Ortega-Rivera Oscar A, Pokorski Jonathan K, Steinmetz Nicole F
Department of NanoEngineering, University of California-San Diego, La Jolla CA 92039, USA.
Center for Nano-ImmunoEngineering, University of California-San Diego, La Jolla CA 92039, USA.
Adv Ther (Weinh). 2021 Aug;4(8). doi: 10.1002/adtp.202100014. Epub 2021 Mar 11.
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 (), 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.
心血管疾病是全球头号死因。降低血浆中的胆固醇水平是主要治疗方法;然而,终身治疗及其不良反应需要改进治疗干预措施。我们研发了一种三价候选疫苗,其靶向作用于前蛋白转化酶枯草溶菌素/kexin-9(PCSK9)、载脂蛋白B(ApoB)和胆固醇酯转运蛋白(CETP)。候选疫苗是利用基于噬菌体Qβ的病毒样颗粒(VLP)分别展示PCKS9、ApoB和CETP的抗原而研发的。候选疫苗混合物采用热熔挤压法制成缓释聚乳酸-羟基乙酸共聚物(PLGA):VLP植入物。通过植入物递送三价候选疫苗产生的针对胆固醇检查点蛋白的抗体水平,与使用可溶性混合物的三剂注射方案相当。实现了血浆中PCSK9和ApoB水平的降低、CETP()的抑制以及总血浆胆固醇的下降。总之,我们展示了一种用于靶向胆固醇检查点蛋白的单剂量多靶点疫苗接种平台的技术。