Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1999-4-13
pubmed:abstractText
CD40 ligand (CD40L) gene-disrupted (CD40L-/-) mice were employed to examine the role of costimulatory signals via CD40L-CD40 interactions in mucosally induced tolerance. CD40L-/- and control (CD40L+/+) mice of the same C57BL/6 x 129/J background were immunized orally with 25 mg of OVA before systemic challenge with OVA in CFA. While CD40L+/+ mice showed reductions in Ag-specific T cell responses including delayed-type hypersensitivity (DTH) and proliferative responses, CD40L-/- mice underwent normal T cell responses. Further, cytokine analysis of splenic CD4+ T cells showed that both Th1-type (e.g., IFN-gamma and IL-2) and Th2-type (e.g., IL-4, IL-5, IL-6, and IL-10) responses were maintained in CD40L-/- mice orally immunized with OVA, whereas these cytokine responses in CD40L+/+ mice were significantly reduced. In addition, splenic CD4+ T cells from CD40L-/- mice orally immunized with OVA provided B cell help in Ag-specific Ab-forming cells when the cells were cultured with naive B cells in the presence of Ag and CD40L-transfected cell lines. In contrast, an identical culture condition containing splenic CD4+ T cells from orally tolerized CD40L+/+ mice did not exhibit helper activity. Taken together, these findings indicate that CD40L and CD40 interactions are essential for the induction of systemic T cell unresponsiveness to orally administered Ag.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0022-1767
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
162
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1904-9
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:9973457-Administration, Oral, pubmed-meshheading:9973457-Animals, pubmed-meshheading:9973457-Antigens, CD40, pubmed-meshheading:9973457-B-Lymphocytes, pubmed-meshheading:9973457-CD4-Positive T-Lymphocytes, pubmed-meshheading:9973457-CD40 Ligand, pubmed-meshheading:9973457-Cytokines, pubmed-meshheading:9973457-Dose-Response Relationship, Immunologic, pubmed-meshheading:9973457-Down-Regulation, pubmed-meshheading:9973457-Immune Tolerance, pubmed-meshheading:9973457-Ligands, pubmed-meshheading:9973457-Lymphocyte Cooperation, pubmed-meshheading:9973457-Membrane Glycoproteins, pubmed-meshheading:9973457-Mice, pubmed-meshheading:9973457-Mice, Inbred C57BL, pubmed-meshheading:9973457-Mice, Inbred Strains, pubmed-meshheading:9973457-Mice, Knockout, pubmed-meshheading:9973457-Mouth Mucosa, pubmed-meshheading:9973457-Ovalbumin, pubmed-meshheading:9973457-T-Lymphocyte Subsets, pubmed-meshheading:9973457-Th1 Cells, pubmed-meshheading:9973457-Th2 Cells, pubmed-meshheading:9973457-Transfection
pubmed:year
1999
pubmed:articleTitle
Mucosally induced systemic T cell unresponsiveness to ovalbumin requires CD40 ligand-CD40 interactions.
pubmed:affiliation
Department of Oral Biology, Immunobiology Vaccine Center, University of Alabama Medical Center, Birmingham 35294, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't