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Immunization with Virus-Like Particle Vaccine Protects Rabbits against Hepatitis E-3 Virus Infection
Here, rabbits were immunized with a virus-like particle (VLP) vaccine prepared by expressing 239 amino acids of the swine hepatitis E virus (HEV)-3 capsid protein using a baculovirus system. Thirty specific-pathogen-free rabbits were divided into five groups (negative and positive control and 10, 50...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322348/ https://www.ncbi.nlm.nih.gov/pubmed/35891413 http://dx.doi.org/10.3390/v14071432 |
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author | Go, Hyeon-Jeong Park, Byung-Joo Ahn, Hee-Seop Han, Sang-Hoon Kim, Dong-Hwi Lyoo, Eu-Lim Kim, Da-Yoon Kim, Jae-Hyeong Lee, Joong-Bok Park, Seung-Yong Song, Chang-Seon Lee, Sang-Won Choi, Yang-Kyu Choi, In-Soo |
author_facet | Go, Hyeon-Jeong Park, Byung-Joo Ahn, Hee-Seop Han, Sang-Hoon Kim, Dong-Hwi Lyoo, Eu-Lim Kim, Da-Yoon Kim, Jae-Hyeong Lee, Joong-Bok Park, Seung-Yong Song, Chang-Seon Lee, Sang-Won Choi, Yang-Kyu Choi, In-Soo |
author_sort | Go, Hyeon-Jeong |
collection | PubMed |
description | Here, rabbits were immunized with a virus-like particle (VLP) vaccine prepared by expressing 239 amino acids of the swine hepatitis E virus (HEV)-3 capsid protein using a baculovirus system. Thirty specific-pathogen-free rabbits were divided into five groups (negative and positive control and 10, 50, and 100 μg VLP-vaccinated). Positive control group rabbits showed viremia and fecal viral shedding, whereas rabbits vaccinated with 10 μg VLP showed transient fecal viral shedding, and rabbits vaccinated with 50 and 100 μg VLP did not show viremia or fecal viral shedding. Serum anti-HEV antibody titers increased in a dose-dependent manner. Anti-HEV antibody titers were significantly higher (p < 0.05) in 100 μg VLP-vaccinated rabbits than in the negative control rabbits at week 4. Anti-HEV antibody titers were significantly higher in 50 and 10 μg VLP-vaccinated rabbits than in the negative control rabbits at weeks 8 and 11, respectively. Serum IFN-γ and IL-12 levels were significantly higher (p < 0.01) in rabbits vaccinated with 50 and 100 μg VLP than in the negative control rabbits at weeks 4 and 6. Liver tissues of 50 and 100 μg VLP-vaccinated rabbits displayed significantly less (p < 0.05) fibrosis than those of the positive control rabbits. The prepared VLP vaccine demonstrated dose-dependent immunogenicity sufficient for inducing anti-HEV antibody production, thus protecting rabbits against swine HEV-3. |
format | Online Article Text |
id | pubmed-9322348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93223482022-07-27 Immunization with Virus-Like Particle Vaccine Protects Rabbits against Hepatitis E-3 Virus Infection Go, Hyeon-Jeong Park, Byung-Joo Ahn, Hee-Seop Han, Sang-Hoon Kim, Dong-Hwi Lyoo, Eu-Lim Kim, Da-Yoon Kim, Jae-Hyeong Lee, Joong-Bok Park, Seung-Yong Song, Chang-Seon Lee, Sang-Won Choi, Yang-Kyu Choi, In-Soo Viruses Article Here, rabbits were immunized with a virus-like particle (VLP) vaccine prepared by expressing 239 amino acids of the swine hepatitis E virus (HEV)-3 capsid protein using a baculovirus system. Thirty specific-pathogen-free rabbits were divided into five groups (negative and positive control and 10, 50, and 100 μg VLP-vaccinated). Positive control group rabbits showed viremia and fecal viral shedding, whereas rabbits vaccinated with 10 μg VLP showed transient fecal viral shedding, and rabbits vaccinated with 50 and 100 μg VLP did not show viremia or fecal viral shedding. Serum anti-HEV antibody titers increased in a dose-dependent manner. Anti-HEV antibody titers were significantly higher (p < 0.05) in 100 μg VLP-vaccinated rabbits than in the negative control rabbits at week 4. Anti-HEV antibody titers were significantly higher in 50 and 10 μg VLP-vaccinated rabbits than in the negative control rabbits at weeks 8 and 11, respectively. Serum IFN-γ and IL-12 levels were significantly higher (p < 0.01) in rabbits vaccinated with 50 and 100 μg VLP than in the negative control rabbits at weeks 4 and 6. Liver tissues of 50 and 100 μg VLP-vaccinated rabbits displayed significantly less (p < 0.05) fibrosis than those of the positive control rabbits. The prepared VLP vaccine demonstrated dose-dependent immunogenicity sufficient for inducing anti-HEV antibody production, thus protecting rabbits against swine HEV-3. MDPI 2022-06-29 /pmc/articles/PMC9322348/ /pubmed/35891413 http://dx.doi.org/10.3390/v14071432 Text en © 2022 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 Go, Hyeon-Jeong Park, Byung-Joo Ahn, Hee-Seop Han, Sang-Hoon Kim, Dong-Hwi Lyoo, Eu-Lim Kim, Da-Yoon Kim, Jae-Hyeong Lee, Joong-Bok Park, Seung-Yong Song, Chang-Seon Lee, Sang-Won Choi, Yang-Kyu Choi, In-Soo Immunization with Virus-Like Particle Vaccine Protects Rabbits against Hepatitis E-3 Virus Infection |
title | Immunization with Virus-Like Particle Vaccine Protects Rabbits against Hepatitis E-3 Virus Infection |
title_full | Immunization with Virus-Like Particle Vaccine Protects Rabbits against Hepatitis E-3 Virus Infection |
title_fullStr | Immunization with Virus-Like Particle Vaccine Protects Rabbits against Hepatitis E-3 Virus Infection |
title_full_unstemmed | Immunization with Virus-Like Particle Vaccine Protects Rabbits against Hepatitis E-3 Virus Infection |
title_short | Immunization with Virus-Like Particle Vaccine Protects Rabbits against Hepatitis E-3 Virus Infection |
title_sort | immunization with virus-like particle vaccine protects rabbits against hepatitis e-3 virus infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322348/ https://www.ncbi.nlm.nih.gov/pubmed/35891413 http://dx.doi.org/10.3390/v14071432 |
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