TABLE 1.
IFN-γ added | WT
|
TNFRp55−/−
|
||||
---|---|---|---|---|---|---|
No. of parasites/100 cells (% infected cells) | NO2− release (μM)
|
No. of parasites/100 cells (% infected cells) | NO2− release (μm)
|
|||
Medium | Medium + l-NIL | Medium | Medium + l-NIL | |||
No | 273 ± 50 (28 ± 7) | 2 ± 2 | 3 ± 2 | 351 ± 58 (35 ± 7) | 11 ± 9 | 5 ± 1 |
Yes | 10 ± 6b (5 ± 3)c | 49 ± 1c | 3 ± 2 | 36 ± 2b (3 ± 1)c | 79 ± 16c | 6 ± 3 |
Recombinant murine IFN-γ (5 U/ml) and/or 0.5 mM l-NIL was added to macrophages 24 h before infection with T. cruzi. Four hours after infection, free parasites were washed and reagents were replenished. The nitrite concentration in the supernatant was measured by the Griess assay 3 days after infection. Supernatants from noninfected cells contained nondetectable levels of nitrite after 4 days in culture. The mean numbers of infected cells and the numbers of parasites per 100 cells ± standard errors of the means from triplicate determinations as recorded 48 h after infection are shown.
Difference from the nontreated infected control value is significant (P < 0.05, Mann-Whitney-U Wilcoxon test).
Difference from the nontreated infected control value is significant (P < 0.05, Pearson chi-square test).