Table III.
Source | Cells | IFN-γ (pg/ml) | TNF-α (pg/ml) |
Aged | PBMC | 70,800 ± 8,500 (p < 0.001) | 35,400 ± 6,200 (p < 0.005) |
Control | PBMC | 20,300 ± 3,000 | 16,900 ± 4,100 |
Aged | CD8+ | 86,300 ± 15,600 (p < 0.001) | 44,200 ± 7,800 (p < 0.005) |
Control | CD8+ | 24,400 ± 6,200 | 19,400 ± 4,300 |
HIV+ | CD8+ | 121,000 ± 15,600 (p < 0.001) | 57,200 ≅ 11,500(p < 0.001) |
Control | CD8+ | 27,300 ± 4,800 | 16,400 ± 4,900 |
PBMC and purified CD8+ T cells were incubated for 66 hrs. as described in Methods, and the media was tested by ELISA. The results are expressed in pg IFN-γ or TNF-α per 105 cells (mean value ± S.D.). The standard deviation is shown and the p valves, determined with Student's t test, compare the IFN-γ or TNF-α secreted by aged or HIV+-derived cells and normal control cells. Eight different aged and HIV+ donors were used, and seven young control donors. In the presence of 5 mM of N-acetylcysteine, the production of both INF-γ and TNF-α was significantly increased in aged, HIV+ and control samples, generally by 1.5 to 2 fold.