Engraftment can be achieved in donor-primed mice by the combination of high numbers of bone marrow cells, in vivo TCD, and megadose mIg with or without splenectomy
Treatment group . | Survival . | Engraftment . |
---|---|---|
Not primed | 16/16* | 16/16* |
Primed | ||
No treatment | 2/16 | 0/16 |
Ig | 1/16 | 1/16 |
TCD | 3/8 | 0/8 |
TCD, Ig | 6/8* | 3/8* |
Ig, Splx | 2/7 | 0/7 |
TCD, Ig, Splx | 13/17* | 10/17* |
Treatment group . | Survival . | Engraftment . |
---|---|---|
Not primed | 16/16* | 16/16* |
Primed | ||
No treatment | 2/16 | 0/16 |
Ig | 1/16 | 1/16 |
TCD | 3/8 | 0/8 |
TCD, Ig | 6/8* | 3/8* |
Ig, Splx | 2/7 | 0/7 |
TCD, Ig, Splx | 13/17* | 10/17* |
B6 recipients were primed on day −56 with 20 × 106 BALB/c splenocytes intraperitoneally. Splenectomy (Splx) was performed on day −28. Mouse Ig (20 mg) was administered intraperitoneally on day −15 and day −7. In vivo TCD was achieved by intraperitoneal administration of 400 μg anti-CD4 and anti-CD8 mAbs on days −2, 0, 2, 4, and 7. Mice were irradiated with 6.0 Gy on day −1 and infused with 100 × 106 BALB/c BM on day 0. All deaths occurred within 2 weeks after transplantation. All engrafted mice were more than 90% donor by peripheral blood leukocyte phenotyping 3 months after BMT.
P < .01 versus primed, no treatment (primed, TCD, Ig vs primed, TCD, Ig, Splx; P = .32.).