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. 1997 Apr 15;94(8):3926–3931. doi: 10.1073/pnas.94.8.3926

Table 2.

Production of IFN-γ and TGF-β by PBMCs of TB patients and control subjects cocultured with optimal concentrations of antibody to TGF-β, decorin, or LAP

Stimulus TB patients
Controls
IFN-γ TGF-β IFN-γ TGF-β
NIL <0.03 1.3  ±  0.5 <0.03 0.7  ±  0.3
PPD 0.224  ±  0.08 13.5  ±  3.6* 2.7  ±  0.6 5.3  ±  1.3
PPD + NAB 0.442  ±  0.12 3.8  ±  1.3 2.6  ±  0.5 2.2  ±  1.3
PPD + DEC 0.556  ±  0.15 4.1  ±  3.6§ 2.5  ±  0.5 2.2  ±  1.2
PPD + LAP 0.803  ±  0.22 3.9  ±  2.3§ 2.8  ±  0.5 1.7  ±  1.3

PBMCs of TB patients and healthy tuberculin-reactive control subjects were cultured for 72 h with or without PPD (10 μg/ml) in the presence or absence of neutralizing antibody to TGF-β (NAB) (10 μg/ml), decorin (DEC) (50 μg/ml), or LAP (100 ng/ml). IFN-γ and TGF-β immunoreactivities in culture supernatants were assessed by ELISA and both are expressed as ng/ml. Results represent mean ± SE, n = 8. 

*

P ≤ 0.0008 compared with TGF-β in supernatants of unstimulated PBMCs from TB patients. 

P ≤ 0.005 compared with IFN-γ in supernatants of PPD-stimulated PBMCs from TB patients. 

P ≤ 0.006 compared with TGF-β in supernatants of PBMCs from TB patients cultured with PPD alone. 

§

P ≤ 0.004 compared with TGF-β in supernatants of PBMCs from TB patients cultured with PPD alone. 

P ≤ 0.03 compared with IFN-γ in supernatants of PPD-stimulated PBMCs from TB patients.