一种新型病毒样颗粒疫苗平台的开发,模拟未成熟形式的甲病毒。

Q2 Biochemistry, Genetics and Molecular Biology Clinical and Vaccine Immunology Pub Date : 2017-07-05 Print Date: 2017-07-01 DOI:10.1128/CVI.00090-17
Akane Urakami, Atsuko Sakurai, Momoko Ishikawa, Moh Lan Yap, Yevel Flores-Garcia, Yasunari Haseda, Taiki Aoshi, Fidel P Zavala, Michael G Rossmann, Sachiko Kuno, Ryuji Ueno, Wataru Akahata
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引用次数: 29

摘要

病毒样颗粒(vlp)是一种非传染性的多蛋白结构,由病毒结构蛋白设计成自组装。在这里,我们利用基孔肯雅病毒的VLPs开发了一种新的基于vlp的疫苗平台。我们在基孔肯雅病毒的包膜蛋白(一种结构成分)内确定了两个区域,外来抗原可以在不损害VLP结构的情况下插入。我们的VLP以高度对称的方式在VLP表面显示480个插入抗原的丰富拷贝,因此能够诱导对任何插入抗原的强免疫反应。此外,通过模拟未成熟病毒的结构,我们改变了VLP的体内动力学并增强了其免疫原性。我们使用恶性疟原虫的环孢子子蛋白(CSP)作为抗原,并证明了基于vlp的疫苗在动物中引起对CSP的强烈免疫反应。免疫猴子的血清保护小鼠免受疟疾感染。同样地,接种含有约氏P. csp的VLPs的小鼠可以免受感染性孢子虫的攻击。因此,我们独特设计的VLP平台可以作为开发针对其他病原体和疾病的疫苗的蓝图。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Development of a Novel Virus-Like Particle Vaccine Platform That Mimics the Immature Form of Alphavirus.

Virus-like particles (VLPs) are noninfectious multiprotein structures that are engineered to self-assemble from viral structural proteins. Here, we developed a novel VLP-based vaccine platform utilizing VLPs from the chikungunya virus. We identified two regions within the envelope protein, a structural component of chikungunya, where foreign antigens can be inserted without compromising VLP structure. Our VLP displays 480 copious copies of an inserted antigen on the VLP surface in a highly symmetric manner and is thus capable of inducing strong immune responses against any inserted antigen. Furthermore, by mimicking the structure of the immature form of the virus, we altered our VLP's in vivo dynamics and enhanced its immunogenicity. We used the circumsporozoite protein (CSP) of the Plasmodium falciparum malaria parasite as an antigen and demonstrated that our VLP-based vaccine elicits strong immune responses against CSP in animals. The sera from immunized monkeys protected mice from malaria infection. Likewise, mice vaccinated with P. yoelii CSP-containing VLPs were protected from an infectious sporozoite challenge. Hence, our uniquely engineered VLP platform can serve as a blueprint for the development of vaccines against other pathogens and diseases.

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来源期刊
Clinical and Vaccine Immunology
Clinical and Vaccine Immunology 医学-传染病学
CiteScore
2.88
自引率
0.00%
发文量
0
审稿时长
1.5 months
期刊介绍: Cessation. First launched as Clinical and Diagnostic Laboratory Immunology (CDLI) in 1994, CVI published articles that enhanced the understanding of the immune response in health and disease and after vaccination by showcasing discoveries in clinical, laboratory, and vaccine immunology. CVI was committed to advancing all aspects of vaccine research and immunization, including discovery of new vaccine antigens and vaccine design, development and evaluation of vaccines in animal models and in humans, characterization of immune responses and mechanisms of vaccine action, controlled challenge studies to assess vaccine efficacy, study of vaccine vectors, adjuvants, and immunomodulators, immune correlates of protection, and clinical trials.
期刊最新文献
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