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Impaired Lymphocyte Profile in Schistosomiasis Patients with Periportal Fibrosis

The Th2 immune response in chronic schistosomiasis is associated with the development of periportal fibrosis. However, little is known about the phenotype and activation status of T cells in the process. Objective. To evaluate the profile of T cells in schistosomiasis patients with periportal fibros...

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Autores principales: Cardoso, Luciana Santos, Barreto, Andréia de Souza Rocha, Fernandes, Jamille Souza, Oliveira, Ricardo Riccio, de Souza, Robson da Paixão, Carvalho, Edgar M., Araujo, Maria Ilma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855942/
https://www.ncbi.nlm.nih.gov/pubmed/24348679
http://dx.doi.org/10.1155/2013/710647
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author Cardoso, Luciana Santos
Barreto, Andréia de Souza Rocha
Fernandes, Jamille Souza
Oliveira, Ricardo Riccio
de Souza, Robson da Paixão
Carvalho, Edgar M.
Araujo, Maria Ilma
author_facet Cardoso, Luciana Santos
Barreto, Andréia de Souza Rocha
Fernandes, Jamille Souza
Oliveira, Ricardo Riccio
de Souza, Robson da Paixão
Carvalho, Edgar M.
Araujo, Maria Ilma
author_sort Cardoso, Luciana Santos
collection PubMed
description The Th2 immune response in chronic schistosomiasis is associated with the development of periportal fibrosis. However, little is known about the phenotype and activation status of T cells in the process. Objective. To evaluate the profile of T cells in schistosomiasis patients with periportal fibrosis. Methods. It was a cross-sectional study, conducted in the village of Agua Preta, Bahia, Brazil, which included 37 subjects with periportal fibrosis determined by ultrasound. Peripheral blood mononuclear cells were obtained by the Ficcol-hypaque gradient and the frequency of T cells expressing the surface markers CD28, CD69, CD25, and CTLA-4 was determined by flow cytometry. Results. The frequency of CD4(+)CD28(+) T lymphocytes was higher in individuals with moderate to severe fibrosis compared to patients with incipient fibrosis. We did not observe any significant difference in the frequency of CD4(+) T cells expressing CD69 among groups of individuals. There was also no significant difference in the frequency of CD8(+) T cells expressing CD28 or CD69 among the studied groups. Individuals with moderate to severe fibrosis presented a lower frequency of CD8(+) T cells, CD4(+)CD25(high) T cells, and CD4(+)CTLA-4(+) T cells when compared to patients without fibrosis or incipient fibrosis. The frequency of CD4(+)CD25(low) cells did not differ between groups. Conclusion. The high frequency of activated T cells coinciding with a low frequency of putative Treg cells may account for the development of periportal fibrosis in human schistosomiasis.
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spelling pubmed-38559422013-12-16 Impaired Lymphocyte Profile in Schistosomiasis Patients with Periportal Fibrosis Cardoso, Luciana Santos Barreto, Andréia de Souza Rocha Fernandes, Jamille Souza Oliveira, Ricardo Riccio de Souza, Robson da Paixão Carvalho, Edgar M. Araujo, Maria Ilma Clin Dev Immunol Research Article The Th2 immune response in chronic schistosomiasis is associated with the development of periportal fibrosis. However, little is known about the phenotype and activation status of T cells in the process. Objective. To evaluate the profile of T cells in schistosomiasis patients with periportal fibrosis. Methods. It was a cross-sectional study, conducted in the village of Agua Preta, Bahia, Brazil, which included 37 subjects with periportal fibrosis determined by ultrasound. Peripheral blood mononuclear cells were obtained by the Ficcol-hypaque gradient and the frequency of T cells expressing the surface markers CD28, CD69, CD25, and CTLA-4 was determined by flow cytometry. Results. The frequency of CD4(+)CD28(+) T lymphocytes was higher in individuals with moderate to severe fibrosis compared to patients with incipient fibrosis. We did not observe any significant difference in the frequency of CD4(+) T cells expressing CD69 among groups of individuals. There was also no significant difference in the frequency of CD8(+) T cells expressing CD28 or CD69 among the studied groups. Individuals with moderate to severe fibrosis presented a lower frequency of CD8(+) T cells, CD4(+)CD25(high) T cells, and CD4(+)CTLA-4(+) T cells when compared to patients without fibrosis or incipient fibrosis. The frequency of CD4(+)CD25(low) cells did not differ between groups. Conclusion. The high frequency of activated T cells coinciding with a low frequency of putative Treg cells may account for the development of periportal fibrosis in human schistosomiasis. Hindawi Publishing Corporation 2013 2013-11-18 /pmc/articles/PMC3855942/ /pubmed/24348679 http://dx.doi.org/10.1155/2013/710647 Text en Copyright © 2013 Luciana Santos Cardoso 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 Research Article
Cardoso, Luciana Santos
Barreto, Andréia de Souza Rocha
Fernandes, Jamille Souza
Oliveira, Ricardo Riccio
de Souza, Robson da Paixão
Carvalho, Edgar M.
Araujo, Maria Ilma
Impaired Lymphocyte Profile in Schistosomiasis Patients with Periportal Fibrosis
title Impaired Lymphocyte Profile in Schistosomiasis Patients with Periportal Fibrosis
title_full Impaired Lymphocyte Profile in Schistosomiasis Patients with Periportal Fibrosis
title_fullStr Impaired Lymphocyte Profile in Schistosomiasis Patients with Periportal Fibrosis
title_full_unstemmed Impaired Lymphocyte Profile in Schistosomiasis Patients with Periportal Fibrosis
title_short Impaired Lymphocyte Profile in Schistosomiasis Patients with Periportal Fibrosis
title_sort impaired lymphocyte profile in schistosomiasis patients with periportal fibrosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855942/
https://www.ncbi.nlm.nih.gov/pubmed/24348679
http://dx.doi.org/10.1155/2013/710647
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