Animals were anesthetized with a mixture selleck screening library of ketamine and xylazine [47] and intra cranially (i.c.) challenged with 30 μl of E199 medium supplemented with 5% FBS containing 4.32 log10 PFU of DENV-2, which corresponds to approximately 3.8 LD50. Animals were monitored for 21 days, and mortality and morbidity rates were recorded. The IFN-γ ELISPOT assay was performed as previously described [40]. Two weeks after the immunization regimen, cells derived from spleens of vaccinated mice were placed (2 × 105 cells/well) in a 96-well micro titer plate (MultiScreen, Millipore) previously coated

with 10 μg/ml of rat anti-mouse INF-γ monoclonal antibody (mAb) (BD Pharmingen). Cells were cultured at 37 °C with 5% CO2 for 18 h in the presence or absence of 5 μg of the H-2d-restricted CD8+ T cell-specific epitope AGPWHLGKL (NS1265–273), a highly conserved epitope among the DENV serotypes

[48]. As a positive control, cells from all groups were pooled and cultured in the presence of concanavalin A, as previously described [49]. After incubation, cells were washed away, and plates were incubated with a biotinylated anti-mouse INF-γ mAb (BD Pharmingen) at a final concentration of 2 μg/ml at 4 °C. After 16–18 h, the plates were incubated VRT752271 manufacturer with diluted peroxidase-conjugated streptavidin (Sigma–Aldrich). The spots were developed using diaminobenzidine (DAB) substrate (Sigma–Aldrich) and counted with a stereo microscope (model SMZ645, Nikon). The in vivo assessment of the cytotoxic activity

of CD8+ T cells induced in the different immunization groups was carried out as previously described [40]. Splenocytes from naive mice were stained with 0.5 μM or 5 μM carboxyfluorescein diacetate succinimidyl ester (CFSE) (Invitrogen) for 15 min at 37 °C. The cells labeled with 5 μM of CFSE were then pulsed with the NS1265–273 next oligopeptide (AGPWHLGKL) [48] and [50]. Both CFSE-labeled cell populations, NS1265–273 pulsed or not, were transferred intravenously to vaccinated mice (2 × 107 cells of each population). One day later, the inoculated animals were euthanized and individual spleens were isolated to identify the two CFSE-labeled cell populations by multivariant FACScan analyses (FACSCalibur from BD Biosciences). The percentages of specific target cell killing were calculated for each individual by comparing the reduction of peptide-pulsed cells relative to that of the non-pulsed cells. The affinity of anti-NS1 antibodies was assessed by the ammonium thiocyanate elution-ELISA method, as previously described [51]. The procedure was similar to that of the standard ELISA with the inclusion of an extra step. After incubation with the pooled sera diluted according to titers obtained by ELISA, the plates were washed and ammonium thiocyanate, diluted in PBS, was added to the wells in concentrations ranging from 0 to 8 M. Plates were maintained at room temperature for 15 min.