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. 2014 Aug 7;110:132–141. doi: 10.1016/j.antiviral.2014.07.013

Fig. 1.

Fig. 1

Protective efficacy of immune-competent mice treated with VNA with or without MCP-1 after infection with DRV. ICR mice (groups of 10) at the age of 4–6 weeks were infected i.m. with 10 IMLD50 DRV-Mexico and then treated intravenously with RABV-negative serum (N) or RABV-antibody positive serum (Ab) with or without recombinant murine MCP-1 (25 μg/mouse, i.c.) at 5 dpi. Infected and treated mice were observed daily for 21 days and survivorship was recorded and analyzed. Asterisks indicate significant differences (p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001) between the indicated experimental groups.