Table 3.

Therapeutic Effect of Anti-GD2 Antibody IL-2 Fusion Protein on Established Experimental Metastasis of NXS2 Cells in C.B-17 SCID Mice

Treatment*Metastatic ScoreMetastatic ScoreWeight (mg)
 Bone Marrow  Liver  Liver  
PBS  2, 2, 2, 2, 2, 2  4, 4, 4, 4, 3, 2  4,502 ± 1,113 
ch14.18 + IL2  2, 2, 2, 2  4, 4, 4, 3  3,145 ± 780 
ch14.18–IL22-153 0, 0, 0, 0  0, 0, 0, 0 1,028 ± 37 
Treatment*Metastatic ScoreMetastatic ScoreWeight (mg)
 Bone Marrow  Liver  Liver  
PBS  2, 2, 2, 2, 2, 2  4, 4, 4, 4, 3, 2  4,502 ± 1,113 
ch14.18 + IL2  2, 2, 2, 2  4, 4, 4, 3  3,145 ± 780 
ch14.18–IL22-153 0, 0, 0, 0  0, 0, 0, 0 1,028 ± 37 

Experimental bone marrow and liver metastases were induced by intravenous injection of 5 × 104 NXS2 hybrid neuroblastoma cells.

*

Treatment was initiated at day 5 after tumor cell inoculation by daily intravenous injections ×6 of either PBS, 40 μg ch14.18 antibody + 120,000 IU rhIL-2, or 40 μg ch14.18–IL-2 fusion protein.

Bone marrow metastases were staged according to results obtained by high- and low-sensitivity tyrosine hydroxylase RT-PCR as described in Materials and Methods.

Liver metastases were staged according to the percentage of metastatic liver surface: 0, 0%; 1 <0% to 25%; 2, 25% to 50%; 3, 50% to 75%; 4 ≥75%.

F2-153

Differences in bone marrow staging, numbers of metastatic liver foci, and liver weights between fusion protein treatment and all control groups were statistically significant (P < .001).

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