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

被引:33
作者
Urakami, Akane [1 ]
Sakurai, Atsuko [1 ]
Ishikawa, Momoko [1 ,5 ]
Yap, Moh Lan [2 ]
Flores-Garcia, Yevel [3 ]
Haseda, Yasunari [4 ]
Aoshi, Taiki [4 ]
Zavala, Fidel P. [3 ]
Rossmann, Michael G. [2 ]
Kuno, Sachiko [1 ]
Ueno, Ryuji [1 ]
Akahata, Wataru [1 ]
机构
[1] VLP Therapeut, Gaithersburg, MD 20878 USA
[2] Purdue Univ, Dept Biol Sci, W Lafayette, IN 47907 USA
[3] Johns Hopkins Univ, Dept Mol Microbiol & Immunol, Johns Hopkins Bloomberg Sch Publ Hlth, Baltimore, MD USA
[4] Osaka Univ, Vaccine Dynam Project, BIKEN Innovat Vaccine Res Alliance Labs, Microbial Dis Res Inst, Suita, Osaka, Japan
[5] Tohoku Univ, Grad Sch Dent, Dept Oral Hlth & Dev Sci, Sendai, Miyagi, Japan
基金
美国国家卫生研究院;
关键词
alphavirus; chikungunya virus; malaria; vaccines; virus-like particle; MALARIA VACCINE; MICROSCOPY; RTS; S; IMPLEMENTATION; NANOPARTICLES; ORGANIZATION; MECHANISMS; EPITOPE; CELLS; ENTRY;
D O I
10.1128/CVI.00090-17
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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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页数:14
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