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Low Frequency of Circulating CD8(+) T Stem Cell Memory Cells in Chronic Chagasic Patients with Severe Forms of the Disease

BACKGROUND: CD8+ T cells have been shown to play a crucial role in Trypanosoma cruzi infection. Memory CD8+ T cells can be categorised based on their distinct differentiation stages and functional activities as follows: stem cell memory (TSCM), central memory (TCM), transitional memory (TTM), effect...

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Autores principales: Mateus, Jose, Lasso, Paola, Pavia, Paula, Rosas, Fernando, Roa, Nubia, Valencia-Hernández, Carlos Andrés, González, John Mario, Puerta, Concepción J., Cuéllar, Adriana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4287481/
https://www.ncbi.nlm.nih.gov/pubmed/25569149
http://dx.doi.org/10.1371/journal.pntd.0003432
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author Mateus, Jose
Lasso, Paola
Pavia, Paula
Rosas, Fernando
Roa, Nubia
Valencia-Hernández, Carlos Andrés
González, John Mario
Puerta, Concepción J.
Cuéllar, Adriana
author_facet Mateus, Jose
Lasso, Paola
Pavia, Paula
Rosas, Fernando
Roa, Nubia
Valencia-Hernández, Carlos Andrés
González, John Mario
Puerta, Concepción J.
Cuéllar, Adriana
author_sort Mateus, Jose
collection PubMed
description BACKGROUND: CD8+ T cells have been shown to play a crucial role in Trypanosoma cruzi infection. Memory CD8+ T cells can be categorised based on their distinct differentiation stages and functional activities as follows: stem cell memory (TSCM), central memory (TCM), transitional memory (TTM), effector memory (TEM) and terminal effector (TTE) cells. Currently, the immune mechanisms that control T. cruzi in the chronic phase of the infection are unknown. METHODOLOGY/PRINCIPAL FINDINGS: To characterise the CD8+ T cell subsets that could be participating in the control of T. cruzi infection, in this study, we compared total and T. cruzi-specific circulating CD8+ T cells with distinctive phenotypic and functional features in chronic chagasic patients (CCPs) with different degrees of cardiac dysfunction. We observed a decreased frequency of total TSCM along with an increased frequency of TTE in CCPs with severe disease. Antigen-specific TSCM cells were not detectable in CCPs with severe forms of the disease. A functional profile of CD8+ T cell subsets among CCPs revealed a high frequency of monofunctional CD8+ T cells in the most severe patients with IFN-γ+- or TNF-α+-producing cells. CONCLUSIONS/SIGNIFICANCE: These findings suggest that CD8+ TSCM cells may be associated with the immune response to T. cruzi and outcome of Chagas disease, given that these cells may be involved in repopulating the T cell pool that controls infection.
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spelling pubmed-42874812015-01-12 Low Frequency of Circulating CD8(+) T Stem Cell Memory Cells in Chronic Chagasic Patients with Severe Forms of the Disease Mateus, Jose Lasso, Paola Pavia, Paula Rosas, Fernando Roa, Nubia Valencia-Hernández, Carlos Andrés González, John Mario Puerta, Concepción J. Cuéllar, Adriana PLoS Negl Trop Dis Research Article BACKGROUND: CD8+ T cells have been shown to play a crucial role in Trypanosoma cruzi infection. Memory CD8+ T cells can be categorised based on their distinct differentiation stages and functional activities as follows: stem cell memory (TSCM), central memory (TCM), transitional memory (TTM), effector memory (TEM) and terminal effector (TTE) cells. Currently, the immune mechanisms that control T. cruzi in the chronic phase of the infection are unknown. METHODOLOGY/PRINCIPAL FINDINGS: To characterise the CD8+ T cell subsets that could be participating in the control of T. cruzi infection, in this study, we compared total and T. cruzi-specific circulating CD8+ T cells with distinctive phenotypic and functional features in chronic chagasic patients (CCPs) with different degrees of cardiac dysfunction. We observed a decreased frequency of total TSCM along with an increased frequency of TTE in CCPs with severe disease. Antigen-specific TSCM cells were not detectable in CCPs with severe forms of the disease. A functional profile of CD8+ T cell subsets among CCPs revealed a high frequency of monofunctional CD8+ T cells in the most severe patients with IFN-γ+- or TNF-α+-producing cells. CONCLUSIONS/SIGNIFICANCE: These findings suggest that CD8+ TSCM cells may be associated with the immune response to T. cruzi and outcome of Chagas disease, given that these cells may be involved in repopulating the T cell pool that controls infection. Public Library of Science 2015-01-08 /pmc/articles/PMC4287481/ /pubmed/25569149 http://dx.doi.org/10.1371/journal.pntd.0003432 Text en © 2015 Mateus et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Mateus, Jose
Lasso, Paola
Pavia, Paula
Rosas, Fernando
Roa, Nubia
Valencia-Hernández, Carlos Andrés
González, John Mario
Puerta, Concepción J.
Cuéllar, Adriana
Low Frequency of Circulating CD8(+) T Stem Cell Memory Cells in Chronic Chagasic Patients with Severe Forms of the Disease
title Low Frequency of Circulating CD8(+) T Stem Cell Memory Cells in Chronic Chagasic Patients with Severe Forms of the Disease
title_full Low Frequency of Circulating CD8(+) T Stem Cell Memory Cells in Chronic Chagasic Patients with Severe Forms of the Disease
title_fullStr Low Frequency of Circulating CD8(+) T Stem Cell Memory Cells in Chronic Chagasic Patients with Severe Forms of the Disease
title_full_unstemmed Low Frequency of Circulating CD8(+) T Stem Cell Memory Cells in Chronic Chagasic Patients with Severe Forms of the Disease
title_short Low Frequency of Circulating CD8(+) T Stem Cell Memory Cells in Chronic Chagasic Patients with Severe Forms of the Disease
title_sort low frequency of circulating cd8(+) t stem cell memory cells in chronic chagasic patients with severe forms of the disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4287481/
https://www.ncbi.nlm.nih.gov/pubmed/25569149
http://dx.doi.org/10.1371/journal.pntd.0003432
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