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Enhancement of Immune Response of Bioconjugate Nanovaccine by Loading of CpG through Click Chemistry

CpG is a widely used adjuvant that enhances the cellular immune response by entering antigen-presenting cells and binding with receptors. The traditional physical mixing of the antigen and CpG adjuvant results in a low adjuvant utilization rate. Considering the efficient delivery capacity of nanovac...

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Autores principales: Mo, Mengting, Li, Xiang, Li, Caixia, Wang, Kangfeng, Li, Shulei, Guo, Yan, Sun, Peng, Wu, Jun, Lu, Ying, Pan, Chao, Wang, Hengliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052328/
https://www.ncbi.nlm.nih.gov/pubmed/36983689
http://dx.doi.org/10.3390/jpm13030507
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author Mo, Mengting
Li, Xiang
Li, Caixia
Wang, Kangfeng
Li, Shulei
Guo, Yan
Sun, Peng
Wu, Jun
Lu, Ying
Pan, Chao
Wang, Hengliang
author_facet Mo, Mengting
Li, Xiang
Li, Caixia
Wang, Kangfeng
Li, Shulei
Guo, Yan
Sun, Peng
Wu, Jun
Lu, Ying
Pan, Chao
Wang, Hengliang
author_sort Mo, Mengting
collection PubMed
description CpG is a widely used adjuvant that enhances the cellular immune response by entering antigen-presenting cells and binding with receptors. The traditional physical mixing of the antigen and CpG adjuvant results in a low adjuvant utilization rate. Considering the efficient delivery capacity of nanovaccines, we developed an attractive strategy to covalently load CpG onto the nanovaccine, which realized the co-delivery of both CpG and the antigen. Briefly, the azide-modified CpG was conjugated to a bioconjugate nanovaccine (NP-OPS) against Shigella flexneri through a simple two-step reaction. After characterization of the novel vaccine (NP-OPS-CpG), a series of in vitro and in vivo experiments were performed, including in vivo imaging, lymph node sectioning, and dendritic cell stimulation, and the results showed that more CpG reached the lymph nodes after covalent coupling. Subsequent flow cytometry analysis of lymph nodes from immunized mice showed that the cellular immune response was greatly promoted by the nanovaccine coupled with CpG. Moreover, by analyzing the antibody subtypes of immunized mice, NP-OPS-CpG was found to further promote a Th1-biased immune response. Thus, we developed an attractive method to load CpG on a nanovaccine that is simple, convenient, and is especially suitable for immune enhancement of vaccines against intracellular bacteria.
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spelling pubmed-100523282023-03-30 Enhancement of Immune Response of Bioconjugate Nanovaccine by Loading of CpG through Click Chemistry Mo, Mengting Li, Xiang Li, Caixia Wang, Kangfeng Li, Shulei Guo, Yan Sun, Peng Wu, Jun Lu, Ying Pan, Chao Wang, Hengliang J Pers Med Article CpG is a widely used adjuvant that enhances the cellular immune response by entering antigen-presenting cells and binding with receptors. The traditional physical mixing of the antigen and CpG adjuvant results in a low adjuvant utilization rate. Considering the efficient delivery capacity of nanovaccines, we developed an attractive strategy to covalently load CpG onto the nanovaccine, which realized the co-delivery of both CpG and the antigen. Briefly, the azide-modified CpG was conjugated to a bioconjugate nanovaccine (NP-OPS) against Shigella flexneri through a simple two-step reaction. After characterization of the novel vaccine (NP-OPS-CpG), a series of in vitro and in vivo experiments were performed, including in vivo imaging, lymph node sectioning, and dendritic cell stimulation, and the results showed that more CpG reached the lymph nodes after covalent coupling. Subsequent flow cytometry analysis of lymph nodes from immunized mice showed that the cellular immune response was greatly promoted by the nanovaccine coupled with CpG. Moreover, by analyzing the antibody subtypes of immunized mice, NP-OPS-CpG was found to further promote a Th1-biased immune response. Thus, we developed an attractive method to load CpG on a nanovaccine that is simple, convenient, and is especially suitable for immune enhancement of vaccines against intracellular bacteria. MDPI 2023-03-11 /pmc/articles/PMC10052328/ /pubmed/36983689 http://dx.doi.org/10.3390/jpm13030507 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mo, Mengting
Li, Xiang
Li, Caixia
Wang, Kangfeng
Li, Shulei
Guo, Yan
Sun, Peng
Wu, Jun
Lu, Ying
Pan, Chao
Wang, Hengliang
Enhancement of Immune Response of Bioconjugate Nanovaccine by Loading of CpG through Click Chemistry
title Enhancement of Immune Response of Bioconjugate Nanovaccine by Loading of CpG through Click Chemistry
title_full Enhancement of Immune Response of Bioconjugate Nanovaccine by Loading of CpG through Click Chemistry
title_fullStr Enhancement of Immune Response of Bioconjugate Nanovaccine by Loading of CpG through Click Chemistry
title_full_unstemmed Enhancement of Immune Response of Bioconjugate Nanovaccine by Loading of CpG through Click Chemistry
title_short Enhancement of Immune Response of Bioconjugate Nanovaccine by Loading of CpG through Click Chemistry
title_sort enhancement of immune response of bioconjugate nanovaccine by loading of cpg through click chemistry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052328/
https://www.ncbi.nlm.nih.gov/pubmed/36983689
http://dx.doi.org/10.3390/jpm13030507
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