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Oral Tolerance Induced by OVA Intake Ameliorates TNBS-Induced Colitis in Mice

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...

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Published in:PloS one 2017-01, Vol.12 (1), p.e0170205
Main Authors: Paiatto, Lisiery N, Silva, Fernanda G D, Bier, Julia, Brochetto-Braga, Márcia R, Yamada, Áureo T, Tamashiro, Wirla M S C, Simioni, Patricia U
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creator Paiatto, Lisiery N
Silva, Fernanda G D
Bier, Julia
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Tamashiro, Wirla M S C
Simioni, Patricia U
description 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. 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-γ. 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-γ) were lower in supernatants of cells from tolerant colitic mice, whereas IL-10 levels were higher. 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.
doi_str_mv 10.1371/journal.pone.0170205
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immunology</topic><topic>Interleukin-10 - metabolism</topic><topic>Interleukin-17 - immunology</topic><topic>Interleukin-17 - metabolism</topic><topic>Interleukin-6 - immunology</topic><topic>Interleukin-6 - metabolism</topic><topic>Laboratory animals</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Medicine and Health Sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Modulation</topic><topic>Mucous membrane</topic><topic>Organs</topic><topic>Ovalbumin</topic><topic>Ovalbumin - immunology</topic><topic>Ovalbumin - pharmacology</topic><topic>Proteins</topic><topic>Rodents</topic><topic>Spleen</topic><topic>T-Lymphocytes, Regulatory - immunology</topic><topic>Transcription factors</topic><topic>Tumor Necrosis Factor-alpha - immunology</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><topic>Tumor necrosis factor-α</topic><topic>Weight reduction</topic><topic>γ-Interferon</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Paiatto, Lisiery N</creatorcontrib><creatorcontrib>Silva, Fernanda G D</creatorcontrib><creatorcontrib>Bier, Julia</creatorcontrib><creatorcontrib>Brochetto-Braga, Márcia R</creatorcontrib><creatorcontrib>Yamada, Áureo T</creatorcontrib><creatorcontrib>Tamashiro, Wirla M S C</creatorcontrib><creatorcontrib>Simioni, Patricia U</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing &amp; Allied Health Database (ProQuest)</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological &amp; Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database (Proquest)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - 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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. 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-γ. 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-γ) were lower in supernatants of cells from tolerant colitic mice, whereas IL-10 levels were higher. 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.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>28099498</pmid><doi>10.1371/journal.pone.0170205</doi><tpages>e0170205</tpages><orcidid>https://orcid.org/0000-0002-6951-5040</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1932-6203
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issn 1932-6203
1932-6203
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source PubMed Central (Open Access); Publicly Available Content Database
subjects Abnormalities
Analysis
Animals
Antigens
Arthritis
Biology
Biology and Life Sciences
Body weight
Body weight gain
Bystander Effect - immunology
Care and treatment
Causes of
CD4 antigen
Cell proliferation
Colitis
Colitis - chemically induced
Colitis - immunology
Colon
Crohn's disease
Cytokines
Dendritic cells
Diet
Drinking behavior
Drinking water
Ethanol
Evolution
Female
Free water
Genetic aspects
Histology
Immune response
Immune system
Immune Tolerance - immunology
Immunological tolerance
Immunomodulation
Immunoregulation
Inflammation
Inflammatory bowel disease
Inflammatory diseases
Ingestion
Interferon
Interferon-gamma - immunology
Interferon-gamma - metabolism
Interleukin 10
Interleukin 17
Interleukin 6
Interleukin-10 - immunology
Interleukin-10 - metabolism
Interleukin-17 - immunology
Interleukin-17 - metabolism
Interleukin-6 - immunology
Interleukin-6 - metabolism
Laboratory animals
Lymphocytes
Lymphocytes T
Medicine and Health Sciences
Mice
Mice, Inbred BALB C
Modulation
Mucous membrane
Organs
Ovalbumin
Ovalbumin - immunology
Ovalbumin - pharmacology
Proteins
Rodents
Spleen
T-Lymphocytes, Regulatory - immunology
Transcription factors
Tumor Necrosis Factor-alpha - immunology
Tumor Necrosis Factor-alpha - metabolism
Tumor necrosis factor-α
Weight reduction
γ-Interferon
title Oral Tolerance Induced by OVA Intake Ameliorates TNBS-Induced Colitis in Mice
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