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pH-Responsive Micelle-Based Cytoplasmic Delivery System for Induction of Cellular Immunity

(1) Background: Cytoplasmic delivery of antigens is crucial for the induction of cellular immunity, which is an important immune response for the treatment of cancer and infectious diseases. To date, fusogenic protein-incorporated liposomes and pH-responsive polymer-modified liposomes have been used...

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Autores principales: Yuba, Eiji, Sakaguchi, Naoki, Kanda, Yuhei, Miyazaki, Maiko, Koiwai, Kazunori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748608/
https://www.ncbi.nlm.nih.gov/pubmed/29113042
http://dx.doi.org/10.3390/vaccines5040041
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author Yuba, Eiji
Sakaguchi, Naoki
Kanda, Yuhei
Miyazaki, Maiko
Koiwai, Kazunori
author_facet Yuba, Eiji
Sakaguchi, Naoki
Kanda, Yuhei
Miyazaki, Maiko
Koiwai, Kazunori
author_sort Yuba, Eiji
collection PubMed
description (1) Background: Cytoplasmic delivery of antigens is crucial for the induction of cellular immunity, which is an important immune response for the treatment of cancer and infectious diseases. To date, fusogenic protein-incorporated liposomes and pH-responsive polymer-modified liposomes have been used to achieve cytoplasmic delivery of antigen via membrane rupture or fusion with endosomes. However, a more versatile cytoplasmic delivery system is desired for practical use. For this study, we developed pH-responsive micelles composed of dilauroyl phosphatidylcholine (DLPC) and deoxycholic acid and investigated their cytoplasmic delivery performance and immunity-inducing capability. (2) Methods: Interaction of micelles with fluorescence dye-loaded liposomes, intracellular distribution of micelles, and antigenic proteins were observed. Finally, antigen-specific cellular immune response was evaluated in vivo using ELIspot assay. (3) Results: Micelles induced leakage of contents from liposomes via lipid mixing at low pH. Micelles were taken up by dendritic cells mainly via macropinocytosis and delivered ovalbumin (OVA) into the cytosol. After intradermal injection of micelles and OVA, OVA-specific cellular immunity was induced in the spleen. (4) Conclusions: pH-responsive micelles composed of DLPC and deoxycholic acid are promising as enhancers of cytosol delivery of antigens and the induction capability of cellular immunity for the treatment of cancer immunotherapy and infectious diseases.
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spelling pubmed-57486082018-01-07 pH-Responsive Micelle-Based Cytoplasmic Delivery System for Induction of Cellular Immunity Yuba, Eiji Sakaguchi, Naoki Kanda, Yuhei Miyazaki, Maiko Koiwai, Kazunori Vaccines (Basel) Article (1) Background: Cytoplasmic delivery of antigens is crucial for the induction of cellular immunity, which is an important immune response for the treatment of cancer and infectious diseases. To date, fusogenic protein-incorporated liposomes and pH-responsive polymer-modified liposomes have been used to achieve cytoplasmic delivery of antigen via membrane rupture or fusion with endosomes. However, a more versatile cytoplasmic delivery system is desired for practical use. For this study, we developed pH-responsive micelles composed of dilauroyl phosphatidylcholine (DLPC) and deoxycholic acid and investigated their cytoplasmic delivery performance and immunity-inducing capability. (2) Methods: Interaction of micelles with fluorescence dye-loaded liposomes, intracellular distribution of micelles, and antigenic proteins were observed. Finally, antigen-specific cellular immune response was evaluated in vivo using ELIspot assay. (3) Results: Micelles induced leakage of contents from liposomes via lipid mixing at low pH. Micelles were taken up by dendritic cells mainly via macropinocytosis and delivered ovalbumin (OVA) into the cytosol. After intradermal injection of micelles and OVA, OVA-specific cellular immunity was induced in the spleen. (4) Conclusions: pH-responsive micelles composed of DLPC and deoxycholic acid are promising as enhancers of cytosol delivery of antigens and the induction capability of cellular immunity for the treatment of cancer immunotherapy and infectious diseases. MDPI 2017-11-04 /pmc/articles/PMC5748608/ /pubmed/29113042 http://dx.doi.org/10.3390/vaccines5040041 Text en © 2017 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
Yuba, Eiji
Sakaguchi, Naoki
Kanda, Yuhei
Miyazaki, Maiko
Koiwai, Kazunori
pH-Responsive Micelle-Based Cytoplasmic Delivery System for Induction of Cellular Immunity
title pH-Responsive Micelle-Based Cytoplasmic Delivery System for Induction of Cellular Immunity
title_full pH-Responsive Micelle-Based Cytoplasmic Delivery System for Induction of Cellular Immunity
title_fullStr pH-Responsive Micelle-Based Cytoplasmic Delivery System for Induction of Cellular Immunity
title_full_unstemmed pH-Responsive Micelle-Based Cytoplasmic Delivery System for Induction of Cellular Immunity
title_short pH-Responsive Micelle-Based Cytoplasmic Delivery System for Induction of Cellular Immunity
title_sort ph-responsive micelle-based cytoplasmic delivery system for induction of cellular immunity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748608/
https://www.ncbi.nlm.nih.gov/pubmed/29113042
http://dx.doi.org/10.3390/vaccines5040041
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