Table 1.

Prevention of Marrow Graft Rejection by Cultured CD8 Blasts

T Cells Added Number of T Cells IL-2Recipients Tested Recipients Engrafted Percent Engrafted
None  —  No  10  0  0  
None —  Yes  10  0  0  
CD8 blasts 5.0 × 104 No  5  0  0  
CD8 blasts 5.0 × 104 Yes  10  0  0  
CD8 blasts 2.5 × 105 No  9  3  33  
CD8 blasts 2.5 × 105 Yes  15  6  40  
CD8 blasts  1.0 to 1.2 × 106 No  9  100  
CD8 blasts  1.0 to 1.2 × 106 Yes 10  10  100  
LN T  1.0 to 1.2 × 106 No  9  9  100 
T Cells Added Number of T Cells IL-2Recipients Tested Recipients Engrafted Percent Engrafted
None  —  No  10  0  0  
None —  Yes  10  0  0  
CD8 blasts 5.0 × 104 No  5  0  0  
CD8 blasts 5.0 × 104 Yes  10  0  0  
CD8 blasts 2.5 × 105 No  9  3  33  
CD8 blasts 2.5 × 105 Yes  15  6  40  
CD8 blasts  1.0 to 1.2 × 106 No  9  100  
CD8 blasts  1.0 to 1.2 × 106 Yes 10  10  100  
LN T  1.0 to 1.2 × 106 No  9  9  100 

Groups of five irradiated (800 cGy) CB6 recipients were transplanted with T-cell–depleted marrow (5.0 × 106cells) from B6C3 donors. Grafts contained no added T cells (negative control), 1.0 to 1.25 × 106 freshly isolated B6C3 lymph node T cells (LN T) (positive control), or the indicated numbers of CD8 blasts recovered on day 5 from MLC in which B6C3 LN T cells were stimulated with irradiated CB6 spleen cells. IL-2 (2,000 U IP) was administered daily for 6 days starting on the day of the transplant. Engrafted recipients had 86% to 99% (mean, 95.4%) H2k-positive donor-derived granulocytes in the blood at 2 months after transplantation, whereas recipients with rejection had 0% to 9% (mean, 1.9%) H2k-positive granulocytes when last tested at 1 to 2 months after transplantation. The table shows results pooled from three experiments.

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