Fig. 3.
Fig. 3. Complete protection from hepatic neuroblastoma metastases induced by an mTH-based DNA vaccine with posttranscriptionally enhanced gene expression by WPRE and boosts with ch14.18–IL-2. / (A) Mice were immunized twice by oral gavage at 2-week intervals with 108 attenuated salmonella that contained either the empty vector, pcDNA3.1; pcDNA3.1 plus mTH; or pcDNA3.1 plus mTH-WPRE. All animals were injected intravenously with a lethal challenge of 5 × 105 NXS2 wild-type tumor cells 1 week after the second immunization and boosted 2 days thereafter with 10 μg ch14.18–IL-2 for 4 consecutive days. (B) Mice were killed 4 weeks after tumor cell challenge, and hepatic metastases were assessed by liver weight in milligrams and counting of individual metastatic foci. Ruler below images is marked in centimeters.

Complete protection from hepatic neuroblastoma metastases induced by an mTH-based DNA vaccine with posttranscriptionally enhanced gene expression by WPRE and boosts with ch14.18–IL-2.

(A) Mice were immunized twice by oral gavage at 2-week intervals with 108 attenuated salmonella that contained either the empty vector, pcDNA3.1; pcDNA3.1 plus mTH; or pcDNA3.1 plus mTH-WPRE. All animals were injected intravenously with a lethal challenge of 5 × 105 NXS2 wild-type tumor cells 1 week after the second immunization and boosted 2 days thereafter with 10 μg ch14.18–IL-2 for 4 consecutive days. (B) Mice were killed 4 weeks after tumor cell challenge, and hepatic metastases were assessed by liver weight in milligrams and counting of individual metastatic foci. Ruler below images is marked in centimeters.

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