Table 2.

Effect of NK cells on systemic tumor-protective immunity induced by the mTH-WPRE vaccine and the ch14.18–IL-2 fusion protein

TreatmentLiver weight, mgMetastatic foci
Empty vector + anti–asialo-GM1 5200 ± 500 >250, >250, >250, >250  
mTH + ch14.18–IL-2 +
anti–asialo-GM1 
5450 ± 421 >250, >250, >250, >250 
mTH-WPRE + anti–asialo-GM1 3700 ± 200 >250, >250, >250, >250  
mTH-WPRE + ch14.18–IL-2 +
anti–asialo-GM1 
4693 ± 200 >250, >250, >250, >250 
mTH-WPRE 1250 ± 113 7, 3, 0, 0  
mTH-WPRE + ch14.18–IL-2 1073 ± 103 0, 0, 0, 0 
TreatmentLiver weight, mgMetastatic foci
Empty vector + anti–asialo-GM1 5200 ± 500 >250, >250, >250, >250  
mTH + ch14.18–IL-2 +
anti–asialo-GM1 
5450 ± 421 >250, >250, >250, >250 
mTH-WPRE + anti–asialo-GM1 3700 ± 200 >250, >250, >250, >250  
mTH-WPRE + ch14.18–IL-2 +
anti–asialo-GM1 
4693 ± 200 >250, >250, >250, >250 
mTH-WPRE 1250 ± 113 7, 3, 0, 0  
mTH-WPRE + ch14.18–IL-2 1073 ± 103 0, 0, 0, 0 

Mice were treated by oral vaccination with 1 × 108 salmonella containing pcDNA3.1, pcDNA3.1mTH, or pcDNA3.1mTH-WPRE on day 0 (prime) and day 14 (boost); challenged with 5 × 105 NXS2 wild-type tumor cells on day 21; and treated with 10 μg ch14.18–IL-2 2 days thereafter for 4 consecutive days. Mice (n = 4) were humanely killed 28 days after tumor cell challenge, and metastases to the liver were assessed. NK-cell depletion was performed with injection of 100 μL anti–asialo-GM1 weekly for 4 weeks, starting 1 day prior to tumor cell challenge. Differences in liver weights between mice of all experimental groups depleted with anti–asialo-GM1 as compared with nondepleted mice were statistically significant (P ≤ .001). Treatment protocol as described for Figure 3.

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