Effects of anti-CD70 mAb on Theiler's murine encephalomyelitis virus-induced demyelinating disease

Brain Res. 2010 Mar 4:1317:236-45. doi: 10.1016/j.brainres.2009.12.058. Epub 2010 Jan 4.

Abstract

Ligation of CD27, a member of the tumor necrosis factor (TNF) receptor family, by its ligand CD70 is thought to be important in T cell activation, expansion and survival, B cell activation, and NK cell activation. We examined the role of CD70 in Theiler's murine encephalomyelitis virus-induced demyelinating disease (TMEV-IDD) mice. Blocking of CD70 in effector phase by anti-CD70 monoclonal antibody (mAb) suppressed the development of TMEV-IDD. The number of IFN-gamma- or TNF-alpha-producing cells in the spleen and mRNA levels of IFN-gamma and TNF-alpha in spinal cord were decreased in mice treated with anti-CD70 mAb at the effector phase. In contrast, treatment with anti-CD70 mAb in induction phase failed to reduce these responses, compared to nonspecific IgG-treated control mice. These data suggest that CD70 is critically involved in the pathogenesis of TMEV-IDD and that antibodies against CD70 could be a novel therapeutic approach in the clinical treatment of demyelinating diseases such as human multiple sclerosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / therapeutic use*
  • CD27 Ligand / immunology*
  • CD27 Ligand / physiology
  • Cardiovirus Infections / immunology
  • Cardiovirus Infections / metabolism
  • Cardiovirus Infections / prevention & control*
  • Cytokines / metabolism
  • Demyelinating Diseases / immunology
  • Demyelinating Diseases / metabolism
  • Demyelinating Diseases / prevention & control*
  • Female
  • Immunologic Factors / therapeutic use*
  • Interferon-gamma / metabolism
  • Mice
  • RNA, Messenger / metabolism
  • Spinal Cord / immunology
  • Spinal Cord / metabolism
  • Spleen / immunology
  • Spleen / metabolism
  • Theilovirus*
  • Time Factors
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Antibodies, Monoclonal
  • CD27 Ligand
  • Cytokines
  • Immunologic Factors
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma