Literature DB >> 16220047

Oral tolerance and inflammatory bowel disease.

Thomas A Kraus1, Lloyd Mayer.   

Abstract

PURPOSE OF REVIEW: Oral tolerance refers to the ability of the mucosal immune system to actively inhibit systemic immune responses to fed antigens. Recently, clinical trials have used oral tolerance as a therapy for certain chronic inflammatory and autoimmune diseases such as multiple sclerosis and type I diabetes. Inflammatory bowel disease is now widely thought to be caused by the breakdown of oral tolerance through a combination of genetic and environmental factors. Therefore, it seems incongruous that clinicians would try to use oral tolerance therapy to alleviate the symptoms of inflammatory bowel disease. Yet, armed with the results of select animal models, trials have begun for oral tolerance therapy for Crohn's disease. This review will outline the recent advances in understanding oral tolerance, explore the relation between oral tolerance and inflammatory bowel disease, and comment on the likelihood of successful oral tolerance therapy for inflammatory bowel disease. RECENT
FINDINGS: The results of an oral tolerance trial in Crohn's disease patients in Israel have shown some promising results, whereas the results of studies of experimentally induced oral tolerance in patients with inflammatory bowel disease from the authors' laboratory have shown that feeding a neoantigen in an attempt to induce oral tolerance is not successful in patients with inflammatory bowel disease.
SUMMARY: The fundamental difference in the mechanisms of oral tolerance in mice and humans requires a more focused effort to understand the human mucosal immune system before oral tolerance therapy for autoimmune and chronic inflammatory disorders reaches its full potential.

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Year:  2005        PMID: 16220047     DOI: 10.1097/01.mog.0000182862.88798.28

Source DB:  PubMed          Journal:  Curr Opin Gastroenterol        ISSN: 0267-1379            Impact factor:   3.287


  10 in total

1.  Regulation of induced colonic inflammation by Lactobacillus acidophilus deficient in lipoteichoic acid.

Authors:  Mansour Mohamadzadeh; Erika A Pfeiler; Jeffrey B Brown; Mojgan Zadeh; Matthew Gramarossa; Elizabeth Managlia; Praveen Bere; Bara Sarraj; Mohammad W Khan; Krishna Chaitanya Pakanati; M Javeed Ansari; Sarah O'Flaherty; Terrence Barrett; Todd R Klaenhammer
Journal:  Proc Natl Acad Sci U S A       Date:  2011-01-31       Impact factor: 11.205

Review 2.  Do we really understand what the immunological disturbances in inflammatory bowel disease mean?

Authors:  Epameinondas V Tsianos; Konstantinos Katsanos
Journal:  World J Gastroenterol       Date:  2009-02-07       Impact factor: 5.742

3.  Induction of antigen-specific tolerance by oral administration of Lactococcus lactis delivered immunodominant DQ8-restricted gliadin peptide in sensitized nonobese diabetic Abo Dq8 transgenic mice.

Authors:  Inge L Huibregtse; Eric V Marietta; Shadi Rashtak; Frits Koning; Pieter Rottiers; Chella S David; Sander J H van Deventer; Joseph A Murray
Journal:  J Immunol       Date:  2009-07-27       Impact factor: 5.422

Review 4.  Current view of the immunopathogenesis in inflammatory bowel disease and its implications for therapy.

Authors:  M-I Torres; A Rios
Journal:  World J Gastroenterol       Date:  2008-04-07       Impact factor: 5.742

5.  SAMP1/YitFc mice develop ileitis via loss of CCL21 and defects in dendritic cell migration.

Authors:  Zbigniew Mikulski; Rebecca Johnson; Iftach Shaked; Gisen Kim; Heba Nowyhed; Wendy Goodman; Grzegorz Chodaczek; Theresa T Pizarro; Fabio Cominelli; Klaus Ley
Journal:  Gastroenterology       Date:  2015-01-22       Impact factor: 22.682

Review 6.  Age-related changes in ocular mucosal tolerance: Lessons learned from gut and respiratory tract immunity.

Authors:  Jeremias G Galletti; Cintia S de Paiva
Journal:  Immunology       Date:  2021-05-02       Impact factor: 7.215

7.  Crotoxin from Crotalus durissus terrificus is able to down-modulate the acute intestinal inflammation in mice.

Authors:  Caroline de Souza Almeida; Vinicius Andrade-Oliveira; Niels Olsen Saraiva Câmara; Jacqueline F Jacysyn; Eliana L Faquim-Mauro
Journal:  PLoS One       Date:  2015-04-08       Impact factor: 3.240

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

Authors:  Lisiery N Paiatto; Fernanda G D Silva; Julia Bier; Márcia R Brochetto-Braga; Áureo T Yamada; Wirla M S C Tamashiro; Patricia U Simioni
Journal:  PLoS One       Date:  2017-01-18       Impact factor: 3.240

Review 9.  Reactive oxygen species and antioxidant defense in human gastrointestinal diseases.

Authors:  Peter Patlevič; Janka Vašková; Pavol Švorc; Ladislav Vaško; Pavol Švorc
Journal:  Integr Med Res       Date:  2016-07-29

10.  Treatment of Intestinal Inflammation With Epicutaneous Immunotherapy Requires TGF-β and IL-10 but Not Foxp3+ Tregs.

Authors:  Xin Chen; M Cecilia Berin; Virginia L Gillespie; Hugh A Sampson; David Dunkin
Journal:  Front Immunol       Date:  2021-02-26       Impact factor: 7.561

  10 in total

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