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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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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
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author 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
author_facet 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
author_sort Lasso, Paola
collection PubMed
description 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.
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spelling pubmed-35112232012-12-01 Chagasic patients are able to respond against a viral antigen from influenza virus 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 BMC Infect Dis Research Article 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. BioMed Central 2012-08-24 /pmc/articles/PMC3511223/ /pubmed/22920436 http://dx.doi.org/10.1186/1471-2334-12-198 Text en Copyright ©2012 Lasso et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
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
Chagasic patients are able to respond against a viral antigen from influenza virus
title Chagasic patients are able to respond against a viral antigen from influenza virus
title_full Chagasic patients are able to respond against a viral antigen from influenza virus
title_fullStr Chagasic patients are able to respond against a viral antigen from influenza virus
title_full_unstemmed Chagasic patients are able to respond against a viral antigen from influenza virus
title_short Chagasic patients are able to respond against a viral antigen from influenza virus
title_sort chagasic patients are able to respond against a viral antigen from influenza virus
topic Research Article
url 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
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