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Recent vaccine technology in industrial animals
Various new technologies have been applied for developing vaccines against various animal diseases. Virus-like particle (VLP) vaccine technology was used for manufacturing the porcine circovirus type 2 and RNA particle vaccines based on an alphavirus vector for porcine epidemic diarrhea (PED). Altho...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Vaccine Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742593/ https://www.ncbi.nlm.nih.gov/pubmed/26866019 http://dx.doi.org/10.7774/cevr.2016.5.1.12 |
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author | Kim, Hyunil Lee, Yoo-kyoung Kang, Sang Chul Han, Beom Ku Choi, Ki Myung |
author_facet | Kim, Hyunil Lee, Yoo-kyoung Kang, Sang Chul Han, Beom Ku Choi, Ki Myung |
author_sort | Kim, Hyunil |
collection | PubMed |
description | Various new technologies have been applied for developing vaccines against various animal diseases. Virus-like particle (VLP) vaccine technology was used for manufacturing the porcine circovirus type 2 and RNA particle vaccines based on an alphavirus vector for porcine epidemic diarrhea (PED). Although VLP is classified as a killed-virus vaccine, because its structure is similar to the original virus, it can induce long-term and cell-mediated immunity. The RNA particle vaccine used a Venezuela equine encephalitis (VEE) virus gene as a vector. The VEE virus partial gene can be substituted with the PED virus spike gene. Recombinant vaccines can be produced by substitution of the target gene in the VEE vector. Both of these new vaccine technologies made it possible to control the infectious disease efficiently in a relatively short time. |
format | Online Article Text |
id | pubmed-4742593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Korean Vaccine Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-47425932016-02-10 Recent vaccine technology in industrial animals Kim, Hyunil Lee, Yoo-kyoung Kang, Sang Chul Han, Beom Ku Choi, Ki Myung Clin Exp Vaccine Res Review Article Various new technologies have been applied for developing vaccines against various animal diseases. Virus-like particle (VLP) vaccine technology was used for manufacturing the porcine circovirus type 2 and RNA particle vaccines based on an alphavirus vector for porcine epidemic diarrhea (PED). Although VLP is classified as a killed-virus vaccine, because its structure is similar to the original virus, it can induce long-term and cell-mediated immunity. The RNA particle vaccine used a Venezuela equine encephalitis (VEE) virus gene as a vector. The VEE virus partial gene can be substituted with the PED virus spike gene. Recombinant vaccines can be produced by substitution of the target gene in the VEE vector. Both of these new vaccine technologies made it possible to control the infectious disease efficiently in a relatively short time. The Korean Vaccine Society 2016-01 2016-01-27 /pmc/articles/PMC4742593/ /pubmed/26866019 http://dx.doi.org/10.7774/cevr.2016.5.1.12 Text en © Korean Vaccine Society. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Kim, Hyunil Lee, Yoo-kyoung Kang, Sang Chul Han, Beom Ku Choi, Ki Myung Recent vaccine technology in industrial animals |
title | Recent vaccine technology in industrial animals |
title_full | Recent vaccine technology in industrial animals |
title_fullStr | Recent vaccine technology in industrial animals |
title_full_unstemmed | Recent vaccine technology in industrial animals |
title_short | Recent vaccine technology in industrial animals |
title_sort | recent vaccine technology in industrial animals |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742593/ https://www.ncbi.nlm.nih.gov/pubmed/26866019 http://dx.doi.org/10.7774/cevr.2016.5.1.12 |
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