Skip to main content
. 2014 Dec 23;59(1):299–309. doi: 10.1128/AAC.03918-14

TABLE 2.

CFU recovery in skin homogenates following SF-8300 challenge and treatment with vancomycin, linezolid, MEDI4893*, combination therapy, or R347

Drug (dose, mg/kg/day)a MAb (dose, mg/kg/day)a Log10 CFU/ml ± SEM at postchallenge time (h):
24 72 168
Vancomycin (200) None 8.44 ± 0.30 7.92 ± 0.20b,d 7.54 ± 0.11b
MEDI4893* (2.5) 8.49 ± 0.06 7.63 ± 0.12b,d 6.18 ± 0.25b,c,d
Linezolid (10) None 8.52 ± 0.16 8.40 ± 0.07 7.21 ± 0.44b
MEDI4893* (2.5) 8.58 ± 0.31 8.13 ± 0.10b 7.23 ± 0.15b
None MEDI4893* (2.5) 8.00 ± 0.01 8.98 ± 0.15e 7.66 ± 0.31b
R347 (15.0) 8.52 ± 0.11 8.76 ± 0.16 8.53 ± 0.19
a

Vancomycin and linezolid were dosed at 3, 8, 24, and 32 h postinfection. MEDI4893* and R347 were dosed at 3 h postinfection. See Materials and Methods for further details.

b

The CFU value is significantly lower than that for the R347 control (P < 0.05).

c

Vancomycin combination therapy is significantly different from vancomycin monotherapy (P < 0.05).

d

Significantly different from MEDI4893* monotherapy (P < 0.05).

e

Significantly different from vancomycin monotherapy and vancomycin-MEDI4893* therapy (P < 0.05).