CD4(+) T helper cells and regulatory T cells in active lupus nephritis: an imbalance towards a predominant Th1 response?

Detalhes bibliográficos
Autor(a) principal: Mesquita, D., Jr.
Data de Publicação: 2018
Outros Autores: Mastroianni Kirsztajn, G., Franco, M. F. [UNIFESP], Reis, L. A., Perazzio, S. F., Mesquita, F. V., da Silva Ferreira, V., Coelho Andrade, L. E., Silva de Souza, A. W.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1111/cei.13050
https://repositorio.unifesp.br/handle/11600/53971
Resumo: The objective of this study was to evaluate the frequency of CD4(+) T cell subsets in peripheral blood mononuclear cells (PBMC), urine and renal tissue from patients with lupus nephritis (LN). PBMC and urinary cells were collected from 17 patients with active LN, 20 disease controls (DC) with primary glomerulonephritis and 10 healthy controls (HC) and were analysed by flow cytometry with markers for T helper type 1 (Th1), Th2, Th17 and regulatory T cells (T-reg) cells. T cell subsets were assessed by immunohistochemistry from LN biopsy specimens from 12 LN patients. T cell subtypes in PBMC were re-evaluated at 6 months of therapy. CD4(+) T cells were decreased in PBMC in LN compared with DC and HC (P=0<bold></bold>0001). No differences were observed in urinary CD4(+) T cell subsets between LN and DC. The frequency of urinary Th17 cells was higher in patients with non-proliferative than in proliferative LN (P=0<bold></bold>041). CD3(+) and T-box 21 ( <mml:msubsup>Tbet+</mml:msubsup>) cells were found in glomeruli and interstitium of LN patients, while forkhead box protein 3 (FoxP3), retinoid-related orphan receptor gamma (ROR-) and GATA binding protein 3 (GATA-3) were present only in glomeruli. Th1 cells in PBMC were correlated negatively with urinary Th1 cells (Rho=-0<bold></bold>531
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spelling CD4(+) T helper cells and regulatory T cells in active lupus nephritis: an imbalance towards a predominant Th1 response?glomerulonephritishelper T cellslupus nephritisregulatory T cellssystemic lupus erythematosusThe objective of this study was to evaluate the frequency of CD4(+) T cell subsets in peripheral blood mononuclear cells (PBMC), urine and renal tissue from patients with lupus nephritis (LN). PBMC and urinary cells were collected from 17 patients with active LN, 20 disease controls (DC) with primary glomerulonephritis and 10 healthy controls (HC) and were analysed by flow cytometry with markers for T helper type 1 (Th1), Th2, Th17 and regulatory T cells (T-reg) cells. T cell subsets were assessed by immunohistochemistry from LN biopsy specimens from 12 LN patients. T cell subtypes in PBMC were re-evaluated at 6 months of therapy. CD4(+) T cells were decreased in PBMC in LN compared with DC and HC (P=0<bold></bold>0001). No differences were observed in urinary CD4(+) T cell subsets between LN and DC. The frequency of urinary Th17 cells was higher in patients with non-proliferative than in proliferative LN (P=0<bold></bold>041). CD3(+) and T-box 21 ( <mml:msubsup>Tbet+</mml:msubsup>) cells were found in glomeruli and interstitium of LN patients, while forkhead box protein 3 (FoxP3), retinoid-related orphan receptor gamma (ROR-) and GATA binding protein 3 (GATA-3) were present only in glomeruli. Th1 cells in PBMC were correlated negatively with urinary Th1 cells (Rho=-0<bold></bold>531P=0<bold></bold>028) and with T-bet in renal interstitium (Rho=-0<bold></bold>782P=0<bold></bold>004). At 6 months, LN patients showed an increase in Th17 cells in PBMC. In conclusion, the inverse association between Th1 cells from PBMC and urinary/renal tissue indicate a role for Th1 in LN pathophysiology. Urinary Th17 cells were associated with less severe LN, and Th17 increased in PBMC during therapy. Urinary CD4(+) T cells were not different between LN and DC.Rheumatol Div, Sao Paulo, SP, BrazilNephrol Div, Sao Paulo, SP, BrazilUniv Fed Sao Paulo, Escola Paulista Med, Dept Pathol, Sao Paulo, SP, BrazilUniv Fed Sao Paulo, Escola Paulista Med, Dept Pathol, Sao Paulo, SP, BrazilWeb of ScienceFAPESP (Fundacao de Amparo a Pesquisa do Estado de Sao Paulo) [10/51088-7]FAPESP [10/51088-7]Wiley2020-07-02T18:52:14Z2020-07-02T18:52:14Z2018info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion50-59application/pdfhttp://dx.doi.org/10.1111/cei.13050Clinical And Experimental Immunology. Hoboken, v. 191, n. 1, p. 50-59, 2018.10.1111/cei.13050WOS000417564300006.pdf0009-9104https://repositorio.unifesp.br/handle/11600/53971WOS:000417564300006engClinical And Experimental ImmunologyHobokeninfo:eu-repo/semantics/openAccessMesquita, D., Jr.Mastroianni Kirsztajn, G.Franco, M. F. [UNIFESP]Reis, L. A.Perazzio, S. F.Mesquita, F. V.da Silva Ferreira, V.Coelho Andrade, L. E.Silva de Souza, A. W.reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-03T05:18:56Zoai:repositorio.unifesp.br/:11600/53971Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-03T05:18:56Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv CD4(+) T helper cells and regulatory T cells in active lupus nephritis: an imbalance towards a predominant Th1 response?
title CD4(+) T helper cells and regulatory T cells in active lupus nephritis: an imbalance towards a predominant Th1 response?
spellingShingle CD4(+) T helper cells and regulatory T cells in active lupus nephritis: an imbalance towards a predominant Th1 response?
Mesquita, D., Jr.
glomerulonephritis
helper T cells
lupus nephritis
regulatory T cells
systemic lupus erythematosus
title_short CD4(+) T helper cells and regulatory T cells in active lupus nephritis: an imbalance towards a predominant Th1 response?
title_full CD4(+) T helper cells and regulatory T cells in active lupus nephritis: an imbalance towards a predominant Th1 response?
title_fullStr CD4(+) T helper cells and regulatory T cells in active lupus nephritis: an imbalance towards a predominant Th1 response?
title_full_unstemmed CD4(+) T helper cells and regulatory T cells in active lupus nephritis: an imbalance towards a predominant Th1 response?
title_sort CD4(+) T helper cells and regulatory T cells in active lupus nephritis: an imbalance towards a predominant Th1 response?
author Mesquita, D., Jr.
author_facet Mesquita, D., Jr.
Mastroianni Kirsztajn, G.
Franco, M. F. [UNIFESP]
Reis, L. A.
Perazzio, S. F.
Mesquita, F. V.
da Silva Ferreira, V.
Coelho Andrade, L. E.
Silva de Souza, A. W.
author_role author
author2 Mastroianni Kirsztajn, G.
Franco, M. F. [UNIFESP]
Reis, L. A.
Perazzio, S. F.
Mesquita, F. V.
da Silva Ferreira, V.
Coelho Andrade, L. E.
Silva de Souza, A. W.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Mesquita, D., Jr.
Mastroianni Kirsztajn, G.
Franco, M. F. [UNIFESP]
Reis, L. A.
Perazzio, S. F.
Mesquita, F. V.
da Silva Ferreira, V.
Coelho Andrade, L. E.
Silva de Souza, A. W.
dc.subject.por.fl_str_mv glomerulonephritis
helper T cells
lupus nephritis
regulatory T cells
systemic lupus erythematosus
topic glomerulonephritis
helper T cells
lupus nephritis
regulatory T cells
systemic lupus erythematosus
description The objective of this study was to evaluate the frequency of CD4(+) T cell subsets in peripheral blood mononuclear cells (PBMC), urine and renal tissue from patients with lupus nephritis (LN). PBMC and urinary cells were collected from 17 patients with active LN, 20 disease controls (DC) with primary glomerulonephritis and 10 healthy controls (HC) and were analysed by flow cytometry with markers for T helper type 1 (Th1), Th2, Th17 and regulatory T cells (T-reg) cells. T cell subsets were assessed by immunohistochemistry from LN biopsy specimens from 12 LN patients. T cell subtypes in PBMC were re-evaluated at 6 months of therapy. CD4(+) T cells were decreased in PBMC in LN compared with DC and HC (P=0<bold></bold>0001). No differences were observed in urinary CD4(+) T cell subsets between LN and DC. The frequency of urinary Th17 cells was higher in patients with non-proliferative than in proliferative LN (P=0<bold></bold>041). CD3(+) and T-box 21 ( <mml:msubsup>Tbet+</mml:msubsup>) cells were found in glomeruli and interstitium of LN patients, while forkhead box protein 3 (FoxP3), retinoid-related orphan receptor gamma (ROR-) and GATA binding protein 3 (GATA-3) were present only in glomeruli. Th1 cells in PBMC were correlated negatively with urinary Th1 cells (Rho=-0<bold></bold>531
publishDate 2018
dc.date.none.fl_str_mv 2018
2020-07-02T18:52:14Z
2020-07-02T18:52:14Z
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/10.1111/cei.13050
Clinical And Experimental Immunology. Hoboken, v. 191, n. 1, p. 50-59, 2018.
10.1111/cei.13050
WOS000417564300006.pdf
0009-9104
https://repositorio.unifesp.br/handle/11600/53971
WOS:000417564300006
url http://dx.doi.org/10.1111/cei.13050
https://repositorio.unifesp.br/handle/11600/53971
identifier_str_mv Clinical And Experimental Immunology. Hoboken, v. 191, n. 1, p. 50-59, 2018.
10.1111/cei.13050
WOS000417564300006.pdf
0009-9104
WOS:000417564300006
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Clinical And Experimental Immunology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 50-59
application/pdf
dc.coverage.none.fl_str_mv Hoboken
dc.publisher.none.fl_str_mv Wiley
publisher.none.fl_str_mv Wiley
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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