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. 1999 Mar;73(3):2401–2409. doi: 10.1128/jvi.73.3.2401-2409.1999

TABLE 3.

HSV-1 and cytokine titers in PWF and serum from vehicle- and IL-18-administered BALB/c mice treated with NRS or anti-asialo GM1 antibody 26 h after i.p. inoculation with 104 PFU of HSV-1

In vivo treatment PWF
Serum
HSV-1a (log10 PFU/ml) Antiviral activityb (mIFN-α IU/ml) IFN-γc (101 pg/ml) Antiviral activity (mIFN-α IU/ml) IFN-γ (101 pg/ml)
NRSd + vehiclee 1.7 ± 0.2f 17.6 ± 6.0 <6 ± 0 29.7 ± 13.4 <30 ± 0
AGMh + vehicle 1.8 ± 0.2 14.7 ± 5.5 <6 ± 0 18.3 ± 8.5 <30 ± 0
NRS + IL-18 <0.7 ± 0.0 <1.0 ± 0.0 48 ± 20g <10.0 ± 0.0 <30 ± 0
AGM + IL-18 <0.7 ± 0.0 <1.0 ± 0.0 <6 ± 0 <10.0 ± 0.0 <52 ± 28
a

HSV-1 was titrated by plaque assay with Vero cells. 

b

Antiviral activity was measured by using VSV and mouse L929 cells and is expressed as the mIFN-α titer. 

c

Measured by ELISA. 

d

NRS or anti-asialo GM1 antibody was injected i.p. on days 3 and 1 before infection. 

e

On days 2 and 1 before infection and days 0 and 1 of infection, 1 μg of IL-18 was injected i.p. into each mouse (n = 3 per group), and the mice were sacrificed to prepare PWF and serum 2 h after the final injection with the vehicle or IL-18. 

f

Mean ± standard deviation. 

g

Significantly increased values compared to those of mice treated with anti-asialo GM1 antibody plus IL-18 (P < 0.01). 

h

AGM, anti-asialo GM1 antibody.