Direct adenovirus-mediated gene transfer of interleukin 1 and tumor necrosis factor alpha soluble receptors to rabbit knees with experimental arthritis has local and distal anti-arthritic effects

Proc Natl Acad Sci U S A. 1998 Apr 14;95(8):4613-8. doi: 10.1073/pnas.95.8.4613.

Abstract

Adenoviral vectors were used to deliver genes encoding a soluble interleukin 1 (IL-1)-type I receptor-IgG fusion protein and/or a soluble type I tumor necrosis factor alpha (TNFalpha) receptor-IgG fusion protein directly to the knees of rabbits with antigen-induced arthritis. When tested individually, knees receiving the soluble IL-1 receptor had significantly reduced cartilage matrix degradation and white blood cell infiltration into the joint space. Delivery of the soluble TNFalpha receptor was less effective, having only a moderate effect on white blood cell infiltration and no effect on cartilage breakdown. When both soluble receptors were used together, there was a greater inhibition of white blood cell infiltration and cartilage breakdown with a considerable reduction of synovitis. Interestingly, anti-arthritic effects were also seen in contralateral control knees receiving only a marker gene, suggesting that sustained local inhibition of disease activity in one joint may confer an anti-arthritic effect on other joints. These results suggest that local intra-articular gene transfer could be used to treat systemic polyarticular arthritides.

Publication types

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

MeSH terms

  • Adenoviridae
  • Animals
  • Arthritis, Experimental / pathology
  • Arthritis, Experimental / therapy*
  • Cartilage, Articular / pathology
  • Enzyme-Linked Immunosorbent Assay
  • Gene Transfer Techniques
  • Genes, Reporter
  • Genetic Markers
  • Genetic Therapy*
  • Genetic Vectors
  • Immunoglobulin G
  • Joints / pathology
  • Leukocytes / physiology
  • Luciferases / biosynthesis
  • Mice
  • Organ Specificity
  • Rabbits
  • Receptors, Interleukin-1 / biosynthesis*
  • Receptors, Interleukin-1 / genetics
  • Recombinant Fusion Proteins / biosynthesis
  • Synovial Membrane / pathology
  • Tumor Necrosis Factor-alpha / biosynthesis*
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Genetic Markers
  • Immunoglobulin G
  • Receptors, Interleukin-1
  • Recombinant Fusion Proteins
  • Tumor Necrosis Factor-alpha
  • Luciferases