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. Author manuscript; available in PMC: 2015 Feb 1.
Published in final edited form as: Virology. 2014 Jan 9;0:243–249. doi: 10.1016/j.virol.2013.12.029

Figure 2. Vaccine Efficacy in Pre-exposure and Post-exposure Regimens.

Figure 2

[A] Dose Escalation: Cynomologous monkeys were vaccinated once with various doses (109–1011 vp) of the AdC68rab.gp vector, a control AdC68 vector given at 1011 vp, or three doses of commercial human raies vaccine, HDCV. Additional control animals received PBS only. Animals were challenged with canine rabies vius at 18 weeks after AdC68 vaccination. [B] Effect of pre-existing HAd-V5 neutralizing antibodies: Groups of monkeys were injected with 1012 vp of an AdHu5 vector expressing a reporter protein, or they were left untreated.. Four weeks later, pre-treated, as well as untreated animals, were vaccinated with 1010 vp of AdC68rab.gp. A positive control group received commercial human rabies vaccine, HDCV given 3 times, a negative control group received PBS. Animals were challenged with canine rabies virus 18 weeks after AdC vaccination and survival was recorded. [C] Post-exposure prophylaxis: Nonhuman primates were infected with canine rabies virus. Six hours later, one group was vaccinated with 1010 vp of AdC68rab.gp and received commercial HRIG infiltrated at the rabies virus inoculation site. An additional group was vaccinated with AdC68rab.gp, but without HRIG. A positive control group was treated with the traditional vaccine regimen, i.e., HRIG combined with 4 doses of commercial PCEC human rabies vaccine, the latter given on days 1, 8, 15 and 29 relative to challenge. Additional control groups only received HRIG, a control AdC68 vector or PBS. Survival was recorded. [NB: need to change the vaccine in @C from HDCV to PCEC.

Graphs A–C show percent of animals that survived without developing signs of rabies. Numbers of animals per group are shown within each graph above the bars.