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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 structu...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498722/ https://www.ncbi.nlm.nih.gov/pubmed/28515133 http://dx.doi.org/10.1128/CVI.00090-17 |
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author | Urakami, Akane Sakurai, Atsuko Ishikawa, Momoko Yap, Moh Lan Flores-Garcia, Yevel Haseda, Yasunari Aoshi, Taiki Zavala, Fidel P. Rossmann, Michael G. Kuno, Sachiko Ueno, Ryuji Akahata, Wataru |
author_facet | Urakami, Akane Sakurai, Atsuko Ishikawa, Momoko Yap, Moh Lan Flores-Garcia, Yevel Haseda, Yasunari Aoshi, Taiki Zavala, Fidel P. Rossmann, Michael G. Kuno, Sachiko Ueno, Ryuji Akahata, Wataru |
author_sort | Urakami, Akane |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5498722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-54987222017-07-14 Development of a Novel Virus-Like Particle Vaccine Platform That Mimics the Immature Form of Alphavirus Urakami, Akane Sakurai, Atsuko Ishikawa, Momoko Yap, Moh Lan Flores-Garcia, Yevel Haseda, Yasunari Aoshi, Taiki Zavala, Fidel P. Rossmann, Michael G. Kuno, Sachiko Ueno, Ryuji Akahata, Wataru Clin Vaccine Immunol Vaccines 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. American Society for Microbiology 2017-07-05 /pmc/articles/PMC5498722/ /pubmed/28515133 http://dx.doi.org/10.1128/CVI.00090-17 Text en Copyright © 2017 Urakami et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Vaccines Urakami, Akane Sakurai, Atsuko Ishikawa, Momoko Yap, Moh Lan Flores-Garcia, Yevel Haseda, Yasunari Aoshi, Taiki Zavala, Fidel P. Rossmann, Michael G. Kuno, Sachiko Ueno, Ryuji Akahata, Wataru Development of a Novel Virus-Like Particle Vaccine Platform That Mimics the Immature Form of Alphavirus |
title | Development of a Novel Virus-Like Particle Vaccine Platform That Mimics the Immature Form of Alphavirus |
title_full | Development of a Novel Virus-Like Particle Vaccine Platform That Mimics the Immature Form of Alphavirus |
title_fullStr | Development of a Novel Virus-Like Particle Vaccine Platform That Mimics the Immature Form of Alphavirus |
title_full_unstemmed | Development of a Novel Virus-Like Particle Vaccine Platform That Mimics the Immature Form of Alphavirus |
title_short | Development of a Novel Virus-Like Particle Vaccine Platform That Mimics the Immature Form of Alphavirus |
title_sort | development of a novel virus-like particle vaccine platform that mimics the immature form of alphavirus |
topic | Vaccines |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498722/ https://www.ncbi.nlm.nih.gov/pubmed/28515133 http://dx.doi.org/10.1128/CVI.00090-17 |
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