Table 5.

Growth of MK in Liquid Culture From ET and PMF CD34+ Cells

0 PEG-rhuMGDF sMpl-Fc PEG-rhuMGDF + sMpl-Fc
A  
t1  15     26   3   22  
t6 12    120   1   90  
t7  48    203  61 167  
t10   9     60   4   30  
t11  39    75  23   50  
t12  38 ± 6  77 ± 7  3   47  
t16  14 1,000   0  400  
t17 11 ± 1  67 ± 7  1.5 ± 0.5  26 ± 6  
t18 16 ± 4  101 ± 4  0.3 ± 0.5  57 ± 3  
m1 13 ± 1  196 ± 23  1 ± 0.5  64 ± 12  
m2 333 ± 230  1,700 ± 333   0  633 ± 152 
m3  53 ± 15  181 ± 83  12 ± 8 33 ± 11  
B  
t15  128 ± 18 441 ± 6  71 ± 15  233 ± 16  
m2  42 ± 2 260 ± 15  4 ± 0.5  178 ± 13  
m3 993 ± 205  3,746 ± 272  279 ± 55 1,039 ± 207 
0 PEG-rhuMGDF sMpl-Fc PEG-rhuMGDF + sMpl-Fc
A  
t1  15     26   3   22  
t6 12    120   1   90  
t7  48    203  61 167  
t10   9     60   4   30  
t11  39    75  23   50  
t12  38 ± 6  77 ± 7  3   47  
t16  14 1,000   0  400  
t17 11 ± 1  67 ± 7  1.5 ± 0.5  26 ± 6  
t18 16 ± 4  101 ± 4  0.3 ± 0.5  57 ± 3  
m1 13 ± 1  196 ± 23  1 ± 0.5  64 ± 12  
m2 333 ± 230  1,700 ± 333   0  633 ± 152 
m3  53 ± 15  181 ± 83  12 ± 8 33 ± 11  
B  
t15  128 ± 18 441 ± 6  71 ± 15  233 ± 16  
m2  42 ± 2 260 ± 15  4 ± 0.5  178 ± 13  
m3 993 ± 205  3,746 ± 272  279 ± 55 1,039 ± 207 

Mean number of MKs ± SEM, quantified after 10 days of liquid culture with an inverted microscope (A) or by flow cytometry (B) after labeling with an R-PE or FITC-conjugated anti–CD-41 monoclonal antibody. Culture conditions were no growth factor (0), 10 ng/mL PEG-rhuMGDF, sMpl-Fc at 5 μg/mL, or a combination of sMpl-Fc (5 μg/mL) and PEG-rhuMGDF (10 ng/mL) (PEG-rhuMGDF + sMpl-Fc). Results are expressed for 1 × 103 CD34+ cells from TE (t) or PMF (m) patients.

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