Anti-CD2 + 48 MoAb Inhibit Long-Term Alloengraftment in Irradiated B6 Recipients of T-Cell–Depleted BALB/c or DBA/1 Donor BM
Group . | No. H2 Typed . | Day Post-BMT . | % Donor . | % Host . |
---|---|---|---|---|
A. BALB/c Donors | ||||
Irrelevant IgG | 28 | 40-57 | 60 ± 7 | 40 ± 7 |
αCD2 + 48 MoAb | 29 | 40-57 | 20 ± 6* | 80 ± 6* |
Irrelevant IgG | 20 | 110-145 | 74 ± 7 | 26 ± 7 |
αCD2 + 48 MoAb | 23 | 110-145 | 38 ± 9* | 62 ± 9* |
B. DBA/1 Donors | ||||
Irrelevant IgG | 9 | 40 | 60 ± 12 | 39 ± 12 |
αCD2 + 48 MoAb | 11 | 40 | 13 ± 8* | 87 ± 8* |
αCD2 MoAb | 13 | 40 | 66 ± 7 | 34 ± 7 |
αCD48 MoAb | 2 | 40 | 0 ± 0† | 100 ± 0† |
Irrelevant MoAb | 8 | 104 | 80 ± 12 | 20 ± 12 |
αCD2 + 48 MoAb | 8 | 104 | 22 ± 14* | 87 ± 14* |
αCD2 MoAb | 8 | 104 | 81 ± 12 | 19 ± 12 |
αCD48 MoAb | 1 | 104 | 0 | 100 |
Group . | No. H2 Typed . | Day Post-BMT . | % Donor . | % Host . |
---|---|---|---|---|
A. BALB/c Donors | ||||
Irrelevant IgG | 28 | 40-57 | 60 ± 7 | 40 ± 7 |
αCD2 + 48 MoAb | 29 | 40-57 | 20 ± 6* | 80 ± 6* |
Irrelevant IgG | 20 | 110-145 | 74 ± 7 | 26 ± 7 |
αCD2 + 48 MoAb | 23 | 110-145 | 38 ± 9* | 62 ± 9* |
B. DBA/1 Donors | ||||
Irrelevant IgG | 9 | 40 | 60 ± 12 | 39 ± 12 |
αCD2 + 48 MoAb | 11 | 40 | 13 ± 8* | 87 ± 8* |
αCD2 MoAb | 13 | 40 | 66 ± 7 | 34 ± 7 |
αCD48 MoAb | 2 | 40 | 0 ± 0† | 100 ± 0† |
Irrelevant MoAb | 8 | 104 | 80 ± 12 | 20 ± 12 |
αCD2 + 48 MoAb | 8 | 104 | 22 ± 14* | 87 ± 14* |
αCD2 MoAb | 8 | 104 | 81 ± 12 | 19 ± 12 |
αCD48 MoAb | 1 | 104 | 0 | 100 |
B6 recipients were administered 6.0 or 6.5 Gy TBI on day −1 followed by 107 T-cell–depleted BM from the indicated donor strain on day 0. Mice received αCD2 + 48 MoAb (300 μg/dose each) or irrelevant IgG IP on days −1 and +2 and then twice weekly through day 14 post-BMT. Data in A are pooled from three experiments consisting of 40 mice per group. Data in B are derived from an experiment in which 15 mice per group were transplanted. All surviving mice were H2 phenotyped at the indicated time periods post-BMT. The % donor and % host cells are the mean ± 1 SEM.
P ≤ .01 as compared with irrelevant IgG control group.
P ≤ .05 as compared with irrelevant IgG control group.