Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
1995-7-13
pubmed:abstractText
The mechanisms underlying the induction of immunological tolerance after feeding soluble exogenous antigens, including proteins and haptens, are still unclear. Using a model of oral tolerance to the contact-sensitizing hapten 2,4-dinitrochlorobenzene (DNCB), we have compared the ability-of intestinal epithelial cells and of Peyer's patch APC to present DNCB in vitro or ex vivo after oral feeding, to specific peripheral lymph node T cells from DNCB-sensitized mice. In contrast to Peyer's patch APC, which induce efficient hapten-specific T cell activation upon exposure to the hapten either in vitro or in vivo, mature MHC class-II-positive intestinal epithelial cells were unable to induce T cell activation in either case. Interestingly, enterocytes from DNCB-fed mice exerted a dramatic inhibitory effect on the proliferative response of hapten-primed T cells in response to dinitrobenzene sulfonate presented by syngeneic spleen cells. This inhibitory effect, which was also observed with supernatant of intestinal epithelial cells from DNCB-fed mice, could be reversed by neutralizing anti-transforming growth factor (TGF)-beta antibodies. In addition, pre-incubation of hapten-sensitized T cells with enterocytes from DNCB-fed mice induced T cell anergy, which could be reversed by exogenous interleukin-2 or interleukin-4. These data demonstrate that intestinal epithelial cells activated in vivo by oral administration of DNCB are able to block proliferation of activated T cells through secretion of immunosuppressive cytokines such as TGF-beta. It is proposed that intestinal epithelial cells may play a significant role in oral tolerance by limiting T cell-mediated hypersensitivity responses.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0014-2980
pubmed:author
pubmed:issnType
Print
pubmed:volume
25
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1385-90
pubmed:dateRevised
2003-11-14
pubmed:meshHeading
pubmed-meshheading:7774642-Administration, Oral, pubmed-meshheading:7774642-Animals, pubmed-meshheading:7774642-Antigen-Presenting Cells, pubmed-meshheading:7774642-Culture Media, Conditioned, pubmed-meshheading:7774642-Dermatitis, Allergic Contact, pubmed-meshheading:7774642-Dinitrochlorobenzene, pubmed-meshheading:7774642-Dinitrofluorobenzene, pubmed-meshheading:7774642-Epithelial Cells, pubmed-meshheading:7774642-Female, pubmed-meshheading:7774642-Haptens, pubmed-meshheading:7774642-Histocompatibility Antigens Class II, pubmed-meshheading:7774642-Immune Tolerance, pubmed-meshheading:7774642-Immunization, pubmed-meshheading:7774642-Interleukin-2, pubmed-meshheading:7774642-Interleukin-4, pubmed-meshheading:7774642-Intestinal Absorption, pubmed-meshheading:7774642-Intestinal Mucosa, pubmed-meshheading:7774642-Lymph Nodes, pubmed-meshheading:7774642-Lymphocyte Activation, pubmed-meshheading:7774642-Mice, pubmed-meshheading:7774642-Mice, Inbred C3H, pubmed-meshheading:7774642-Peyer's Patches, pubmed-meshheading:7774642-Spleen, pubmed-meshheading:7774642-T-Lymphocyte Subsets, pubmed-meshheading:7774642-Transforming Growth Factor beta
pubmed:year
1995
pubmed:articleTitle
Oral tolerance to haptens: intestinal epithelial cells from 2,4-dinitrochlorobenzene-fed mice inhibit hapten-specific T cell activation in vitro.
pubmed:affiliation
INSERM U404, Immunité et Vaccination, Institut Pasteur de Lyon, France.
pubmed:publicationType
Journal Article