Figure 1
Figure 1. Hematopoietic cells are involved in SRA/CD204 deficiency-enhanced antitumor immunity after OVA-MPL vaccination. (A) Enhanced antitumor efficacy in immunized SRA−/− mice. Age-matched WT and SRA−/− C57BL/6 mice (n = 5) were immunized twice at a weekly interval with 50 μg of OVA protein mixed with 10 μg of MPL. One week after booster immunization, mice were challenged with 3 × 105 B16-OVA tumor cells (*P < .001, SRA−/− vs WT mice, ANOVA test). Experiments were performed twice, and a representative experiment is shown. (B) Hematopoietic cells required for the enhanced vaccine activities in SRA−/− mice. Recipient SRA−/− mice (n = 5) were whole body irradiated and received 107 total BM cells from donor WT or SRA−/− mice. Eight weeks later, recipient mice were immunized with OVA-MPL and challenged with 2 × 105 B16-OVA cells (P < .001, SRA−/− BM vs WT BM, ANOVA test). Results are representative of 2 separate experiments.

Hematopoietic cells are involved in SRA/CD204 deficiency-enhanced antitumor immunity after OVA-MPL vaccination. (A) Enhanced antitumor efficacy in immunized SRA−/− mice. Age-matched WT and SRA−/− C57BL/6 mice (n = 5) were immunized twice at a weekly interval with 50 μg of OVA protein mixed with 10 μg of MPL. One week after booster immunization, mice were challenged with 3 × 105 B16-OVA tumor cells (*P < .001, SRA−/− vs WT mice, ANOVA test). Experiments were performed twice, and a representative experiment is shown. (B) Hematopoietic cells required for the enhanced vaccine activities in SRA−/− mice. Recipient SRA−/− mice (n = 5) were whole body irradiated and received 107 total BM cells from donor WT or SRA−/− mice. Eight weeks later, recipient mice were immunized with OVA-MPL and challenged with 2 × 105 B16-OVA cells (P < .001, SRA−/− BM vs WT BM, ANOVA test). Results are representative of 2 separate experiments.

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