Broad-spectrum CC-chemokine blockade by gene transfer inhibits macrophage recruitment and atherosclerotic plaque formation in apolipoprotein E-knockout mice

Circulation. 2004 Oct 19;110(16):2460-6. doi: 10.1161/01.CIR.0000145122.58420.CO. Epub 2004 Oct 11.

Abstract

Background: The CC-chemokines (CKs) recruit monocytes/macrophages to sites of inflammation; several different CC-CKs play a role in the pathogenesis of atherosclerosis. The vaccinia virus expresses a 35-kDa soluble protein (35K) that binds to and inactivates nearly all of the CC-CKs, providing a potentially useful therapeutic strategy for broad-spectrum CC-CK inhibition in atherosclerosis. A recombinant adenovirus encoding soluble 35K (Ad35K) was generated to investigate the effect of 35K gene transfer on atherosclerosis in Western diet-fed apolipoprotein E-knockout (ApoE KO) mice.

Methods and results: ApoE KO mice received tail-vein injections of phosphate-buffered saline, Ad35K, or control adenovirus AdGFP encoding green fluorescence protein. Two weeks after Ad35K gene transfer, atherosclerotic lesion area was significantly reduced in aortic roots by 55% compared with PBS or AdGFP control mice (P<0.05). Furthermore, 35K gene transfer strikingly reduced the macrophage content in aortic root lesions by 85% (P<0.01) and reduced lipid deposition in descending aortas by more than half (P<0.05). By an in vitro chemotaxis assay, plasma and aortic homogenates from 35K gene transfer mice promoted significantly less CC-CK-induced cell migration than did PBS or AdGFP controls.

Conclusions: These findings show that a single intravenous injection of a recombinant adenovirus encoding the broad-spectrum CC-CK inhibitor 35K can reduce atherosclerosis by inhibiting CC-CK-induced macrophage recruitment in atherosclerotic ApoE KO mice. These experiments suggest that CC-CKs play an important role in atherogenesis and are a rational target for therapeutic intervention.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae / genetics
  • Animals
  • Aortic Diseases / etiology
  • Aortic Diseases / pathology
  • Aortic Diseases / prevention & control
  • Aortic Diseases / therapy
  • Apolipoproteins E / deficiency*
  • Apolipoproteins E / genetics
  • Arteriosclerosis / etiology
  • Arteriosclerosis / pathology
  • Arteriosclerosis / prevention & control*
  • Arteriosclerosis / therapy
  • Cell Movement
  • Chemokines, CC / antagonists & inhibitors
  • Chemokines, CC / physiology*
  • Chemotaxis
  • Diet, Atherogenic
  • Genetic Therapy*
  • Genetic Vectors / therapeutic use*
  • Hyperlipoproteinemia Type II / etiology
  • Hyperlipoproteinemia Type II / genetics
  • Macrophages / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Recombinant Fusion Proteins / physiology
  • Transduction, Genetic
  • Vaccinia virus / genetics
  • Viral Proteins / genetics
  • Viral Proteins / physiology*
  • Virulence Factors

Substances

  • Apolipoproteins E
  • CCI protein, Cowpox virus
  • Chemokines, CC
  • Recombinant Fusion Proteins
  • Viral Proteins
  • Virulence Factors