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A Toll-like Receptor-Activating, Self-Adjuvant Glycan Nanocarrier
The global pandemic of COVID-19 highlights the importance of vaccination, which remains the most efficient measure against many diseases. Despite the progress in vaccine design, concerns with suboptimal antigen immunogenicity and delivery efficiency prevail. Self-adjuvant carriers–vehicles that can...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110926/ https://www.ncbi.nlm.nih.gov/pubmed/35592309 http://dx.doi.org/10.3389/fchem.2022.864206 |
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author | Xie, Daping Niu, Yiming Mu, Ruoyu Campos de Souza, Senio Yin, Xiaoyu Dong, Lei Wang, Chunming |
author_facet | Xie, Daping Niu, Yiming Mu, Ruoyu Campos de Souza, Senio Yin, Xiaoyu Dong, Lei Wang, Chunming |
author_sort | Xie, Daping |
collection | PubMed |
description | The global pandemic of COVID-19 highlights the importance of vaccination, which remains the most efficient measure against many diseases. Despite the progress in vaccine design, concerns with suboptimal antigen immunogenicity and delivery efficiency prevail. Self-adjuvant carriers–vehicles that can simultaneously deliver antigens and act as adjuvants–may improve efficacies in these aspects. Here, we developed a self-adjuvant carrier based on an acetyl glucomannan (acGM), which can activate toll-like receptor 2 (TLR2) and encapsulate the model antigen ovalbumin (OVA) via a double-emulsion process. In vitro tests showed that these OVA@acGM-8k nanoparticles (NPs) enhanced cellular uptake and activated TLR2 on the surface of dendritic cells (DCs), with increased expression of co-stimulatory molecules (e.g. CD80 and CD86) and pro-inflammatory cytokines (e.g. TNF-α and IL12p70). In vivo experiments in mice demonstrated that OVA@acGM-8k NPs accumulated in the lymph nodes and promoted DCs’ maturation. The immunization also boosted the humoral and cellular immune responses. Our findings suggest that this self-adjuvant polysaccharide carrier could be a promising approach for vaccine development. |
format | Online Article Text |
id | pubmed-9110926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91109262022-05-18 A Toll-like Receptor-Activating, Self-Adjuvant Glycan Nanocarrier Xie, Daping Niu, Yiming Mu, Ruoyu Campos de Souza, Senio Yin, Xiaoyu Dong, Lei Wang, Chunming Front Chem Chemistry The global pandemic of COVID-19 highlights the importance of vaccination, which remains the most efficient measure against many diseases. Despite the progress in vaccine design, concerns with suboptimal antigen immunogenicity and delivery efficiency prevail. Self-adjuvant carriers–vehicles that can simultaneously deliver antigens and act as adjuvants–may improve efficacies in these aspects. Here, we developed a self-adjuvant carrier based on an acetyl glucomannan (acGM), which can activate toll-like receptor 2 (TLR2) and encapsulate the model antigen ovalbumin (OVA) via a double-emulsion process. In vitro tests showed that these OVA@acGM-8k nanoparticles (NPs) enhanced cellular uptake and activated TLR2 on the surface of dendritic cells (DCs), with increased expression of co-stimulatory molecules (e.g. CD80 and CD86) and pro-inflammatory cytokines (e.g. TNF-α and IL12p70). In vivo experiments in mice demonstrated that OVA@acGM-8k NPs accumulated in the lymph nodes and promoted DCs’ maturation. The immunization also boosted the humoral and cellular immune responses. Our findings suggest that this self-adjuvant polysaccharide carrier could be a promising approach for vaccine development. Frontiers Media S.A. 2022-05-03 /pmc/articles/PMC9110926/ /pubmed/35592309 http://dx.doi.org/10.3389/fchem.2022.864206 Text en Copyright © 2022 Xie, Niu, Mu, Campos de Souza, Yin, Dong and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Xie, Daping Niu, Yiming Mu, Ruoyu Campos de Souza, Senio Yin, Xiaoyu Dong, Lei Wang, Chunming A Toll-like Receptor-Activating, Self-Adjuvant Glycan Nanocarrier |
title | A Toll-like Receptor-Activating, Self-Adjuvant Glycan Nanocarrier |
title_full | A Toll-like Receptor-Activating, Self-Adjuvant Glycan Nanocarrier |
title_fullStr | A Toll-like Receptor-Activating, Self-Adjuvant Glycan Nanocarrier |
title_full_unstemmed | A Toll-like Receptor-Activating, Self-Adjuvant Glycan Nanocarrier |
title_short | A Toll-like Receptor-Activating, Self-Adjuvant Glycan Nanocarrier |
title_sort | toll-like receptor-activating, self-adjuvant glycan nanocarrier |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110926/ https://www.ncbi.nlm.nih.gov/pubmed/35592309 http://dx.doi.org/10.3389/fchem.2022.864206 |
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