Table 3.

HPC and CFU Escape SLT-1 Toxicity

(A) Analysis of HPC
Patient Source of Mobilized Blood Percentage of CD34+45lo HPC at Day 6-7
UntreatedSLT-1–Treated
Breast cancer  
 Unfractionated   2.8%  2.6%  
 HPC-enriched  39.5%  60.2%  
Lymphoma 
 Unfractionated   1.1%   1.4%  
 HPC-enriched 71.1%  39.5%  
Myeloma  
 HPC-enriched   5.0% 28.4%  
(B) Analysis of CFC  
Patient Source of Mobilized Blood  No. of Colonies/100-200 Cells Plated at Day 203-150 
Untreated  SLT-1–Treated  
Breast cancer  
 HPC-enriched  15 ± 1  13 ± 1   
Lymphoma 
 HPC-enriched  17 ± 1   20 ± 1.5  
Myeloma 
 HPC-enriched  17 ± 1  19 ± 1  
(A) Analysis of HPC
Patient Source of Mobilized Blood Percentage of CD34+45lo HPC at Day 6-7
UntreatedSLT-1–Treated
Breast cancer  
 Unfractionated   2.8%  2.6%  
 HPC-enriched  39.5%  60.2%  
Lymphoma 
 Unfractionated   1.1%   1.4%  
 HPC-enriched 71.1%  39.5%  
Myeloma  
 HPC-enriched   5.0% 28.4%  
(B) Analysis of CFC  
Patient Source of Mobilized Blood  No. of Colonies/100-200 Cells Plated at Day 203-150 
Untreated  SLT-1–Treated  
Breast cancer  
 HPC-enriched  15 ± 1  13 ± 1   
Lymphoma 
 HPC-enriched  17 ± 1   20 ± 1.5  
Myeloma 
 HPC-enriched  17 ± 1  19 ± 1  

Mobilized MNC were treated with 5 μg/mL SLT-1 for 60 minutes, washed, and cultured. For HPC assays, toxin-treated or untreated cells were cultured in Myelocult + 10% Hemostim culture medium for 7 days, followed by harvest of cultured cells and staining with anti-CD34-PE and anti-CD45-QR conjugates. Mobilized MNC were enriched for HPC by negative selection after antibody coating and magnetic bead depletion resulting in a cell population in which 40% to 60% of cells display the HPC phenotype.

F3-150

Cells were plated in microtiter wells. Values listed represent the average number of colonies (±SE) calculated from 6 to 12 replicate wells for each condition tested.

or Create an Account

Close Modal
Close Modal