Table 1.

Effect of rD-mPGPtide on Donor/Host Chimerism in BM Engraftment Across MHC Barriers

Strain CombinationGenetic DifferenceTreatmentPhenotype, Day 30 (% donor/host)Phenotype, Day 60 (% donor/host)
B10.BR → B6 (750 cGy) Full MHC PBS 19/65  
  rD-mPGPtide 53/38 ND 
  Anti-CD4 MoAb 53/37  
(B6D2)F1 → (B6CB)F1 (800 cGy) Haplo-MHC PBS 8/87 17/76 
  rD-mPGPtide 71/21 84/13 
  Anti-CD4 MoAb 75/19 86/12 
bm12 → B6-Ly5.2 (750 cGy) MHC class II PBS 9/73 7/85 
  rD-mPGPtide 66/26 71/20 
  Anti-CD4 MoAb 62/27 69/21 
Strain CombinationGenetic DifferenceTreatmentPhenotype, Day 30 (% donor/host)Phenotype, Day 60 (% donor/host)
B10.BR → B6 (750 cGy) Full MHC PBS 19/65  
  rD-mPGPtide 53/38 ND 
  Anti-CD4 MoAb 53/37  
(B6D2)F1 → (B6CB)F1 (800 cGy) Haplo-MHC PBS 8/87 17/76 
  rD-mPGPtide 71/21 84/13 
  Anti-CD4 MoAb 75/19 86/12 
bm12 → B6-Ly5.2 (750 cGy) MHC class II PBS 9/73 7/85 
  rD-mPGPtide 66/26 71/20 
  Anti-CD4 MoAb 62/27 69/21 

Data from one experiment representative of three separate experiments are presented as the percentage of positive splenocytes as analyzed by flow cytometry. Chimerism was determined using the following MoAb pairs: FITC-anti-H2Kk (B10.BR) and PE-anti-H2Kb (B6); PE-anti-H2Kb (bm12 and B6-Ly5.2) and FITC-anti-CD45.1 (anti-Ly5.1; B6-Ly5.2); and FITC-anti-H2Kk [(B6CB)F1] and PE-anti-H2Kd [(B6D2)F1]. The mean of samples from five mice per group is presented for each individual treatment. The values in all rD-mPGPtide and anti-CD4 MoAb treatment groups were significantly different from those in the PBS control group, P ≤ .001.

Abbreviation: ND, not done.

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