TABLE 2.
TNF production in Q fever endocarditisa
| Group | No. of TNF copies/ ng of RNAb
|
TNF secretion (pg/ml)b
|
||
|---|---|---|---|---|
| Without C. burnetii | With C. burnetii | Without C. burnetii | With C. burnetii | |
| Controls | 7.4 ± 0.8 | 146 ± 25 | 185 ± 16 | 1,999 ± 430 |
| Active patients | 13.6 ± 1.4* | 440 ± 95*** | 396 ± 59*** | 4,826 ± 897** |
| Cured patients | 11.2 ± 3.2 | 229 ± 79 | 195 ± 49 | 2,202 ± 506 |
Monocytes were stimulated or not stimulated with C. burnetii at a bacterium-to-cell ratio of 200:1 for 3 h. RNA was extracted and incubated with a reverse transcriptase mixture. After incubation with specific primers, the cDNAs were amplified and the expression of TNF transcripts was quantitated. Supernatants of monocyte cultures were collected after 24 h and assayed for the presence of TNF by immunoassay.
Results are expressed as means ± SEs. *, P < 0.05; **, P < 0.04; ***, P < 0.01 (for the comparison of active patient values with control values). Each group contained 10 individuals.