Altered pathological progression of diaphragm and quadriceps muscle in TNF-deficient, dystrophin-deficient mice

Neuromuscul Disord. 2000 Dec;10(8):612-9. doi: 10.1016/s0960-8966(00)00160-7.


We have previously demonstrated a role for T cells in Duchenne muscular dystrophy (DMD) using the mdx mouse and have shown that T cell killing of dystrophic muscle can occur through perforin-dependent and perforin-independent mechanisms. In this investigation, we explore the possibility that one perforin-independent mechanism utilized by the T cells is cytokine-based killing, specifically by tumor necrosis factor (TNF). We tested this hypothesis by generating mice that are TNF-deficient and dystrophin-deficient (TNF-/mdx). Body mass and muscle mass of the TNF-/mdx mice were significantly less than TNF+/mdx mice at 8 weeks of age. Creatine kinase levels and overall muscle strength were unchanged. Histopathology measurements showed different results in the diaphragm and quadriceps muscles. These data suggest that removal of TNF in vivo in dystrophic mice has differential effects on diaphragm and quadriceps suggesting that TNF is an unfavorable target for immunotherapy for DMD.

Publication types

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

MeSH terms

  • Age Factors
  • Animals
  • Body Weight / physiology
  • Creatine Kinase / metabolism
  • Diaphragm / metabolism*
  • Diaphragm / pathology*
  • Diaphragm / physiopathology
  • Disease Models, Animal
  • Dystrophin / deficiency*
  • Dystrophin / genetics
  • Female
  • Immunotherapy / methods
  • Inflammation / immunology
  • Inflammation / metabolism
  • Inflammation / pathology
  • Leg / pathology*
  • Leg / physiopathology
  • Male
  • Mice
  • Mice, Knockout / anatomy & histology
  • Mice, Knockout / metabolism
  • Muscle Weakness / diagnosis
  • Muscle, Skeletal / metabolism*
  • Muscle, Skeletal / pathology*
  • Muscle, Skeletal / physiopathology
  • Muscular Dystrophy, Duchenne / immunology*
  • Muscular Dystrophy, Duchenne / metabolism
  • Muscular Dystrophy, Duchenne / pathology
  • T-Lymphocytes / immunology
  • Tumor Necrosis Factor-alpha / deficiency*
  • Tumor Necrosis Factor-alpha / genetics


  • Dystrophin
  • Tumor Necrosis Factor-alpha
  • Creatine Kinase