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

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 dise...

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Detalles Bibliográficos
Autores principales: Lasso, Paola, Mesa, Diana, Bolaños, Natalia, Cuéllar, Adriana, Guzmán, Fanny, Cucunuba, Zulma, Rosas, Fernando, Velasco, Víctor, Thomas, Maria C, López, Manuel Carlos, González, John Mario, Puerta, Concepción Judith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511223/
https://www.ncbi.nlm.nih.gov/pubmed/22920436
http://dx.doi.org/10.1186/1471-2334-12-198
Descripción
Sumario: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 T(EM) (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.