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

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 protect...

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Detalles Bibliográficos
Autores principales: Chyu, Kuang-Yuh, Shah, Prediman K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4555973/
https://www.ncbi.nlm.nih.gov/pubmed/26388776
http://dx.doi.org/10.3389/fphar.2015.00187
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author Chyu, Kuang-Yuh
Shah, Prediman K.
author_facet Chyu, Kuang-Yuh
Shah, Prediman K.
author_sort Chyu, Kuang-Yuh
collection PubMed
description 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.
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spelling pubmed-45559732015-09-18 HDL/ApoA-1 infusion and ApoA-1 gene therapy in atherosclerosis Chyu, Kuang-Yuh Shah, Prediman K. Front Pharmacol Pharmacology 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. Frontiers Media S.A. 2015-09-01 /pmc/articles/PMC4555973/ /pubmed/26388776 http://dx.doi.org/10.3389/fphar.2015.00187 Text en Copyright © 2015 Chyu and Shah. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Chyu, Kuang-Yuh
Shah, Prediman K.
HDL/ApoA-1 infusion and ApoA-1 gene therapy in atherosclerosis
title HDL/ApoA-1 infusion and ApoA-1 gene therapy in atherosclerosis
title_full HDL/ApoA-1 infusion and ApoA-1 gene therapy in atherosclerosis
title_fullStr HDL/ApoA-1 infusion and ApoA-1 gene therapy in atherosclerosis
title_full_unstemmed HDL/ApoA-1 infusion and ApoA-1 gene therapy in atherosclerosis
title_short HDL/ApoA-1 infusion and ApoA-1 gene therapy in atherosclerosis
title_sort hdl/apoa-1 infusion and apoa-1 gene therapy in atherosclerosis
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4555973/
https://www.ncbi.nlm.nih.gov/pubmed/26388776
http://dx.doi.org/10.3389/fphar.2015.00187
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