IFN-γ and perforin without any differences. These findings support that K1 peptide is a promiscuous epitope presented by HLA-A2 supertype molecules and is highly recognized by chagasic patients.

Idioma originalInglés
Páginas (desde-hasta)494-502
Número de páginas9
PublicaciónParasite Immunology
Volumen32
N.º7
DOI
EstadoPublicada - jul 2010

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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