Table 1.

Differentiation of amplified peripheral blood B cells into CD20/CD38++ cells

Healthy donorsCD20/
CD38++(%)
Annexin-V (%)Amplification factor from day 4 to 6Overall amplification factor
 1 57 18 2.6 6.8 
 2 50 30 4.2 9.5  
 3 41 24 6.4 
 4 60 22 3.7 15.6  
 5 41 30 2.6 7.7 
 6 42 32 9  
 7 51 26 9.4 
 8 46 29 2.8 7.6  
 9 56 22 3.5 
10 51 23 2.5 11  
Mean ± SD 50 ± 7 25.6 ± 4.5 3.2 ± 0.6 9.1 ± 2.7 
Healthy donorsCD20/
CD38++(%)
Annexin-V (%)Amplification factor from day 4 to 6Overall amplification factor
 1 57 18 2.6 6.8 
 2 50 30 4.2 9.5  
 3 41 24 6.4 
 4 60 22 3.7 15.6  
 5 41 30 2.6 7.7 
 6 42 32 9  
 7 51 26 9.4 
 8 46 29 2.8 7.6  
 9 56 22 3.5 
10 51 23 2.5 11  
Mean ± SD 50 ± 7 25.6 ± 4.5 3.2 ± 0.6 9.1 ± 2.7 

Purified peripheral blood B cells from 10 healthy donors were cultured for 4 days with CD40 + IL-2 + IL-4 + IL-10 + IL-12. Amplified B cells were then harvested, washed, and cultured for 2 additional days with IL-2 + IL-10 + IL-12 + IL-6. At day 6 of culture, the viability was evaluated by annexin V staining, and the percentage of CD20/CD38++ plasma cells was determined by flow cytometry.

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