Table 1.

Phenotypic characteristics of B-acute Ph1-ALL

Patient No. FAB Subtype Age/ Sex Level of Engraftment of NOD/SCID Mice With 10 × 106 MNCs% CD34+ in MNCs % CD34++CD38 in MNCs Estimated Frequency of SL-ICs/106 MNCs
1  L2  16/M 35 ± 6  94  18  41  
2  L2  34/F 70 ± 8  90  24  12  
3  L1  42/M 61 ± 6  78  19  3  
4  L2  24/M  43 ± 7 85  20  2  
5  L1  37/F  71 ± 9  93  0.2  
6  L2  29/M  27 ± 8  94  21  9  
L2  33/M  26 ± 6  84  26  19 
Patient No. FAB Subtype Age/ Sex Level of Engraftment of NOD/SCID Mice With 10 × 106 MNCs% CD34+ in MNCs % CD34++CD38 in MNCs Estimated Frequency of SL-ICs/106 MNCs
1  L2  16/M 35 ± 6  94  18  41  
2  L2  34/F 70 ± 8  90  24  12  
3  L1  42/M 61 ± 6  78  19  3  
4  L2  24/M  43 ± 7 85  20  2  
5  L1  37/F  71 ± 9  93  0.2  
6  L2  29/M  27 ± 8  94  21  9  
L2  33/M  26 ± 6  84  26  19 

FAB criteria18 and NOD/SCID mice were used.

Patient Nos. 1, 2, 4, and 7 showed expression of myeloid antigens. The MNCs of all patients were transplanted at the dose indicated into 56 NOD/SCID mice using conditions previously described.

The level of human cell engraftment of the mice transplanted was determined by Southern blot analysis, using a human-specific α-satellite probe, and compared with the intensity of the bands of the human/mouse mixtures.

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