Thymopoiesis and regulatory T cells in healthy children and adolescents
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
dARK ID: | ark:/48912/001300000q33n |
DOI: | 10.6061/clinics/2012(05)04 |
Texto Completo: | http://dx.doi.org/10.6061/clinics/2012(05)04 http://repositorio.unifesp.br/handle/11600/6806 |
Resumo: | OBJECTIVES: The purpose of this study was to investigate the association between T cell receptor excision circle levels in peripheral blood mononuclear cells and regulatory T cells that co-express CD25 and Foxp3 in healthy children and adolescents of different ages. MATERIALS AND METHODS: The quantification of signal-joint T-cell receptor excision circle levels in the genomic DNA of peripheral blood mononuclear cells was performed using real-time quantitative PCR. The analysis of CD4, CD8, CD25, and Foxp3 expression was performed using flow cytometry. RESULTS: Ninety-five healthy controls (46 females and 49 males) ranging in age from 1 to 18 years were analyzed. The mean T-cell receptor excision circle count in all individuals was 89.095¡36.790 T-cell receptor excision circles per microgram of DNA. There was an inverse correlation between T-cell receptor excision circles counts and age (r = -0.846; p<0.001) as well as between the proportion of CD4+CD25+Foxp3+ T cells and age (r = -0.467; p = 0.04). In addition, we observed a positive correlation between the amount of CD4+CD25+Foxp3+ T cells and the amount of Tcell receptor excision circles per microgram of DNA in individuals of all ages (r = -0.529; p = 0.02). CONCLUSIONS: In this study, we observed a decrease in the thymic function with age based on the fact that the level of T-cell receptor excision circles in the peripheral blood positively correlated with the proportion of regulatory T cells in healthy children and adolescents. These findings indicate that although T-cell receptor excision circles and regulatory T cells levels decrease with age, homeostasis of the immune system and relative regulatory T cells population levels are maintained in the peripheral blood. |
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Thymopoiesis and regulatory T cells in healthy children and adolescentsT lymphocytesThymusFoxp3T-cell ReceptorOBJECTIVES: The purpose of this study was to investigate the association between T cell receptor excision circle levels in peripheral blood mononuclear cells and regulatory T cells that co-express CD25 and Foxp3 in healthy children and adolescents of different ages. MATERIALS AND METHODS: The quantification of signal-joint T-cell receptor excision circle levels in the genomic DNA of peripheral blood mononuclear cells was performed using real-time quantitative PCR. The analysis of CD4, CD8, CD25, and Foxp3 expression was performed using flow cytometry. RESULTS: Ninety-five healthy controls (46 females and 49 males) ranging in age from 1 to 18 years were analyzed. The mean T-cell receptor excision circle count in all individuals was 89.095¡36.790 T-cell receptor excision circles per microgram of DNA. There was an inverse correlation between T-cell receptor excision circles counts and age (r = -0.846; p<0.001) as well as between the proportion of CD4+CD25+Foxp3+ T cells and age (r = -0.467; p = 0.04). In addition, we observed a positive correlation between the amount of CD4+CD25+Foxp3+ T cells and the amount of Tcell receptor excision circles per microgram of DNA in individuals of all ages (r = -0.529; p = 0.02). CONCLUSIONS: In this study, we observed a decrease in the thymic function with age based on the fact that the level of T-cell receptor excision circles in the peripheral blood positively correlated with the proportion of regulatory T cells in healthy children and adolescents. These findings indicate that although T-cell receptor excision circles and regulatory T cells levels decrease with age, homeostasis of the immune system and relative regulatory T cells population levels are maintained in the peripheral blood.Instituto da Criança Departamento de PediatriaUniversidade de São Paulo Faculdade de MedicinaUniversidade Federal de São Paulo (UNIFESP) Escola Paulista de MedicinaUNIFESP, EPMSciELOFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)2008/58238-4Faculdade de Medicina / USPInstituto da Criança Departamento de PediatriaUniversidade de São Paulo (USP)Universidade Federal de São Paulo (UNIFESP)Arismendi, Maria IzabelKallas, Esper Georges [UNIFESP]Santos, Bianca Almeida Natali dosCarneiro-Sampaio, Magda Maria SalesKayser, Cristiane [UNIFESP]2015-06-14T13:43:27Z2015-06-14T13:43:27Z2012-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion425-429application/pdfhttp://dx.doi.org/10.6061/clinics/2012(05)04Clinics. Faculdade de Medicina / USP, v. 67, n. 5, p. 425-429, 2012.10.6061/clinics/2012(05)04S1807-59322012000500004.pdf1807-5932S1807-59322012000500004http://repositorio.unifesp.br/handle/11600/6806WOS:000304827700004ark:/48912/001300000q33nengClinicsinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-04T09:11:14Zoai:repositorio.unifesp.br/:11600/6806Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-12-11T20:30:35.500762Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Thymopoiesis and regulatory T cells in healthy children and adolescents |
title |
Thymopoiesis and regulatory T cells in healthy children and adolescents |
spellingShingle |
Thymopoiesis and regulatory T cells in healthy children and adolescents Thymopoiesis and regulatory T cells in healthy children and adolescents Arismendi, Maria Izabel T lymphocytes Thymus Foxp3 T-cell Receptor Arismendi, Maria Izabel T lymphocytes Thymus Foxp3 T-cell Receptor |
title_short |
Thymopoiesis and regulatory T cells in healthy children and adolescents |
title_full |
Thymopoiesis and regulatory T cells in healthy children and adolescents |
title_fullStr |
Thymopoiesis and regulatory T cells in healthy children and adolescents Thymopoiesis and regulatory T cells in healthy children and adolescents |
title_full_unstemmed |
Thymopoiesis and regulatory T cells in healthy children and adolescents Thymopoiesis and regulatory T cells in healthy children and adolescents |
title_sort |
Thymopoiesis and regulatory T cells in healthy children and adolescents |
author |
Arismendi, Maria Izabel |
author_facet |
Arismendi, Maria Izabel Arismendi, Maria Izabel Kallas, Esper Georges [UNIFESP] Santos, Bianca Almeida Natali dos Carneiro-Sampaio, Magda Maria Sales Kayser, Cristiane [UNIFESP] Kallas, Esper Georges [UNIFESP] Santos, Bianca Almeida Natali dos Carneiro-Sampaio, Magda Maria Sales Kayser, Cristiane [UNIFESP] |
author_role |
author |
author2 |
Kallas, Esper Georges [UNIFESP] Santos, Bianca Almeida Natali dos Carneiro-Sampaio, Magda Maria Sales Kayser, Cristiane [UNIFESP] |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Instituto da Criança Departamento de Pediatria Universidade de São Paulo (USP) Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Arismendi, Maria Izabel Kallas, Esper Georges [UNIFESP] Santos, Bianca Almeida Natali dos Carneiro-Sampaio, Magda Maria Sales Kayser, Cristiane [UNIFESP] |
dc.subject.por.fl_str_mv |
T lymphocytes Thymus Foxp3 T-cell Receptor |
topic |
T lymphocytes Thymus Foxp3 T-cell Receptor |
description |
OBJECTIVES: The purpose of this study was to investigate the association between T cell receptor excision circle levels in peripheral blood mononuclear cells and regulatory T cells that co-express CD25 and Foxp3 in healthy children and adolescents of different ages. MATERIALS AND METHODS: The quantification of signal-joint T-cell receptor excision circle levels in the genomic DNA of peripheral blood mononuclear cells was performed using real-time quantitative PCR. The analysis of CD4, CD8, CD25, and Foxp3 expression was performed using flow cytometry. RESULTS: Ninety-five healthy controls (46 females and 49 males) ranging in age from 1 to 18 years were analyzed. The mean T-cell receptor excision circle count in all individuals was 89.095¡36.790 T-cell receptor excision circles per microgram of DNA. There was an inverse correlation between T-cell receptor excision circles counts and age (r = -0.846; p<0.001) as well as between the proportion of CD4+CD25+Foxp3+ T cells and age (r = -0.467; p = 0.04). In addition, we observed a positive correlation between the amount of CD4+CD25+Foxp3+ T cells and the amount of Tcell receptor excision circles per microgram of DNA in individuals of all ages (r = -0.529; p = 0.02). CONCLUSIONS: In this study, we observed a decrease in the thymic function with age based on the fact that the level of T-cell receptor excision circles in the peripheral blood positively correlated with the proportion of regulatory T cells in healthy children and adolescents. These findings indicate that although T-cell receptor excision circles and regulatory T cells levels decrease with age, homeostasis of the immune system and relative regulatory T cells population levels are maintained in the peripheral blood. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-01-01 2015-06-14T13:43:27Z 2015-06-14T13:43:27Z |
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/10.6061/clinics/2012(05)04 Clinics. Faculdade de Medicina / USP, v. 67, n. 5, p. 425-429, 2012. 10.6061/clinics/2012(05)04 S1807-59322012000500004.pdf 1807-5932 S1807-59322012000500004 http://repositorio.unifesp.br/handle/11600/6806 WOS:000304827700004 |
dc.identifier.dark.fl_str_mv |
ark:/48912/001300000q33n |
url |
http://dx.doi.org/10.6061/clinics/2012(05)04 http://repositorio.unifesp.br/handle/11600/6806 |
identifier_str_mv |
Clinics. Faculdade de Medicina / USP, v. 67, n. 5, p. 425-429, 2012. 10.6061/clinics/2012(05)04 S1807-59322012000500004.pdf 1807-5932 S1807-59322012000500004 WOS:000304827700004 ark:/48912/001300000q33n |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Clinics |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
425-429 application/pdf |
dc.publisher.none.fl_str_mv |
Faculdade de Medicina / USP |
publisher.none.fl_str_mv |
Faculdade de Medicina / USP |
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 |
_version_ |
1822178966842114048 |
dc.identifier.doi.none.fl_str_mv |
10.6061/clinics/2012(05)04 |