The imbalance between Treg and Th17 cells caused by FTY720 treatment in skin allograft rejection
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:/48912/001300001391h |
Texto Completo: | http://dx.doi.org/10.6061/clinics/2012(07)17 http://repositorio.unifesp.br/handle/11600/34416 |
Resumo: | OBJECTIVES: FTY720 modulates CD4(+)T cells by the augmentation of regulatory T cell activity, secretion of suppressive cytokines and suppression of IL-17 secretion by Th17 cells. To further understand the process of graft rejection/acceptance, we evaluated skin allograft survival and associated events after FTY720 treatment.METHODS: F1 mice (C57BL/6xBALB/c) and C57BL/6 mice were used as donors for and recipients of skin transplantation, respectively. the recipients were transplanted and either not treated or treated with FTY720 by gavage for 21 days to evaluate the allograft survival. in another set of experiments, the immunological evaluation was performed five days post-transplantation. the spleens, axillary lymph nodes and skin allografts of the recipient mice were harvested for phenotyping (flow cytometry), gene expression (real-time PCR) and cytokine (Bio-Plex) analysis.RESULTS: the FTY720 treatment significantly increased skin allograft survival, reduced the number of cells in the lymph nodes and decreased the percentage of Tregs at this site in the C57BL/6 recipients. Moreover, the treatment reduced the number of graft-infiltrating cells and the percentage of CD4(+) graft-infiltrating cells. the cytokine analysis (splenocytes) showed decreased levels of IL-10, IL-6 and IL-17 in the FTY720-treated mice. We also observed a decrease in the IL-10, IL-6 and IL-23 mRNA levels, as well as an increase in the IL-27 mRNA levels, in the splenocytes of the treated group. the FTY720-treated mice exhibited increased mRNA levels of IL-10, IL-27 and IL-23 in the skin graft.CONCLUSIONS: Our results demonstrated prolonged but not indefinite skin allograft survival by FTY720 treatment. This finding indicates that the drug did not prevent the imbalance between Tr1 and Th17 cells in the graft that led to rejection. |
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The imbalance between Treg and Th17 cells caused by FTY720 treatment in skin allograft rejectionTransplantationRejectionToleranceFTY720Foxp3Th17OBJECTIVES: FTY720 modulates CD4(+)T cells by the augmentation of regulatory T cell activity, secretion of suppressive cytokines and suppression of IL-17 secretion by Th17 cells. To further understand the process of graft rejection/acceptance, we evaluated skin allograft survival and associated events after FTY720 treatment.METHODS: F1 mice (C57BL/6xBALB/c) and C57BL/6 mice were used as donors for and recipients of skin transplantation, respectively. the recipients were transplanted and either not treated or treated with FTY720 by gavage for 21 days to evaluate the allograft survival. in another set of experiments, the immunological evaluation was performed five days post-transplantation. the spleens, axillary lymph nodes and skin allografts of the recipient mice were harvested for phenotyping (flow cytometry), gene expression (real-time PCR) and cytokine (Bio-Plex) analysis.RESULTS: the FTY720 treatment significantly increased skin allograft survival, reduced the number of cells in the lymph nodes and decreased the percentage of Tregs at this site in the C57BL/6 recipients. Moreover, the treatment reduced the number of graft-infiltrating cells and the percentage of CD4(+) graft-infiltrating cells. the cytokine analysis (splenocytes) showed decreased levels of IL-10, IL-6 and IL-17 in the FTY720-treated mice. We also observed a decrease in the IL-10, IL-6 and IL-23 mRNA levels, as well as an increase in the IL-27 mRNA levels, in the splenocytes of the treated group. the FTY720-treated mice exhibited increased mRNA levels of IL-10, IL-27 and IL-23 in the skin graft.CONCLUSIONS: Our results demonstrated prolonged but not indefinite skin allograft survival by FTY720 treatment. This finding indicates that the drug did not prevent the imbalance between Tr1 and Th17 cells in the graft that led to rejection.Fed Univ São Paulo UNIFESP, Vis Inst, São Paulo, BrazilHosp Israelita Albert Einstein, São Paulo, BrazilFed Univ São Paulo UNIFESP, Div Nephrol, São Paulo, BrazilUniv São Paulo, Fac Med, Dept Immunol, São Paulo, BrazilFed Univ São Paulo UNIFESP, Div Immunol, São Paulo, BrazilFed Univ São Paulo UNIFESP, Vis Inst, São Paulo, BrazilFed Univ São Paulo UNIFESP, Div Nephrol, São Paulo, BrazilFed Univ São Paulo UNIFESP, Div Immunol, São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Hospital Clinicas, Univ São PauloUniversidade Federal de São Paulo (UNIFESP)Hosp Israelita Albert EinsteinUniversidade de São Paulo (USP)Commodaro, Alessandra Goncalves [UNIFESP]Pedregosa, Juliana Figueredo [UNIFESP]Peron, Jean PierreBrandao, WesleyRizzo, Luiz VicenteBueno, Valquiria [UNIFESP]2016-01-24T14:17:40Z2016-01-24T14:17:40Z2012-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion805-813application/pdfhttp://dx.doi.org/10.6061/clinics/2012(07)17Clinics. São Paulo: Hospital Clinicas, Univ São Paulo, v. 67, n. 7, p. 805-813, 2012.10.6061/clinics/2012(07)17S1807-59322012000700017.pdf1807-5932S1807-59322012000700017http://repositorio.unifesp.br/handle/11600/34416WOS:000307723100017ark:/48912/001300001391hengClinicsinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-31T23:34:48Zoai:repositorio.unifesp.br/:11600/34416Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-12-11T20:53:05.010957Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
The imbalance between Treg and Th17 cells caused by FTY720 treatment in skin allograft rejection |
title |
The imbalance between Treg and Th17 cells caused by FTY720 treatment in skin allograft rejection |
spellingShingle |
The imbalance between Treg and Th17 cells caused by FTY720 treatment in skin allograft rejection Commodaro, Alessandra Goncalves [UNIFESP] Transplantation Rejection Tolerance FTY720 Foxp3 Th17 |
title_short |
The imbalance between Treg and Th17 cells caused by FTY720 treatment in skin allograft rejection |
title_full |
The imbalance between Treg and Th17 cells caused by FTY720 treatment in skin allograft rejection |
title_fullStr |
The imbalance between Treg and Th17 cells caused by FTY720 treatment in skin allograft rejection |
title_full_unstemmed |
The imbalance between Treg and Th17 cells caused by FTY720 treatment in skin allograft rejection |
title_sort |
The imbalance between Treg and Th17 cells caused by FTY720 treatment in skin allograft rejection |
author |
Commodaro, Alessandra Goncalves [UNIFESP] |
author_facet |
Commodaro, Alessandra Goncalves [UNIFESP] Pedregosa, Juliana Figueredo [UNIFESP] Peron, Jean Pierre Brandao, Wesley Rizzo, Luiz Vicente Bueno, Valquiria [UNIFESP] |
author_role |
author |
author2 |
Pedregosa, Juliana Figueredo [UNIFESP] Peron, Jean Pierre Brandao, Wesley Rizzo, Luiz Vicente Bueno, Valquiria [UNIFESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) Hosp Israelita Albert Einstein Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Commodaro, Alessandra Goncalves [UNIFESP] Pedregosa, Juliana Figueredo [UNIFESP] Peron, Jean Pierre Brandao, Wesley Rizzo, Luiz Vicente Bueno, Valquiria [UNIFESP] |
dc.subject.por.fl_str_mv |
Transplantation Rejection Tolerance FTY720 Foxp3 Th17 |
topic |
Transplantation Rejection Tolerance FTY720 Foxp3 Th17 |
description |
OBJECTIVES: FTY720 modulates CD4(+)T cells by the augmentation of regulatory T cell activity, secretion of suppressive cytokines and suppression of IL-17 secretion by Th17 cells. To further understand the process of graft rejection/acceptance, we evaluated skin allograft survival and associated events after FTY720 treatment.METHODS: F1 mice (C57BL/6xBALB/c) and C57BL/6 mice were used as donors for and recipients of skin transplantation, respectively. the recipients were transplanted and either not treated or treated with FTY720 by gavage for 21 days to evaluate the allograft survival. in another set of experiments, the immunological evaluation was performed five days post-transplantation. the spleens, axillary lymph nodes and skin allografts of the recipient mice were harvested for phenotyping (flow cytometry), gene expression (real-time PCR) and cytokine (Bio-Plex) analysis.RESULTS: the FTY720 treatment significantly increased skin allograft survival, reduced the number of cells in the lymph nodes and decreased the percentage of Tregs at this site in the C57BL/6 recipients. Moreover, the treatment reduced the number of graft-infiltrating cells and the percentage of CD4(+) graft-infiltrating cells. the cytokine analysis (splenocytes) showed decreased levels of IL-10, IL-6 and IL-17 in the FTY720-treated mice. We also observed a decrease in the IL-10, IL-6 and IL-23 mRNA levels, as well as an increase in the IL-27 mRNA levels, in the splenocytes of the treated group. the FTY720-treated mice exhibited increased mRNA levels of IL-10, IL-27 and IL-23 in the skin graft.CONCLUSIONS: Our results demonstrated prolonged but not indefinite skin allograft survival by FTY720 treatment. This finding indicates that the drug did not prevent the imbalance between Tr1 and Th17 cells in the graft that led to rejection. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-01-01 2016-01-24T14:17:40Z 2016-01-24T14:17:40Z |
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(07)17 Clinics. São Paulo: Hospital Clinicas, Univ São Paulo, v. 67, n. 7, p. 805-813, 2012. 10.6061/clinics/2012(07)17 S1807-59322012000700017.pdf 1807-5932 S1807-59322012000700017 http://repositorio.unifesp.br/handle/11600/34416 WOS:000307723100017 |
dc.identifier.dark.fl_str_mv |
ark:/48912/001300001391h |
url |
http://dx.doi.org/10.6061/clinics/2012(07)17 http://repositorio.unifesp.br/handle/11600/34416 |
identifier_str_mv |
Clinics. São Paulo: Hospital Clinicas, Univ São Paulo, v. 67, n. 7, p. 805-813, 2012. 10.6061/clinics/2012(07)17 S1807-59322012000700017.pdf 1807-5932 S1807-59322012000700017 WOS:000307723100017 ark:/48912/001300001391h |
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 |
805-813 application/pdf |
dc.publisher.none.fl_str_mv |
Hospital Clinicas, Univ São Paulo |
publisher.none.fl_str_mv |
Hospital Clinicas, Univ São Paulo |
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_ |
1818602561992654848 |