Thymopoiesis and regulatory T cells in healthy children and adolescents

Detalhes bibliográficos
Autor(a) principal: Arismendi, Maria Izabel
Data de Publicação: 2012
Outros Autores: Kallas, Esper Georges [UNIFESP], Santos, Bianca Almeida Natali dos, Carneiro-Sampaio, Magda Maria Sales, Kayser, Cristiane [UNIFESP]
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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spelling 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