Table 1.

Cdk5 activity in donor T cells is primarily responsible for reductions in GVHD

GroupGVHD scoreSurvival, %
Week 4Week 5Week 6
F1 → F1 0.2 ± 0.2 0.0 ± 0.0 0.0 ± 0.0 100 
Allo WT T + Allo WT BM → F1 5.0 ± 0.4 5.2 ± 0.5 5.8 ± 0.1 13 
Allo WT T + Allo KO BM → F1 4.8 ± 0.6 4.6 ± 0.6 4.5 ± 0.5 33 
Allo KO T + Allo KO BM → F1 2.4 ± 0.3* 2.5 ± 0.4* 3.0 ± 0.5* 73* 
Allo KO T + Allo WT BM → F1 3.2 ± 0.8* 2.6 ± 0.5* 2.7 ± 0.4* 60* 
GroupGVHD scoreSurvival, %
Week 4Week 5Week 6
F1 → F1 0.2 ± 0.2 0.0 ± 0.0 0.0 ± 0.0 100 
Allo WT T + Allo WT BM → F1 5.0 ± 0.4 5.2 ± 0.5 5.8 ± 0.1 13 
Allo WT T + Allo KO BM → F1 4.8 ± 0.6 4.6 ± 0.6 4.5 ± 0.5 33 
Allo KO T + Allo KO BM → F1 2.4 ± 0.3* 2.5 ± 0.4* 3.0 ± 0.5* 73* 
Allo KO T + Allo WT BM → F1 3.2 ± 0.8* 2.6 ± 0.5* 2.7 ± 0.4* 60* 

Lethally irradiated B6D2F1 received HCT from either syngeneic B6D2F1 or allogeneic Cdk5+/+C (Allo WT) or Cdk5−/−C (Allo KO) donors as described in Figure 2. Two additional allogeneic groups were evaluated in this “mixing” experiment as described in “Methods”: allogeneic KO BM cells mixed with allogeneic WT T cells and allogeneic WT BM cells mixed with allogeneic KO T cells. Survival was monitored daily and GVHD clinical scores were assessed weekly as described; n = 8 to 16 per group.

*

P < .01 compared with recipients of Cdk5+/+C HCT.

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