Oral tolerance induced by OVA intake ameliorates TNBS-induced colitis in Mice

Detalhes bibliográficos
Autor(a) principal: Paiatto, Lisiery N. [UNESP]
Data de Publicação: 2017
Outros Autores: Silva, Fernanda G. D., Bier, Julia, Brochetto-Braga, Márcia R. [UNESP], Yamada, Áureo T., Tamashiro, Wirla M. S. C., Simioni, Patricia U. [UNESP]
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.
id UNSP_5464ef91a9bb5cfd2a44bc0005d49336
oai_identifier_str oai:repositorio.unesp.br:11449/169372
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling 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
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1808129560098635776