spiralis infected mice. rTs-Hsp70-activated DCs were passively transferred into naive mice three times with intervals of 14

days. The levels of anti-Ts-Hsp70-specific IgG in the sera of these mice were significantly elevated, and these elevations lasted more than 11 weeks without declining ( Fig. 3A). The selleckchem levels of the IgG subtypes were measured, and the results revealed that both IgG1 and IgG2a were induced at similar levels, which indicates that the Ts-Hsp70-activated DCs induced a mixed Th1 and Th2 response in the mice ( Fig. 3B). No anti-Ts-Hsp70 IgG was detected in the mice that received the DCs that were incubated with PBS, the non-relevant protein (Ts-Pmy-N) or LPS. The cytokines IFN-γ, IL-2, IL-4, and IL-6 that were secreted

by the splenocytes that were collected from the mice that were passively transferred with rTs-Hsp70-activated DCs were also measured. The secretions of the Th1 (IFN-γ and IL-2) and Th2 cytokines (IL-4 and IL-6) were significantly elevated in the mice that received the Ts-Hsp70-activated DCs compared those of the groups that received PBS- or non-relevant protein (Ts-Pmy-N)-incubated DCs ( Fig. 4). To determine whether the Ts-Hsp70-activated selleck kinase inhibitor DCs were able to induce protective immunity against T. spiralis infection, the mice that received the DCs were challenged with T. spiralis infective larvae, and the worm burdens were examined at the end of the experiment. The mice that received the rTs-Hsp70-activated DCs exhibited a statistically significant 38.4% reduction in muscle larvae burden compared to the mice that received the PBS-incubated DCs ( Fig. 5). The mice that received recombinant Ts-Pmy-N-incubated DCs did not exhibit a significant reduction in worm burden upon T. spiralis larval challenge.

DCs are central players in the induction and maintenance of immune responses Megestrol Acetate and play a prominent role in helminth infections. The infection itself stimulates DC activity, and the infection-induced DC responses are critical for controlling and eliminating the invading agent [26]. In recent years, considerable progress has been made in elucidating the mechanisms behind the interplay between DCs and helminthes [18], [19] and [26]. After interacting with some inhibitors parasitic helminth antigens, DCs become mature [22], [27] and [28]. The research into the activation and maturation of DCs that are stimulated by helminth antigens has provided a novel approach for the development of vaccines that directly target the antigen-presenting cells [13]. Our previous results indicated that Ts-Hsp70 is a potential vaccine candidate for T. spiralis infection. In the present study, we confirmed that Ts-Hsp70 was able to directly activate mouse bone marrow-derived DCs to mature as characterized by the expressions of typical mature DC cytokines (i.e., IL-1β, IL-6, IL-12p70, and TNF-α) and surface markers (i.e., MHC II, CD40, CD80, and CD86). These results are consistent with the previous observations that T.