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Tumour-derived extracellular vesicle based vaccines for melanoma treatment
The interest of extracellular vesicles (EVs) in cancer immunotherapy is increasing every day. EVs are lipid bilayer vesicles released by most cells, which contain the molecular signature of their parent cell. Melanoma-derived EVs present antigens specific to this aggressive type of cancer, but they...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10102154/ https://www.ncbi.nlm.nih.gov/pubmed/37022605 http://dx.doi.org/10.1007/s13346-023-01328-5 |
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author | Gonzalez-Melero, Lorena Hernandez, Rosa Maria Santos-Vizcaino, Edorta Igartua, Manoli |
author_facet | Gonzalez-Melero, Lorena Hernandez, Rosa Maria Santos-Vizcaino, Edorta Igartua, Manoli |
author_sort | Gonzalez-Melero, Lorena |
collection | PubMed |
description | The interest of extracellular vesicles (EVs) in cancer immunotherapy is increasing every day. EVs are lipid bilayer vesicles released by most cells, which contain the molecular signature of their parent cell. Melanoma-derived EVs present antigens specific to this aggressive type of cancer, but they also exert immunomodulatory and pro-metastatic activity. Until now, most reviews focus on the immunoevasive characteristics of tumour-derived EVs, but do not help to overcome the issues related to them. In this review, we describe isolation methods of EVs from melanoma patients and most interesting markers to oversee their effect if they are used as antigen carriers. We also discuss the methods developed so far to overcome the lack of immunogenicity of melanoma-derived EVs, which includes EV modification or adjuvant co-administration. In summary, we conclude that EVs can be an interesting antigen source for immunotherapy development once EV obtaining is optimised and the understanding of the mechanisms behind their multiple effects is further understood. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-10102154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-101021542023-04-15 Tumour-derived extracellular vesicle based vaccines for melanoma treatment Gonzalez-Melero, Lorena Hernandez, Rosa Maria Santos-Vizcaino, Edorta Igartua, Manoli Drug Deliv Transl Res Original Article The interest of extracellular vesicles (EVs) in cancer immunotherapy is increasing every day. EVs are lipid bilayer vesicles released by most cells, which contain the molecular signature of their parent cell. Melanoma-derived EVs present antigens specific to this aggressive type of cancer, but they also exert immunomodulatory and pro-metastatic activity. Until now, most reviews focus on the immunoevasive characteristics of tumour-derived EVs, but do not help to overcome the issues related to them. In this review, we describe isolation methods of EVs from melanoma patients and most interesting markers to oversee their effect if they are used as antigen carriers. We also discuss the methods developed so far to overcome the lack of immunogenicity of melanoma-derived EVs, which includes EV modification or adjuvant co-administration. In summary, we conclude that EVs can be an interesting antigen source for immunotherapy development once EV obtaining is optimised and the understanding of the mechanisms behind their multiple effects is further understood. GRAPHICAL ABSTRACT: [Image: see text] Springer US 2023-04-06 2023 /pmc/articles/PMC10102154/ /pubmed/37022605 http://dx.doi.org/10.1007/s13346-023-01328-5 Text en © The Author(s) 2023 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 Gonzalez-Melero, Lorena Hernandez, Rosa Maria Santos-Vizcaino, Edorta Igartua, Manoli Tumour-derived extracellular vesicle based vaccines for melanoma treatment |
title | Tumour-derived extracellular vesicle based vaccines for melanoma treatment |
title_full | Tumour-derived extracellular vesicle based vaccines for melanoma treatment |
title_fullStr | Tumour-derived extracellular vesicle based vaccines for melanoma treatment |
title_full_unstemmed | Tumour-derived extracellular vesicle based vaccines for melanoma treatment |
title_short | Tumour-derived extracellular vesicle based vaccines for melanoma treatment |
title_sort | tumour-derived extracellular vesicle based vaccines for melanoma treatment |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10102154/ https://www.ncbi.nlm.nih.gov/pubmed/37022605 http://dx.doi.org/10.1007/s13346-023-01328-5 |
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