CD11c-specific bio-nanocapsule enhances vaccine immunogenicity by targeting immune cells
Abstract Background Various nanocarriers have been used to deliver subunit vaccines specifically to dendritic cells (DCs) for the improvement of immunogenicity. However, due to their insufficient DC priming ability, these vaccines could not elicit effective innate immunity. We have recently develope...
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doaj-81e749a58d104ce4aefe4a8ccc2d29dd2020-11-25T02:11:16ZengBMCJournal of Nanobiotechnology1477-31552018-08-0116111210.1186/s12951-018-0386-6CD11c-specific bio-nanocapsule enhances vaccine immunogenicity by targeting immune cellsHidenori Matsuo0Masaharu Somiya1Masumi Iijima2Takeshi Arakawa3Shun’ichi Kuroda4Graduate School of Bioagricultural Sciences, Nagoya UniversityDepartment of Biomolecular Science and Reaction, The Institute of Scientific and Industrial Research, Osaka UniversityGraduate School of Bioagricultural Sciences, Nagoya UniversityCOMB, Tropical Biosphere Research Center, University of the RyukyusGraduate School of Bioagricultural Sciences, Nagoya UniversityAbstract Background Various nanocarriers have been used to deliver subunit vaccines specifically to dendritic cells (DCs) for the improvement of immunogenicity. However, due to their insufficient DC priming ability, these vaccines could not elicit effective innate immunity. We have recently developed a DC-targeting bio-nanocapsule (BNC) by displaying anti-CD11c IgGs via protein A-derived IgG Fc-binding Z domain on the hepatitis B virus envelope L protein particles (α-DC-ZZ-BNC). Results After the chemical modification with antigens (Ags), the α-DC-ZZ-BNC-Ag complex could deliver Ags to DCs efficiently, leading to effective DC maturation and efficient endosomal escape of Ags, followed by Ag-specific T cell responses and IgG productions. Moreover, the α-DC-ZZ-BNC modified with Japanese encephalitis virus (JEV) envelope-derived D3 Ags could confer protection against 50-fold lethal dose of JEV injection on mice. Conclusion The α-DC-ZZ-BNC-Ag platform was shown to induce humoral and cellular immunities effectively without any adjuvant.http://link.springer.com/article/10.1186/s12951-018-0386-6Bio-nanocapsuleHepatitis B virusVaccineDendritic cellIn vivo targetingProtective immunity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hidenori Matsuo Masaharu Somiya Masumi Iijima Takeshi Arakawa Shun’ichi Kuroda |
spellingShingle |
Hidenori Matsuo Masaharu Somiya Masumi Iijima Takeshi Arakawa Shun’ichi Kuroda CD11c-specific bio-nanocapsule enhances vaccine immunogenicity by targeting immune cells Journal of Nanobiotechnology Bio-nanocapsule Hepatitis B virus Vaccine Dendritic cell In vivo targeting Protective immunity |
author_facet |
Hidenori Matsuo Masaharu Somiya Masumi Iijima Takeshi Arakawa Shun’ichi Kuroda |
author_sort |
Hidenori Matsuo |
title |
CD11c-specific bio-nanocapsule enhances vaccine immunogenicity by targeting immune cells |
title_short |
CD11c-specific bio-nanocapsule enhances vaccine immunogenicity by targeting immune cells |
title_full |
CD11c-specific bio-nanocapsule enhances vaccine immunogenicity by targeting immune cells |
title_fullStr |
CD11c-specific bio-nanocapsule enhances vaccine immunogenicity by targeting immune cells |
title_full_unstemmed |
CD11c-specific bio-nanocapsule enhances vaccine immunogenicity by targeting immune cells |
title_sort |
cd11c-specific bio-nanocapsule enhances vaccine immunogenicity by targeting immune cells |
publisher |
BMC |
series |
Journal of Nanobiotechnology |
issn |
1477-3155 |
publishDate |
2018-08-01 |
description |
Abstract Background Various nanocarriers have been used to deliver subunit vaccines specifically to dendritic cells (DCs) for the improvement of immunogenicity. However, due to their insufficient DC priming ability, these vaccines could not elicit effective innate immunity. We have recently developed a DC-targeting bio-nanocapsule (BNC) by displaying anti-CD11c IgGs via protein A-derived IgG Fc-binding Z domain on the hepatitis B virus envelope L protein particles (α-DC-ZZ-BNC). Results After the chemical modification with antigens (Ags), the α-DC-ZZ-BNC-Ag complex could deliver Ags to DCs efficiently, leading to effective DC maturation and efficient endosomal escape of Ags, followed by Ag-specific T cell responses and IgG productions. Moreover, the α-DC-ZZ-BNC modified with Japanese encephalitis virus (JEV) envelope-derived D3 Ags could confer protection against 50-fold lethal dose of JEV injection on mice. Conclusion The α-DC-ZZ-BNC-Ag platform was shown to induce humoral and cellular immunities effectively without any adjuvant. |
topic |
Bio-nanocapsule Hepatitis B virus Vaccine Dendritic cell In vivo targeting Protective immunity |
url |
http://link.springer.com/article/10.1186/s12951-018-0386-6 |
work_keys_str_mv |
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