A cell-free assay to estimate the neutralizing capacity of granulocyte-macrophage colony-stimulating factor autoantibodies

J Immunol Methods. 2010 Aug 31;360(1-2):141-8. doi: 10.1016/j.jim.2010.07.001. Epub 2010 Jul 16.

Abstract

The aim of the project is to develop a novel method estimating granulocyte-macrophage colony-stimulating factor (GM-CSF) neutralizing capacity with high-throughput and good reproducibility. For that purpose, we designed a cell-free receptor binding assay consisting of a solid-phase recombinant soluble GM-CSF receptor alpha (GMRalpha) and a biotinylated GM-CSF (bGM-CSF). Using this system, competitive inhibition of bGM-CSF binding to soluble GM-CSF receptor alpha (sGMRalpha) by GM-CSF autoantibody or IgG fractions from the sera of patients with pulmonary alveolar proteinosis was examined, resulting in excellent reproducibility. Binding inhibition was correlated with growth inhibition of TF-1 cells, a GM-CSF dependent cell line. These results suggest that our cell-free system can be applied to estimate the neutralizing capacity of GM-CSF autoantibodies ex vivo.

MeSH terms

  • Autoantibodies / isolation & purification
  • Autoantibodies / metabolism*
  • Binding, Competitive / drug effects*
  • Binding, Competitive / immunology
  • Biotin / metabolism
  • Cell Line
  • Cell Proliferation / drug effects
  • Cell-Free System
  • Granulocyte-Macrophage Colony-Stimulating Factor / immunology
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology*
  • High-Throughput Screening Assays
  • Humans
  • Pulmonary Alveolar Proteinosis / blood
  • Pulmonary Alveolar Proteinosis / diagnosis
  • Pulmonary Alveolar Proteinosis / immunology*
  • Receptors, Granulocyte-Macrophage Colony-Stimulating Factor / metabolism
  • Reproducibility of Results

Substances

  • Autoantibodies
  • Receptors, Granulocyte-Macrophage Colony-Stimulating Factor
  • Biotin
  • Granulocyte-Macrophage Colony-Stimulating Factor