TABLE 4.
Effect of IL-18 treatment in vitro on IFN-γ production by peritoneal cells from uninfected BALB/c mice treated with or without anti-asialo GM1 antibody
| Expt and in vivo treatment | IFN-γ (ng/ml)a
|
Increase (fold)b | |
|---|---|---|---|
| IL-18(−) | IL-18(+) | ||
| 1 | |||
| Vehiclec | 1.9 | 7.0 | 3.7 |
| IL-18 | 0.7 | 0.7 | 1.0 |
| 2 | |||
| NRSd + vehicle | 1.1 | 11.5 | 10.5 |
| NRS + IL-18 | 2.9 | 6.5 | 2.2 |
| AGMe + vehicle | 1.9 | 5.0 | 2.6 |
| AGM + IL-18 | <0.2 | 0.6 | >3.0 |
Peritoneal cells were incubated in the presence or absence of IL-18 (1 ng/ml), and the culture supernatants were harvested 24 h later. IFN-γ in the supernatant pooled from duplicate or triplicate samples was measured by ELISA.
IFN-γ amount after IL-18(+) treatment/IFN-γ amount after IL-18(−) treatment.
The vehicle or IL-18 (1 μg per mouse a day) was administered i.p. to mice for 3 days, and peritoneal cells were prepared 1 day after the last administration.
NRS or anti-asialo GM1 antibody was injected i.p. into mice twice, 1 day each before and after the first administration of the vehicle or IL-18.
AGM, anti-asialo GM1 antibody.