Table 1.

Dd-ζ cells inhibit the generation of anti-Dd cytotoxicity in MLC




P815

EL4
Responder
Stimulator
40:1*
20:1
10:1
40:1
20:1
10:1
FVB pr  Dd-ζ irr  100   100   100   67   31   23  
FVB pr   Dd-ζ   34   19   11   100   100   98  
Dd-ζ   FVB pr irr   33   28   23   100   100   100  
FVB pr   MHC-Dd irr   100   100   99   57   38   25  
FVB pr
 
MHC-Dd
 
100
 
100
 
85
 
49
 
37
 
22
 



P815

EL4
Responder
Stimulator
40:1*
20:1
10:1
40:1
20:1
10:1
FVB pr  Dd-ζ irr  100   100   100   67   31   23  
FVB pr   Dd-ζ   34   19   11   100   100   98  
Dd-ζ   FVB pr irr   33   28   23   100   100   100  
FVB pr   MHC-Dd irr   100   100   99   57   38   25  
FVB pr
 
MHC-Dd
 
100
 
100
 
85
 
49
 
37
 
22
 

Stimulator and responder splenocytes were incubated in MLC at a 1:1 ratio for 5 days, harvested, and tested against 51Cr-labeled P815 or EL4 target cells. The Dd-ζ cells were obtained from homozygous 130 strain mice.

*

Chromium release cytotoxicity assay results are listed as the percentage of specific lysis at the indicated effector-to-target cell ratios.

Stimulators or responders marked “pr” were primed at least 4 weeks prior to use with an intraperitoneal injection of 20 million splenocytes from an MHC-Dd transgenic mouse.

Stimulators marked “irr” were irradiated at a dose of 2000 rad.

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