Your browser doesn't support javascript.
loading
Identification of Trypanosoma cruzi trans-sialidase family members as targets of protective CD8+ TC1 responses.
Wizel, B; Nunes, M; Tarleton, R L.
Afiliación
  • Wizel B; Department of Cellular Biology, University of Georgia, Athens 30602, USA.
J Immunol ; 159(12): 6120-30, 1997 Dec 15.
Article en En | MEDLINE | ID: mdl-9550413
ABSTRACT
CD8+ T lymphocytes play a critical role in immunity to Trypanosoma cruzi. However, the target molecules of this T cell subset have not been elucidated. In this work, we report the identification of an H-2Kb-restricted CTL epitope within two trypomastigote surface Ags encoded by members of the T. cruzi sialidase/trans-sialidase gene superfamily. Octapeptide VDYNFTIV sensitized target cells for lysis by CD8+ CTL generated from spleens of T. cruzi-infected mice. Peptide-specific CD8+ T cell lines were cytotoxic, secreted IFN-gamma and TNF-alpha, but low to undetectable levels of IL-4 and IL-5, and were able, upon adoptive transfer, to confer a high degree of protection against challenge infection. Finally, the protective determinant appears to be conserved among parasites from diverse geographic locations. This constitutes the first identified class I MHC-restricted epitope in T. cruzi and provides the basis for the search of additional targets to be considered in the development of vaccines against Chagas' disease.
Asunto(s)
Buscar en Google
Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trypanosoma cruzi / Glicoproteínas / Enfermedad de Chagas / Linfocitos T CD8-positivos / Antígenos de Protozoos / Neuraminidasa Tipo de estudio: Diagnostic_studies Límite: Animals / Female / Humans Idioma: En Revista: J Immunol Año: 1997 Tipo del documento: Article País de afiliación: Estados Unidos
Buscar en Google
Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trypanosoma cruzi / Glicoproteínas / Enfermedad de Chagas / Linfocitos T CD8-positivos / Antígenos de Protozoos / Neuraminidasa Tipo de estudio: Diagnostic_studies Límite: Animals / Female / Humans Idioma: En Revista: J Immunol Año: 1997 Tipo del documento: Article País de afiliación: Estados Unidos