| Literature DB >> 14670304 |
Pau Serra1, Abdelaziz Amrani, Jun Yamanouchi, Bingye Han, Shari Thiessen, Toshihiro Utsugi, Joan Verdaguer, Pere Santamaria.
Abstract
We report that disruption of CD154 in nonobese diabetic (NOD) mice abrogates the helper function of CD4+CD25- T cells without impairing the regulatory activity of CD4+CD25+ T cells. Whereas CD4+ T cells from NOD mice enhanced a diabetogenic CD8+ T cell response in monoclonal TCR-transgenic NOD mice, CD4+ T cells from NOD.CD154(-/-) mice actively suppressed it. Suppression was mediated by regulatory CD4+CD25+ T cells capable of inhibiting CD8+ T cell responses induced by peptide-pulsed dendritic cells (DCs), but not peptide/MHC monomers. It involved inhibition of DC maturation, did not occur in the presence of CD154+ T-helper cells, and could be inhibited by activation of DCs with LPS, CpG DNA, or an agonistic anti-CD40 mAb. Thus, in at least some genetic backgrounds, CD154-CD40 interactions and innate stimuli release immature DCs from suppression by CD4+CD25+ T cells.Entities:
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Year: 2003 PMID: 14670304 DOI: 10.1016/s1074-7613(03)00327-3
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745