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. Author manuscript; available in PMC: 2008 Aug 1.
Published in final edited form as: Antiviral Res. 2006 Dec 20;75(2):104–112. doi: 10.1016/j.antiviral.2006.11.013

Table 2.

Effects of a single dose of Ampligen administered at various times in relation to virus exposure on survival and brain virus titers in BALB/c mice inoculated with Banzi virus or Semliki Forest virus. All mice received an approximately LD90 dose of virus inoculum.

Uninfected toxicity control Infected, treated

Compound
Virus
Virus Dose Surv/Total Surv/Total MDDa Brain Virus
Titersbc

Ampligen (24 h pre) Banzi 1 mg/kg 3/3 9/10*** 14.0 2.3 ± 0.1***
Ampligen (4-6 h pre) Banzi 1 mg/kg 3/3 7/10*** 12.3 ± 1.5 3.8 ± 1.0***
Ampligen (24 h post) Banzi 1 mg/kg 3/3 0/10 12.8 ± 3.1* 7.0 ± 2.1
Placebo (24 h pre) Banzi - 3/3 0/20 10.4 ± 1.8 9.1 ± 0.1

Normal Control - - 3/3 - - -

Ampligen (24 h pre) Semliki Forest 1 mg/kg 3/3 4/10 9.0 ± 1.1* 6.2 ± 1.9
Ampligen (4-6 h pre) Semliki Forest 1 mg/kg 3/3 7/10*** 7.7 ± 1.5 5.5 ± 1.5+
Ampligen (24 h post) Semliki Forest 1 mg/kg 3/3 3/10 7.4 ± 1.8 7.9 ± 1.1
Placebo (24 h pre) Semliki Forest - 3/3 2/20 7.6 ± 1.3 7.4 ± 1.2

Normal Control - - 3/3 - - -
a

Mean day to death of mice dying before day 21

b

Log10 infectious doses/g of tissue.

c

Banzi virus inoculated animals assayed on 8 dpi. Semliki Forest virus inoculated animals assayed on 6 dpi.

*

p<0.05,

***

p<0.001 compared to placebo treated controls,

+

p<0.05 compared to Ampligen treatment 24 h after virus inoculation