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基于病毒样颗粒的新型疫苗设计

Design of Novel Vaccines Based on Virus-Like Particles.

作者信息

Bárcena Juan, Zamora-Ceballos María, Blanco Esther

机构信息

Centro de Investigación en Sanidad Animal (CISA-INIA/CSIC), Madrid, Spain.

出版信息

Subcell Biochem. 2024;105:785-821. doi: 10.1007/978-3-031-65187-8_21.


DOI:10.1007/978-3-031-65187-8_21
PMID:39738963
Abstract

Virus-like particles (VLPs) are formed by viral proteins that, when overexpressed, spontaneously self-assemble into particles that structurally are similar to infectious virus or subviral particles (e.g. the viral capsid). VLPs are appealing as vaccine candidates because their inherent properties (i.e. virus-sized, multimeric antigens, highly organised and repetitive structure, not infectious) are suitable for the induction of safe and efficient humoral and cellular immune responses. VLP-based vaccines have already been licensed for human and veterinary use, and many more vaccine candidates are currently in late stages of evaluation. Moreover, the development of VLPs as platforms for foreign antigen display has further broadened their potential applicability both as prophylactic and therapeutic vaccines. This chapter provides an overview on the design and use of VLPs for the development of new-generation vaccines.

摘要

病毒样颗粒(VLPs)由病毒蛋白形成,当这些病毒蛋白过度表达时,会自发地自我组装成在结构上与感染性病毒或亚病毒颗粒(如病毒衣壳)相似的颗粒。VLPs作为疫苗候选物很有吸引力,因为它们的固有特性(即病毒大小、多聚体抗原、高度有序且重复的结构、无感染性)适合诱导安全有效的体液免疫和细胞免疫反应。基于VLP的疫苗已获许可用于人类和兽医领域,目前还有更多的候选疫苗正处于评估后期。此外,将VLPs开发为外源抗原展示平台进一步拓宽了它们作为预防性和治疗性疫苗的潜在应用范围。本章概述了VLPs在新一代疫苗开发中的设计与应用。

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引用本文的文献

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Enterovirus A71 priorities, challenges, and future opportunities in humoral immunity and vaccine development.

NPJ Vaccines. 2025-8-15

[2]
Integrated in-silico design and in vivo validation of multi-epitope vaccines for norovirus.

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本文引用的文献

[1]
Chimaeric plant-produced bluetongue virus particles as potential vaccine candidates.

Arch Virol. 2023-6-13

[2]
Historical Advances in Structural and Molecular Biology and How They Impacted Vaccine Development.

J Mol Biol. 2023-7-1

[3]
Platforms, advances, and technical challenges in virus-like particles-based vaccines.

Front Immunol. 2023

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Virus-like particle vaccinology, from bench to bedside.

Cell Mol Immunol. 2022-9

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Mechanisms of cellular and humoral immunity through the lens of VLP-based vaccines.

Expert Rev Vaccines. 2022-4

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NPJ Vaccines. 2021-5-13

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Nat Rev Immunol. 2021-2

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Disulfide stabilization of human norovirus GI.1 virus-like particles focuses immune response toward blockade epitopes.

NPJ Vaccines. 2020-12-14

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First human efficacy study of a plant-derived influenza vaccine.

Lancet. 2020-11-7

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