No clinical signs could be detected in group 11, vaccinated i.n. with recNcPDI associated with chitosan/alginate nanogels (1PDI-Alg-CT; Table 2). Quantitative real-time PCR of cerebral tissues from all animals was performed to investigate the cerebral parasite loads (Figure 2). While infection of the CNS took place in all groups, there were distinct www.selleckchem.com/products/bgj398-nvp-bgj398.html differences in the intensity of infection. With the i.p. vaccinated animals (Figure 2a), no differences were found among those groups receiving

the antigen (10PDI-SAP, 10PDI-Alg-SAP, 10PDI-Man-SAP) and those groups receiving only the nanogels (Alg-SAP, Man-SAP). In contrast, the i.n. delivery showed significantly lower (P < 0·05) cerebral parasite burdens in the groups receiving recNcPDI (10PDI-CT, 1PDI-CT) and the groups receiving chitosan/alginate

or recNcPDI-chitosan/alginate nanogels (Alg-CT, 1PDI-Alg-CT; Figure 2b). This was observed with mice receiving 1 or 10 μg recNcPDI. For the latter, the group vaccinated selleck chemicals llc with recNcPDI incorporated into chitosan/alginate nanogels (1PDI-Alg-CT) had a slightly lower parasite load compared to the group immunized with nanogels alone (Alg-CT). Although there was a reduced cerebral parasite loads in mice vaccinated with recNcPDI incorporated into chitosan/alginate-mannose nanogels (1PDI-Man-CT), this was not statistically significant compared to the chitosan/alginate-mannose groups (Man-CT) Wilson disease protein or to the cholera toxin control group (CT). Serological

responses against recNcPDI as well as against crude N. caninum tachyzoite extract antigen (Nc. extract) were measured by ELISA. Total IgG, IgG1 and IgG2a reactivities of sera were measured prior to vaccination (PrI), after vaccination prior to challenge infection (BI) and after challenge infection prior to euthanasia (PI). The PrI sera of all mice were negative for antibody reactivity against either Nc. extract or recNcPDI (data not shown). BI and PI sera showed the different levels of reactivity with recNcPDI as shown in Figure 3, and the reactivities with Nc. extract are shown in Figure 4.