| Literature DB >> 34541299 |
Oscar A Ortega-Rivera1,2, Jonathan K Pokorski1,2,3, Nicole F Steinmetz1,2,3,4,5,6.
Abstract
Cardiovascular disease is the number one cause of death globally. Lowering cholesterol levels in plasma is the mainstay therapy; however lifelong treatment and adverse effects call for improved therapeutic interventions. We developed a trivalent vaccine candidate targeting proprotein convertase subtilisin/kexin-9 (PCSK9), apolipoprotein B (ApoB), and cholesteryl ester transfer protein (CETP). Vaccine candidates were developed using bacteriophage Qβ-based virus-like particles (VLPs) displaying antigens of PCKS9, ApoB, and CETP, respectively. Vaccine candidate mixtures were formulated as slow-release PLGA:VLP implants using hot-melt extrusion. The delivery of the trivalent vaccine candidate via the implant produced antibodies against the cholesterol checkpoint proteins at levels comparable to a three-dose injection schedule with soluble mixtures. The reduction in PCSK9 and ApoB levels in plasma, inhibition of CETP (in vitro), and total plasma cholesterol decrease was achieved. All-together, we present a platform technology for a single-dose multi-target vaccination platform targeting cholesterol checkpoint proteins.Entities:
Keywords: ApoB; CETP; Cardiovascular disease; PCSK9; cholesterol; trivalent vaccine; virus-like particle (VLP)
Year: 2021 PMID: 34541299 PMCID: PMC8447230 DOI: 10.1002/adtp.202100014
Source DB: PubMed Journal: Adv Ther (Weinh) ISSN: 2366-3987