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- Title
Interferon-γ and Interleukin-17 production from PPD-stimulated PBMCss of patients with pulmonary tuberculosis.
- Authors
Nunnari, Giuseppe; Pinzone, Marilia R.; Vancheri, Carlo; Palermo, Filippo; Cacopardo, Bruno
- Abstract
Purpose: The purpose of this study was to evaluate Interferon (IFN)-γ and Interleukin(IL)-17 profiles in patients with different clinical presentations of pulmonary tuberculosis (TB) and to compare them with those of tuberculin-negative and tuberculinreactive healthy controls Methods: Peripheral blood mononuclear cells (PBMCss), isolated from patients (n=52) and controls (n=30), were stimulated ex viγo with purified protein derivative (PPD) and IFN-γ and IL-17 levels in the supernatant were measured. Results: At baseline, PBMCss from patients with TB released a significantly lower amount of IL-17 (p=0.043) than PBMCss from healthy controls, whereas IFN-γ levels were similar in the two groups. After PPD stimulation, a significant rise in IL-17 levels was found only among healthy controls (p=0.02). This rise in IL-17 levels was similar between tuberculinreactive and tuberculin-negative subjects. After PPD stimulation, patients with infiltrative TB secreted higher levels of IL-17 and IFN-γ than those affected with chronic, miliary and cavitary TB (p<0.01). IFN-γ production from patients with infiltrative TB was even higher than for healthy controls (p<0.01). PBMCss from tuberculin-reactive patients released higher levels of IFN-γ than tuberculin-negative subjects after PPD stimulation (p<0.01). Conclusion: Ex viγo PPD stimulation of PBMCs from patients with pulmonary TB does not significantly stimulate IL-17 release; however, higher IL-17 and IFN-γ levels are found in patients with infiltrative disease, in comparison with those affected with miliary, cavitary and chronic TB.
- Subjects
TUBERCULOSIS patients; INTERLEUKINS; INTERFERONS; TUBERCULIN test; TUBERCULOSIS diagnosis
- Publication
Clinical & Investigative Medicine, 2013, Vol 36, Issue 2, pE64
- ISSN
0147-958X
- Publication type
Article
- DOI
10.25011/cim.v36i2.19568