Oral tolerance induced by OVA intake ameliorates TNBS-induced colitis in Mice
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1371/journal.pone.0170205 http://hdl.handle.net/11449/169372 |
Resumo: | Introduction Literature data have shown that the consumption of dietary proteins may cause modulatory effects on the host immune system, process denominated oral tolerance by bystander suppression. It has been shown that the bystander suppression induced by dietary proteins can improve inflammatory diseases such as experimental arthritis. Here, we evaluated the effects of oral tolerance induced by ingestion of ovalbumin (OVA) on TNBS-induced colitis in mice, an experimental model for human Crohn's disease. Methods and Results Colitis was induced in BALB/c mice by instilling a single dose of TNBS (100 mg/kg) in ethanol into the colon. Tolerized mice received OVA (4mg/mL) dissolved in the drinking water for seven consecutive days, prior to or concomitantly with the intrarectal instillation. Control groups received protein-free water and ethanol by intrarectal route. We observed that either the prior or concomitant induction of oral tolerance were able to reduce the severity of colitis as noted by recovery of body weight gain, improvement of clinical signs and reduction of histological abnormalities. The in vitro proliferation of spleen cells from tolerant colitic mice was lower than that of control mice, the same as the frequencies of CD4+ T cells secreting IL-17 and IFN-ã. The frequencies of regulatory T cells and T cells secreting IL-10 have increased significantly in mice orally treated with OVA. The levels of inflammatory cytokines (IL-17A, TNF-α, IL-6 and IFN-ã) were lower in supernatants of cells from tolerant colitic mice, whereas IL-10 levels were higher. Conclusion Our data show that the modulation of immune response induced by oral tolerance reduces the severity of experimental colitis. Such modulation may be partially attributed to the increase of Treg cells and reduction of pro-inflammatory cytokines in peripheral lymphoid organs of tolerant mice by bystander suppression. |
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Repositório Institucional da UNESP |
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Oral tolerance induced by OVA intake ameliorates TNBS-induced colitis in MiceIntroduction Literature data have shown that the consumption of dietary proteins may cause modulatory effects on the host immune system, process denominated oral tolerance by bystander suppression. It has been shown that the bystander suppression induced by dietary proteins can improve inflammatory diseases such as experimental arthritis. Here, we evaluated the effects of oral tolerance induced by ingestion of ovalbumin (OVA) on TNBS-induced colitis in mice, an experimental model for human Crohn's disease. Methods and Results Colitis was induced in BALB/c mice by instilling a single dose of TNBS (100 mg/kg) in ethanol into the colon. Tolerized mice received OVA (4mg/mL) dissolved in the drinking water for seven consecutive days, prior to or concomitantly with the intrarectal instillation. Control groups received protein-free water and ethanol by intrarectal route. We observed that either the prior or concomitant induction of oral tolerance were able to reduce the severity of colitis as noted by recovery of body weight gain, improvement of clinical signs and reduction of histological abnormalities. The in vitro proliferation of spleen cells from tolerant colitic mice was lower than that of control mice, the same as the frequencies of CD4+ T cells secreting IL-17 and IFN-ã. The frequencies of regulatory T cells and T cells secreting IL-10 have increased significantly in mice orally treated with OVA. The levels of inflammatory cytokines (IL-17A, TNF-α, IL-6 and IFN-ã) were lower in supernatants of cells from tolerant colitic mice, whereas IL-10 levels were higher. Conclusion Our data show that the modulation of immune response induced by oral tolerance reduces the severity of experimental colitis. Such modulation may be partially attributed to the increase of Treg cells and reduction of pro-inflammatory cytokines in peripheral lymphoid organs of tolerant mice by bystander suppression.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Department of Genetics Evolution and Bioagents Institute of Biology State University of Campinas UNICAMPInstitute of Biosciences Universidade Estadual Paulista UNESPFaculty of Food Engineering University of Campinas UNICAMPDepartment of Histology and Embryology Institute of Biology State University of Campinas UNICAMPDepartment of Biomedical Science Faculty of Americana FAMInstitute of Biosciences Universidade Estadual Paulista UNESPFAPESP: 2013/20258-2#2014/086192#2015/09326-1#2014/1670102014/08591-0Universidade Estadual de Campinas (UNICAMP)Universidade Estadual Paulista (Unesp)FAMPaiatto, Lisiery N. [UNESP]Silva, Fernanda G. D.Bier, JuliaBrochetto-Braga, Márcia R. [UNESP]Yamada, Áureo T.Tamashiro, Wirla M. S. C.Simioni, Patricia U. [UNESP]2018-12-11T16:45:35Z2018-12-11T16:45:35Z2017-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://dx.doi.org/10.1371/journal.pone.0170205PLoS ONE, v. 12, n. 1, 2017.1932-6203http://hdl.handle.net/11449/16937210.1371/journal.pone.01702052-s2.0-850098576112-s2.0-85009857611.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPLoS ONE1,164info:eu-repo/semantics/openAccess2024-01-24T06:34:45Zoai:repositorio.unesp.br:11449/169372Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T23:52:16.219724Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Oral tolerance induced by OVA intake ameliorates TNBS-induced colitis in Mice |
title |
Oral tolerance induced by OVA intake ameliorates TNBS-induced colitis in Mice |
spellingShingle |
Oral tolerance induced by OVA intake ameliorates TNBS-induced colitis in Mice Paiatto, Lisiery N. [UNESP] |
title_short |
Oral tolerance induced by OVA intake ameliorates TNBS-induced colitis in Mice |
title_full |
Oral tolerance induced by OVA intake ameliorates TNBS-induced colitis in Mice |
title_fullStr |
Oral tolerance induced by OVA intake ameliorates TNBS-induced colitis in Mice |
title_full_unstemmed |
Oral tolerance induced by OVA intake ameliorates TNBS-induced colitis in Mice |
title_sort |
Oral tolerance induced by OVA intake ameliorates TNBS-induced colitis in Mice |
author |
Paiatto, Lisiery N. [UNESP] |
author_facet |
Paiatto, Lisiery N. [UNESP] Silva, Fernanda G. D. Bier, Julia Brochetto-Braga, Márcia R. [UNESP] Yamada, Áureo T. Tamashiro, Wirla M. S. C. Simioni, Patricia U. [UNESP] |
author_role |
author |
author2 |
Silva, Fernanda G. D. Bier, Julia Brochetto-Braga, Márcia R. [UNESP] Yamada, Áureo T. Tamashiro, Wirla M. S. C. Simioni, Patricia U. [UNESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual de Campinas (UNICAMP) Universidade Estadual Paulista (Unesp) FAM |
dc.contributor.author.fl_str_mv |
Paiatto, Lisiery N. [UNESP] Silva, Fernanda G. D. Bier, Julia Brochetto-Braga, Márcia R. [UNESP] Yamada, Áureo T. Tamashiro, Wirla M. S. C. Simioni, Patricia U. [UNESP] |
description |
Introduction Literature data have shown that the consumption of dietary proteins may cause modulatory effects on the host immune system, process denominated oral tolerance by bystander suppression. It has been shown that the bystander suppression induced by dietary proteins can improve inflammatory diseases such as experimental arthritis. Here, we evaluated the effects of oral tolerance induced by ingestion of ovalbumin (OVA) on TNBS-induced colitis in mice, an experimental model for human Crohn's disease. Methods and Results Colitis was induced in BALB/c mice by instilling a single dose of TNBS (100 mg/kg) in ethanol into the colon. Tolerized mice received OVA (4mg/mL) dissolved in the drinking water for seven consecutive days, prior to or concomitantly with the intrarectal instillation. Control groups received protein-free water and ethanol by intrarectal route. We observed that either the prior or concomitant induction of oral tolerance were able to reduce the severity of colitis as noted by recovery of body weight gain, improvement of clinical signs and reduction of histological abnormalities. The in vitro proliferation of spleen cells from tolerant colitic mice was lower than that of control mice, the same as the frequencies of CD4+ T cells secreting IL-17 and IFN-ã. The frequencies of regulatory T cells and T cells secreting IL-10 have increased significantly in mice orally treated with OVA. The levels of inflammatory cytokines (IL-17A, TNF-α, IL-6 and IFN-ã) were lower in supernatants of cells from tolerant colitic mice, whereas IL-10 levels were higher. Conclusion Our data show that the modulation of immune response induced by oral tolerance reduces the severity of experimental colitis. Such modulation may be partially attributed to the increase of Treg cells and reduction of pro-inflammatory cytokines in peripheral lymphoid organs of tolerant mice by bystander suppression. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-01-01 2018-12-11T16:45:35Z 2018-12-11T16:45:35Z |
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://dx.doi.org/10.1371/journal.pone.0170205 PLoS ONE, v. 12, n. 1, 2017. 1932-6203 http://hdl.handle.net/11449/169372 10.1371/journal.pone.0170205 2-s2.0-85009857611 2-s2.0-85009857611.pdf |
url |
http://dx.doi.org/10.1371/journal.pone.0170205 http://hdl.handle.net/11449/169372 |
identifier_str_mv |
PLoS ONE, v. 12, n. 1, 2017. 1932-6203 10.1371/journal.pone.0170205 2-s2.0-85009857611 2-s2.0-85009857611.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
PLoS ONE 1,164 |
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.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
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Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
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1808129560098635776 |