Malignant and tuberculous pleural effusions: immunophenotypic cellular characterization
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Clinics |
DOI: | 10.1590/S1807-59322008000500012 |
Texto Completo: | https://www.revistas.usp.br/clinics/article/view/17754 |
Resumo: | INTRODUCTION AND OBJECTIVES: Tuberculosis and cancer are the main causes of pleural effusion. Pleural involvement is associated with migration of immune cells to the pleural cavity. We sought to characterize the immunophenotype of leukocytes in the pleural effusion and peripheral blood of patients with tuberculosis or malignancy. METHODS: Thirty patients with tuberculosis (14) or malignancy (16) were studied. A control group included 20 healthy blood donors. RESULTS: Malignant phycoerythrin pleural effusions showed higher percentages of CD3, CD4, CD3CD45RO, and CD20CD25 lymphocytes and lower percentages of CD3CD25 and CD20HLA-DR when compared to PB lymphocytes. Compared to PB, tuberculous effusions had a higher percentage of lymphocytes that co-expressed CD3, CD4, CD3CD45RO, CD3TCRαβ, CD3CD28, and CD20 and a lower percentage of CD14, CD8 and CD3TCRγδ-positive lymphocytes. Malignant effusions presented higher expression of CD14 whereas tuberculous effusions had higher expression of CD3 and CD3CD95L. Peripheral blood cells from tuberculosis patients showed higher expression of CD14, CD20CD25 and CD3CD95L. Compared with the control cells, tuberculosis and cancer peripheral blood cells presented a lower percentage of CD3CD4 and CD3CD28-positive cells as well as a higher percentage of CD3CD8, CD3CD25 and CD3CD80-positive cells. CONCLUSIONS: Tuberculous and malignant peripheral blood is enriched with lymphocytes with a helper/inducer T cell phenotype, which are mainly of memory cells. CD14-positive cells were more frequently found in malignant effusions, while CD3-positive cells expressing Fas ligand were more frequently found in tuberculous effusions. |
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oai:revistas.usp.br:article/17754 |
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USP-19 |
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Clinics |
spelling |
Malignant and tuberculous pleural effusions: immunophenotypic cellular characterization Pleural fluidCancerFlow cytometryMonoclonal antibodyTuberculosis INTRODUCTION AND OBJECTIVES: Tuberculosis and cancer are the main causes of pleural effusion. Pleural involvement is associated with migration of immune cells to the pleural cavity. We sought to characterize the immunophenotype of leukocytes in the pleural effusion and peripheral blood of patients with tuberculosis or malignancy. METHODS: Thirty patients with tuberculosis (14) or malignancy (16) were studied. A control group included 20 healthy blood donors. RESULTS: Malignant phycoerythrin pleural effusions showed higher percentages of CD3, CD4, CD3CD45RO, and CD20CD25 lymphocytes and lower percentages of CD3CD25 and CD20HLA-DR when compared to PB lymphocytes. Compared to PB, tuberculous effusions had a higher percentage of lymphocytes that co-expressed CD3, CD4, CD3CD45RO, CD3TCRαβ, CD3CD28, and CD20 and a lower percentage of CD14, CD8 and CD3TCRγδ-positive lymphocytes. Malignant effusions presented higher expression of CD14 whereas tuberculous effusions had higher expression of CD3 and CD3CD95L. Peripheral blood cells from tuberculosis patients showed higher expression of CD14, CD20CD25 and CD3CD95L. Compared with the control cells, tuberculosis and cancer peripheral blood cells presented a lower percentage of CD3CD4 and CD3CD28-positive cells as well as a higher percentage of CD3CD8, CD3CD25 and CD3CD80-positive cells. CONCLUSIONS: Tuberculous and malignant peripheral blood is enriched with lymphocytes with a helper/inducer T cell phenotype, which are mainly of memory cells. CD14-positive cells were more frequently found in malignant effusions, while CD3-positive cells expressing Fas ligand were more frequently found in tuberculous effusions. Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2008-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/1775410.1590/S1807-59322008000500012Clinics; Vol. 63 No. 5 (2008); 637-644 Clinics; v. 63 n. 5 (2008); 637-644 Clinics; Vol. 63 Núm. 5 (2008); 637-644 1980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/17754/19819Aguiar, Lucia Maria Zanatta deAntonangelo, LeilaVargas, Francisco S.Zerbini, Maria Cláudia NogueiraSales, Maria MirtesUip, David E.Saldiva, Paulo Hilário Nascimentoinfo:eu-repo/semantics/openAccess2012-05-22T18:30:46Zoai:revistas.usp.br:article/17754Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2012-05-22T18:30:46Clinics - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Malignant and tuberculous pleural effusions: immunophenotypic cellular characterization |
title |
Malignant and tuberculous pleural effusions: immunophenotypic cellular characterization |
spellingShingle |
Malignant and tuberculous pleural effusions: immunophenotypic cellular characterization Malignant and tuberculous pleural effusions: immunophenotypic cellular characterization Aguiar, Lucia Maria Zanatta de Pleural fluid Cancer Flow cytometry Monoclonal antibody Tuberculosis Aguiar, Lucia Maria Zanatta de Pleural fluid Cancer Flow cytometry Monoclonal antibody Tuberculosis |
title_short |
Malignant and tuberculous pleural effusions: immunophenotypic cellular characterization |
title_full |
Malignant and tuberculous pleural effusions: immunophenotypic cellular characterization |
title_fullStr |
Malignant and tuberculous pleural effusions: immunophenotypic cellular characterization Malignant and tuberculous pleural effusions: immunophenotypic cellular characterization |
title_full_unstemmed |
Malignant and tuberculous pleural effusions: immunophenotypic cellular characterization Malignant and tuberculous pleural effusions: immunophenotypic cellular characterization |
title_sort |
Malignant and tuberculous pleural effusions: immunophenotypic cellular characterization |
author |
Aguiar, Lucia Maria Zanatta de |
author_facet |
Aguiar, Lucia Maria Zanatta de Aguiar, Lucia Maria Zanatta de Antonangelo, Leila Vargas, Francisco S. Zerbini, Maria Cláudia Nogueira Sales, Maria Mirtes Uip, David E. Saldiva, Paulo Hilário Nascimento Antonangelo, Leila Vargas, Francisco S. Zerbini, Maria Cláudia Nogueira Sales, Maria Mirtes Uip, David E. Saldiva, Paulo Hilário Nascimento |
author_role |
author |
author2 |
Antonangelo, Leila Vargas, Francisco S. Zerbini, Maria Cláudia Nogueira Sales, Maria Mirtes Uip, David E. Saldiva, Paulo Hilário Nascimento |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Aguiar, Lucia Maria Zanatta de Antonangelo, Leila Vargas, Francisco S. Zerbini, Maria Cláudia Nogueira Sales, Maria Mirtes Uip, David E. Saldiva, Paulo Hilário Nascimento |
dc.subject.por.fl_str_mv |
Pleural fluid Cancer Flow cytometry Monoclonal antibody Tuberculosis |
topic |
Pleural fluid Cancer Flow cytometry Monoclonal antibody Tuberculosis |
description |
INTRODUCTION AND OBJECTIVES: Tuberculosis and cancer are the main causes of pleural effusion. Pleural involvement is associated with migration of immune cells to the pleural cavity. We sought to characterize the immunophenotype of leukocytes in the pleural effusion and peripheral blood of patients with tuberculosis or malignancy. METHODS: Thirty patients with tuberculosis (14) or malignancy (16) were studied. A control group included 20 healthy blood donors. RESULTS: Malignant phycoerythrin pleural effusions showed higher percentages of CD3, CD4, CD3CD45RO, and CD20CD25 lymphocytes and lower percentages of CD3CD25 and CD20HLA-DR when compared to PB lymphocytes. Compared to PB, tuberculous effusions had a higher percentage of lymphocytes that co-expressed CD3, CD4, CD3CD45RO, CD3TCRαβ, CD3CD28, and CD20 and a lower percentage of CD14, CD8 and CD3TCRγδ-positive lymphocytes. Malignant effusions presented higher expression of CD14 whereas tuberculous effusions had higher expression of CD3 and CD3CD95L. Peripheral blood cells from tuberculosis patients showed higher expression of CD14, CD20CD25 and CD3CD95L. Compared with the control cells, tuberculosis and cancer peripheral blood cells presented a lower percentage of CD3CD4 and CD3CD28-positive cells as well as a higher percentage of CD3CD8, CD3CD25 and CD3CD80-positive cells. CONCLUSIONS: Tuberculous and malignant peripheral blood is enriched with lymphocytes with a helper/inducer T cell phenotype, which are mainly of memory cells. CD14-positive cells were more frequently found in malignant effusions, while CD3-positive cells expressing Fas ligand were more frequently found in tuberculous effusions. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008-01-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/17754 10.1590/S1807-59322008000500012 |
url |
https://www.revistas.usp.br/clinics/article/view/17754 |
identifier_str_mv |
10.1590/S1807-59322008000500012 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/17754/19819 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
dc.source.none.fl_str_mv |
Clinics; Vol. 63 No. 5 (2008); 637-644 Clinics; v. 63 n. 5 (2008); 637-644 Clinics; Vol. 63 Núm. 5 (2008); 637-644 1980-5322 1807-5932 reponame:Clinics instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Clinics |
collection |
Clinics |
repository.name.fl_str_mv |
Clinics - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
||clinics@hc.fm.usp.br |
_version_ |
1822181710323777536 |
dc.identifier.doi.none.fl_str_mv |
10.1590/S1807-59322008000500012 |