Table 2.

Flow cytometric analysis on RCC-reactive CTL clones B5, G16, K34, and J23




B5

G16

K34

J23
CD3   95   99   97   100  
CD8   95   99   97   100  
CD4dim  2   3   73   0  
TCRαβ   91   99   96   100  
TCRγδ   2   1   0   0  
CD16   1   0   0   0  
CD56dim  17   44   46   44  
CD57   1   1   NT   1  
CD45RA   4   1   0   1  
CD45RO   68   99   82   62  
CCR7dim  26   7   18   10  
CD28dim  46   48   NT   52  
CD94   13   33   17   1  
CD158a   3   5   5   2  
CD158b   5   14   4   2  
CD25   67   85   NT   95  
CD69   71   67   NT   93  
HLA-DR
 
90
 
92
 
NT
 
79
 



B5

G16

K34

J23
CD3   95   99   97   100  
CD8   95   99   97   100  
CD4dim  2   3   73   0  
TCRαβ   91   99   96   100  
TCRγδ   2   1   0   0  
CD16   1   0   0   0  
CD56dim  17   44   46   44  
CD57   1   1   NT   1  
CD45RA   4   1   0   1  
CD45RO   68   99   82   62  
CCR7dim  26   7   18   10  
CD28dim  46   48   NT   52  
CD94   13   33   17   1  
CD158a   3   5   5   2  
CD158b   5   14   4   2  
CD25   67   85   NT   95  
CD69   71   67   NT   93  
HLA-DR
 
90
 
92
 
NT
 
79
 

CTL clones were isolated from allogeneic MLTC-1 on blood-derived CD8+ T lymphocytes of healthy donor 860 and the HLA class la—matched RCC line MZ1257-RCC. T cells were stained with FITC- or PE-conjugated monoclonal antibodies directed against indicated cell surface markers and were then analyzed. Results shown represent percentage of cells with positive FITC- or PE-staining. Low staining intensity is marked as “dim.” NT indicates not tested.

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