Table 1

IL-21R expression and clinical characteristics of CLL patient samples

NoAgePrevious therapyInterphase cytogenetics% CD38+% IL-21Rα expressionRMFI of IL-21Rα+cells
55 Nullisomy 13q- (39%), 46 3.89 
66 17P- (76%) 27.37 22.2 
55 11q22.3- (93%) 11 80 19.1 
68 Normal 67 1.85 
45 13q- (68%) 65 
50 11q22.3-(90%), 13q- (93%) 22 60 4.32 
57 10 11q22.3- (93%) 19.4 6.07 
67 Normal 38 16.8 
54 11q22.3 (83.4%), 13q14- (92%) 48 53.6 4.24 
10 64 Normal 64.5 24 
11 77 Normal — 34 3.89 
12 76 13q14- (97%), 11q22.3 (94.3%) 13 49 21 
13 76 11q22.3 (93.3%) 95 30.3 3.5 
14 46 13q14 (28.2%) 15 2.1 
15 53 11q23 (10%) — 0.31 4.32 
16 72 11q22.3 (7.8%) 27.1 21.1 
   17p- (7.8%)    
NoAgePrevious therapyInterphase cytogenetics% CD38+% IL-21Rα expressionRMFI of IL-21Rα+cells
55 Nullisomy 13q- (39%), 46 3.89 
66 17P- (76%) 27.37 22.2 
55 11q22.3- (93%) 11 80 19.1 
68 Normal 67 1.85 
45 13q- (68%) 65 
50 11q22.3-(90%), 13q- (93%) 22 60 4.32 
57 10 11q22.3- (93%) 19.4 6.07 
67 Normal 38 16.8 
54 11q22.3 (83.4%), 13q14- (92%) 48 53.6 4.24 
10 64 Normal 64.5 24 
11 77 Normal — 34 3.89 
12 76 13q14- (97%), 11q22.3 (94.3%) 13 49 21 
13 76 11q22.3 (93.3%) 95 30.3 3.5 
14 46 13q14 (28.2%) 15 2.1 
15 53 11q23 (10%) — 0.31 4.32 
16 72 11q22.3 (7.8%) 27.1 21.1 
   17p- (7.8%)    

Surface staining of B-CLL cells: primary cell samples from 16 B-CLL patients were stained with PE-labeled mouse mAb to human IL-21Rα or a nonbinding isotype control and analyzed by flow cytometry. The percentage of cells expressing receptor was correlated with interphase cytogenetics, CD38 expression, and direct cytotoxicity mediated by IL-21, as examined by annexin+/PI+cells.

RMFI indicates relative mean fluorescent intensity; and —, not detected.

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