| Literature DB >> 26413878 |
Erin Crossey1, Marcelo J A Amar2, Maureen Sampson2, Julianne Peabody1, John T Schiller3, Bryce Chackerian4, Alan T Remaley5.
Abstract
Proprotein convertase subtilisin/kexin type 9 (PCSK9) is a secretory protein that controls cholesterol homeostasis by enhancing endosomal and lysosomal degradation of the low-density lipoprotein receptor (LDL-R). Mutations that cause increased activity of PCSK9 are associated with hypercholesterolemia, atherosclerosis and early cardiovascular disease (CVD), whereas individuals with loss-of-function mutations in PCSK9 are apparently healthy but are hypocholesterolemic and have a dramatically decreased risk of CVD. In this study, we generated virus-like particle (VLP)-based vaccines targeting PCSK9. Mice and macaques vaccinated with bacteriophage VLPs displaying PCSK9-derived peptides developed high titer IgG antibodies that bound to circulating PCSK9. Vaccination was associated with significant reductions in total cholesterol, free cholesterol, phospholipids, and triglycerides. A vaccine targeting PCSK9 may, therefore, be an attractive alternative to monoclonal antibody-based therapies.Entities:
Keywords: LDL Cholesterol; PCSK9; Vaccine; Virus-like particles
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Year: 2015 PMID: 26413878 PMCID: PMC4609631 DOI: 10.1016/j.vaccine.2015.09.044
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641