Literature DB >> 14515264

Functional CD25- and CD25+ mucosal regulatory T cells are induced in gut-draining lymphoid tissue within 48 h after oral antigen application.

Femke Hauet-Broere1, Wendy W J Unger, Johan Garssen, Maarten A Hoijer, Georg Kraal, Janneke N Samsom.   

Abstract

Oral antigen application induces tolerance, leading to suppression of a subsequent systemic challenge with this antigen. The suppression is mediated by mucosal regulatory T (Tr) cells that may differentiate from naive peripheral T cells in the gut-draining lymphoid tissue. However, little is known about the initial steps of this differentiation process. In this study we show that 48 h after oral OVA treatment, antigen-specific T cells in mesenteric lymph nodes (MLN) and Peyer's Patches (PP) were activated and had divided up to four times. The first division was already seen in PP after 24 h. Analysis of surface marker expression and cytokine secretion of the dividing antigen-specific T cells revealed that they sequentially obtained an activation- and memory-like phenotype. These cells secreted IL-2 in most stages of division but only transiently IFN-gamma whereas no IL-4 or IL-10 secretion was detected. Remarkably, 48 h after antigen application, isolated dividing cells were suppressive, as they transferred tolerance to naive mice. Even though CD25 was expressed heterogeneously, both CD25(+) and CD25(-) OVA-specific T cells from MLN could transfer tolerance. Together these findings show that differentiation of functional Tr cells occurs in the MLN and PP within 2 days after antigen ingestion and involves the generation of CD25(+) and CD25(-) antigen-specific T cells.

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Year:  2003        PMID: 14515264     DOI: 10.1002/eji.200324115

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  28 in total

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Review 2.  Dendritic cells at the oral mucosal interface.

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3.  Oral tolerance in the absence of naturally occurring Tregs.

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4.  Induction of antigen-specific regulatory T cells in the liver-draining celiac lymph node following oral antigen administration.

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5.  T cell-mediated oral tolerance is intact in germ-free mice.

Authors:  K L W Walton; J A Galanko; R Balfour Sartor; N C Fisher
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6.  The role of gut microbiota in programming the immune phenotype.

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7.  Oral tolerance induction by mucosal administration of cholera toxin B-coupled antigen involves T-cell proliferation in vivo and is not affected by depletion of CD25+ T cells.

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8.  Gut-tropic T cells that express integrin α4β7 and CCR9 are required for induction of oral immune tolerance in mice.

Authors:  Barbara Cassani; Eduardo J Villablanca; Francisco J Quintana; Paul E Love; Adam Lacy-Hulbert; William S Blaner; Tim Sparwasser; Scott B Snapper; Howard L Weiner; J Rodrigo Mora
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9.  Abnormal apical-to-basal transport of dietary ovalbumin by secretory IgA stimulates a mucosal Th1 response.

Authors:  J Abed; C Lebreton; G Champier; A Cuvillier; M Cogné; B Meresse; C Dugave; M Garfa-Traoré; B Corthésy; N Cerf-Bensussan; M Heyman
Journal:  Mucosal Immunol       Date:  2013-07-10       Impact factor: 7.313

10.  An imbalance of esophageal effector and regulatory T cell subsets in experimental eosinophilic esophagitis in mice.

Authors:  Xiang Zhu; Meiqin Wang; Caleb H Crump; Anil Mishra
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2009-07-01       Impact factor: 4.052

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