American Journal of Respiratory and Critical Care Medicine · 2003 · 106 citations · 41 references
MedicineImmunologyPathologyChemotherapyImmunopathologyInflammationGranulomatous InflammationInflammation In Infectious DiseaseMacrophage BiologyPulmonary TuberculosisActive Pulmonary TuberculosisGranulomatous LesionsInflammatory Lung LesionsInterleukin-12 ResponsesMycobacterium Tuberculosis InfectionNoncollagenous ProteinsOsteopontin FunctionTuberculous Granuloma
Osteopontin (OPN, also known as Eta-1), a noncollagenous matrix protein produced by macrophages and T lymphocytes, is expressed in granulomatous lesions caused by Mycobacterium tuberculosis infection. In the present study, we compared plasma concentrations of OPN in patients with active pulmonary tuberculosis with those of healthy control subjects and patients with sarcoidosis, another disease associated with granuloma formation. Plasma OPN levels were significantly higher in patients with tuberculosis (n = 48) than in control subjects (n = 34) and patients with sarcoidosis (n = 20). OPN levels correlated well with severity of pulmonary tuberculosis, as indicated by the size of lung lesions on chest X-ray films. Furthermore, chemotherapy resulted in a significant fall in plasma OPN levels. In patients with tuberculosis, plasma OPN concentrations correlated significantly with those of interleukin (IL)-12. In vitro experiments showed that OPN production by peripheral blood mononuclear cells infected with Mycobacterium bovis bacillus Calmette-Guérin preceded the synthesis of IL-12 and interferon-gamma and that the neutralizing anti-OPN monoclonal antibody significantly reduced the production of IL-12 and interferon-gamma. Our results suggest that OPN may be involved in the pathologic process associated with active pulmonary tuberculosis by inducing IL-12-mediated type 1 T helper cell responses.
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Eta-1 (Osteopontin): An Early Component of Type-1 (Cell-Mediated) Immunity
Samy Ashkar, Georg F. Weber, Marie Sanchirico et al. · Science · 2000 · 1.1K citations
Life Sciences, Immunology, Pathology +17