2), a time-point at which we found previously that T cells were already primed but anti-TSHR antibodies or hyperthyroidism were not induced [26]. Albeit slightly less effective

Barasertib price than pretreatment (Fig. 3), only 33% of immunized, anti-mCD20 mAb-treated mice became hyperthyroid compared with 73% in immunized, untreated mice (Fig. 4a). Again, the levels of anti-TSHR antibodies were significantly lower in mice that received anti-mCD20 mAb (Fig. 4b). In the third approach, anti-mCD20 mAb was administered to hyperthyroid mice (experiment 3 in Fig. 2). This treatment proved to be ineffective. Thus, the incidences of hyperthyroidism were decreased from 90% in the immunized, untreated mice to 54% in the immunized, anti-mCD20 mAb-treated mice (Fig. 5a), which were statistically insignificantly different. Moreover, the differences in levels of anti-TSHR antibodies selleckchem and TSAb activities were also insignificant between two groups (Fig. 3b,c). Of interest,

immunization with Ad-TSHR289 increased serum concentrations of IgG significantly (Figs 3d and 5d). However, anti-mCD20 mAb had no effect on the basal IgG levels (Fig. 3d). TSHR antigen-specific splenocyte secretion of IFN-γin vitro was used as a measure of T cell activation because we have found previously that this cytokine is indispensable for the pathogenesis of Graves’ disease [27]. In the first experiment, splenocytes were prepared 2 weeks after a single injection of AdTSHR289 from mice which received anti-mCD20 mAb 5 days before immunization (experiment 1 in Fig. 2). Controls were splenocytes from immunized but not B cell-depleted mice, as well as splenocytes from unimmunized mice. In a T cell recall assay, splenocytes from Ad-TSHR289 immunized mice, but not from immunized

and B cell-depleted mice, produced significantly increased amounts of IFN-γ in response to TSHR antigen (Fig. 6a). Thus, anti-mCD20 mAb suppressed antigen-specific IFN-γ synthesis by ∼50%. In the second experiment, T cell recall responses were studied in mice which received anti-mCD20 mAb 10 days after immunization with Ad-TSHR289 (experiment 2 in Fig. 3). Splenocytes were prepared 2 weeks after immunization from these B cell-depleted mice either and from immunized but not B cell-depleted mice, as well as from unimmunized mice. In this case, splenocytes from both the immunized mice and the immunized and B cell-depleted mice produced comparably increased amounts of IFN-γ in response to TSHR antigen (Fig. 6b). Overall, our findings indicate that B cells are important for disease initiation by stimulating T cell function and antibody production. However, B cell depletion prevents disease induction but is not efficacious once disease is manifested clinically. This study was designed to evaluate the prophylactic and therapeutic potentials of B cell depletion on Graves’ hyperthyroidism in a mouse model.