包膜病毒样颗粒作为疫苗开发的平台

Pub Date : 2021-11-01 DOI:10.4103/2468-8827.330656
F. Diaz-Mitoma
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引用次数: 2

摘要

疫苗接种是预防和控制传染病对全球公共卫生威胁的最有效方法。由于包膜病毒样颗粒(evlp)具有自我调节特性,因此与其他亚单位疫苗相比具有优势。它们的最佳尺寸和颗粒结构可以激活抗原呈递细胞。本文介绍的候选疫苗在制造、应用和预防或治疗疾病方面的灵活性和优势。先前的临床前和临床研究证明了两种eVLP候选疫苗的免疫原性,这些疫苗被设计用于预防巨细胞病毒。evlp中病毒包膜蛋白的表达诱导了强大的中和抗体反应,这被认为是许多病毒感染中保护的相关因素。VBI已经开发了两种针对SARS CoV2的候选疫苗,VBI-2902a和VBI-2905a。正在进行的这些候选疫苗的临床开发将在先前接种和未接种疫苗的个体中接种一剂或两剂后评估人体安全性和免疫原性(NCT04773665)。
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Enveloped virus-like particles as a platform for vaccine development
Vaccination is the most effective approach in preventing and controlling the global public health threat of infectious diseases. Enveloped virus-like particles (eVLPs) offer advantages over other subunit vaccines because of their self-adjuvanting properties. Their optimal size and particulate structure activate antigen-presenting cells. The flexibility in manufacturing, applications, and advantages for preventing or treating disease are highlighted by the vaccine candidates described in this review. Previous preclinical and clinical studies demonstrated the immunogenicity of two eVLP vaccine candidates designed to protect against cytomegalovirus. The expression of viral envelope proteins in the eVLPs induces a robust neutralizing antibody response, which is considered a correlate of protection in many viral infections. VBI has developed two vaccine candidates against SARS CoV2, VBI-2902a, and VBI-2905a. Ongoing clinical development of these vaccine candidates will assess human safety and immunogenicity, after one or two doses in previously vaccinated and unvaccinated, individuals (NCT04773665).
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