Taken together, IC pretreatment can significantly inhibit LPS or CpG ODN-induced maturation of DCs in a FcγRIIb-dependent manner. Mature DC-induced Th1 and Th17 responses are involved in the pathogenesis of some autoimmune Panobinostat price diseases, whereas immature DCs contribute to tolerance induction by downregulation of T-cell response and subsequently attenuate the pathogenesis of some autoimmune diseases. Next we investigated whether IC pretreatment could enhance tolerogenecity of immature DCs. OVA-pulsed immature DCs, which were pretreated with IC/Ig and then stimulated with LPS or CpG ODN, were incubated with OVA323–339-specific CD4+ T cells in vitro. We found that IC pretreatment reduced the

ability of LPS or CpG ODN-stimulated DCs to induce the proliferation and IL-17, IFN-γ secretion of antigen-specific CD4+ T cells (Fig. 1C and D). In contrast, IC/Ig pretreatment could not reduce the ability of FcγRIIb−/− DCs to induce proliferation and IL-17 secretion of antigen-specific CD4+ T cells. Altogether, the data suggest that IC pretreatment could enhance tolerogenecity of immature DCs in FcγRIIb-dependent manner. We previously showed that IC can induce massive amount of PGE2 from macrophages, which is responsible for the inhibition of TLR4-triggered inflammatory response. Similar

to macrophages, immature Daporinad research buy DCs produced large amount of PGE2 once stimulated with IC. LPS or CpG ODN could not further promote IC-induced PGE2 production of immature DCs (Fig. 2A). Also, immature FcγRIIb−/− DCs released some PGE2 in response to IC stimulation, but less than the PGE2 secreted by WT DCs in response to IC stimulation (Fig. 2B). To investigate whether PGE2 was responsible

for the hyporesponsiveness of T cells induced by DCs pretreated with IC, we first observed the direct effect of PGE2 on the proliferation of CD4+ T PKC inhibitor cells by anti-CD3/CD28. As expected, PGE2 inhibited the proliferation of T cells in a dose-dependent manner (Supporting Information Fig. 2). Next, OVA323–339-pulsed DCs were incubated with celecoxib, an inhibitor of COX2, 30 min prior to treatment with IC and TLR ligands. The hyporesponsiveness of OVA323–339-specific T cells disappeared when PGE2 secretion was inhibited, and addition of exogenous PGE2 could restore the inhibitory effect on T-cell proliferation in this system (Fig. 2C). Altogether, these data confirmed that IC-induced PGE2 from DCs was responsible for the downregulation of T-cell response by immature DCs that were pretreated with IC and then stimulated with TLR ligands. The data in the previous sections indicated that IC could downregulate DC-initiated T-cell response by inducing PGE2 production from DCs via FcγRIIb. To investigate whether IC could also inhibit in vivo T-cell response triggered by TLR agonists, we i.v. injected mice with OVA323–339-specific CD4+ T cells 24 h and OVA together with IC before i.p. administration of LPS or CpG ODN.