Impact of Donor and Recipient Cytokine Genotypes on Renal Allograft Outcome

Detalhes bibliográficos
Autor(a) principal: Ligeiro, D
Data de Publicação: 2004
Outros Autores: Sancho, MR, Papoila, AL, Barradinhas, AM, Almeida, A, Calão, S, Machado, D, Nolasco, F, Guerra, J, Sampaio, MJ, Trindade, H
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.17/904
Resumo: Allelic differences in gene promoter or codifying regions have been described to affect regulation of gene expression, consequently increasing or decreasing cytokine production and signal transduction responses to a given stimulus. This observation has been reported for interleukin (IL)-10 (-1082 A/G; -819/-592 CT/CA), transforming growth factor (TGF)-beta (codon 10 C/T, codon 25 G/C), tumor necrosis factor (TNF)-alpha (-308 G/A), TNF-beta (+252 A/G), interferon (IFN)-gamma (+874 T/A), IL-6 (-174 G/C), and IL-4R alpha (+1902 G/A). To evaluate the influence of these cytokine genotypes on the development of acute or chronic rejection, we correlated the genotypes of both kidney graft recipients and cadaver donors with the clinical outcome. Kidney recipients had 5 years follow-up, at least 2 HLA-DRB compatibilities, and a maximum of 25% anti-HLA pretransplantation sensitization. The clinical outcomes were grouped as follows: stable functioning graft (NR, n = 35); acute rejection episodes (AR, n = 31); and chronic rejection (CR, n = 31). The cytokine genotype polymorphisms were defined using PCR-SSP typing. A statistical analysis showed a significant prevalence of recipient IL-10 -819/-592 genotype among CR individuals; whereas among donors, the TGF-beta codon 10 CT genotype was significantly associated with the AR cohort and the IL-6 -174 CC genotype with CR. Other albeit not significant observations included a strong predisposition of recipient TGF-beta codon 10 CT genotype with CR, and TNF-beta 252 AA with AR. A low frequency of TNF-alpha -308 AA genotype also was observed among recipients and donors who showed poor allograft outcomes.
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spelling Impact of Donor and Recipient Cytokine Genotypes on Renal Allograft OutcomeCitocinasGenótipoRejeição do TransplanteInterleucina-10Interleucina-6Neoplasias RenaisFactores de Crescimento Transformador BetaTransplante HomólogoResultado de TratamentoFactor de Necrose Tumoral AlfaAllelic differences in gene promoter or codifying regions have been described to affect regulation of gene expression, consequently increasing or decreasing cytokine production and signal transduction responses to a given stimulus. This observation has been reported for interleukin (IL)-10 (-1082 A/G; -819/-592 CT/CA), transforming growth factor (TGF)-beta (codon 10 C/T, codon 25 G/C), tumor necrosis factor (TNF)-alpha (-308 G/A), TNF-beta (+252 A/G), interferon (IFN)-gamma (+874 T/A), IL-6 (-174 G/C), and IL-4R alpha (+1902 G/A). To evaluate the influence of these cytokine genotypes on the development of acute or chronic rejection, we correlated the genotypes of both kidney graft recipients and cadaver donors with the clinical outcome. Kidney recipients had 5 years follow-up, at least 2 HLA-DRB compatibilities, and a maximum of 25% anti-HLA pretransplantation sensitization. The clinical outcomes were grouped as follows: stable functioning graft (NR, n = 35); acute rejection episodes (AR, n = 31); and chronic rejection (CR, n = 31). The cytokine genotype polymorphisms were defined using PCR-SSP typing. A statistical analysis showed a significant prevalence of recipient IL-10 -819/-592 genotype among CR individuals; whereas among donors, the TGF-beta codon 10 CT genotype was significantly associated with the AR cohort and the IL-6 -174 CC genotype with CR. Other albeit not significant observations included a strong predisposition of recipient TGF-beta codon 10 CT genotype with CR, and TNF-beta 252 AA with AR. A low frequency of TNF-alpha -308 AA genotype also was observed among recipients and donors who showed poor allograft outcomes.ElsevierRepositório do Centro Hospitalar Universitário de Lisboa Central, EPELigeiro, DSancho, MRPapoila, ALBarradinhas, AMAlmeida, ACalão, SMachado, DNolasco, FGuerra, JSampaio, MJTrindade, H2012-12-21T17:01:01Z20042004-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.17/904engTransplant Proc. 2004 May;36(4):827-9info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-10T09:28:11Zoai:repositorio.chlc.min-saude.pt:10400.17/904Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:18:31.347217Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Impact of Donor and Recipient Cytokine Genotypes on Renal Allograft Outcome
title Impact of Donor and Recipient Cytokine Genotypes on Renal Allograft Outcome
spellingShingle Impact of Donor and Recipient Cytokine Genotypes on Renal Allograft Outcome
Ligeiro, D
Citocinas
Genótipo
Rejeição do Transplante
Interleucina-10
Interleucina-6
Neoplasias Renais
Factores de Crescimento Transformador Beta
Transplante Homólogo
Resultado de Tratamento
Factor de Necrose Tumoral Alfa
title_short Impact of Donor and Recipient Cytokine Genotypes on Renal Allograft Outcome
title_full Impact of Donor and Recipient Cytokine Genotypes on Renal Allograft Outcome
title_fullStr Impact of Donor and Recipient Cytokine Genotypes on Renal Allograft Outcome
title_full_unstemmed Impact of Donor and Recipient Cytokine Genotypes on Renal Allograft Outcome
title_sort Impact of Donor and Recipient Cytokine Genotypes on Renal Allograft Outcome
author Ligeiro, D
author_facet Ligeiro, D
Sancho, MR
Papoila, AL
Barradinhas, AM
Almeida, A
Calão, S
Machado, D
Nolasco, F
Guerra, J
Sampaio, MJ
Trindade, H
author_role author
author2 Sancho, MR
Papoila, AL
Barradinhas, AM
Almeida, A
Calão, S
Machado, D
Nolasco, F
Guerra, J
Sampaio, MJ
Trindade, H
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório do Centro Hospitalar Universitário de Lisboa Central, EPE
dc.contributor.author.fl_str_mv Ligeiro, D
Sancho, MR
Papoila, AL
Barradinhas, AM
Almeida, A
Calão, S
Machado, D
Nolasco, F
Guerra, J
Sampaio, MJ
Trindade, H
dc.subject.por.fl_str_mv Citocinas
Genótipo
Rejeição do Transplante
Interleucina-10
Interleucina-6
Neoplasias Renais
Factores de Crescimento Transformador Beta
Transplante Homólogo
Resultado de Tratamento
Factor de Necrose Tumoral Alfa
topic Citocinas
Genótipo
Rejeição do Transplante
Interleucina-10
Interleucina-6
Neoplasias Renais
Factores de Crescimento Transformador Beta
Transplante Homólogo
Resultado de Tratamento
Factor de Necrose Tumoral Alfa
description Allelic differences in gene promoter or codifying regions have been described to affect regulation of gene expression, consequently increasing or decreasing cytokine production and signal transduction responses to a given stimulus. This observation has been reported for interleukin (IL)-10 (-1082 A/G; -819/-592 CT/CA), transforming growth factor (TGF)-beta (codon 10 C/T, codon 25 G/C), tumor necrosis factor (TNF)-alpha (-308 G/A), TNF-beta (+252 A/G), interferon (IFN)-gamma (+874 T/A), IL-6 (-174 G/C), and IL-4R alpha (+1902 G/A). To evaluate the influence of these cytokine genotypes on the development of acute or chronic rejection, we correlated the genotypes of both kidney graft recipients and cadaver donors with the clinical outcome. Kidney recipients had 5 years follow-up, at least 2 HLA-DRB compatibilities, and a maximum of 25% anti-HLA pretransplantation sensitization. The clinical outcomes were grouped as follows: stable functioning graft (NR, n = 35); acute rejection episodes (AR, n = 31); and chronic rejection (CR, n = 31). The cytokine genotype polymorphisms were defined using PCR-SSP typing. A statistical analysis showed a significant prevalence of recipient IL-10 -819/-592 genotype among CR individuals; whereas among donors, the TGF-beta codon 10 CT genotype was significantly associated with the AR cohort and the IL-6 -174 CC genotype with CR. Other albeit not significant observations included a strong predisposition of recipient TGF-beta codon 10 CT genotype with CR, and TNF-beta 252 AA with AR. A low frequency of TNF-alpha -308 AA genotype also was observed among recipients and donors who showed poor allograft outcomes.
publishDate 2004
dc.date.none.fl_str_mv 2004
2004-01-01T00:00:00Z
2012-12-21T17:01:01Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.17/904
url http://hdl.handle.net/10400.17/904
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Transplant Proc. 2004 May;36(4):827-9
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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