Table 1.

Secondary adoptive transfer of 205-immune BMT chimera lymphocytes into irradiated recipients does not induce GVHD

Donor Vaccine Treated? # Dead/N # With Signs of Acute GVHD Final Weight Avg. ± SEM
C3H.SW  No 0/5  0/5  25 ± 0.9  
C3H.SW  Yes  2/3* 2/3 16 ± 3 
BMT chimera  No  0/4  0/4 25 ± 0.9  
BMT chimera  Yes  0/4  0/4 25 ± 1.5 
Donor Vaccine Treated? # Dead/N # With Signs of Acute GVHD Final Weight Avg. ± SEM
C3H.SW  No 0/5  0/5  25 ± 0.9  
C3H.SW  Yes  2/3* 2/3 16 ± 3 
BMT chimera  No  0/4  0/4 25 ± 0.9  
BMT chimera  Yes  0/4  0/4 25 ± 1.5 

C3H.SW or long-term surviving C3H.SW → B6 BMT chimeras were either not immunized (nonimmune) or immunized (205-immune) with 5 × 106 irradiated 205IL-2/TK cells twice at a weekly interval. Ten days later, their splenocytes were adoptively transferred to C57BL/6 recipients that were given 850 cGy total body irradiation 1 day earlier. Survival was monitored until day 108. Final weights represent the weight of the surviving mice at day 108 or the weight at death for the 2 dead mice. Secondary transfer recipients were engrafted with C3H.SW T-cells as assessed by flow cytometry, which showed that the majority of Thy1.2+ cells in the spleen after sacrifice were CD5.1+.

*

P = .0431 compared to survival of recipients of nonimmune C3H.SW.

P < .01 compared to final weight of recipients of nonimmune C3H.SW.