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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 |
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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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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.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0170205</identifier><identifier>PMID: 28099498</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>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</subject><ispartof>PloS one, 2017-01, Vol.12 (1), p.e0170205</ispartof><rights>COPYRIGHT 2017 Public Library of Science</rights><rights>2017 Paiatto et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2017 Paiatto et al 2017 Paiatto et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c725t-d7b57f258dcac869edff0a33d11bb9c59e8c91c7a577a035d374c9307ea95c883</citedby><cites>FETCH-LOGICAL-c725t-d7b57f258dcac869edff0a33d11bb9c59e8c91c7a577a035d374c9307ea95c883</cites><orcidid>0000-0002-6951-5040</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1859788223/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1859788223?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28099498$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Ashour, Hossam M</contributor><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><title>Oral Tolerance Induced by OVA Intake Ameliorates TNBS-Induced Colitis in Mice</title><title>PloS one</title><addtitle>PLoS One</addtitle><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.</description><subject>Abnormalities</subject><subject>Analysis</subject><subject>Animals</subject><subject>Antigens</subject><subject>Arthritis</subject><subject>Biology</subject><subject>Biology and Life Sciences</subject><subject>Body weight</subject><subject>Body weight gain</subject><subject>Bystander Effect - immunology</subject><subject>Care and treatment</subject><subject>Causes of</subject><subject>CD4 antigen</subject><subject>Cell proliferation</subject><subject>Colitis</subject><subject>Colitis - chemically induced</subject><subject>Colitis - immunology</subject><subject>Colon</subject><subject>Crohn's disease</subject><subject>Cytokines</subject><subject>Dendritic cells</subject><subject>Diet</subject><subject>Drinking behavior</subject><subject>Drinking water</subject><subject>Ethanol</subject><subject>Evolution</subject><subject>Female</subject><subject>Free water</subject><subject>Genetic aspects</subject><subject>Histology</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Immune Tolerance - immunology</subject><subject>Immunological tolerance</subject><subject>Immunomodulation</subject><subject>Immunoregulation</subject><subject>Inflammation</subject><subject>Inflammatory bowel disease</subject><subject>Inflammatory diseases</subject><subject>Ingestion</subject><subject>Interferon</subject><subject>Interferon-gamma - immunology</subject><subject>Interferon-gamma - metabolism</subject><subject>Interleukin 10</subject><subject>Interleukin 17</subject><subject>Interleukin 6</subject><subject>Interleukin-10 - immunology</subject><subject>Interleukin-10 - metabolism</subject><subject>Interleukin-17 - immunology</subject><subject>Interleukin-17 - metabolism</subject><subject>Interleukin-6 - immunology</subject><subject>Interleukin-6 - metabolism</subject><subject>Laboratory animals</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Medicine and Health Sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Modulation</subject><subject>Mucous membrane</subject><subject>Organs</subject><subject>Ovalbumin</subject><subject>Ovalbumin - immunology</subject><subject>Ovalbumin - pharmacology</subject><subject>Proteins</subject><subject>Rodents</subject><subject>Spleen</subject><subject>T-Lymphocytes, Regulatory - immunology</subject><subject>Transcription factors</subject><subject>Tumor Necrosis Factor-alpha - immunology</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><subject>Tumor necrosis factor-α</subject><subject>Weight reduction</subject><subject>γ-Interferon</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNkl1v0zAUhiMEYmPwDxBEQkJw0eKPOLZvJpWKj0oblVjZrXViO62HG5c4Qezf467p1KJdIF_46znvOT5-s-wlRmNMOf5wE_q2AT_ehMaOEeaIIPYoO8WSklFJEH18sD7JnsV4gxCjoiyfZidEICkLKU6zy3kLPl8Eb1totM1njem1NXl1m8-vJ2nbwU-bT9bWu9BCZ2O--PbxarTHpsG7zsXcNfml0_Z59qQGH-2LYT7Lfnz-tJh-HV3Mv8ymk4uR5oR1I8MrxmvChNGgRSmtqWsElBqMq0pqJq3QEmsOjHNAlBnKCy0p4hYk00LQs-z1TnfjQ1RDJ6LCgkkuBCE0EbMdYQLcqE3r1tDeqgBO3R2Edqmg7Zz2VlkpS0EAm5LXhQApMSMFqipTVwWAYEnrfMjWV2trtG261LQj0eObxq3UMvxWSYcUd-W-GwTa8Ku3sVNrF7X1Hhob-m3dpaAFYWWR0Df_oA-_bqCWkB7gmjqkvHorqiYFF5hSTLZ1jx-g0jB27XSyTe3S-VHA-6OAxHT2T7eEPkY1u_r-_-z8-ph9e8CuLPhuFYPvOxeaeAwWO1C3IcbW1vdNxkhtXb_vhtq6Xg2uT2GvDj_oPmhvc_oXP4v6hg</recordid><startdate>20170118</startdate><enddate>20170118</enddate><creator>Paiatto, Lisiery N</creator><creator>Silva, Fernanda G D</creator><creator>Bier, Julia</creator><creator>Brochetto-Braga, Márcia R</creator><creator>Yamada, Áureo T</creator><creator>Tamashiro, Wirla M S C</creator><creator>Simioni, Patricia U</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-6951-5040</orcidid></search><sort><creationdate>20170118</creationdate><title>Oral Tolerance Induced by OVA Intake Ameliorates TNBS-Induced Colitis in Mice</title><author>Paiatto, Lisiery N ; Silva, Fernanda G D ; Bier, Julia ; Brochetto-Braga, Márcia R ; Yamada, Áureo T ; Tamashiro, Wirla M S C ; Simioni, Patricia U</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c725t-d7b57f258dcac869edff0a33d11bb9c59e8c91c7a577a035d374c9307ea95c883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Abnormalities</topic><topic>Analysis</topic><topic>Animals</topic><topic>Antigens</topic><topic>Arthritis</topic><topic>Biology</topic><topic>Biology and Life Sciences</topic><topic>Body weight</topic><topic>Body weight gain</topic><topic>Bystander Effect - 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Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals (Open Access)</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Paiatto, Lisiery N</au><au>Silva, Fernanda G D</au><au>Bier, Julia</au><au>Brochetto-Braga, Márcia R</au><au>Yamada, Áureo T</au><au>Tamashiro, Wirla M S C</au><au>Simioni, Patricia U</au><au>Ashour, Hossam M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oral Tolerance Induced by OVA Intake Ameliorates TNBS-Induced Colitis in Mice</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2017-01-18</date><risdate>2017</risdate><volume>12</volume><issue>1</issue><spage>e0170205</spage><pages>e0170205-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>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.</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> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2017-01, Vol.12 (1), p.e0170205 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1859788223 |
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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