Table 2.

Combination of anti-CD28 mAb and rapamycin leads to long-term donor T- and B-cell reconstitution




Donor T cells

Donor B cells

Survival, %
%
×106
cpm × 1000
%
×106
cpm × 1000
BM alone   100   18 ± 3   22 ± 5   11 ± 2   60 ± 4   73 ± 10   53 ± 11  
Control   0   —   —   —   —   —   —  
Rapamycin   0   —   —   —   —   —   —  
αCD28   40   25 ± 3*  4 ± 1  5 ± 2  25 ± 10  4 ± 2  34 ± 7 
αCD28 + rapamycin
 
57
 
23 ± 2*
 
13 ± 7
 
9 ± 2*
 
62 ± 7*
 
35 ± 5
 
56 ± 13*
 



Donor T cells

Donor B cells

Survival, %
%
×106
cpm × 1000
%
×106
cpm × 1000
BM alone   100   18 ± 3   22 ± 5   11 ± 2   60 ± 4   73 ± 10   53 ± 11  
Control   0   —   —   —   —   —   —  
Rapamycin   0   —   —   —   —   —   —  
αCD28   40   25 ± 3*  4 ± 1  5 ± 2  25 ± 10  4 ± 2  34 ± 7 
αCD28 + rapamycin
 
57
 
23 ± 2*
 
13 ± 7
 
9 ± 2*
 
62 ± 7*
 
35 ± 5
 
56 ± 13*
 

Lethally irradiated (1200 cGy) B10.BR recipients were given transplants of 15 × 106 T-cell-depleted marrow cells plus 25 × 106 splenocytes from C57BL/6 donors. Recipients were treated intraperitoneally with either anti-CD28 mAb (αCD28) at 100 μg × 1 or rapamycin (rapamycin) at 1.5 mg/kg × 14 days or both (αCD28 + rapamycin). Surviving recipients were killed on day 120 after transplantation. Splenocytes were stained for expression of CD4, CD8, B220 and H2Kb. T-cell function was measured by stimulating splenocytes with Concanavalin A for 3 days, and B cell function was measured by stimulating splenocytes with LPS for 3 days. Data are presented as average counts per minute (cpm) ± SD. Results are representative of 2 replicate experiments. — indicates that no data are available, because all mice in this group died before day 120.

*

P > .05 compared with BM alone

P < .05 compared with BM alone

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