Evaluation of Experimental Autoimmune Uveitis in Mice Treated with FTY720

Detalhes bibliográficos
Autor(a) principal: Commodaro, Alessandra Goncalves [UNIFESP]
Data de Publicação: 2010
Outros Autores: Peron, Jean Pierre S., Lopes, Camila Takao, Arslanian, Christina, Belfort, Rubens Junior [UNIFESP], Rizzo, Luiz Vicente, Bueno, Valquiria [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/32492
http://dx.doi.org/10.1167/iovs.09-4769
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
id UFSP_837de562e0b447d56dfdaef9c4a40f60
oai_identifier_str oai:repositorio.unifesp.br:11600/32492
network_acronym_str UFSP
network_name_str Repositório Institucional da UNIFESP
repository_id_str 3465
spelling Commodaro, Alessandra Goncalves [UNIFESP]Peron, Jean Pierre S.Lopes, Camila TakaoArslanian, ChristinaBelfort, Rubens Junior [UNIFESP]Rizzo, Luiz VicenteBueno, Valquiria [UNIFESP]Universidade Federal de São Paulo (UNIFESP)Universidade de São Paulo (USP)Albert Einstein Jewish Inst Educ & Res2016-01-24T13:59:37Z2016-01-24T13:59:37Z2010-05-01Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 51, n. 5, p. 2568-2574, 2010.0146-0404http://repositorio.unifesp.br/handle/11600/32492http://dx.doi.org/10.1167/iovs.09-476910.1167/iovs.09-4769WOS:000277180500038PURPOSE. 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.09-4769Fundação 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 PauloUniversidade 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, BrazilFAPESP: 04/14727-0Pan-American Ophthalmological Foundation: 2007Web of Science2568-2574engAssoc Research Vision Ophthalmology IncInvestigative Ophthalmology & Visual ScienceEvaluation of Experimental Autoimmune Uveitis in Mice Treated with FTY720info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/324922022-11-03 15:00:32.585metadata only accessoai:repositorio.unifesp.br:11600/32492Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-05-25T12:28:10.685137Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.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.institution.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.issued.fl_str_mv 2010-05-01
dc.date.accessioned.fl_str_mv 2016-01-24T13:59:37Z
dc.date.available.fl_str_mv 2016-01-24T13:59:37Z
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.citation.fl_str_mv Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 51, n. 5, p. 2568-2574, 2010.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/32492
http://dx.doi.org/10.1167/iovs.09-4769
dc.identifier.issn.none.fl_str_mv 0146-0404
dc.identifier.doi.none.fl_str_mv 10.1167/iovs.09-4769
dc.identifier.wos.none.fl_str_mv WOS:000277180500038
identifier_str_mv Investigative Ophthalmology & Visual Science. Rockville: Assoc Research Vision Ophthalmology Inc, v. 51, n. 5, p. 2568-2574, 2010.
0146-0404
10.1167/iovs.09-4769
WOS:000277180500038
url http://repositorio.unifesp.br/handle/11600/32492
http://dx.doi.org/10.1167/iovs.09-4769
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.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
_version_ 1783460294881705984