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Oral administration of PPC enhances antigen-specific CD8(+ )T cell responses while reducing IgE levels in sensitized mice

BACKGROUND: For almost 2000 years it has been recognized that aqueous extracts from pine cones possess medicinal properties beneficial for the treatment of a broad variety of diseases and conditions. In this report, the ability of an orally administered poly phenylpropanoid-polysaccharide rich extra...

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Autores principales: Burrows, Mike, Assundani, Deepak, Celis, Esteban, Tufaro, Frank, Tanaka, Akiko, Bradley, W Guy
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2794845/
https://www.ncbi.nlm.nih.gov/pubmed/19948039
http://dx.doi.org/10.1186/1472-6882-9-49
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author Burrows, Mike
Assundani, Deepak
Celis, Esteban
Tufaro, Frank
Tanaka, Akiko
Bradley, W Guy
author_facet Burrows, Mike
Assundani, Deepak
Celis, Esteban
Tufaro, Frank
Tanaka, Akiko
Bradley, W Guy
author_sort Burrows, Mike
collection PubMed
description BACKGROUND: For almost 2000 years it has been recognized that aqueous extracts from pine cones possess medicinal properties beneficial for the treatment of a broad variety of diseases and conditions. In this report, the ability of an orally administered poly phenylpropanoid-polysaccharide rich extract of pine cones (PPC) to suppress the generation of IgE and to significantly enhance antigen-specific cellular responses to a variety of vaccines was tested. METHODS: A variety of vaccine protocols were utilized to determine the affects of orally administered PPC on the Th1/Th2 cytokine balance, the production of IgE antibodies, and the generation of antigen-specific cytotoxic T cells. The effect of PPC on the Th1/Th2 balance in aged mice was also investigated. RESULTS: Oral delivery of PPC was found to significantly suppress serum IgE levels in naïve mice and in mice sensitized to ovalbumin. PPC was also found to enhance the generation of antigen-specific CD8(+ )T cells in mice immunized with DNA, dendritic cell, and soluble protein vaccines. The suppression of IgE was associated with reduction of IL-4 secretion and the enhanced production of IL-12 and IFN(γ )by antigen-stimulated splenocytes from PPC treated mice. PPC also suppressed the Th2 response and enhanced the Th1 response of splenocytes from aged mice. CONCLUSION: Oral delivery of PPC enhances the generation of an antigen-specific CD8(+ )T cell responses induced by soluble protein, DNA, and dendritic cell vaccines while at the same time suppressing the generation of a Th2 dominant IgE response. This effect on the Th1/Th2 balance was also observed in aged mice.
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spelling pubmed-27948452009-12-17 Oral administration of PPC enhances antigen-specific CD8(+ )T cell responses while reducing IgE levels in sensitized mice Burrows, Mike Assundani, Deepak Celis, Esteban Tufaro, Frank Tanaka, Akiko Bradley, W Guy BMC Complement Altern Med Research article BACKGROUND: For almost 2000 years it has been recognized that aqueous extracts from pine cones possess medicinal properties beneficial for the treatment of a broad variety of diseases and conditions. In this report, the ability of an orally administered poly phenylpropanoid-polysaccharide rich extract of pine cones (PPC) to suppress the generation of IgE and to significantly enhance antigen-specific cellular responses to a variety of vaccines was tested. METHODS: A variety of vaccine protocols were utilized to determine the affects of orally administered PPC on the Th1/Th2 cytokine balance, the production of IgE antibodies, and the generation of antigen-specific cytotoxic T cells. The effect of PPC on the Th1/Th2 balance in aged mice was also investigated. RESULTS: Oral delivery of PPC was found to significantly suppress serum IgE levels in naïve mice and in mice sensitized to ovalbumin. PPC was also found to enhance the generation of antigen-specific CD8(+ )T cells in mice immunized with DNA, dendritic cell, and soluble protein vaccines. The suppression of IgE was associated with reduction of IL-4 secretion and the enhanced production of IL-12 and IFN(γ )by antigen-stimulated splenocytes from PPC treated mice. PPC also suppressed the Th2 response and enhanced the Th1 response of splenocytes from aged mice. CONCLUSION: Oral delivery of PPC enhances the generation of an antigen-specific CD8(+ )T cell responses induced by soluble protein, DNA, and dendritic cell vaccines while at the same time suppressing the generation of a Th2 dominant IgE response. This effect on the Th1/Th2 balance was also observed in aged mice. BioMed Central 2009-11-30 /pmc/articles/PMC2794845/ /pubmed/19948039 http://dx.doi.org/10.1186/1472-6882-9-49 Text en Copyright ©2009 Burrows et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Burrows, Mike
Assundani, Deepak
Celis, Esteban
Tufaro, Frank
Tanaka, Akiko
Bradley, W Guy
Oral administration of PPC enhances antigen-specific CD8(+ )T cell responses while reducing IgE levels in sensitized mice
title Oral administration of PPC enhances antigen-specific CD8(+ )T cell responses while reducing IgE levels in sensitized mice
title_full Oral administration of PPC enhances antigen-specific CD8(+ )T cell responses while reducing IgE levels in sensitized mice
title_fullStr Oral administration of PPC enhances antigen-specific CD8(+ )T cell responses while reducing IgE levels in sensitized mice
title_full_unstemmed Oral administration of PPC enhances antigen-specific CD8(+ )T cell responses while reducing IgE levels in sensitized mice
title_short Oral administration of PPC enhances antigen-specific CD8(+ )T cell responses while reducing IgE levels in sensitized mice
title_sort oral administration of ppc enhances antigen-specific cd8(+ )t cell responses while reducing ige levels in sensitized mice
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2794845/
https://www.ncbi.nlm.nih.gov/pubmed/19948039
http://dx.doi.org/10.1186/1472-6882-9-49
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