The imbalance between Treg and Th17 cells caused by FTY720 treatment in skin allograft rejection

Detalhes bibliográficos
Autor(a) principal: Commodaro, Alessandra Gonçalves
Data de Publicação: 2012
Outros Autores: Pedregosa, Juliana Figueredo, Peron, Jean Pierre, Brandão, Wesley, Rizzo, Luiz Vicente, Bueno, Valquiria
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/40158
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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spelling 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.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2012-07-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/4015810.6061/clinics/2012(07)17Clinics; Vol. 67 No. 7 (2012); 805-813Clinics; v. 67 n. 7 (2012); 805-813Clinics; Vol. 67 Núm. 7 (2012); 805-8131980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/40158/43024Commodaro, Alessandra GonçalvesPedregosa, Juliana FigueredoPeron, Jean PierreBrandão, WesleyRizzo, Luiz VicenteBueno, Valquiriainfo:eu-repo/semantics/openAccess2012-08-23T18:32:18Zoai:revistas.usp.br:article/40158Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2012-08-23T18:32:18Clinics - Universidade de São Paulo (USP)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 Gonçalves
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 Gonçalves
author_facet Commodaro, Alessandra Gonçalves
Pedregosa, Juliana Figueredo
Peron, Jean Pierre
Brandão, Wesley
Rizzo, Luiz Vicente
Bueno, Valquiria
author_role author
author2 Pedregosa, Juliana Figueredo
Peron, Jean Pierre
Brandão, Wesley
Rizzo, Luiz Vicente
Bueno, Valquiria
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Commodaro, Alessandra Gonçalves
Pedregosa, Juliana Figueredo
Peron, Jean Pierre
Brandão, Wesley
Rizzo, Luiz Vicente
Bueno, Valquiria
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 2012-07-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/40158
10.6061/clinics/2012(07)17
url https://www.revistas.usp.br/clinics/article/view/40158
identifier_str_mv 10.6061/clinics/2012(07)17
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/40158/43024
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 Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 67 No. 7 (2012); 805-813
Clinics; v. 67 n. 7 (2012); 805-813
Clinics; Vol. 67 Núm. 7 (2012); 805-813
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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