Th17 cells and cd4(+) multifunctional t cells in patients with systemic lupus erythematosus

Detalhes bibliográficos
Autor(a) principal: Pereira Araujo, Julio Antonio [UNIFESP]
Data de Publicação: 2016
Outros Autores: Mesquita, Danilo, Jr. [UNIFESP], Cruvinel, Wilson de Melo [UNIFESP], Salmazi, Karina Inacio, Kallas, Esper Georges, Coelho Andrade, Luis Eduardo [UNIFESP]
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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spelling 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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