Macrophage nitric oxide synthase (NOS) activation by Nocardia opaca fractions and 15- and 56-kD isolated antigens

Clin Exp Immunol. 1996 May;104(2):215-20. doi: 10.1046/j.1365-2249.1996.23730.x.

Abstract

The Gram-positive bacterium, Nocardia opaca, is a source of substances with adjuvant effect, ability to stimulate macrophages and natural killer cells for enhanced cytotoxity and cytokine production and B lymphocytes for polyclonal immunoglobulin secretion. We determined the immunogenicity of isolated N. opaca fractions and prepared MoAbs against immunogenic water-soluble mitogen (NWSM). Two main proteins of molecular mass 15 and 56 kD were detected in western blot analysis and isolated by affinity chromatography using anti-NWSM MoAb B7/7. Both these isolated nocardial antigens were found to stimulate mouse peritoneal macrophage NOS. The effect of 5 micrograms NWSM was comparable to that of 5 micrograms lipopolysaccharide (LPS) or 20 U of interferon-gamma (IFN-gamma) added to cell cultures. The MoAb B7/7 decreased No2- production induced by NWSM or by isolated nocardial antigens, but did not significantly influence the production elicited by LPS or IFN-gamma. On the other hand, NOS activation by NWSM was not affected by anti-IFN-gamma MoAb. The possible independent pathway for IFN-gamma and NWSM macrophage activation is discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / biosynthesis
  • Antibodies, Monoclonal / chemistry
  • Antibodies, Monoclonal / pharmacology
  • Antigens, Bacterial / isolation & purification*
  • Antigens, Bacterial / pharmacology
  • Binding, Competitive / immunology
  • Enzyme Activation / immunology
  • Female
  • Interferon-gamma / immunology
  • Macrophages, Peritoneal / enzymology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mitogens / immunology
  • Nitric Oxide Synthase / metabolism*
  • Nocardia / chemistry*
  • Nocardia / immunology*

Substances

  • Antibodies, Monoclonal
  • Antigens, Bacterial
  • Mitogens
  • Interferon-gamma
  • Nitric Oxide Synthase