Endogenous VSIG4 negatively regulates the helper T cell-mediated antibody response

Immunol Lett. 2015 Jun;165(2):78-83. doi: 10.1016/j.imlet.2015.04.004. Epub 2015 Apr 27.

Abstract

VSIG4 acts as a co-inhibitory ligand to negatively regulate T cell proliferation and cytokine production, and its expression is restricted to macrophages. We hypothesized that endogenous VSIG4 impairs helper T cell functions and then inhibits the subsequent antibody response. Isotype switching of ovalbumin (OVA)-specific antibody subclasses to IgG1, IgG2a, IgG2b, and IgG3 was enhanced in OVA-immunized VSIG4 knockout (KO) mice. 2,4,6-Trinitrophenyl hapten (TNP) - Keyhole Limpet Hemocyanin (KLH)-primed B cells cocultured with OVA-primed CD4(+) T cells from OVA-immunized VSIG4 KO mice in the presence of TNP-OVA showed enhanced isotype switching to IgG subclasses compared to those cocultured with cells isolated from OVA-immunized wild-type (WT) mice. Furthermore, the levels of CD40L expression, the frequency of memory CD4(+) T cells, and the production of isotype switching-inducing cytokines increased significantly in OVA-primed CD4(+) T cells from VSIG4 KO mice. T cells from OVA-specific T cell receptor (TCR) transgenic mice produced more IFN-γ when cocultured with macrophages from VSIG4 KO mice compared to WT mice. Thus, our results demonstrate that macrophage-associated VSIG4 plays a negative role in helper T cell-dependent isotype switching by inhibiting helper T cell activation and differentiation, and suppressing the isotype switching-inducing cytokine production in antigen-primed CD4(+) helper T cells.

Keywords: B cells; CD40L; Co-inhibition; Isotype switching; VSIG4.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibody Formation / genetics
  • CD40 Ligand / metabolism
  • Cell Differentiation / genetics
  • Coculture Techniques
  • Cytokines / metabolism
  • HEK293 Cells
  • Humans
  • Immunoglobulin Class Switching / genetics
  • Immunologic Memory / genetics
  • Lymphocyte Activation / genetics
  • Macrophages / physiology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Receptors, Complement / genetics
  • Receptors, Complement / metabolism*
  • T-Lymphocytes, Helper-Inducer / physiology*

Substances

  • Cytokines
  • Receptors, Complement
  • VSIG4 protein, mouse
  • CD40 Ligand