Th17 cells and cd4(+) multifunctional t cells in patients with systemic lupus erythematosus
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1016/j.rbr.2015.08.008 http://repositorio.unifesp.br/handle/11600/49529 |
Resumo: | Introduction/Objective: Recent evidence suggests that abnormalities involving Th17 lymphocytes are associated with the pathophysiology of systemic lupus erythematosus (SLE). In addition, multifunctional T cells (MFT), i.e., those producing multiple cytokines simultaneously, are present in the inflammatory milieu and may be implicated in the autoimmune process observed in SLE. In the present study, we aimed to characterize the functional status of CD4(+) T cells in SLE by simultaneously determining the concentration of IL-2, IFN-gamma and IL-17 in lymphocyte cultures under exogenous and self-antigenic stimuli. Patients and methods: Eighteen patients with active disease, 18 with inactive disease, and 14 healthy controls had functional status of CD4(+) T cells analyzed. Results: We found that SLE patients presented a decreased number of total CD4(+) cells, an increased number of activated T cells, and an increased frequency of Th17 cells compared to healthy controls (HC). MFT cells had increased frequency in SLE patients and there was an increased frequency of tri-functional MFT in patients with active SLE compared with those with inactive SLE. Interestingly, MTF cells produced larger amounts of IFN gamma than mono-functional T cells in patients and controls. Conclusion: Taken together these data indicate the participation of recently activated Th17 cells and MTF cells in the SLE pathophysiology. (C) 2015 Elsevier Editora Ltda. All rights reserved. |
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Th17 cells and cd4(+) multifunctional t cells in patients with systemic lupus erythematosusLinfócitos Th17 e linfócitos T CD4+ multifuncionais em pacientes com lúpus eritematoso sistêmicoSystemic Lupus ErythematosusT LymphocytesTh17Multifunctional T CellsDisease-ActivityIl-17CytokineProfilesSubsetsBalanceIl-23Introduction/Objective: Recent evidence suggests that abnormalities involving Th17 lymphocytes are associated with the pathophysiology of systemic lupus erythematosus (SLE). In addition, multifunctional T cells (MFT), i.e., those producing multiple cytokines simultaneously, are present in the inflammatory milieu and may be implicated in the autoimmune process observed in SLE. In the present study, we aimed to characterize the functional status of CD4(+) T cells in SLE by simultaneously determining the concentration of IL-2, IFN-gamma and IL-17 in lymphocyte cultures under exogenous and self-antigenic stimuli. Patients and methods: Eighteen patients with active disease, 18 with inactive disease, and 14 healthy controls had functional status of CD4(+) T cells analyzed. Results: We found that SLE patients presented a decreased number of total CD4(+) cells, an increased number of activated T cells, and an increased frequency of Th17 cells compared to healthy controls (HC). MFT cells had increased frequency in SLE patients and there was an increased frequency of tri-functional MFT in patients with active SLE compared with those with inactive SLE. Interestingly, MTF cells produced larger amounts of IFN gamma than mono-functional T cells in patients and controls. Conclusion: Taken together these data indicate the participation of recently activated Th17 cells and MTF cells in the SLE pathophysiology. (C) 2015 Elsevier Editora Ltda. All rights reserved.Departamento de Reumatologia, Universidade Federal de São Paulo (Unifesp), São Paulo, SP, BrasilDepartamento de Biomedicina, Pontifícia Universidade Católica de Goiás (PUC-GO), Goiânia, GO, BrasilDepartamento de Imunologia Clínica e Alergia, Universidade de São Paulo (USP), São Paulo, SP, BrasilDepartamento de Reumatologia, Universidade Federal de São Paulo (Unifesp), São Paulo, SP, BrasilWeb of ScienceElsevier science inc2019-01-21T10:30:00Z2019-01-21T10:30:00Z2016info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion28-36http://dx.doi.org/10.1016/j.rbr.2015.08.008Revista Brasileira De Reumatologia. New york, v. 56, n. 1, p. 28-36, 2016.10.1016/j.rbr.2015.08.008S0482-50042016000100028.pdf0482-5004S0482-50042016000100028http://repositorio.unifesp.br/handle/11600/49529WOS:000374895300006porRevista Brasileira De Reumatologiainfo:eu-repo/semantics/openAccessPereira Araujo, Julio Antonio [UNIFESP]Mesquita, Danilo, Jr. [UNIFESP]Cruvinel, Wilson de Melo [UNIFESP]Salmazi, Karina InacioKallas, Esper GeorgesCoelho Andrade, Luis Eduardo [UNIFESP]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2022-02-09T10:20:36Zoai:repositorio.unifesp.br/:11600/49529Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652022-02-09T10:20:36Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Th17 cells and cd4(+) multifunctional t cells in patients with systemic lupus erythematosus Linfócitos Th17 e linfócitos T CD4+ multifuncionais em pacientes com lúpus eritematoso sistêmico |
title |
Th17 cells and cd4(+) multifunctional t cells in patients with systemic lupus erythematosus |
spellingShingle |
Th17 cells and cd4(+) multifunctional t cells in patients with systemic lupus erythematosus Pereira Araujo, Julio Antonio [UNIFESP] Systemic Lupus Erythematosus T Lymphocytes Th17 Multifunctional T CellsDisease-Activity Il-17 Cytokine Profiles Subsets Balance Il-23 |
title_short |
Th17 cells and cd4(+) multifunctional t cells in patients with systemic lupus erythematosus |
title_full |
Th17 cells and cd4(+) multifunctional t cells in patients with systemic lupus erythematosus |
title_fullStr |
Th17 cells and cd4(+) multifunctional t cells in patients with systemic lupus erythematosus |
title_full_unstemmed |
Th17 cells and cd4(+) multifunctional t cells in patients with systemic lupus erythematosus |
title_sort |
Th17 cells and cd4(+) multifunctional t cells in patients with systemic lupus erythematosus |
author |
Pereira Araujo, Julio Antonio [UNIFESP] |
author_facet |
Pereira Araujo, Julio Antonio [UNIFESP] Mesquita, Danilo, Jr. [UNIFESP] Cruvinel, Wilson de Melo [UNIFESP] Salmazi, Karina Inacio Kallas, Esper Georges Coelho Andrade, Luis Eduardo [UNIFESP] |
author_role |
author |
author2 |
Mesquita, Danilo, Jr. [UNIFESP] Cruvinel, Wilson de Melo [UNIFESP] Salmazi, Karina Inacio Kallas, Esper Georges Coelho Andrade, Luis Eduardo [UNIFESP] |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Pereira Araujo, Julio Antonio [UNIFESP] Mesquita, Danilo, Jr. [UNIFESP] Cruvinel, Wilson de Melo [UNIFESP] Salmazi, Karina Inacio Kallas, Esper Georges Coelho Andrade, Luis Eduardo [UNIFESP] |
dc.subject.por.fl_str_mv |
Systemic Lupus Erythematosus T Lymphocytes Th17 Multifunctional T CellsDisease-Activity Il-17 Cytokine Profiles Subsets Balance Il-23 |
topic |
Systemic Lupus Erythematosus T Lymphocytes Th17 Multifunctional T CellsDisease-Activity Il-17 Cytokine Profiles Subsets Balance Il-23 |
description |
Introduction/Objective: Recent evidence suggests that abnormalities involving Th17 lymphocytes are associated with the pathophysiology of systemic lupus erythematosus (SLE). In addition, multifunctional T cells (MFT), i.e., those producing multiple cytokines simultaneously, are present in the inflammatory milieu and may be implicated in the autoimmune process observed in SLE. In the present study, we aimed to characterize the functional status of CD4(+) T cells in SLE by simultaneously determining the concentration of IL-2, IFN-gamma and IL-17 in lymphocyte cultures under exogenous and self-antigenic stimuli. Patients and methods: Eighteen patients with active disease, 18 with inactive disease, and 14 healthy controls had functional status of CD4(+) T cells analyzed. Results: We found that SLE patients presented a decreased number of total CD4(+) cells, an increased number of activated T cells, and an increased frequency of Th17 cells compared to healthy controls (HC). MFT cells had increased frequency in SLE patients and there was an increased frequency of tri-functional MFT in patients with active SLE compared with those with inactive SLE. Interestingly, MTF cells produced larger amounts of IFN gamma than mono-functional T cells in patients and controls. Conclusion: Taken together these data indicate the participation of recently activated Th17 cells and MTF cells in the SLE pathophysiology. (C) 2015 Elsevier Editora Ltda. All rights reserved. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016 2019-01-21T10:30:00Z 2019-01-21T10:30:00Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.rbr.2015.08.008 Revista Brasileira De Reumatologia. New york, v. 56, n. 1, p. 28-36, 2016. 10.1016/j.rbr.2015.08.008 S0482-50042016000100028.pdf 0482-5004 S0482-50042016000100028 http://repositorio.unifesp.br/handle/11600/49529 WOS:000374895300006 |
url |
http://dx.doi.org/10.1016/j.rbr.2015.08.008 http://repositorio.unifesp.br/handle/11600/49529 |
identifier_str_mv |
Revista Brasileira De Reumatologia. New york, v. 56, n. 1, p. 28-36, 2016. 10.1016/j.rbr.2015.08.008 S0482-50042016000100028.pdf 0482-5004 S0482-50042016000100028 WOS:000374895300006 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
Revista Brasileira De Reumatologia |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
28-36 |
dc.publisher.none.fl_str_mv |
Elsevier science inc |
publisher.none.fl_str_mv |
Elsevier science inc |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1814268361281896448 |