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A Novel Recombinant Virus-Like Particles Displaying B and T Cell Epitopes of Japanese Encephalitis Virus Offers Protective Immunity in Mice and Guinea Pigs
Virus-like particles (VLPs) are non-replicative vectors for the delivery of heterologous epitopes and are considered one of the most potent inducers of cellular and humoral immune responses in mice and guinea pigs. In the present study, VLP-JEVe was constructed by the insertion of six Japanese encep...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473392/ https://www.ncbi.nlm.nih.gov/pubmed/34579217 http://dx.doi.org/10.3390/vaccines9090980 |
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author | Anwar, Muhammad Naveed Jiang, Chunying Di, Di Zhang, Junjie Guo, Shuang Wang, Xin Hameed, Muddassar Wahaab, Abdul Shao, Donghua Li, Zongjie Liu, Ke Li, Beibei Qiu, Yafeng Ma, Zhiyong Wei, Jianchao |
author_facet | Anwar, Muhammad Naveed Jiang, Chunying Di, Di Zhang, Junjie Guo, Shuang Wang, Xin Hameed, Muddassar Wahaab, Abdul Shao, Donghua Li, Zongjie Liu, Ke Li, Beibei Qiu, Yafeng Ma, Zhiyong Wei, Jianchao |
author_sort | Anwar, Muhammad Naveed |
collection | PubMed |
description | Virus-like particles (VLPs) are non-replicative vectors for the delivery of heterologous epitopes and are considered one of the most potent inducers of cellular and humoral immune responses in mice and guinea pigs. In the present study, VLP-JEVe was constructed by the insertion of six Japanese encephalitis virus (JEV) envelope protein epitopes into different surface loop regions of PPV VP2 by the substitution of specific amino acid sequences without altering the assembly of the virus; subsequently, the protective efficacy of this VLP-JEVe was evaluated against JEV challenge in mice and guinea pigs. Mice immunized with the VLP-JEVe antigen developed high titers of neutralizing antibodies and 100% protection against lethal JEV challenge. The neutralizing and hemagglutination inhibition (HI) antibody responses were also induced in guinea pigs vaccinated with VLP-JEVe. In addition, immunization with VLP-JEVe in mice induced effective neutralizing antibodies and protective immunity against PPV (porcine parvovirus) challenge in guinea pigs. These studies suggest that VLP-JEVe produced as described here could be a potential candidate for vaccine development. |
format | Online Article Text |
id | pubmed-8473392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84733922021-09-28 A Novel Recombinant Virus-Like Particles Displaying B and T Cell Epitopes of Japanese Encephalitis Virus Offers Protective Immunity in Mice and Guinea Pigs Anwar, Muhammad Naveed Jiang, Chunying Di, Di Zhang, Junjie Guo, Shuang Wang, Xin Hameed, Muddassar Wahaab, Abdul Shao, Donghua Li, Zongjie Liu, Ke Li, Beibei Qiu, Yafeng Ma, Zhiyong Wei, Jianchao Vaccines (Basel) Article Virus-like particles (VLPs) are non-replicative vectors for the delivery of heterologous epitopes and are considered one of the most potent inducers of cellular and humoral immune responses in mice and guinea pigs. In the present study, VLP-JEVe was constructed by the insertion of six Japanese encephalitis virus (JEV) envelope protein epitopes into different surface loop regions of PPV VP2 by the substitution of specific amino acid sequences without altering the assembly of the virus; subsequently, the protective efficacy of this VLP-JEVe was evaluated against JEV challenge in mice and guinea pigs. Mice immunized with the VLP-JEVe antigen developed high titers of neutralizing antibodies and 100% protection against lethal JEV challenge. The neutralizing and hemagglutination inhibition (HI) antibody responses were also induced in guinea pigs vaccinated with VLP-JEVe. In addition, immunization with VLP-JEVe in mice induced effective neutralizing antibodies and protective immunity against PPV (porcine parvovirus) challenge in guinea pigs. These studies suggest that VLP-JEVe produced as described here could be a potential candidate for vaccine development. MDPI 2021-09-02 /pmc/articles/PMC8473392/ /pubmed/34579217 http://dx.doi.org/10.3390/vaccines9090980 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Anwar, Muhammad Naveed Jiang, Chunying Di, Di Zhang, Junjie Guo, Shuang Wang, Xin Hameed, Muddassar Wahaab, Abdul Shao, Donghua Li, Zongjie Liu, Ke Li, Beibei Qiu, Yafeng Ma, Zhiyong Wei, Jianchao A Novel Recombinant Virus-Like Particles Displaying B and T Cell Epitopes of Japanese Encephalitis Virus Offers Protective Immunity in Mice and Guinea Pigs |
title | A Novel Recombinant Virus-Like Particles Displaying B and T Cell Epitopes of Japanese Encephalitis Virus Offers Protective Immunity in Mice and Guinea Pigs |
title_full | A Novel Recombinant Virus-Like Particles Displaying B and T Cell Epitopes of Japanese Encephalitis Virus Offers Protective Immunity in Mice and Guinea Pigs |
title_fullStr | A Novel Recombinant Virus-Like Particles Displaying B and T Cell Epitopes of Japanese Encephalitis Virus Offers Protective Immunity in Mice and Guinea Pigs |
title_full_unstemmed | A Novel Recombinant Virus-Like Particles Displaying B and T Cell Epitopes of Japanese Encephalitis Virus Offers Protective Immunity in Mice and Guinea Pigs |
title_short | A Novel Recombinant Virus-Like Particles Displaying B and T Cell Epitopes of Japanese Encephalitis Virus Offers Protective Immunity in Mice and Guinea Pigs |
title_sort | novel recombinant virus-like particles displaying b and t cell epitopes of japanese encephalitis virus offers protective immunity in mice and guinea pigs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473392/ https://www.ncbi.nlm.nih.gov/pubmed/34579217 http://dx.doi.org/10.3390/vaccines9090980 |
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