Table 2.

Therapeutic Effect of Anti-GD2Antibody–IL-2 Fusion Protein on Experimental Liver Metastasis of NXS2 Cells in Immunocompetent and In Vivo–Depleted A/J Mice

Depletion*TreatmentNo. of FociLiver Weight (mg)
None  PBS  >250, >250, >250, >250, >250, >250  4,356 ± 459  
 ch14.18 + IL-2  >250, 240, 189, 165, 120, 98  2,670 ± 361  
 ch14.18–IL-2 fusion protein  0, 0, 0, 0, 0, 0  1,040 ± 52  
Anti-asialo  GM1 ch14.18–IL-2 fusion protein  >250, >250, >250, >250 3,913 ± 464  
Anti-CD8  ch14.18–IL-2 fusion protein 0, 0, 0, 7  1,208 ± 108 
Depletion*TreatmentNo. of FociLiver Weight (mg)
None  PBS  >250, >250, >250, >250, >250, >250  4,356 ± 459  
 ch14.18 + IL-2  >250, 240, 189, 165, 120, 98  2,670 ± 361  
 ch14.18–IL-2 fusion protein  0, 0, 0, 0, 0, 0  1,040 ± 52  
Anti-asialo  GM1 ch14.18–IL-2 fusion protein  >250, >250, >250, >250 3,913 ± 464  
Anti-CD8  ch14.18–IL-2 fusion protein 0, 0, 0, 7  1,208 ± 108 

Experimental liver metastases were induced by intravenous injection of 10 6 NXS2 hybrid neuroblastoma cells.

*

At day 3 and 1 before tumor cell inoculation and then once weekly for 3 weeks animals were injected intraperitoneally with either 350 μg anti-CD8 antibody or 100 μl anti-asialo GM1 antiserum, respectively.

Treatment was initiated 24 hours after tumor cell inoculation by daily intravenous injections for 5 days of either PBS, 10 μg ch14.18 antibody + 30,000 IU rIL-2 or 10 μg ch14.18–IL-2 fusion protein.

Differences in numbers of metastatic foci and liver weights between immunocompetent mice receiving fusion protein treatment and such animals depleted of CD8+ T cells and all control groups were statistically significant (P < .001).

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