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. Author manuscript; available in PMC: 2011 Jan 22.
Published in final edited form as: Vaccine. 2009 Nov 13;28(4):1031. doi: 10.1016/j.vaccine.2009.10.126

Table 2.

Induction of Immune Responses and Protection Against VEEV TrD Challenges in Mice Immunized with gV3526 Formulations

Vaccine
Formulation
Route of
Vaccination
Dosaged
(µg/dosage)
Percent Seroconversiona
PRN
Day 21
Post-
vaccinationb
Day 49
Post-
vaccinationb
gV3526 SC 0.2 35 85
gV3526 IM
IM
0.02
0.04e
0
30
40
80
gV3526/ CpG SC 0.2 35 75
gV3526/ CpG IM
IM
0.02
0.04e
10
30
55
78c
gV3526/ AlOH SC 0.2 55 90
gV3526/ AlOH IM
IM
0.02
0.04e
20
50
60
90
gV3526 / CpG +
AlOH
IM 0.04e 60 100
C-84 (3 dosage) SC 4 60 100
CpG alone
AlOH alone
CpG + AlOH
alone
SC and IM
SC and IM
SC and IM
0
0
0
0
0
0
0
0
0
Saline SC
IM
0
0
0
0
0
0
a

Percent seroconversion is defined as follows: PRNT, the percentage of mice with PRN titers ≥20; ELISA, the percentage of mice with ELISA titers ≥100.

b

Percent seroconversion was calculated by combining groups of similarly vaccinated mice making a total of 20 mice per group. Groups were later split into 10 mice challenged by the aerosol route and 10 challenged by the SC route.

c

The total number of mice in this group was 19 at the time of the 49 day blood draw. One mouse succumbed to a non-study related reason between study day 21 and 49.

d

All dosages were administered on a 2 dose schedule (day 0 and 28) except for C-84 which was administered on a 3 dose schedule (day 0, 7 and 28).

e

To double the IM dosage, both hind limb muscles were injected with 0.05 mL of inoculum (0.02 µg gV3526).