Malignant and tuberculous pleural effusions: immunophenotypic cellular characterization

Detalhes bibliográficos
Autor(a) principal: Aguiar, Lucia Maria Zanatta de
Data de Publicação: 2008
Outros Autores: Antonangelo, Leila, Vargas, Francisco S., Zerbini, Maria Cláudia Nogueira, Sales, Maria Mirtes, Uip, David E., Saldiva, Paulo Hilário Nascimento
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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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
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dc.identifier.doi.none.fl_str_mv 10.1590/S1807-59322008000500012