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Mannose-modified hyaluronic acid nanocapsules for the targeting of tumor-associated macrophages
Tumor-associated macrophages (TAMs), a class of immune cells that play a key role in tumor immunosuppression, are recognized as important targets to improve cancer prognosis and treatment. Consequently, the engineering of drug delivery nanocarriers that can reach TAMs has acquired special relevance....
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238357/ https://www.ncbi.nlm.nih.gov/pubmed/36472784 http://dx.doi.org/10.1007/s13346-022-01265-9 |
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author | Fernández-Mariño, Iago Anfray, Clément Crecente-Campo, Jose Maeda, Akihiro Ummarino, Aldo Teijeiro-Valiño, Carmen Blanco-Martinez, Dario Mpambani, Francis Poul, Laurence Devalliere, Julie Germain, Matthieu Correa, Juan Fernandez-Villamarin, Marcos Allavena, Paola Fernandez-Megia, Eduardo Alonso, María José Andón, Fernando Torres |
author_facet | Fernández-Mariño, Iago Anfray, Clément Crecente-Campo, Jose Maeda, Akihiro Ummarino, Aldo Teijeiro-Valiño, Carmen Blanco-Martinez, Dario Mpambani, Francis Poul, Laurence Devalliere, Julie Germain, Matthieu Correa, Juan Fernandez-Villamarin, Marcos Allavena, Paola Fernandez-Megia, Eduardo Alonso, María José Andón, Fernando Torres |
author_sort | Fernández-Mariño, Iago |
collection | PubMed |
description | Tumor-associated macrophages (TAMs), a class of immune cells that play a key role in tumor immunosuppression, are recognized as important targets to improve cancer prognosis and treatment. Consequently, the engineering of drug delivery nanocarriers that can reach TAMs has acquired special relevance. This work describes the development and biological evaluation of a panel of hyaluronic acid (HA) nanocapsules (NCs), with different compositions and prepared by different techniques, designed to target macrophages. The results showed that plain HA NCs did not significantly influence the polarization of M0 and M2-like macrophages towards an M1-like pro-inflammatory phenotype; however, the chemical functionalization of HA with mannose (HA-Man) led to a significant increase of NCs uptake by M2 macrophages in vitro and to an improved biodistribution in a MN/MNCA1 fibrosarcoma mouse model with high infiltration of TAMs. These functionalized HA-Man NCs showed a higher accumulation in the tumor compared to non-modified HA NCs. Finally, the pre-administration of the liposomal liver occupying agent Nanoprimer™ further increased the accumulation of the HA-Man NCs in the tumor. This work highlights the promise shown by the HA-Man NCs to target TAMs and thus provides new options for the development of nanomedicine and immunotherapy-based cancer treatments. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13346-022-01265-9. |
format | Online Article Text |
id | pubmed-10238357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-102383572023-06-04 Mannose-modified hyaluronic acid nanocapsules for the targeting of tumor-associated macrophages Fernández-Mariño, Iago Anfray, Clément Crecente-Campo, Jose Maeda, Akihiro Ummarino, Aldo Teijeiro-Valiño, Carmen Blanco-Martinez, Dario Mpambani, Francis Poul, Laurence Devalliere, Julie Germain, Matthieu Correa, Juan Fernandez-Villamarin, Marcos Allavena, Paola Fernandez-Megia, Eduardo Alonso, María José Andón, Fernando Torres Drug Deliv Transl Res Original Article Tumor-associated macrophages (TAMs), a class of immune cells that play a key role in tumor immunosuppression, are recognized as important targets to improve cancer prognosis and treatment. Consequently, the engineering of drug delivery nanocarriers that can reach TAMs has acquired special relevance. This work describes the development and biological evaluation of a panel of hyaluronic acid (HA) nanocapsules (NCs), with different compositions and prepared by different techniques, designed to target macrophages. The results showed that plain HA NCs did not significantly influence the polarization of M0 and M2-like macrophages towards an M1-like pro-inflammatory phenotype; however, the chemical functionalization of HA with mannose (HA-Man) led to a significant increase of NCs uptake by M2 macrophages in vitro and to an improved biodistribution in a MN/MNCA1 fibrosarcoma mouse model with high infiltration of TAMs. These functionalized HA-Man NCs showed a higher accumulation in the tumor compared to non-modified HA NCs. Finally, the pre-administration of the liposomal liver occupying agent Nanoprimer™ further increased the accumulation of the HA-Man NCs in the tumor. This work highlights the promise shown by the HA-Man NCs to target TAMs and thus provides new options for the development of nanomedicine and immunotherapy-based cancer treatments. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13346-022-01265-9. Springer US 2022-12-06 2023 /pmc/articles/PMC10238357/ /pubmed/36472784 http://dx.doi.org/10.1007/s13346-022-01265-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Fernández-Mariño, Iago Anfray, Clément Crecente-Campo, Jose Maeda, Akihiro Ummarino, Aldo Teijeiro-Valiño, Carmen Blanco-Martinez, Dario Mpambani, Francis Poul, Laurence Devalliere, Julie Germain, Matthieu Correa, Juan Fernandez-Villamarin, Marcos Allavena, Paola Fernandez-Megia, Eduardo Alonso, María José Andón, Fernando Torres Mannose-modified hyaluronic acid nanocapsules for the targeting of tumor-associated macrophages |
title | Mannose-modified hyaluronic acid nanocapsules for the targeting of tumor-associated macrophages |
title_full | Mannose-modified hyaluronic acid nanocapsules for the targeting of tumor-associated macrophages |
title_fullStr | Mannose-modified hyaluronic acid nanocapsules for the targeting of tumor-associated macrophages |
title_full_unstemmed | Mannose-modified hyaluronic acid nanocapsules for the targeting of tumor-associated macrophages |
title_short | Mannose-modified hyaluronic acid nanocapsules for the targeting of tumor-associated macrophages |
title_sort | mannose-modified hyaluronic acid nanocapsules for the targeting of tumor-associated macrophages |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238357/ https://www.ncbi.nlm.nih.gov/pubmed/36472784 http://dx.doi.org/10.1007/s13346-022-01265-9 |
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