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In Situ Expression of Regulatory Cytokines by Heart Inflammatory Cells in Chagas' Disease Patients with Heart Failure
Chagas' disease is caused by the protozoan parasite Trypanosoma cruzi. The immune system plays an important role in the reduction of parasite load, but may also contribute to the development of lesions observed during the chronic phase of the disease. We analyzed cytokines produced by inflammat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397162/ https://www.ncbi.nlm.nih.gov/pubmed/22811738 http://dx.doi.org/10.1155/2012/361730 |
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author | Rodrigues, Denise Bertulucci Rocha dos Reis, Marlene Antonia Romano, Audrey Pereira, Sanívia Aparecida de Lima Teixeira, Vicente de Paula Antunes Tostes Junior, Sebastião Rodrigues, Virmondes |
author_facet | Rodrigues, Denise Bertulucci Rocha dos Reis, Marlene Antonia Romano, Audrey Pereira, Sanívia Aparecida de Lima Teixeira, Vicente de Paula Antunes Tostes Junior, Sebastião Rodrigues, Virmondes |
author_sort | Rodrigues, Denise Bertulucci Rocha |
collection | PubMed |
description | Chagas' disease is caused by the protozoan parasite Trypanosoma cruzi. The immune system plays an important role in the reduction of parasite load, but may also contribute to the development of lesions observed during the chronic phase of the disease. We analyzed cytokines produced by inflammatory heart cells in 21 autopsy samples obtained from patients with Chagas' disease divided according to the presence or absence of heart failure (HF). Left ventricular sections were analyzed by immunohistochemistry using antibodies against human IL-4, IFN-γ, TGF-β, TNF-α, and NOS2. In situ mRNA expression was quantified by a Low Density Array. The number of IFN-γ-positive cells was significantly higher than IL-4 positive cells. TNF-α, TGF-β and NOS2 were detected in 65%, 62% and 94% of samples respectively. There was an association between TNF-α-producing cells and the presence of HF. Subjects with HF presented higher levels of STAT4 mRNA, whereas FoxP3 and STAT6 levels were similar in the two groups. A Th1 cytokine pattern predominated in the cardiac inflammatory cell infiltrate of Chagas' disease patients associated with HF. High degree of fibrosis was associated with low NOS2 expression. These results support the idea that Th1 immune responses are involved in heart lesions of Chagas' disease patients. |
format | Online Article Text |
id | pubmed-3397162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-33971622012-07-18 In Situ Expression of Regulatory Cytokines by Heart Inflammatory Cells in Chagas' Disease Patients with Heart Failure Rodrigues, Denise Bertulucci Rocha dos Reis, Marlene Antonia Romano, Audrey Pereira, Sanívia Aparecida de Lima Teixeira, Vicente de Paula Antunes Tostes Junior, Sebastião Rodrigues, Virmondes Clin Dev Immunol Clinical Study Chagas' disease is caused by the protozoan parasite Trypanosoma cruzi. The immune system plays an important role in the reduction of parasite load, but may also contribute to the development of lesions observed during the chronic phase of the disease. We analyzed cytokines produced by inflammatory heart cells in 21 autopsy samples obtained from patients with Chagas' disease divided according to the presence or absence of heart failure (HF). Left ventricular sections were analyzed by immunohistochemistry using antibodies against human IL-4, IFN-γ, TGF-β, TNF-α, and NOS2. In situ mRNA expression was quantified by a Low Density Array. The number of IFN-γ-positive cells was significantly higher than IL-4 positive cells. TNF-α, TGF-β and NOS2 were detected in 65%, 62% and 94% of samples respectively. There was an association between TNF-α-producing cells and the presence of HF. Subjects with HF presented higher levels of STAT4 mRNA, whereas FoxP3 and STAT6 levels were similar in the two groups. A Th1 cytokine pattern predominated in the cardiac inflammatory cell infiltrate of Chagas' disease patients associated with HF. High degree of fibrosis was associated with low NOS2 expression. These results support the idea that Th1 immune responses are involved in heart lesions of Chagas' disease patients. Hindawi Publishing Corporation 2012 2012-07-03 /pmc/articles/PMC3397162/ /pubmed/22811738 http://dx.doi.org/10.1155/2012/361730 Text en Copyright © 2012 Denise Bertulucci Rocha Rodrigues et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Rodrigues, Denise Bertulucci Rocha dos Reis, Marlene Antonia Romano, Audrey Pereira, Sanívia Aparecida de Lima Teixeira, Vicente de Paula Antunes Tostes Junior, Sebastião Rodrigues, Virmondes In Situ Expression of Regulatory Cytokines by Heart Inflammatory Cells in Chagas' Disease Patients with Heart Failure |
title |
In Situ Expression of Regulatory Cytokines by Heart Inflammatory Cells in Chagas' Disease Patients with Heart Failure |
title_full |
In Situ Expression of Regulatory Cytokines by Heart Inflammatory Cells in Chagas' Disease Patients with Heart Failure |
title_fullStr |
In Situ Expression of Regulatory Cytokines by Heart Inflammatory Cells in Chagas' Disease Patients with Heart Failure |
title_full_unstemmed |
In Situ Expression of Regulatory Cytokines by Heart Inflammatory Cells in Chagas' Disease Patients with Heart Failure |
title_short |
In Situ Expression of Regulatory Cytokines by Heart Inflammatory Cells in Chagas' Disease Patients with Heart Failure |
title_sort | in situ expression of regulatory cytokines by heart inflammatory cells in chagas' disease patients with heart failure |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397162/ https://www.ncbi.nlm.nih.gov/pubmed/22811738 http://dx.doi.org/10.1155/2012/361730 |
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