Membrane-bound IgE on B cells is increased during Clonorchis sinensis infection

Immunobiology. 2019 May;224(3):347-352. doi: 10.1016/j.imbio.2019.03.004. Epub 2019 Mar 31.

Abstract

A high level of serum IgE is a hallmark of helminthic disease. Secretory IgE can bind FcεRI or FcεRII/CD23. The combination of IgE and FcεRI, a high-affinity interaction, has long received attention and is believed to facilitate helminth control, while the properties of CD23-bound IgE have long been unexplored. Here, we established a Clonorchis sinensis (C. sinensis) infection model with different mouse strains and investigated membrane-bound IgE on B cells during infection. We show that after infection, the increase in CD23 expression on B cells was obvious, even in relatively resistant C57BL/6 mice, as well as in susceptible BALB/c and FVB mice. Although the serum IgE amount was lower in C57BL/6 mice than in BALB/c and FVB mice, the level of IgE binding to peripheral B cells was also elevated. Additionally, the IgE on B cells was soon undetectable in vitro due to dissociable binding. The results of the present study demonstrate the dramatic increase in CD23-bound IgE on B cells after C. sinensis infection. The significance of CD23-bound IgE in Ag transport and presentation has gained consideration in allergy development for its potential ability to promote the Th2 response. Therefore, even though the association of IgE and CD23 is not as substantial as that of IgE and FcεRI, membrane-bound IgE on B cells may be worth further study regarding clonorchiasis and other parasitic infections.

Keywords: CD23; Clonorchis sinensis; Ig E.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Helminth
  • Antigen Presentation
  • B-Lymphocytes / metabolism*
  • Clonorchiasis / immunology*
  • Clonorchis sinensis / physiology*
  • Disease Models, Animal
  • Disease Susceptibility
  • Female
  • Humans
  • Hypersensitivity / immunology*
  • Immunoglobulin E / metabolism*
  • Membrane Proteins / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Receptors, IgE / metabolism
  • Th2 Cells / immunology*

Substances

  • Antibodies, Helminth
  • Membrane Proteins
  • Receptors, IgE
  • Immunoglobulin E