Cargando…
T Lymphocytes from Chagasic Patients Are Activated but Lack Proliferative Capacity and Down-Regulate CD28 and CD3ζ
BACKGROUND: Chronic persistent infections have been associated with T lymphocytes functional impairment. The aim of this study was to compare the activation status, the proliferative potential and the expression of CD28 and CD3ζ chain on T lymphocytes between chronic chagasic patients and uninfected...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3561132/ https://www.ncbi.nlm.nih.gov/pubmed/23383358 http://dx.doi.org/10.1371/journal.pntd.0002038 |
_version_ | 1782257909682405376 |
---|---|
author | Giraldo, Nicolás A. Bolaños, Natalia I. Cuellar, Adriana Roa, Nubia Cucunubá, Zulma Rosas, Fernando Velasco, Víctor Puerta, Concepción J. González, John M. |
author_facet | Giraldo, Nicolás A. Bolaños, Natalia I. Cuellar, Adriana Roa, Nubia Cucunubá, Zulma Rosas, Fernando Velasco, Víctor Puerta, Concepción J. González, John M. |
author_sort | Giraldo, Nicolás A. |
collection | PubMed |
description | BACKGROUND: Chronic persistent infections have been associated with T lymphocytes functional impairment. The aim of this study was to compare the activation status, the proliferative potential and the expression of CD28 and CD3ζ chain on T lymphocytes between chronic chagasic patients and uninfected controls. METHODOLOGY/PRINCIPAL FINDINGS: Forty-two chronic chagasic patients, 28 healthy individuals and 32 non-chagasic cardiomyopathy donors were included. Peripheral blood was marked for CD3, CD4, CD8, HLA-DR, CD28, CD38 and intracellular CD3ζ. Peripheral blood mononuclear cells were stained with carboxyfluorescein diacetate succinimidylester and incubated with T. cruzi lysate or phytohemagglutinin for five days. Cells from 3 healthy controls were incubated with T. cruzi trypomastigotes separated with transwells; and the expression of CD3ζ chain and proliferation index was determined. Heart-infiltrating cells from two chronic chagasic patients were tested for the aforementioned cellular markers. Chagasic patients displayed higher frequencies of CD4+/HLA-DR+/CD38+ (8.1%±6.1) and CD8+/HLA-DR+/CD38+ (19.8±8.9) T cells in comparison with healthy (1.6±1.0; 10.6±8.0) and non-chagasic cardiomyopathy donors (2.9±2.9; 5.8±6.8). Furthermore, the percentage of CD4+ activated T cells was higher in chagasic patients with cardiac involvement. CD8+ T cells proliferation index in chagasic donors (1.7±0.3) was lower when compared with healthy (2.3±0.3) and non-chagasic cardiomyopathy individuals (3.1±1.1). The frequencies of CD4+/CD28+ and CD8+/CD28+ T cells, as well as the CD3ζ(bright)/CD3ζ(dim)% ratios in CD4+ and CD8+ were lower in chagasic patients when compared with both control groups. The CD3ζ(bright)/CD3ζ(dim)% ratio and proliferative indexes for CD4+ and CD8+ T lymphocytes decreased gradually in those cells cultivated with parasites and displayed lower values than those incubated with medium alone. Finally, heart-infiltrating T cells from two T. cruzi infected patients also expressed activation markers and down-regulate CD28 and CD3ζ. CONCLUSIONS: CD8+ T lymphocytes from chagasic donors displayed reduced proliferative capacity, which might be associated with CD3ζ down-regulation and diminished CD28 expression on CD4 T cells. |
format | Online Article Text |
id | pubmed-3561132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35611322013-02-04 T Lymphocytes from Chagasic Patients Are Activated but Lack Proliferative Capacity and Down-Regulate CD28 and CD3ζ Giraldo, Nicolás A. Bolaños, Natalia I. Cuellar, Adriana Roa, Nubia Cucunubá, Zulma Rosas, Fernando Velasco, Víctor Puerta, Concepción J. González, John M. PLoS Negl Trop Dis Research Article BACKGROUND: Chronic persistent infections have been associated with T lymphocytes functional impairment. The aim of this study was to compare the activation status, the proliferative potential and the expression of CD28 and CD3ζ chain on T lymphocytes between chronic chagasic patients and uninfected controls. METHODOLOGY/PRINCIPAL FINDINGS: Forty-two chronic chagasic patients, 28 healthy individuals and 32 non-chagasic cardiomyopathy donors were included. Peripheral blood was marked for CD3, CD4, CD8, HLA-DR, CD28, CD38 and intracellular CD3ζ. Peripheral blood mononuclear cells were stained with carboxyfluorescein diacetate succinimidylester and incubated with T. cruzi lysate or phytohemagglutinin for five days. Cells from 3 healthy controls were incubated with T. cruzi trypomastigotes separated with transwells; and the expression of CD3ζ chain and proliferation index was determined. Heart-infiltrating cells from two chronic chagasic patients were tested for the aforementioned cellular markers. Chagasic patients displayed higher frequencies of CD4+/HLA-DR+/CD38+ (8.1%±6.1) and CD8+/HLA-DR+/CD38+ (19.8±8.9) T cells in comparison with healthy (1.6±1.0; 10.6±8.0) and non-chagasic cardiomyopathy donors (2.9±2.9; 5.8±6.8). Furthermore, the percentage of CD4+ activated T cells was higher in chagasic patients with cardiac involvement. CD8+ T cells proliferation index in chagasic donors (1.7±0.3) was lower when compared with healthy (2.3±0.3) and non-chagasic cardiomyopathy individuals (3.1±1.1). The frequencies of CD4+/CD28+ and CD8+/CD28+ T cells, as well as the CD3ζ(bright)/CD3ζ(dim)% ratios in CD4+ and CD8+ were lower in chagasic patients when compared with both control groups. The CD3ζ(bright)/CD3ζ(dim)% ratio and proliferative indexes for CD4+ and CD8+ T lymphocytes decreased gradually in those cells cultivated with parasites and displayed lower values than those incubated with medium alone. Finally, heart-infiltrating T cells from two T. cruzi infected patients also expressed activation markers and down-regulate CD28 and CD3ζ. CONCLUSIONS: CD8+ T lymphocytes from chagasic donors displayed reduced proliferative capacity, which might be associated with CD3ζ down-regulation and diminished CD28 expression on CD4 T cells. Public Library of Science 2013-01-31 /pmc/articles/PMC3561132/ /pubmed/23383358 http://dx.doi.org/10.1371/journal.pntd.0002038 Text en © 2013 Giraldo 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 Giraldo, Nicolás A. Bolaños, Natalia I. Cuellar, Adriana Roa, Nubia Cucunubá, Zulma Rosas, Fernando Velasco, Víctor Puerta, Concepción J. González, John M. T Lymphocytes from Chagasic Patients Are Activated but Lack Proliferative Capacity and Down-Regulate CD28 and CD3ζ |
title | T Lymphocytes from Chagasic Patients Are Activated but Lack Proliferative Capacity and Down-Regulate CD28 and CD3ζ |
title_full | T Lymphocytes from Chagasic Patients Are Activated but Lack Proliferative Capacity and Down-Regulate CD28 and CD3ζ |
title_fullStr | T Lymphocytes from Chagasic Patients Are Activated but Lack Proliferative Capacity and Down-Regulate CD28 and CD3ζ |
title_full_unstemmed | T Lymphocytes from Chagasic Patients Are Activated but Lack Proliferative Capacity and Down-Regulate CD28 and CD3ζ |
title_short | T Lymphocytes from Chagasic Patients Are Activated but Lack Proliferative Capacity and Down-Regulate CD28 and CD3ζ |
title_sort | t lymphocytes from chagasic patients are activated but lack proliferative capacity and down-regulate cd28 and cd3ζ |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3561132/ https://www.ncbi.nlm.nih.gov/pubmed/23383358 http://dx.doi.org/10.1371/journal.pntd.0002038 |
work_keys_str_mv | AT giraldonicolasa tlymphocytesfromchagasicpatientsareactivatedbutlackproliferativecapacityanddownregulatecd28andcd3z AT bolanosnataliai tlymphocytesfromchagasicpatientsareactivatedbutlackproliferativecapacityanddownregulatecd28andcd3z AT cuellaradriana tlymphocytesfromchagasicpatientsareactivatedbutlackproliferativecapacityanddownregulatecd28andcd3z AT roanubia tlymphocytesfromchagasicpatientsareactivatedbutlackproliferativecapacityanddownregulatecd28andcd3z AT cucunubazulma tlymphocytesfromchagasicpatientsareactivatedbutlackproliferativecapacityanddownregulatecd28andcd3z AT rosasfernando tlymphocytesfromchagasicpatientsareactivatedbutlackproliferativecapacityanddownregulatecd28andcd3z AT velascovictor tlymphocytesfromchagasicpatientsareactivatedbutlackproliferativecapacityanddownregulatecd28andcd3z AT puertaconcepcionj tlymphocytesfromchagasicpatientsareactivatedbutlackproliferativecapacityanddownregulatecd28andcd3z AT gonzalezjohnm tlymphocytesfromchagasicpatientsareactivatedbutlackproliferativecapacityanddownregulatecd28andcd3z |