Table 1.

The effect of CTX treatment on IFN-γ or IL-4 production and proliferative activity of spleen cells stimulated with T-Cell mitogens

Treatment Stimuli*IFN-γ (ng/mL)IL-4 (pg/mL) Proliferation (×10−3 cpm)
 None <0.3  <7  2.1 ± 0.5  
PBS  Con A 8.2 ± 0.6  73.7 ± 2.3  122.3 ± 16.1 
 CD3 + IL-2  21.1 ± 1.9  198.4 ± 1.6 103.4 ± 11.5  
 None  <0.3  <7 1.4 ± 0.2  
CTX  Con A  8.0 ± 0.0 99.2 ± 4.1 15.1 ± 4.4 
 CD3 + IL-2 12.1 ± 0.0 203.9 ± 6.1  12.4 ± 5.1 
Treatment Stimuli*IFN-γ (ng/mL)IL-4 (pg/mL) Proliferation (×10−3 cpm)
 None <0.3  <7  2.1 ± 0.5  
PBS  Con A 8.2 ± 0.6  73.7 ± 2.3  122.3 ± 16.1 
 CD3 + IL-2  21.1 ± 1.9  198.4 ± 1.6 103.4 ± 11.5  
 None  <0.3  <7 1.4 ± 0.2  
CTX  Con A  8.0 ± 0.0 99.2 ± 4.1 15.1 ± 4.4 
 CD3 + IL-2 12.1 ± 0.0 203.9 ± 6.1  12.4 ± 5.1 

CTX-SC were obtained 10 days after the last dose of CTX (100 mg/kg) was administered to mice.

*

Spleen cells were cultured in 96 flat-bottomed wells (0.4 × 106 cells/well) and stimulated at culture initiation with Con A (1 μg/mL) or anti-CD3 (2 μg/mL) plus IL-2 (50 units/mL).

Culture supernatants for cytokine quantification were recovered after 24 hours of culture. Proliferative activity was estimated by [3H]TdR incorporation after 72 hours of culture.

Values were significantly (P < .05) different from PBS-treated controls.

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