Table 3.

C1498/B7-2 induced immunologic memory against C1498 and C1498/B7-1

Priming tumor3-150Challenge tumor (1 × 106cells)3-151No. tumor progressors/injected mice (%)3-152MST ± SD (d)3-153
None C1498 5/5  (100) 27 ± 7  
C1498/B7-2 C1498 2/14  (14)3-155 19 ± 1  
None C1498/B7-1 6/6  (100) 34 ± 5  
C1498/B7-2 C1498/B7-1 0/5  (0)3-155 —  
C1498/B7-2 and C1498 C1498/B7-1 0/12  (0)3-155 — 
Priming tumor3-150Challenge tumor (1 × 106cells)3-151No. tumor progressors/injected mice (%)3-152MST ± SD (d)3-153
None C1498 5/5  (100) 27 ± 7  
C1498/B7-2 C1498 2/14  (14)3-155 19 ± 1  
None C1498/B7-1 6/6  (100) 34 ± 5  
C1498/B7-2 C1498/B7-1 0/5  (0)3-155 —  
C1498/B7-2 and C1498 C1498/B7-1 0/12  (0)3-155 — 
F3-150

C1498 challenge experiment: C1498/B7-2 “primed” B6 mice had rejected a subcutaneous challenge of 1 × 106live C1498/B7-2 tumor cells 16 to 22 weeks before this experiment. On day 0, a group of naive B6 mice and the C1498/B7-2-primed mice were challenged subcutaneously with 1 × 106 parental C1498 tumor cells.

C1498/B7-1 challenge experiment: C1498/B7-2-primed B6 mice had rejected a subcutaneous challenge of 1 × 106 C1498/B7-2 tumor cells 11 weeks earlier, whereas B6 mice primed to both C1498/B7-2 and C1498 had rejected challenges of live C1498/B7-2 (1 × 106) 36 to 43 weeks earlier and of live C1498 tumor cells (1 × 106) 21 weeks earlier. On day 0 of this experiment, naive B6 mice and primed mice noted above were challenged subcutaneously with C1498/B7-1.

F3-151

C57BL/6 mice were injected subcutaneously with 1 × 106 live tumor cells, as indicated.

F3-152

Percentages of mice that developed progressive tumors within 60 days after tumor injection.

F3-153

MST of mice that developed tumor.

F3-155

Significantly different from the naive control groups challenged with either C1498 or C1498/B7-1 (Fischer exact test;P ≤ .002).

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