We found Tem cells highly expressing OX40, even if at lower level than Treg cells (Fig. 3C); thus intratumoral OX86 injection could directly target Tem cells at this site. Conversely, Tem cells obtained after immunization check details of naïve BALB/c mice with two consecutive injections of BM-derived dendritic cells (BMDCs) activated with LPS, as previously described 17, expressed low or absent OX40, even after in vitro activation (Supporting Information Fig. 3). In BMDC-injected animals, Tem cells were shown to constitutively express CD40L at sufficient levels to induce DC activation 17. The CD40/CD40L interaction is crucial for DC activation,

survival and proliferation 26. Many data suggest that this axis is involved in inducing protective anti-tumor immune response 18, 19, 27, 28 and that activation of this pathway may represent a strategy for tumor treatment. To investigate whether OX86-induced tumor rejection was dependent on the CD40/CD40L axis, WT and CD40−/− mice were inoculated subcutaneously

with CT26 cells and treated intratumorally with OX86. As shown in Fig. 4A, OX86 treatment was ineffective in CD40-deficient mice, while inducing tumor rejection or impaired tumor growth in CD40-sufficient mice. Such failure to induce anti-tumor response in the absence of CD40 could be either due to defective licensing of DC reactivation and migration from the tumor or due to impaired T-cell priming at the dLNs by DCs licensed, but not competent, for optimal T-cell costimulation. Methane monooxygenase To discriminate between these

two possibilities, an in vivo DC migration assay was performed. Tumors Selleckchem Trichostatin A growing in WT and CD40−/− mice were treated with OX86 or rat IgG co-injected with green fluorescent microbeads. Only DCs that have up-taken the beads at the tumor site can be detected as fluorescent in dLNs. Although OX86 rescued DC migration from tumor to dLNs in WT mice, the same treatment was ineffective in CD40−/− mice (Fig. 4B), a finding implying that in absence of the CD40/CD40L axis tumor-associated DCs cannot be reactivated. We also confirmed that, in CD40−/− mice, the OX40 expression by tumor-infiltrating Tem cells was not defective, indicating that the CD40/CD40L system did not affect the T-cell activation status at the tumor site or Tem-cell responsiveness to OX86 treatment (Supporting Information Fig. 4). We hypothesized that, in the immunosuppressive tumor microenvironment, Tem cells were inhibited in their ability to license DCs via CD40L, and that OX40 triggering might provide the right signal for Tem cells to supply an effective CD40/CD40L mediated co-stimulation. Although the intratumoral injection of OX86 did not change the percentage of Tem cells (Fig. 4C), it significantly upregulated CD40L expression on Tem cells (Fig. 4D). Such CD40L up-modulation was specific for Tem cells, as no other T-cell subsets and especially CD44lowCD62Llow recently activated T (Tact) cells responded accordingly (Fig. 4E).