Somatic gene transfer of human ApoA-I inhibits atherosclerosis progression in mouse models

Circulation. 1999 Jan;99(1):105-10. doi: 10.1161/01.cir.99.1.105.

Abstract

Background: Apolipoprotein (apo) A-I is the major component of HDL, and it displays antiatherogenic properties.

Methods and results: The human apoA-I gene has been transferred into different mouse models by use of a recombinant adenovirus under the control of an RSV-LTR promoter (AV RSV apoA-I). Administration of AV RSV apoA-I to C57BL/6 mice resulted in moderate expression of human apoA-I for 3 weeks, leading to a transient elevation (40% at day 11 after injection) of HDL cholesterol concentration. In contrast, administration of AV RSV apoA-I to human apoA-I-transgenic mice induced a large increase of human apoA-I and HDL cholesterol concentrations (300% and 360%, respectively, at day 14 after injection) for 10 weeks, indicating that an immune response to the transgene was one major hurdle for long-term duration of expression. Recombinant adenovirus expressing human apolipoprotein A-I (AV RSV apoA-I) was also injected into human apoA-I-transgenic/apoE-deficient mice, which are prone to develop atherosclerosis. Over a 6-week period, overexpression of human apoA-I inhibited fatty streak lesion formation by 56% in comparison with control.

Conclusions: Somatic gene transfer of human apoA-I prevents the development of atherosclerosis in the mouse model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae / genetics
  • Animals
  • Apolipoprotein A-I / genetics*
  • Apolipoproteins E / deficiency
  • Arteriosclerosis / therapy*
  • Disease Models, Animal
  • Disease Progression
  • Gene Transfer Techniques*
  • Genetic Vectors
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Reference Values

Substances

  • Apolipoprotein A-I
  • Apolipoproteins E