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J Clin Lab Immunol ; 49(2): 59-75, 1997.
Article in English | MEDLINE | ID: mdl-9819674

ABSTRACT

In humans, tuberculosis is associated with suppression of T-cell responses to antigens of Mycobacterium tuberculosis. Recently, the macrophage product, transforming growth factor-beta (TGF-beta) has been implicated in suppression of T-cell proliferation and cytokine production during tuberculosis. We studied the effect of TGF-beta on production of IL-12, and on the augmentation of M. tuberculosis-induced IFN gamma production by IL-12, in patients with pulmonary tuberculosis and by M. tuberculosis. Induction of IL-12 p35, but not IL-12 p40, by M. tuberculosis in monocytes was dependent on prior priming of the cells with IFN gamma. Expression of both IL-12 p40 and p35, however, was suppressed by TGF-beta. Further, TGF-beta interfered with the bioactivity of IL-12 in the enhancement of M. tuberculosis-induced IFN gamma mRNA expression and cytokine production. However, in mononuclear cells from patients with tuberculosis the main effect of TGF-beta on IL-12 appeared to be counter action to IL-12 induced IFN gamma production in response to M. tuberculosis.


Subject(s)
Interferon-gamma/physiology , Interleukin-12/biosynthesis , Monocytes/drug effects , Mycobacterium tuberculosis/physiology , Transforming Growth Factor beta/pharmacology , Tuberculosis, Pulmonary/pathology , Gene Expression Regulation/drug effects , Interferon-gamma/biosynthesis , Interferon-gamma/genetics , Interferon-gamma/pharmacology , Interleukin-12/chemistry , Interleukin-12/genetics , Monocytes/metabolism , Monocytes/microbiology , RNA, Messenger/biosynthesis , Recombinant Fusion Proteins/pharmacology , T-Lymphocytes/immunology , Transforming Growth Factor beta/biosynthesis , Tuberculosis, Pulmonary/immunology
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