Análise de células T regulatórias FoxP3+ no líquen plano oral

Detalhes bibliográficos
Ano de defesa: 2010
Autor(a) principal: Pereira, Joabe dos Santos
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal do Rio Grande do Norte
BR
UFRN
Programa de Pós-Graduação em Patologia Oral
Odontologia
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: https://repositorio.ufrn.br/jspui/handle/123456789/17110
Resumo: T regulatory cells have the function of controlling immune responses and maintaining self-tolerance. The FoxP3 has been considered the most specific marker for Treg cells. The aiming of this paper was to evaluate the immunoexpression of FoxP3 in the inflammatory infiltrate from oral lichen planus (OLP) and to compare it with the infiltrate in fibrous inflammatory hyperplasia (FIH) and then, between reticular and erosive forms of OLP. The samples were composed by 32 cases of OLP (17 reticular and 15 erosive) beyond 10 cases of FIH that were submitted to immunohistochemistry staining for FoxP3. Localization of the staining was classified in underepithelial and intraepithelial and the amount of FoxP3+ cells was evaluated through cells counting in 10 consecutive fields, at 400x power magnification. The values were expressed in mean ± standart deviation, and submitted to statistical tests with 5% of significance level. It was observed a statistical significant difference in the amount of FoxP3+ Treg cells between the two combined forms of OLP (1,6 ± 2,2) and the FIH (0,5 ±0,4) (P<0,05). This maybe could be explained by immunological mechanism of OLP, which involves a permanent antigenic induction likely with consequent perpetuation of lesion, eliciting the proliferation and constant recruitment of Treg cells. Otherwise, FIH presents a different etiopathogenesis, in which there is also generation of a variable inflammatory infiltrate, however qualitatively distinct from that seen in OLP. The erosive form of OLP exhibited a greater number (1,7 ± 2,4) of FoxP3+ Treg cells than reticular form (1,5 ± 2,1). These alterations could have relation with the great disease activity verified in erosive OLP, or also, with abnormalities in the regulatory function of Treg cells that could cause the increase observed. Considering the capacity already well established in the literature, both about Treg cells in modulating immune responses, as in the oral mucosa in showing great potential for regeneration, it is suggested that the possibility of development and implantation of immunotherapeutic strategies that regulate the frequency and function of these cells, may help in future treatment of immune-mediated inflammatory diseases such as OLP
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spelling Análise de células T regulatórias FoxP3+ no líquen plano oralLíquen plano oralImunoistoquímicaCélula T regulatóriaFoxP3Oral lichen planusImmunohistochemistryRegulatory T cellsFoxP3CNPQ::CIENCIAS DA SAUDE::ODONTOLOGIAT regulatory cells have the function of controlling immune responses and maintaining self-tolerance. The FoxP3 has been considered the most specific marker for Treg cells. The aiming of this paper was to evaluate the immunoexpression of FoxP3 in the inflammatory infiltrate from oral lichen planus (OLP) and to compare it with the infiltrate in fibrous inflammatory hyperplasia (FIH) and then, between reticular and erosive forms of OLP. The samples were composed by 32 cases of OLP (17 reticular and 15 erosive) beyond 10 cases of FIH that were submitted to immunohistochemistry staining for FoxP3. Localization of the staining was classified in underepithelial and intraepithelial and the amount of FoxP3+ cells was evaluated through cells counting in 10 consecutive fields, at 400x power magnification. The values were expressed in mean ± standart deviation, and submitted to statistical tests with 5% of significance level. It was observed a statistical significant difference in the amount of FoxP3+ Treg cells between the two combined forms of OLP (1,6 ± 2,2) and the FIH (0,5 ±0,4) (P<0,05). This maybe could be explained by immunological mechanism of OLP, which involves a permanent antigenic induction likely with consequent perpetuation of lesion, eliciting the proliferation and constant recruitment of Treg cells. Otherwise, FIH presents a different etiopathogenesis, in which there is also generation of a variable inflammatory infiltrate, however qualitatively distinct from that seen in OLP. The erosive form of OLP exhibited a greater number (1,7 ± 2,4) of FoxP3+ Treg cells than reticular form (1,5 ± 2,1). These alterations could have relation with the great disease activity verified in erosive OLP, or also, with abnormalities in the regulatory function of Treg cells that could cause the increase observed. Considering the capacity already well established in the literature, both about Treg cells in modulating immune responses, as in the oral mucosa in showing great potential for regeneration, it is suggested that the possibility of development and implantation of immunotherapeutic strategies that regulate the frequency and function of these cells, may help in future treatment of immune-mediated inflammatory diseases such as OLPCoordenação de Aperfeiçoamento de Pessoal de Nível SuperiorAs células T regulatórias (Treg) possuem a função de controlar respostas imunes e manter a autotolerância. O FoxP3 tem sido considerado o marcador mais específico para células Treg. O objetivo deste estudo foi avaliar a imunoexpressão do FoxP3 no infiltrado inflamatório do líquen plano oral (LPO) comparado ao da hiperplasia fibrosa inflamatória (HFI) e posteriormente entre as formas reticular e erosiva do LPO. A amostra foi composta por 32 casos de LPO (17 reticulares e 15 erosivos) além de 10 casos de HFI que foram submetidos à marcação imunoistoquímica para o FoxP3. A localização da marcação foi classificada em justaepitelial ou intraepitelial e a quantidade das células FoxP3+ foi avaliada através da contagem destas em 10 campos consecutivos, com aumento de 400x. Os valores foram expressos em média ± desvio-padrão, e submetidos aos testes estatísticos com nível de significância de 5%. Observou-se uma diferença estatisticamente significativa na quantidade de células Treg FoxP3+ entre os dois tipos de LPO reunidos (1,6 ± 2,2) e a HFI (0,5 ± 0,4) (P<0,05). Isto talvez possa ser explicado pelo mecanismo imunológico do LPO, que envolve uma provável indução antigênica permanente com conseqüente perpetuação da lesão, suscitando a proliferação e recrutamento constante das células Treg. Em contrapartida, a HFI apresenta uma etiopatogenia diferente, na qual também há geração de um infiltrado inflamatório variável, porém qualitativamente distinto do verificado no LPO. A forma erosiva do LPO exibiu um maior número (1,7 ± 2,4) de células Treg FoxP3+ que a forma reticular (1,5 ± 2,1). Estas alterações podem ter relação com a maior atividade da doença verificada no LPO erosivo, ou ainda, com anormalidades na função reguladora das células Treg que ocasionariam o aumento observado. Considerando-se a capacidade já bem estabelecida na literatura, tanto das células Treg modularem as respostas imunológicas, quanto da mucosa oral em exibir um grande potencial de regeneração, sugere-se que a possibilidade de desenvolvimento e implantação de estratégias imunoterapêuticas que regulem a freqüência e a função destas células, possa futuramente auxiliar no tratamento de doenças inflamatórias mediadas imunologicamente, como o LPOUniversidade Federal do Rio Grande do NorteBRUFRNPrograma de Pós-Graduação em Patologia OralOdontologiaMiguel, Márcia Cristina da Costahttp://lattes.cnpq.br/6228325319211685http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4707501Z3&dataRevisao=nullGodoy, Gustavo Pinahttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4751939A2Souza, Lélia Batista dehttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4787927Z7&dataRevisao=nullPereira, Joabe dos Santos2014-12-17T15:32:18Z2010-05-032014-12-17T15:32:18Z2010-03-15info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfapplication/pdfPEREIRA, Joabe dos Santos. Análise de células T regulatórias FoxP3+ no líquen plano oral. 2010. 109 f. Dissertação (Mestrado em Odontologia) - Universidade Federal do Rio Grande do Norte, Natal, 2010.https://repositorio.ufrn.br/jspui/handle/123456789/17110porinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRN2017-11-04T16:14:35Zoai:repositorio.ufrn.br:123456789/17110Repositório InstitucionalPUBhttp://repositorio.ufrn.br/oai/repositorio@bczm.ufrn.bropendoar:2017-11-04T16:14:35Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false
dc.title.none.fl_str_mv Análise de células T regulatórias FoxP3+ no líquen plano oral
title Análise de células T regulatórias FoxP3+ no líquen plano oral
spellingShingle Análise de células T regulatórias FoxP3+ no líquen plano oral
Pereira, Joabe dos Santos
Líquen plano oral
Imunoistoquímica
Célula T regulatória
FoxP3
Oral lichen planus
Immunohistochemistry
Regulatory T cells
FoxP3
CNPQ::CIENCIAS DA SAUDE::ODONTOLOGIA
title_short Análise de células T regulatórias FoxP3+ no líquen plano oral
title_full Análise de células T regulatórias FoxP3+ no líquen plano oral
title_fullStr Análise de células T regulatórias FoxP3+ no líquen plano oral
title_full_unstemmed Análise de células T regulatórias FoxP3+ no líquen plano oral
title_sort Análise de células T regulatórias FoxP3+ no líquen plano oral
author Pereira, Joabe dos Santos
author_facet Pereira, Joabe dos Santos
author_role author
dc.contributor.none.fl_str_mv Miguel, Márcia Cristina da Costa

http://lattes.cnpq.br/6228325319211685

http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4707501Z3&dataRevisao=null
Godoy, Gustavo Pina

http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4751939A2
Souza, Lélia Batista de
http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4787927Z7&dataRevisao=null
dc.contributor.author.fl_str_mv Pereira, Joabe dos Santos
dc.subject.por.fl_str_mv Líquen plano oral
Imunoistoquímica
Célula T regulatória
FoxP3
Oral lichen planus
Immunohistochemistry
Regulatory T cells
FoxP3
CNPQ::CIENCIAS DA SAUDE::ODONTOLOGIA
topic Líquen plano oral
Imunoistoquímica
Célula T regulatória
FoxP3
Oral lichen planus
Immunohistochemistry
Regulatory T cells
FoxP3
CNPQ::CIENCIAS DA SAUDE::ODONTOLOGIA
description T regulatory cells have the function of controlling immune responses and maintaining self-tolerance. The FoxP3 has been considered the most specific marker for Treg cells. The aiming of this paper was to evaluate the immunoexpression of FoxP3 in the inflammatory infiltrate from oral lichen planus (OLP) and to compare it with the infiltrate in fibrous inflammatory hyperplasia (FIH) and then, between reticular and erosive forms of OLP. The samples were composed by 32 cases of OLP (17 reticular and 15 erosive) beyond 10 cases of FIH that were submitted to immunohistochemistry staining for FoxP3. Localization of the staining was classified in underepithelial and intraepithelial and the amount of FoxP3+ cells was evaluated through cells counting in 10 consecutive fields, at 400x power magnification. The values were expressed in mean ± standart deviation, and submitted to statistical tests with 5% of significance level. It was observed a statistical significant difference in the amount of FoxP3+ Treg cells between the two combined forms of OLP (1,6 ± 2,2) and the FIH (0,5 ±0,4) (P<0,05). This maybe could be explained by immunological mechanism of OLP, which involves a permanent antigenic induction likely with consequent perpetuation of lesion, eliciting the proliferation and constant recruitment of Treg cells. Otherwise, FIH presents a different etiopathogenesis, in which there is also generation of a variable inflammatory infiltrate, however qualitatively distinct from that seen in OLP. The erosive form of OLP exhibited a greater number (1,7 ± 2,4) of FoxP3+ Treg cells than reticular form (1,5 ± 2,1). These alterations could have relation with the great disease activity verified in erosive OLP, or also, with abnormalities in the regulatory function of Treg cells that could cause the increase observed. Considering the capacity already well established in the literature, both about Treg cells in modulating immune responses, as in the oral mucosa in showing great potential for regeneration, it is suggested that the possibility of development and implantation of immunotherapeutic strategies that regulate the frequency and function of these cells, may help in future treatment of immune-mediated inflammatory diseases such as OLP
publishDate 2010
dc.date.none.fl_str_mv 2010-05-03
2010-03-15
2014-12-17T15:32:18Z
2014-12-17T15:32:18Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv PEREIRA, Joabe dos Santos. Análise de células T regulatórias FoxP3+ no líquen plano oral. 2010. 109 f. Dissertação (Mestrado em Odontologia) - Universidade Federal do Rio Grande do Norte, Natal, 2010.
https://repositorio.ufrn.br/jspui/handle/123456789/17110
identifier_str_mv PEREIRA, Joabe dos Santos. Análise de células T regulatórias FoxP3+ no líquen plano oral. 2010. 109 f. Dissertação (Mestrado em Odontologia) - Universidade Federal do Rio Grande do Norte, Natal, 2010.
url https://repositorio.ufrn.br/jspui/handle/123456789/17110
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Universidade Federal do Rio Grande do Norte
BR
UFRN
Programa de Pós-Graduação em Patologia Oral
Odontologia
publisher.none.fl_str_mv Universidade Federal do Rio Grande do Norte
BR
UFRN
Programa de Pós-Graduação em Patologia Oral
Odontologia
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFRN
instname:Universidade Federal do Rio Grande do Norte (UFRN)
instacron:UFRN
instname_str Universidade Federal do Rio Grande do Norte (UFRN)
instacron_str UFRN
institution UFRN
reponame_str Repositório Institucional da UFRN
collection Repositório Institucional da UFRN
repository.name.fl_str_mv Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)
repository.mail.fl_str_mv repositorio@bczm.ufrn.br
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