Table 1.

Phenotypic characterization of cells transduced by a lentiviral vector after stimulation with IL-2, IL-7, and IL-15



IL-2, %

IL-7, %

IL-15, %

TCR-activated, %

Surface marker
LNGFr+
LNGFr-
LNGFr+
LNGFr-
LNGFr+
LNGFr-
LNGFr+
LNGFr-
PBMC, %
CD3   >90   >90   >90   >90   >90   >90   >90   >90   87  
CD4   47   47   48   53   36   44   42   17   53  
CD8   20   38   26   35   41   35   47   60   32  
CD56   8   5   4   9   13   18   96   24   12  
CD62L   56   60   54   69   23   45   88   70   33  
CD95   83   89   90   93   91   91   99   96   40  
CD25   20   6   23   26   52   43   77   78   1  
CD16   7   4   5   2   5   7   1   5   5  
CD14   0   0   0   0   0   0   0   0   1  
CD45RA   50   30   52   40   38   38   11   30   50  
CD45RO
 
26
 
59
 
28
 
46
 
41
 
46
 
92
 
70
 
49
 


IL-2, %

IL-7, %

IL-15, %

TCR-activated, %

Surface marker
LNGFr+
LNGFr-
LNGFr+
LNGFr-
LNGFr+
LNGFr-
LNGFr+
LNGFr-
PBMC, %
CD3   >90   >90   >90   >90   >90   >90   >90   >90   87  
CD4   47   47   48   53   36   44   42   17   53  
CD8   20   38   26   35   41   35   47   60   32  
CD56   8   5   4   9   13   18   96   24   12  
CD62L   56   60   54   69   23   45   88   70   33  
CD95   83   89   90   93   91   91   99   96   40  
CD25   20   6   23   26   52   43   77   78   1  
CD16   7   4   5   2   5   7   1   5   5  
CD14   0   0   0   0   0   0   0   0   1  
CD45RA   50   30   52   40   38   38   11   30   50  
CD45RO
 
26
 
59
 
28
 
46
 
41
 
46
 
92
 
70
 
49
 

Transduced T cells previously stimulated with IL-2, IL-7, and IL-15 or TCR-triggered were characterized for the expression of lineage and activation markers and for transgene expression by flow cytometry. Unmodified PBMCs from the same donors were stained as controls. Transduced and untransduced cells were analyzed and compared by gating on LNGFr+ and LNGFr- cell populations. A representative experiment is shown.

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