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Transcutaneous pollinosis immunotherapy using a solid‐in‐oil nanodispersion system carrying T cell epitope peptide and R848

Antigen‐specific immunotherapy is the only curative approach for the treatment of allergic diseases such as Japanese cedar pollinosis. Immunotherapy using a T cell epitope vaccine in combination with the adjuvant R848 is of particular interest as a safe and effective approach to treat allergic disea...

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Autores principales: Kitaoka, Momoko, Naritomi, Ayaka, Kawabe, Yoshinori, Kamihira, Masamichi, Kamiya, Noriho, Goto, Masahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689524/
https://www.ncbi.nlm.nih.gov/pubmed/29313026
http://dx.doi.org/10.1002/btm2.10048
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author Kitaoka, Momoko
Naritomi, Ayaka
Kawabe, Yoshinori
Kamihira, Masamichi
Kamiya, Noriho
Goto, Masahiro
author_facet Kitaoka, Momoko
Naritomi, Ayaka
Kawabe, Yoshinori
Kamihira, Masamichi
Kamiya, Noriho
Goto, Masahiro
author_sort Kitaoka, Momoko
collection PubMed
description Antigen‐specific immunotherapy is the only curative approach for the treatment of allergic diseases such as Japanese cedar pollinosis. Immunotherapy using a T cell epitope vaccine in combination with the adjuvant R848 is of particular interest as a safe and effective approach to treat allergic diseases. Herein, we propose a simple and easy to handle vaccine administration method using the original solid‐in‐oil (S/O) nanodispersion system that permeates through the skin. The S/O nanodispersion system is composed of nanoparticles of hydrophilic molecules surrounded with hydrophobic surfactants that are dispersed in an oil vehicle. The system has potential to carry and deliver both hydrophilic and hydrophobic bioactives. Hydrophilic T cell epitope peptide was efficiently delivered through mouse skin using the S/O nanodispersion system and lowered antigen‐specific IgE levels in pollinosis model mice. Addition of the hydrophobic adju1vant R848 significantly lowered the antibody secretion and shifted the Th1/Th2‐balance toward Th1‐type immunity in the model mice, showing the potential to alleviate Japanese cedar pollinosis.
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spelling pubmed-56895242018-01-08 Transcutaneous pollinosis immunotherapy using a solid‐in‐oil nanodispersion system carrying T cell epitope peptide and R848 Kitaoka, Momoko Naritomi, Ayaka Kawabe, Yoshinori Kamihira, Masamichi Kamiya, Noriho Goto, Masahiro Bioeng Transl Med Research Reports Antigen‐specific immunotherapy is the only curative approach for the treatment of allergic diseases such as Japanese cedar pollinosis. Immunotherapy using a T cell epitope vaccine in combination with the adjuvant R848 is of particular interest as a safe and effective approach to treat allergic diseases. Herein, we propose a simple and easy to handle vaccine administration method using the original solid‐in‐oil (S/O) nanodispersion system that permeates through the skin. The S/O nanodispersion system is composed of nanoparticles of hydrophilic molecules surrounded with hydrophobic surfactants that are dispersed in an oil vehicle. The system has potential to carry and deliver both hydrophilic and hydrophobic bioactives. Hydrophilic T cell epitope peptide was efficiently delivered through mouse skin using the S/O nanodispersion system and lowered antigen‐specific IgE levels in pollinosis model mice. Addition of the hydrophobic adju1vant R848 significantly lowered the antibody secretion and shifted the Th1/Th2‐balance toward Th1‐type immunity in the model mice, showing the potential to alleviate Japanese cedar pollinosis. John Wiley and Sons Inc. 2017-02-03 /pmc/articles/PMC5689524/ /pubmed/29313026 http://dx.doi.org/10.1002/btm2.10048 Text en © 2017 The Authors. Bioengineering & Translational Medicine is published by Wiley Periodicals, Inc. on behalf of The American Institute of Chemical Engineers This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Reports
Kitaoka, Momoko
Naritomi, Ayaka
Kawabe, Yoshinori
Kamihira, Masamichi
Kamiya, Noriho
Goto, Masahiro
Transcutaneous pollinosis immunotherapy using a solid‐in‐oil nanodispersion system carrying T cell epitope peptide and R848
title Transcutaneous pollinosis immunotherapy using a solid‐in‐oil nanodispersion system carrying T cell epitope peptide and R848
title_full Transcutaneous pollinosis immunotherapy using a solid‐in‐oil nanodispersion system carrying T cell epitope peptide and R848
title_fullStr Transcutaneous pollinosis immunotherapy using a solid‐in‐oil nanodispersion system carrying T cell epitope peptide and R848
title_full_unstemmed Transcutaneous pollinosis immunotherapy using a solid‐in‐oil nanodispersion system carrying T cell epitope peptide and R848
title_short Transcutaneous pollinosis immunotherapy using a solid‐in‐oil nanodispersion system carrying T cell epitope peptide and R848
title_sort transcutaneous pollinosis immunotherapy using a solid‐in‐oil nanodispersion system carrying t cell epitope peptide and r848
topic Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689524/
https://www.ncbi.nlm.nih.gov/pubmed/29313026
http://dx.doi.org/10.1002/btm2.10048
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