Modulation of IL-12 by transforming growth factor-beta (TGF-beta) in Mycobacterium tuberculosis-infected mononuclear phagocytes and in patients with active tuberculosis

J Clin Lab Immunol. 1997;49(2):59-75.

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.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

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

Substances

  • RNA, Messenger
  • Recombinant Fusion Proteins
  • Transforming Growth Factor beta
  • Interleukin-12
  • Interferon-gamma