Table 4.

Absence of CTLA-4 in vivo leads to CD8+T-cell-mediated C1498/B7-1 regression at tumor cell numbers that normally lead to tumor progression

Tumor hosts4-150Tumor injected4-151CD8+depletion4-151No. tumor progressors/mice injected (%)
CTLA-4 BM chimeras C1498/B7-1 No 7/24  (29)4-153 
CTLA-4 BM chimeras C1498/B7-1 Yes 7/7  (100)  
CTLA-4+ BM chimeras C1498/B7-1 No 21/23  (91)  
CTLA-4+ BM chimeras C1498/B7-1 Yes 7/7  (100)  
Normal B6 mice C1498/B7-1 No 7/7  (100)  
CTLA-4 BM chimeras C1498 No 7/7  (100)  
CTLA-4+ BM chimeras C1498 No 4/4  (100)  
Normal B6 mice C1498 No 7/7  (100) 
Tumor hosts4-150Tumor injected4-151CD8+depletion4-151No. tumor progressors/mice injected (%)
CTLA-4 BM chimeras C1498/B7-1 No 7/24  (29)4-153 
CTLA-4 BM chimeras C1498/B7-1 Yes 7/7  (100)  
CTLA-4+ BM chimeras C1498/B7-1 No 21/23  (91)  
CTLA-4+ BM chimeras C1498/B7-1 Yes 7/7  (100)  
Normal B6 mice C1498/B7-1 No 7/7  (100)  
CTLA-4 BM chimeras C1498 No 7/7  (100)  
CTLA-4+ BM chimeras C1498 No 4/4  (100)  
Normal B6 mice C1498 No 7/7  (100) 
F4-150

Normal B6 or Thy1 congenic B6.PL-Thy1amice were conditioned with 1100 cGy of γ-radiation 1 day before intravenous infusion of 5.0 to 8.5 × 106 BM cells from CTLA-4 (−/−) or CTLA-4+ donors (either +/− or +/+).

F4-151

Mice were injected subcutaneously with 1 × 106 tumor cells.

Mice were observed up to 70 to 96 days after bone marrow transplantation (approximately 40-60 days after tumor injection).

F4-153

Significantly lower than in CTLA-4+ BM chimeras (P < .001) and normal B6 mice given C1498/B7-1 as well as CTLA-4 BM chimeras given C1498 (P < .005) (Fischer exact test).

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