Cutting edge: human B cell function is regulated by interaction with soluble CD14: opposite effects on IgG1 and IgE production

J Immunol. 2000 Apr 1;164(7):3480-6. doi: 10.4049/jimmunol.164.7.3480.

Abstract

The mechanism(s) controlling activation of naive B cells, their proliferation, Ag receptor affinity maturation, isotype switching, and their fate as memory or plasma cells is not fully elucidated. Here we show that between 24 and 60% of CD19+ cells in PBMC bind soluble CD14 (sCD14). Tonsillar B cells also bind sCD14, but preferentially the CD38-ve/low cells. Interaction of sCD14 with B cells resulted in higher levels of IgG1 and marked inhibition of IgE production by activated tonsillar B cells and Ag-stimulated PBMC. We found that sCD14 interfered with CD40 signaling in B cells, inhibited IL-6 production by activated B cells, and increased the kinetics and magnitude of CD40 ligand expression on T cells. Together with the previously reported effects on T cells, these findings define sCD14 as a novel soluble regulatory factor capable of modulating cellular and humoral immune responses by interacting directly with T and B cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • B-Lymphocyte Subsets / immunology*
  • B-Lymphocyte Subsets / metabolism*
  • CD40 Antigens / metabolism
  • CD40 Antigens / physiology
  • CD40 Ligand
  • Cell Communication / immunology*
  • Cells, Cultured
  • DNA-Binding Proteins / antagonists & inhibitors
  • DNA-Binding Proteins / metabolism
  • Humans
  • I-kappa B Proteins*
  • Immune Tolerance
  • Immunoglobulin E / biosynthesis*
  • Immunoglobulin G / biosynthesis*
  • Interleukin-6 / antagonists & inhibitors
  • Interleukin-6 / biosynthesis
  • Kinetics
  • Leukocytes, Mononuclear / immunology
  • Leukocytes, Mononuclear / metabolism
  • Ligands
  • Lipopolysaccharide Receptors / blood
  • Lipopolysaccharide Receptors / metabolism*
  • Lipopolysaccharide Receptors / physiology
  • Lymphocyte Activation
  • Membrane Glycoproteins / biosynthesis
  • NF-KappaB Inhibitor alpha
  • Palatine Tonsil / cytology
  • Protein Binding / immunology
  • Solubility

Substances

  • CD40 Antigens
  • DNA-Binding Proteins
  • I-kappa B Proteins
  • Immunoglobulin G
  • Interleukin-6
  • Ligands
  • Lipopolysaccharide Receptors
  • Membrane Glycoproteins
  • NFKBIA protein, human
  • NF-KappaB Inhibitor alpha
  • CD40 Ligand
  • Immunoglobulin E