Inhibition of joint inflammation and destruction induced by anti-type II collagen antibody/lipopolysaccharide (LPS)-induced arthritis in mice due to deletion of macrophage migration inhibitory factor (MIF)

Cytokine. 2004 Jun 7;26(5):187-94. doi: 10.1016/j.cyto.2004.02.007.

Abstract

Objective: Previous studies have demonstrated that neutralization of macrophage migration inhibitory factor (MIF) by anti-MIF antibody decreases joint destruction in the collagen-induced arthritis model. The present study was undertaken to investigate whether selective deletion of MIF inhibits inflammation and joint destruction of the anti-type II collagen antibody (anti-CII Ab)/lipopolysaccharide (LPS)-induced arthritis in mice, in order to determine the role of this cytokine in inflammatory arthritis.

Design: Anti-CII Ab/LPS-induced arthritis was induced in MIF-deficient and wild-type mice. The effects of anti-MIF polyclonal antibody administration on anti-CII Ab-induced arthritis were also evaluated.

Results: The expression of MIF protein and mRNA was induced in anti-CII Ab/LPS-induced arthritis joint tissues. Histopathological arthritis scores for synovial inflammation induced by anti-CII Ab/LPS -induced arthritis were significantly decreased in anti-MIF Ab-treated mice and in MIF-deficient mice compared to wild-type mice. In addition, mRNA levels of MMP-13 and MIP-2 in anti-CII Ab/LPS-induced arthritis joint tissues were significantly reduced in MIF-deficient mice compared to wild-type control mice.

Conclusions: These results indicate that MIF plays a critical role in inflammation and joint destruction in the anti-CII Ab/LPS-induced arthritis model in mice, in part via induction of MMP-13 and neutrophil infiltration through the induction of MIP-2.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / immunology
  • Arthritis, Rheumatoid / immunology*
  • Chemokine CXCL2
  • Chemokines / genetics
  • Chemokines / metabolism
  • Collagen Type II / immunology*
  • Collagenases / genetics
  • Collagenases / metabolism
  • Intramolecular Oxidoreductases
  • Lipopolysaccharides / immunology*
  • Macrophage Migration-Inhibitory Factors / deficiency
  • Macrophage Migration-Inhibitory Factors / genetics*
  • Macrophage Migration-Inhibitory Factors / metabolism
  • Matrix Metalloproteinase 13
  • Mice
  • RNA, Messenger / metabolism
  • Synovial Membrane / immunology
  • Synovial Membrane / metabolism
  • Time Factors

Substances

  • Antibodies, Monoclonal
  • Chemokine CXCL2
  • Chemokines
  • Collagen Type II
  • Cxcl2 protein, mouse
  • Lipopolysaccharides
  • Macrophage Migration-Inhibitory Factors
  • RNA, Messenger
  • Collagenases
  • Matrix Metalloproteinase 13
  • Mmp13 protein, mouse
  • Intramolecular Oxidoreductases
  • Mif protein, mouse