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Application of red clover isoflavone extract as an adjuvant in mice

In the present study, the safety of red clover isoflavone extract (RCIE) and its potential adjuvant effects on the cellular and humoral immune responses to ovalbumin (OVA) were evaluated using an ICR mouse model. On day 1, the mice were first subcutaneously immunized with 100 µg OVA, 100 µg OVA + 20...

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Autores principales: Chen, Hongbo, Zhang, Xue, Liu, Longsi, Cai, Mingqin, Guo, Zhijun, Qiu, Longxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966154/
https://www.ncbi.nlm.nih.gov/pubmed/32010286
http://dx.doi.org/10.3892/etm.2019.8315
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author Chen, Hongbo
Zhang, Xue
Liu, Longsi
Cai, Mingqin
Guo, Zhijun
Qiu, Longxin
author_facet Chen, Hongbo
Zhang, Xue
Liu, Longsi
Cai, Mingqin
Guo, Zhijun
Qiu, Longxin
author_sort Chen, Hongbo
collection PubMed
description In the present study, the safety of red clover isoflavone extract (RCIE) and its potential adjuvant effects on the cellular and humoral immune responses to ovalbumin (OVA) were evaluated using an ICR mouse model. On day 1, the mice were first subcutaneously immunized with 100 µg OVA, 100 µg OVA + 200 µg aluminum hydroxide gel (alum) or OVA + 50, 100 or 200 µg RCIE (RCIE + OVA), following which booster immunization was performed on day 15. After 2 weeks, the stimulation of splenocyte proliferation and levels of serum antibodies were measured. No notable stress responses were observed after the initial and booster immunization. Splenocyte proliferation was significantly increased in mice immunized with OVA + 100 µg RCIE (P<0.01). The levels of IgG, IgG1 and IgG2a antibodies in serum were also significantly increased in OVA + RCIE groups compared with the OVA control group (P<0.05). In the OVA + RCIE groups, serum levels of interleukin (IL)-2, interferon-γ (IFN-γ) and IL-10 were increased, and the mRNA expression levels of IL-2, IFN-γ, IL-4, IL-10, T-bet and GATA-3 were also significantly increased compared with the OVA control group (P<0.05) in splenocytes. In addition, as an adjuvant, RCIE significantly increased the survival rates of mice inoculated with an E. coli vaccine and enhanced the early immune protection against pathogenic E. coli. In conclusion, these findings suggest that RCIE can be used as a safe vaccine adjuvant and supports its use in clinical applications.
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spelling pubmed-69661542020-01-31 Application of red clover isoflavone extract as an adjuvant in mice Chen, Hongbo Zhang, Xue Liu, Longsi Cai, Mingqin Guo, Zhijun Qiu, Longxin Exp Ther Med Articles In the present study, the safety of red clover isoflavone extract (RCIE) and its potential adjuvant effects on the cellular and humoral immune responses to ovalbumin (OVA) were evaluated using an ICR mouse model. On day 1, the mice were first subcutaneously immunized with 100 µg OVA, 100 µg OVA + 200 µg aluminum hydroxide gel (alum) or OVA + 50, 100 or 200 µg RCIE (RCIE + OVA), following which booster immunization was performed on day 15. After 2 weeks, the stimulation of splenocyte proliferation and levels of serum antibodies were measured. No notable stress responses were observed after the initial and booster immunization. Splenocyte proliferation was significantly increased in mice immunized with OVA + 100 µg RCIE (P<0.01). The levels of IgG, IgG1 and IgG2a antibodies in serum were also significantly increased in OVA + RCIE groups compared with the OVA control group (P<0.05). In the OVA + RCIE groups, serum levels of interleukin (IL)-2, interferon-γ (IFN-γ) and IL-10 were increased, and the mRNA expression levels of IL-2, IFN-γ, IL-4, IL-10, T-bet and GATA-3 were also significantly increased compared with the OVA control group (P<0.05) in splenocytes. In addition, as an adjuvant, RCIE significantly increased the survival rates of mice inoculated with an E. coli vaccine and enhanced the early immune protection against pathogenic E. coli. In conclusion, these findings suggest that RCIE can be used as a safe vaccine adjuvant and supports its use in clinical applications. D.A. Spandidos 2020-02 2019-12-11 /pmc/articles/PMC6966154/ /pubmed/32010286 http://dx.doi.org/10.3892/etm.2019.8315 Text en Copyright: © Chen et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Chen, Hongbo
Zhang, Xue
Liu, Longsi
Cai, Mingqin
Guo, Zhijun
Qiu, Longxin
Application of red clover isoflavone extract as an adjuvant in mice
title Application of red clover isoflavone extract as an adjuvant in mice
title_full Application of red clover isoflavone extract as an adjuvant in mice
title_fullStr Application of red clover isoflavone extract as an adjuvant in mice
title_full_unstemmed Application of red clover isoflavone extract as an adjuvant in mice
title_short Application of red clover isoflavone extract as an adjuvant in mice
title_sort application of red clover isoflavone extract as an adjuvant in mice
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966154/
https://www.ncbi.nlm.nih.gov/pubmed/32010286
http://dx.doi.org/10.3892/etm.2019.8315
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