A novel human macrophage-activating factor: distinction from interferon-gamma (IFN-gamma) and granulocyte-macrophage colony-stimulating factor (GMCSF)

Cell Immunol. 1988 May;113(2):361-75. doi: 10.1016/0008-8749(88)90034-2.

Abstract

Culture supernatant from a human T-cell leukemia virus type I (HTLV-1)-infected cell line, DGA-1, contained a novel macrophage-activating factor (MAF). This MAF was antigenically and functionally distinct from interferon-gamma (IFN-gamma) and from granulocyte-monocyte colony-stimulating factor (GMCSF). Potential contaminants such as bacterial lipopolysaccharide (LPS), Mycoplasma spp, and HTLV-1 were not responsible for this MAF activity. The DGA-1 MAF was secreted constitutively and the cell line grew well in the absence of growth factors such as interleukin-2, mitogen, or antigen. This cell line should provide a good source of this MAF for further purification and characterization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Differentiation / analysis
  • Antigens, Surface / analysis
  • Cell Line
  • Colony-Stimulating Factors / pharmacology
  • Deltaretrovirus / physiology
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Growth Substances / pharmacology
  • Humans
  • Hydrogen Peroxide / metabolism
  • Interferon-gamma / pharmacology
  • Lymphokines*
  • Macrophage Activation*
  • Mice
  • Species Specificity
  • T-Lymphocytes / physiology*

Substances

  • Antigens, Differentiation
  • Antigens, Surface
  • Colony-Stimulating Factors
  • Growth Substances
  • Lymphokines
  • Interferon-gamma
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Hydrogen Peroxide