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. 1997 Apr 7;185(7):1261–1274. doi: 10.1084/jem.185.7.1261

Table 3.

IL-12 and IFN-γ Synthesis by Cells Harvested from iNOS ko and C57BL/6 Mice at 5 d after i.p. Challenge with T. gondii

Peritoneal exudate Spleen Serum
Mean ± SE n Range Mean ± SE n Range Mean ± SE n Range
IL-12p40 C57BL/6 bkg    1.4 ± 0.5 6      0–3.5    5.4 ± 1.8 7  2.3–12.7 17.1 ± 3.9 3 15.6–23.2
STAg   10.9 ± 3.3 6 0.3–19.5 35.4 ± 6.0 7 20.7–53.5
iNOS ko bkg    1.9 ± 0.4 6  1.2–4.1 10.3 ± 2.8 9  3.6–17.6   19.5 ± 9 3 13.7–27.3
STAg   11.9 ± 4.3 6 4.3 ± 25.9 56.4 ± 9.1 9 38.0–93.6
IFN-γ C57BL/6 bkg    0.1 ± 0.06 6    0–0.3    0.6 ± 0.5 7      0–3.1  5.1 ± 0.5 3 4.4–5.8
STAg  1.0 ± 0.3 6  0.2–2.1    8.3 ± 2.1 7  1.3–17.9
iNOS ko bkg  6.0 ± 2.9 6 0.3–15.4    1.1 ± 0.7 9      0–3.9  3.4 ± 0.3 3 2.9–3.8
STAg  8.2 ± 4.0 6 0.8–2.13 10.4 ± 2.7 9  1.8–19.2

Mice were infected with 20 ME49 cysts each, killed 5 d later, and then peritoneal and spleen cells were isolated. Cell suspensions from each animal were cultured for 72 h in medium alone or in the presence of STAG (5 μg/ml). Supernatants were then assayed by ELISA for IL-12p40 and IFN-γ as described in Materials and Methods. The data shown are pooled from three experiments employing the number of animals indicated.