Human recombinant granulocyte-macrophage colony-stimulating factor and interleukin 3 cause basophil histamine release

J Clin Invest. 1988 Jul;82(1):17-20. doi: 10.1172/JCI113567.

Abstract

Histamine-releasing factors (HRFs) have been shown to be released from a variety of human cells, including T lymphocytes and alveolar macrophages. We considered the possibility that known cytokines might possess such activity on human basophils and/or mast cells and therefore tested preparations of human recombinant IL 3, IL 4, IL 5, granulocyte colony-stimulating factor (G-CSF) and granulocyte-macrophage colony-stimulating factor (GM-CSF) upon a panel of basophil donors. IL 3 and GM-CSF possessed significant histamine-releasing activity in 8 of 10 and 12 of 14 subjects, respectively. In each instance, a dose response could be demonstrated. IL 4 and G-CSF had no such activity, whereas IL 5 had activity in only 2 of 14 donors tested. We conclude that IL 3 and GM-CSF represent two effective HRFs, and suggest that HRF, as isolated based upon histamine-releasing activity, is likely to be heterogeneous in terms of molecular identity. Whether previously described HRFs relate specifically to IL 3 or GM-CSF must await primary sequence analysis of HRF and/or studies with monospecific antisera.

MeSH terms

  • Basophils / drug effects
  • Basophils / immunology*
  • Biomarkers, Tumor*
  • Colony-Stimulating Factors / pharmacology*
  • Drug Synergism
  • Granulocyte-Macrophage Colony-Stimulating Factor
  • Growth Substances / pharmacology*
  • Histamine Release / drug effects*
  • Humans
  • Hypersensitivity, Immediate / metabolism
  • Interleukin-3 / pharmacology*
  • Kinetics
  • Lymphokines / pharmacology
  • Recombinant Proteins / pharmacology*
  • Tumor Protein, Translationally-Controlled 1

Substances

  • Biomarkers, Tumor
  • Colony-Stimulating Factors
  • Growth Substances
  • Interleukin-3
  • Lymphokines
  • Recombinant Proteins
  • Tumor Protein, Translationally-Controlled 1
  • Granulocyte-Macrophage Colony-Stimulating Factor