Evaluation of Experimental Autoimmune Uveitis in Mice Treated with FTY720
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1167/iovs.09-4769 http://repositorio.unifesp.br/handle/11600/32492 |
Resumo: | PURPOSE. FTY720 (fingolimod) is an immunomodulatory drug capable of preventing T-cell migration to inflammatory sites by binding to and subsequently downregulating the expression of sphingosine-1 phosphate receptor 1 (S1P(1)) leading in turn to T-cell retention in lymphoid organs. Additional effects of FTY720 by increasing functional activity of regulatory T cells have recently been demonstrated, raising the conversion of conventional T cells into regulatory T cells and affecting the sequestration of regulatory T cells in normal mice. in this study, the action of FTY720 in the ocular autoimmune model in mice was investigated.METHODS. Mice were immunized with 161-180 peptide and pertussis toxin and were treated with 1 mg/kg/d FTY720 by gavage (7-21 days postimmunization [dpi]) or left untreated. Spleen cells, harvested 21 dpi, were cultured and assayed for cytokine production. Draining lymph node, spleen, and eye cells 21 dpi were assayed for quantification of T-cell populations. Disease severity was evaluated by histologic examination of the enucleated eyes at 21 and 49 dpi. in addition, anti-IRBP antibodies were analyzed by ELISA.RESULTS. FTY720 was effective in suppressing the experimental autoimmune uveitis score. Although there was a reduction in the number of eye-infiltrating cells, FTY did not prevent Treg accumulation at this site. FTY720 leads to a significant increase of CD4(+)IFN-gamma(+) and CD4(+)Foxp3(+) cell percentages in lymph nodes, suggesting that this site could be the source of Treg cells found in the eye.CONCLUSIONS. the data showed that treatment in vivo with FTY720 was able to suppress EAU in mice. These results are indicative of the possible therapeutic use of FTY720 in ocular autoimmune processes. (Invest Ophthalmol Vis Sci. 2010;51:2568-2574) DOI:10.1167/iovs.09-4769 |
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Evaluation of Experimental Autoimmune Uveitis in Mice Treated with FTY720PURPOSE. FTY720 (fingolimod) is an immunomodulatory drug capable of preventing T-cell migration to inflammatory sites by binding to and subsequently downregulating the expression of sphingosine-1 phosphate receptor 1 (S1P(1)) leading in turn to T-cell retention in lymphoid organs. Additional effects of FTY720 by increasing functional activity of regulatory T cells have recently been demonstrated, raising the conversion of conventional T cells into regulatory T cells and affecting the sequestration of regulatory T cells in normal mice. in this study, the action of FTY720 in the ocular autoimmune model in mice was investigated.METHODS. Mice were immunized with 161-180 peptide and pertussis toxin and were treated with 1 mg/kg/d FTY720 by gavage (7-21 days postimmunization [dpi]) or left untreated. Spleen cells, harvested 21 dpi, were cultured and assayed for cytokine production. Draining lymph node, spleen, and eye cells 21 dpi were assayed for quantification of T-cell populations. Disease severity was evaluated by histologic examination of the enucleated eyes at 21 and 49 dpi. in addition, anti-IRBP antibodies were analyzed by ELISA.RESULTS. FTY720 was effective in suppressing the experimental autoimmune uveitis score. Although there was a reduction in the number of eye-infiltrating cells, FTY did not prevent Treg accumulation at this site. FTY720 leads to a significant increase of CD4(+)IFN-gamma(+) and CD4(+)Foxp3(+) cell percentages in lymph nodes, suggesting that this site could be the source of Treg cells found in the eye.CONCLUSIONS. the data showed that treatment in vivo with FTY720 was able to suppress EAU in mice. These results are indicative of the possible therapeutic use of FTY720 in ocular autoimmune processes. (Invest Ophthalmol Vis Sci. 2010;51:2568-2574) DOI:10.1167/iovs.09-4769Universidade Federal de São Paulo, Div Immunol, Expt Immunol Lab, São Paulo, BrazilUniversidade Federal de São Paulo, Vis Inst, São Paulo, BrazilUniv São Paulo, Dept Immunol, São Paulo, BrazilAlbert Einstein Jewish Inst Educ & Res, São Paulo, BrazilUniversidade Federal de São Paulo, Div Immunol, Expt Immunol Lab, São Paulo, BrazilUniversidade Federal de São Paulo, Vis Inst, São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Pan-American Ophthalmological FoundationFADA-Universidade Federal de São PauloFAPESP: 04/14727-0Pan-American Ophthalmological Foundation: 2007Assoc Research Vision Ophthalmology IncUniversidade Federal de São Paulo (UNIFESP)Universidade de São Paulo (USP)Albert Einstein Jewish Inst Educ & ResCommodaro, Alessandra Goncalves [UNIFESP]Peron, Jean Pierre S.Lopes, Camila TakaoArslanian, ChristinaBelfort, Rubens Junior [UNIFESP]Rizzo, Luiz VicenteBueno, Valquiria [UNIFESP]2016-01-24T13:59:37Z2016-01-24T13:59:37Z2010-05-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion2568-2574http://dx.doi.org/10.1167/iovs.09-4769Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 51, n. 5, p. 2568-2574, 2010.10.1167/iovs.09-47690146-0404http://repositorio.unifesp.br/handle/11600/32492WOS:000277180500038engInvestigative Ophthalmology & Visual Scienceinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2022-11-03T15:00:32Zoai:repositorio.unifesp.br/:11600/32492Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652022-11-03T15:00:32Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Evaluation of Experimental Autoimmune Uveitis in Mice Treated with FTY720 |
title |
Evaluation of Experimental Autoimmune Uveitis in Mice Treated with FTY720 |
spellingShingle |
Evaluation of Experimental Autoimmune Uveitis in Mice Treated with FTY720 Commodaro, Alessandra Goncalves [UNIFESP] |
title_short |
Evaluation of Experimental Autoimmune Uveitis in Mice Treated with FTY720 |
title_full |
Evaluation of Experimental Autoimmune Uveitis in Mice Treated with FTY720 |
title_fullStr |
Evaluation of Experimental Autoimmune Uveitis in Mice Treated with FTY720 |
title_full_unstemmed |
Evaluation of Experimental Autoimmune Uveitis in Mice Treated with FTY720 |
title_sort |
Evaluation of Experimental Autoimmune Uveitis in Mice Treated with FTY720 |
author |
Commodaro, Alessandra Goncalves [UNIFESP] |
author_facet |
Commodaro, Alessandra Goncalves [UNIFESP] Peron, Jean Pierre S. Lopes, Camila Takao Arslanian, Christina Belfort, Rubens Junior [UNIFESP] Rizzo, Luiz Vicente Bueno, Valquiria [UNIFESP] |
author_role |
author |
author2 |
Peron, Jean Pierre S. Lopes, Camila Takao Arslanian, Christina Belfort, Rubens Junior [UNIFESP] Rizzo, Luiz Vicente Bueno, Valquiria [UNIFESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) Universidade de São Paulo (USP) Albert Einstein Jewish Inst Educ & Res |
dc.contributor.author.fl_str_mv |
Commodaro, Alessandra Goncalves [UNIFESP] Peron, Jean Pierre S. Lopes, Camila Takao Arslanian, Christina Belfort, Rubens Junior [UNIFESP] Rizzo, Luiz Vicente Bueno, Valquiria [UNIFESP] |
description |
PURPOSE. FTY720 (fingolimod) is an immunomodulatory drug capable of preventing T-cell migration to inflammatory sites by binding to and subsequently downregulating the expression of sphingosine-1 phosphate receptor 1 (S1P(1)) leading in turn to T-cell retention in lymphoid organs. Additional effects of FTY720 by increasing functional activity of regulatory T cells have recently been demonstrated, raising the conversion of conventional T cells into regulatory T cells and affecting the sequestration of regulatory T cells in normal mice. in this study, the action of FTY720 in the ocular autoimmune model in mice was investigated.METHODS. Mice were immunized with 161-180 peptide and pertussis toxin and were treated with 1 mg/kg/d FTY720 by gavage (7-21 days postimmunization [dpi]) or left untreated. Spleen cells, harvested 21 dpi, were cultured and assayed for cytokine production. Draining lymph node, spleen, and eye cells 21 dpi were assayed for quantification of T-cell populations. Disease severity was evaluated by histologic examination of the enucleated eyes at 21 and 49 dpi. in addition, anti-IRBP antibodies were analyzed by ELISA.RESULTS. FTY720 was effective in suppressing the experimental autoimmune uveitis score. Although there was a reduction in the number of eye-infiltrating cells, FTY did not prevent Treg accumulation at this site. FTY720 leads to a significant increase of CD4(+)IFN-gamma(+) and CD4(+)Foxp3(+) cell percentages in lymph nodes, suggesting that this site could be the source of Treg cells found in the eye.CONCLUSIONS. the data showed that treatment in vivo with FTY720 was able to suppress EAU in mice. These results are indicative of the possible therapeutic use of FTY720 in ocular autoimmune processes. (Invest Ophthalmol Vis Sci. 2010;51:2568-2574) DOI:10.1167/iovs.09-4769 |
publishDate |
2010 |
dc.date.none.fl_str_mv |
2010-05-01 2016-01-24T13:59:37Z 2016-01-24T13:59:37Z |
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/10.1167/iovs.09-4769 Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 51, n. 5, p. 2568-2574, 2010. 10.1167/iovs.09-4769 0146-0404 http://repositorio.unifesp.br/handle/11600/32492 WOS:000277180500038 |
url |
http://dx.doi.org/10.1167/iovs.09-4769 http://repositorio.unifesp.br/handle/11600/32492 |
identifier_str_mv |
Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 51, n. 5, p. 2568-2574, 2010. 10.1167/iovs.09-4769 0146-0404 WOS:000277180500038 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Investigative Ophthalmology & Visual Science |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
2568-2574 |
dc.publisher.none.fl_str_mv |
Assoc Research Vision Ophthalmology Inc |
publisher.none.fl_str_mv |
Assoc Research Vision Ophthalmology Inc |
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 |
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1824718200794775552 |