Differential effects of interleukin-4 in peptide induced autoimmunity

Clin Immunol. 2003 Aug;108(2):80-8. doi: 10.1016/s1521-6616(03)00096-2.

Abstract

BALB/c mice immunized with multimeric DWEYSVWLSN develop IgG1 anti-DNA antibodies and glomerular immunoglobulin deposits, leading us to investigate the role of IL-4 in this model of antigen induced lupus. Splenocytes from DWEYSVWLSN immunized mice secreted IL-4 but not gamma-interferon. Following peptide immunization, IgG1 anti-peptide and anti-DNA antibodies were significantly higher in IL-4 wild type mice, while IgM and IgG3 anti-DNA levels were significantly higher in IL-4 knockout mice. Titers of IgG anti-laminin and anti-histone, but not anti-Sm/RNP and anti-cardiolipin antibodies, were significantly higher in the IL-4 wild type group. Glomerular immunoglobulin deposition was substantially decreased in IL-4 knockout mice. We conclude that while IL-4 does not materially affect the generation of some autoantibody responses associated with peptide induced autoimmunity, IL-4 deficiency inhibits kidney immunoglobulin deposition. The effect of IL-4 on humoral autoimmunity in lupus is complex, and is dependent on genetic background, the antigenic trigger and stage of disease.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Autoantibodies / analysis
  • Autoantibodies / blood
  • Autoimmunity
  • Cells, Cultured
  • DNA / immunology
  • Disease Models, Animal
  • Female
  • Histones / immunology
  • Immunoglobulin G / analysis
  • Immunoglobulin G / blood
  • Immunoglobulin M / blood
  • Immunohistochemistry
  • Interleukin-4 / biosynthesis
  • Interleukin-4 / deficiency
  • Interleukin-4 / immunology*
  • Kidney Glomerulus / immunology
  • Laminin / immunology
  • Lupus Erythematosus, Systemic / etiology
  • Lupus Erythematosus, Systemic / immunology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • Peptides
  • Spleen / cytology
  • Spleen / metabolism

Substances

  • Autoantibodies
  • Histones
  • Immunoglobulin G
  • Immunoglobulin M
  • Laminin
  • Peptides
  • Interleukin-4
  • DNA