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Table 1 Efficacy Study 1. Summary of outcomes based on clinical and laboratory results

From: Efficacy of an adenovirus-vectored foot-and-mouth disease virus serotype A subunit vaccine in cattle using a direct contact transmission model

Treatment Group

N

Percent Protected from Lesions (21 dpcc)

Geometric mean FMDV A24/Cruzeiro/BRA/55 VNT titer (log10) ± SD on 7 dpv/0 dpcc (range)

Percent Positive for FMDV A24/Cruzeiro/BRA/55 VNT on 7 dpv/0 dpcc

Percent Protected from FMDV RNA in oral and nasal cavities (0–5 dpcc)

Percent Positive for FMDV NSP Antibodies

Pedal only

Pedal and Oronasal

T1: 1o vaccinated

AdtA24 5 × 1010 PU

(high dose)

Contact Challenge

6

83%

50%

2.2 ± 0.2a,b

(1.8–2.4)

100%

0%

0% - 0 dpcc

67% - 14 dpcc

T2: 1o vaccinated

AdtA24 1.25 × 1010 PU (medium dose)

Contact Challenge

6

100%

33%

1.5 ± 0.5a

(0.9–2.1)

100%

0%

0% - 0 dpcc

100% - 14 dpcc

T3: 1o vaccinated

AdtA24 3.125 × 109 PU (low dose)

Contact Challenge

6

67%

0%

1.1 ± 0.5b

(0.6–1.8)

67%

0%

0% - 0 dpcc

100% - 14 dpcc

T4: 1o naïve

Contact Challenge

(control)

4

0%

0%

0.6 ± 0.0*

0%

0%

ND

T5 (IDL challenged seeder steers) 1 day prior to contact with T1-T4

8

0%

0%

0.6 ± 0.0*

0%

0%

ND

  1. Dpcc days post contact challenge, DPV days post vaccination, VNT virus neutralization test, 1o primary, PU particle units, IDL intradermolingual challenge, ND Not Determined
  2. *A positive VNT is ≥0.9 log10. a, p = 0.01 for T1 > T2. b, p = < 0.001 for T1 > T3. p = 0.1 for T2 and T3