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. 2005 Sep;73(9):6017–6025. doi: 10.1128/IAI.73.9.6017-6025.2005

TABLE 1.

Trypomastigote-induced parasitemia and mortality in mice immunized with either ASP-2 DNA or recombinant protein administered individually or sequentially (DNA priming/protein boosting)

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
a

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.

b

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).

c

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).