Table 2

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 groupSurvivalEngraftment
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 groupSurvivalEngraftment
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.).

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