TABLE 1.
Mouse group no. | Immunogena | Peak parasitemia (log ± SD)b | No. of mice alive/total no. challengedc | % Protection |
---|---|---|---|---|
I | pcDNA3 | 6.35 ± 0.08 | 0/16 | 0 |
II | Alum | 6.53 ± 0.05 | 0/8 | 0 |
III | ASP-2 DNA | 5.42 ± 0.09 | 12/16 | 75.00 |
IV | Alum/His-65kDa | 5.62 ± 0.32 | 8/15 | 53.31 |
V | ASP-2 DNA plus alum/His-65kDa | 5.55 ± 0.23 | 11/15 | 73.74 |
Groups of seven or eight mice were immunized at 0, 3, and 5 weeks with pcDNA3, ASP-2 DNA, alum, or the formulation alum/His-65kDa. A fifth group of mice was injected with two doses of ASP-2 DNA at 0 and 3 weeks. A third immunizing dose was administered after 5 weeks and consisted of the formulation alum/His-65kDa.
Two weeks after the last dose, mice were challenged i.p. with 250 bloodstream trypomastigotes. The values of peak parasitemia of mouse groups III, IV, and V were lower than those for mouse groups I and II (P < 0.05 in all cases). The peak parasitemias of groups III, IV, and V were not statistically different (P > 0.05).
The number of mice alive was recorded 60 days after challenge. Animals from groups III, IV, and V survived longer than mice from groups I and II (P < 0.0001 in all cases by the log rank test). There was no significant statistical difference among groups III, IV, and V (P > 0.05).