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Early IgG Response to Foot and Mouth Disease Vaccine Formulated with a Vegetable Oil Adjuvant
The present study evaluated soybean oil (SO) containing vitamin E (VE) and ginseng saponins (GS) (SO-VE-GS) for their adjuvant effect on foot-and-mouth disease (FMD) vaccine. Since mineral oil ISA 206 is a common adjuvant used in the FMD vaccine, it was used as a control adjuvant in this study. VE a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963984/ https://www.ncbi.nlm.nih.gov/pubmed/31600943 http://dx.doi.org/10.3390/vaccines7040143 |
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author | Cui, Xuemei Wang, Yong Maqbool, Babar Yuan, Lijia He, Shanshan Zhang, Cenrong Xu, Wei Hu, Songhua |
author_facet | Cui, Xuemei Wang, Yong Maqbool, Babar Yuan, Lijia He, Shanshan Zhang, Cenrong Xu, Wei Hu, Songhua |
author_sort | Cui, Xuemei |
collection | PubMed |
description | The present study evaluated soybean oil (SO) containing vitamin E (VE) and ginseng saponins (GS) (SO-VE-GS) for their adjuvant effect on foot-and-mouth disease (FMD) vaccine. Since mineral oil ISA 206 is a common adjuvant used in the FMD vaccine, it was used as a control adjuvant in this study. VE and GS were found to have a synergistic adjuvant effect. When mice were immunized with the FMD vaccine emulsified in SO with VE and GS, significantly higher serum IgG, IgG1, and IgG2a were found than VE and GS used alone. SO-VE-GS and ISA 206 behaved differently in adjuvant activities. When mice were immunized with the FMD vaccine adjuvanted with SO-VE-GS, significantly higher and earlier production of serum IgG was found than that adjuvanted with ISA 206. Although both adjuvants significantly increased the number of bone marrow plasma cells, a stimulation index of lymphocytes (SI) as well as the production of IL-4 and IL-6, SO-VE-GS promoted significantly higher SI and the ratio of CD4(+)/CD8(+) T cells with production of increased IFN-γ and decreased TGF-β1 as compared with the ISA 206 group. The data suggested that SO-VE-GS activated Th1/Th2 immune responses. Transcriptome analysis of splenocytes showed that differentially expressed genes (DEGs), immune-related gene ontology (GO) terms, and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways were significantly enriched in the SO-VE-GS group. Therefore, the potent adjuvant effect of SO-VE-GS on the FMD vaccine may be attributed to the immune-related gene profile expressed in lymphocytes. Due to its plant origin and due to being much cheaper than imported mineral oil ISA 206, SO-VE-GS deserves further study in relation to vaccines used in food animals. |
format | Online Article Text |
id | pubmed-6963984 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69639842020-01-27 Early IgG Response to Foot and Mouth Disease Vaccine Formulated with a Vegetable Oil Adjuvant Cui, Xuemei Wang, Yong Maqbool, Babar Yuan, Lijia He, Shanshan Zhang, Cenrong Xu, Wei Hu, Songhua Vaccines (Basel) Article The present study evaluated soybean oil (SO) containing vitamin E (VE) and ginseng saponins (GS) (SO-VE-GS) for their adjuvant effect on foot-and-mouth disease (FMD) vaccine. Since mineral oil ISA 206 is a common adjuvant used in the FMD vaccine, it was used as a control adjuvant in this study. VE and GS were found to have a synergistic adjuvant effect. When mice were immunized with the FMD vaccine emulsified in SO with VE and GS, significantly higher serum IgG, IgG1, and IgG2a were found than VE and GS used alone. SO-VE-GS and ISA 206 behaved differently in adjuvant activities. When mice were immunized with the FMD vaccine adjuvanted with SO-VE-GS, significantly higher and earlier production of serum IgG was found than that adjuvanted with ISA 206. Although both adjuvants significantly increased the number of bone marrow plasma cells, a stimulation index of lymphocytes (SI) as well as the production of IL-4 and IL-6, SO-VE-GS promoted significantly higher SI and the ratio of CD4(+)/CD8(+) T cells with production of increased IFN-γ and decreased TGF-β1 as compared with the ISA 206 group. The data suggested that SO-VE-GS activated Th1/Th2 immune responses. Transcriptome analysis of splenocytes showed that differentially expressed genes (DEGs), immune-related gene ontology (GO) terms, and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways were significantly enriched in the SO-VE-GS group. Therefore, the potent adjuvant effect of SO-VE-GS on the FMD vaccine may be attributed to the immune-related gene profile expressed in lymphocytes. Due to its plant origin and due to being much cheaper than imported mineral oil ISA 206, SO-VE-GS deserves further study in relation to vaccines used in food animals. MDPI 2019-10-09 /pmc/articles/PMC6963984/ /pubmed/31600943 http://dx.doi.org/10.3390/vaccines7040143 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Cui, Xuemei Wang, Yong Maqbool, Babar Yuan, Lijia He, Shanshan Zhang, Cenrong Xu, Wei Hu, Songhua Early IgG Response to Foot and Mouth Disease Vaccine Formulated with a Vegetable Oil Adjuvant |
title | Early IgG Response to Foot and Mouth Disease Vaccine Formulated with a Vegetable Oil Adjuvant |
title_full | Early IgG Response to Foot and Mouth Disease Vaccine Formulated with a Vegetable Oil Adjuvant |
title_fullStr | Early IgG Response to Foot and Mouth Disease Vaccine Formulated with a Vegetable Oil Adjuvant |
title_full_unstemmed | Early IgG Response to Foot and Mouth Disease Vaccine Formulated with a Vegetable Oil Adjuvant |
title_short | Early IgG Response to Foot and Mouth Disease Vaccine Formulated with a Vegetable Oil Adjuvant |
title_sort | early igg response to foot and mouth disease vaccine formulated with a vegetable oil adjuvant |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963984/ https://www.ncbi.nlm.nih.gov/pubmed/31600943 http://dx.doi.org/10.3390/vaccines7040143 |
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