CD4(+) T helper cells and regulatory T cells in active lupus nephritis: an imbalance towards a predominant Th1 response?
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , , |
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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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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1814268407127736320 |