Figure 4.
Figure 4. Therapeutic study of karpas299 lymphoma-bearing SCID/NOD wild-type mice with HeFi-1 and daclizumab (n = 10). (A) Serum sIL-2Rα levels in different groups at day 21 after treatment. Data represent mean ± SD. (B) Kaplan-Meier survival plot of the mice. The animals treated with HeFi-1 at a dose of 100 μg weekly for 4 weeks had decreased serum values of sIL-2Rα (P < .01) and prolonged survival (P < .01) when compared with the mice in the control group. Daclizumab treatment also prolonged the survival of the mice as compared with that in the control group (P < .05) and reduced the serum concentration of sIL-2Rα, although the difference in serum sIL-2Rα levels between the daclizumab treatment group and the control group was not statistically significant at day 21.

Therapeutic study of karpas299 lymphoma-bearing SCID/NOD wild-type mice with HeFi-1 and daclizumab (n = 10). (A) Serum sIL-2Rα levels in different groups at day 21 after treatment. Data represent mean ± SD. (B) Kaplan-Meier survival plot of the mice. The animals treated with HeFi-1 at a dose of 100 μg weekly for 4 weeks had decreased serum values of sIL-2Rα (P < .01) and prolonged survival (P < .01) when compared with the mice in the control group. Daclizumab treatment also prolonged the survival of the mice as compared with that in the control group (P < .05) and reduced the serum concentration of sIL-2Rα, although the difference in serum sIL-2Rα levels between the daclizumab treatment group and the control group was not statistically significant at day 21.

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