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基于病毒样颗粒、脂质体和聚合物颗粒的 HIV-1 疫苗。

Virus-Like Particle, Liposome, and Polymeric Particle-Based Vaccines against HIV-1.

机构信息

Department of Microbiology and Immunology, University of Western Ontario, London, ON, Canada.

出版信息

Front Immunol. 2018 Feb 28;9:345. doi: 10.3389/fimmu.2018.00345. eCollection 2018.


DOI:10.3389/fimmu.2018.00345
PMID:29541072
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5835502/
Abstract

It is acknowledged that vaccines remain the best hope for eliminating the HIV-1 epidemic. However, the failure to produce effective vaccine immunogens and the inability of conventional delivery strategies to elicit the desired immune responses remains a central theme and has ultimately led to a significant roadblock in HIV vaccine development. Consequently, significant efforts have been applied to generate novel vaccine antigens and delivery agents, which mimic viral structures for optimal immune induction. Here, we review the latest developments that have occurred in the nanoparticle vaccine field, with special emphasis on strategies that are being utilized to attain highly immunogenic, systemic, and mucosal anti-HIV humoral and cellular immune responses. This includes the design of novel immunogens, the central role of antigen-presenting cells, delivery routes, and biodistribution of nanoparticles to lymph nodes. In particular, we will focus on virus-like-particle formulations and their preclinical uses within the HIV prophylactic vaccine setting.

摘要

人们认识到,疫苗仍然是消除 HIV-1 流行的最佳希望。然而,未能生产出有效的疫苗免疫原,以及常规传递策略无法引发所需的免疫反应,仍然是一个核心主题,并最终导致 HIV 疫苗开发的重大障碍。因此,人们已经投入了大量精力来开发新型疫苗抗原和传递剂,这些抗原和传递剂模拟病毒结构,以实现最佳的免疫诱导。在这里,我们回顾了纳米颗粒疫苗领域的最新进展,特别强调了用于实现高度免疫原性、全身性和黏膜抗 HIV 体液和细胞免疫反应的策略。这包括新型免疫原的设计、抗原呈递细胞的核心作用、纳米颗粒的传递途径和生物分布到淋巴结。特别是,我们将重点介绍病毒样颗粒制剂及其在 HIV 预防性疫苗中的临床前应用。

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本文引用的文献

[1]
A heterogeneous human immunodeficiency virus-like particle (VLP) formulation produced by a novel vector system.

NPJ Vaccines. 2018-1-19

[2]
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Blood Adv. 2017-11-17

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PLoS One. 2017-10-11

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AIDS Res Ther. 2017-9-12

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Covalent Linkage of HIV-1 Trimers to Synthetic Liposomes Elicits Improved B Cell and Antibody Responses.

J Virol. 2017-7-27

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Co-utilization of a TLR5 agonist and nano-formulation of HIV-1 vaccine candidate leads to increased vaccine immunogenicity and decreased immunogenic dose: A preliminary study.

Immunol Lett. 2017-7

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J Virol. 2017-6-26

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Intrastructural help: improving the HIV-1 envelope antibody response induced by virus-like particle vaccines.

Curr Opin HIV AIDS. 2017-5

[9]
Particle-based delivery of the HIV envelope protein.

Curr Opin HIV AIDS. 2017-5

[10]
Adjuvants: tailoring humoral immune responses.

Curr Opin HIV AIDS. 2017-5

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