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. 2007 Oct 16;7:118. doi: 10.1186/1471-2334-7-118

Table 3.

Protection against a lethal influenza virus challenge in offspring immunized with DNA vaccine born to the mothers immunized with inactivated vaccinea

Serum IgG titersb in offspring

Dose (μg) of Inactivated vaccine for female mice Plasmid for offspring ELISA (2n)c NI assay (2n)c Lung virus titersb (log10 TCID50) Survival offspring/Tested offspring (3 weeks)

21 days after primary immunization 7 days after booster 21 days after primary immunization 7 days after booster
1.00 30 μg HA 14.8 ± 0.50 13.3 ± 0.30 3.3 ± 0.35* 3/6
0.10 30 μg HA 11.7 ± 0.50 12.5 ± 0.60 3.8 ± 0.23* 3/7
0.01 30 μg HA 11.3 ± 0.60 13.0 ± 0.00 3.0 ± 0.71* 6/7*
1.00 30 μg NA 4.3 ± 0.60 7.0 ± 1.00 1.9 ± 0.58* 7/7*
0.10 30 μg NA 3.7 ± 0.60 7.2 ± 0.80 1.5 ± 0.24* 7/7*
0.01 30 μg NA 4.3 ± 0.60 8.0 ± 1.00 0.9 ± 0.83* 6/6*
Unimmunized Unimmunized <1 <1 <3 <3 5.3 ± 0.35 0/7

a Female mice were immunized twice, 3 weeks apart, with various doses of inactivated vaccine. The offspring were immunized with 30 μg HA or 30 μg NA at ages of 1 and 4 weeks respectively. Serum samples from offspring were collected 3 weeks after primary immunization and 1 week after booster. The anti-HA antibody titers were measured by ELISA. The anti-NA antibody titers were measured by NI assay. One week after booster, the offspring were challenged with a lethal dose of A/PR/8/34 (20 × LD50). Lungs were taken out from at least three mice in each group 3 days after challenge for virus titration by standard MDCK assay. Survival rates of mice were measured 3 weeks after challenge.

b Values represent mean ± S.D. of each group.

c The serum samples were diluted 2-fold serially and "n" represents the dilution factor.

*Significant difference (p < 0.05)