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Immunogenicity of a novel tetravalent vaccine formulation with four recombinant lipidated dengue envelope protein domain IIIs in mice
We developed a novel platform to express high levels of recombinant lipoproteins with intrinsic adjuvant properties. Based on this technology, our group developed recombinant lipidated dengue envelope protein domain IIIs as vaccine candidates against dengue virus. This work aims to evaluate the immu...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965760/ https://www.ncbi.nlm.nih.gov/pubmed/27470096 http://dx.doi.org/10.1038/srep30648 |
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author | Chiang, Chen-Yi Pan, Chien-Hsiung Chen, Mei-Yu Hsieh, Chun-Hsiang Tsai, Jy-Ping Liu, Hsueh-Hung Liu, Shih-Jen Chong, Pele Leng, Chih-Hsiang Chen, Hsin-Wei |
author_facet | Chiang, Chen-Yi Pan, Chien-Hsiung Chen, Mei-Yu Hsieh, Chun-Hsiang Tsai, Jy-Ping Liu, Hsueh-Hung Liu, Shih-Jen Chong, Pele Leng, Chih-Hsiang Chen, Hsin-Wei |
author_sort | Chiang, Chen-Yi |
collection | PubMed |
description | We developed a novel platform to express high levels of recombinant lipoproteins with intrinsic adjuvant properties. Based on this technology, our group developed recombinant lipidated dengue envelope protein domain IIIs as vaccine candidates against dengue virus. This work aims to evaluate the immune responses in mice to the tetravalent formulation. We demonstrate that 4 serotypes of recombinant lipidated dengue envelope protein domain III induced both humoral and cellular immunity against all 4 serotypes of dengue virus on the mixture that formed the tetravalent formulation. Importantly, the immune responses induced by the tetravalent formulation in the absence of the exogenous adjuvant were functional in clearing the 4 serotypes of dengue virus in vivo. We affirm that the tetravalent formulation of recombinant lipidated dengue envelope protein domain III is a potential vaccine candidate against dengue virus and suggest further detailed studies of this formulation in nonhuman primates. |
format | Online Article Text |
id | pubmed-4965760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49657602016-08-08 Immunogenicity of a novel tetravalent vaccine formulation with four recombinant lipidated dengue envelope protein domain IIIs in mice Chiang, Chen-Yi Pan, Chien-Hsiung Chen, Mei-Yu Hsieh, Chun-Hsiang Tsai, Jy-Ping Liu, Hsueh-Hung Liu, Shih-Jen Chong, Pele Leng, Chih-Hsiang Chen, Hsin-Wei Sci Rep Article We developed a novel platform to express high levels of recombinant lipoproteins with intrinsic adjuvant properties. Based on this technology, our group developed recombinant lipidated dengue envelope protein domain IIIs as vaccine candidates against dengue virus. This work aims to evaluate the immune responses in mice to the tetravalent formulation. We demonstrate that 4 serotypes of recombinant lipidated dengue envelope protein domain III induced both humoral and cellular immunity against all 4 serotypes of dengue virus on the mixture that formed the tetravalent formulation. Importantly, the immune responses induced by the tetravalent formulation in the absence of the exogenous adjuvant were functional in clearing the 4 serotypes of dengue virus in vivo. We affirm that the tetravalent formulation of recombinant lipidated dengue envelope protein domain III is a potential vaccine candidate against dengue virus and suggest further detailed studies of this formulation in nonhuman primates. Nature Publishing Group 2016-07-29 /pmc/articles/PMC4965760/ /pubmed/27470096 http://dx.doi.org/10.1038/srep30648 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Chiang, Chen-Yi Pan, Chien-Hsiung Chen, Mei-Yu Hsieh, Chun-Hsiang Tsai, Jy-Ping Liu, Hsueh-Hung Liu, Shih-Jen Chong, Pele Leng, Chih-Hsiang Chen, Hsin-Wei Immunogenicity of a novel tetravalent vaccine formulation with four recombinant lipidated dengue envelope protein domain IIIs in mice |
title | Immunogenicity of a novel tetravalent vaccine formulation with four recombinant lipidated dengue envelope protein domain IIIs in mice |
title_full | Immunogenicity of a novel tetravalent vaccine formulation with four recombinant lipidated dengue envelope protein domain IIIs in mice |
title_fullStr | Immunogenicity of a novel tetravalent vaccine formulation with four recombinant lipidated dengue envelope protein domain IIIs in mice |
title_full_unstemmed | Immunogenicity of a novel tetravalent vaccine formulation with four recombinant lipidated dengue envelope protein domain IIIs in mice |
title_short | Immunogenicity of a novel tetravalent vaccine formulation with four recombinant lipidated dengue envelope protein domain IIIs in mice |
title_sort | immunogenicity of a novel tetravalent vaccine formulation with four recombinant lipidated dengue envelope protein domain iiis in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965760/ https://www.ncbi.nlm.nih.gov/pubmed/27470096 http://dx.doi.org/10.1038/srep30648 |
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