Table 1

In contrast with B6 WT, primed B-cell-deficient recipients engraft if given high donor BM cell doses

Recipient and no. BM cellsSurvivalNo. engraftedMean % donor
B6 WT, 40 × 106 
    Unprimed 10/10 10/10 98 ± 2 
    Primed 0/10* NA NA 
B6 WT, 200 × 106 
    Unprimed 4/4 4/4 100 ± 0 
    Primed 3/4 0/3* 0 ± 0* 
B6 muMT, 200 × 106 
    Unprimed 4/4 4/4 99 ± 1 
    Primed 4/4 4/4 100 ± 2 
B6 muMT, 100 × 106 
    Unprimed 4/4 4/4 98 ± 3 
    Primed 4/4 4/4 100 ± 0 
B6 muMT, 20 × 106 
    Unprimed 8/8 8/8 83 ± 11 
    Primed 11/12 2/11* 16 ± 11* 
Recipient and no. BM cellsSurvivalNo. engraftedMean % donor
B6 WT, 40 × 106 
    Unprimed 10/10 10/10 98 ± 2 
    Primed 0/10* NA NA 
B6 WT, 200 × 106 
    Unprimed 4/4 4/4 100 ± 0 
    Primed 3/4 0/3* 0 ± 0* 
B6 muMT, 200 × 106 
    Unprimed 4/4 4/4 99 ± 1 
    Primed 4/4 4/4 100 ± 2 
B6 muMT, 100 × 106 
    Unprimed 4/4 4/4 98 ± 3 
    Primed 4/4 4/4 100 ± 0 
B6 muMT, 20 × 106 
    Unprimed 8/8 8/8 83 ± 11 
    Primed 11/12 2/11* 16 ± 11* 

B6 WT or B6 muMT mice were primed on day −28 with 20 × 106 BALB/c splenocytes intraperitoneally, irradiated on day −1 (6.0 Gy), and given non-T-cell-depleted BALB/c BM cells at the indicated number on day 0. Survival was monitored. PBLs were phenotyped 6 weeks after transplantation for donor chimerism. All engrafting mice were high-level donor chimeras (> 90%). Shown is percentage of mean group donor chimerism ± 1 SEM.

NA indicates not available.

*

P < .01 versus nonprimed control at same BM cell dose.

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