Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2015 Sep 1:6:187.
doi: 10.3389/fphar.2015.00187. eCollection 2015.

HDL/ApoA-1 infusion and ApoA-1 gene therapy in atherosclerosis

Affiliations
Review

HDL/ApoA-1 infusion and ApoA-1 gene therapy in atherosclerosis

Kuang-Yuh Chyu et al. Front Pharmacol. .

Abstract

The HDL hypothesis stating that simply raising HDL cholesterol (HDL-C) may produce cardiovascular benefits has been questioned recently based on several randomized clinical trials using CETP inhibitors or niacin to raise HDL-C levels. However, extensive pre-clinical data support the vascular protective effects of administration of exogenous ApoA-1 containing preβ-HDL like particles. Several small proof-of-concept clinical trials using such HDL/ApoA-1 infusion therapy have shown encouraging results but definitive proof of efficacy must await large scale clinical trials. In addition to HDL infusion therapy an alternative way to exploit beneficial cardiovascular effects of HDL/ApoA-1 is to use gene transfer. Preclinical studies have shown evidence of benefit using this approach; however clinical validation is yet lacking. This review summarizes our current knowledge of the aforementioned strategies.

Keywords: ApoA-1; HDL; atherosclerosis; gene therapy.

PubMed Disclaimer

References

    1. Ameli S., Hultgardh-Nilsson A., Cercek B., Shah P. K., Forrester J. S., Ageland H., et al. (1994). Recombinant apolipoprotein A-I Milano reduces intimal thickening after balloon injury in hypercholesterolemic rabbits. Circulation 90, 1935–1941. 10.1161/01.CIR.90.4.1935 - DOI - PubMed
    1. Angeli V., Llodrá J., Rong J. X., Satoh K., Ishii S., Shimizu T., et al. . (2004). Dyslipidemia associated with atherosclerotic disease systemically alters dendritic cell mobilization. Immunity 21, 561–574. 10.1016/j.immuni.2004.09.003 - DOI - PubMed
    1. Asokan A., Samulski R. J. (2013). An emerging adeno-associated viral vector pipeline for cardiac gene therapy. Hum. Gene Ther. 24, 906–913. 10.1089/hum.2013.2515 - DOI - PMC - PubMed
    1. Badimon J. J., Badimon L., Fuster V. (1990). Regression of atherosclerotic lesions by high density lipoprotein plasma fraction in the cholesterol-fed rabbit. J. Clin. Invest. 85, 1234–1241. 10.1172/JCI114558 - DOI - PMC - PubMed
    1. Badimon J. J., Badimon L., Galvez A., Dische R., Fuster V. (1989). High density lipoprotein plasma fractions inhibit aortic fatty streaks in cholesterol-fed rabbits. Lab. Invest. 60, 455–461. - PubMed