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Extracellular vesicle–based drug delivery in cancer immunotherapy
Extracellular vesicles (EVs) are a group of nanoscale membrane-bound organelles including exosomes, microvesicles (MVs), membrane particles, and apoptotic bodies, which are released from almost all eukaryotic cells. Owing to their ingredients, EVs can be employed as biomarkers for human diseases. In...
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/PMC10234250/ https://www.ncbi.nlm.nih.gov/pubmed/37261603 http://dx.doi.org/10.1007/s13346-023-01370-3 |
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author | Najafi, Sajad Majidpoor, Jamal Mortezaee, Keywan |
author_facet | Najafi, Sajad Majidpoor, Jamal Mortezaee, Keywan |
author_sort | Najafi, Sajad |
collection | PubMed |
description | Extracellular vesicles (EVs) are a group of nanoscale membrane-bound organelles including exosomes, microvesicles (MVs), membrane particles, and apoptotic bodies, which are released from almost all eukaryotic cells. Owing to their ingredients, EVs can be employed as biomarkers for human diseases. Interestingly, EVs show favorable features as candidates for targeted drug delivery and thus, they are suggested as ideal drug carriers as well as good vaccines for various human diseases including cancer. Among various drugs loaded in EVs for targeted drug delivery, immune checkpoint inhibitors (ICIs), including antibodies against programmed cell death-1 (PD-1), programmed death-ligand 1 (PD-L1), and cytotoxic-T-lymphocyte-associated protein 4 (CTLA-4), have attracted an increasing attention for cancer researchers and clinicians. Animal and clinical studies have shown combination of EVs and immunotherapy antibodies to improve the efficacy and reduce possible side effects in systemic administration of ICIs. In this review, we discuss the EVs and their significance in drug delivery with a focus on cancer immunotherapy agents. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-10234250 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-102342502023-06-01 Extracellular vesicle–based drug delivery in cancer immunotherapy Najafi, Sajad Majidpoor, Jamal Mortezaee, Keywan Drug Deliv Transl Res Review Article Extracellular vesicles (EVs) are a group of nanoscale membrane-bound organelles including exosomes, microvesicles (MVs), membrane particles, and apoptotic bodies, which are released from almost all eukaryotic cells. Owing to their ingredients, EVs can be employed as biomarkers for human diseases. Interestingly, EVs show favorable features as candidates for targeted drug delivery and thus, they are suggested as ideal drug carriers as well as good vaccines for various human diseases including cancer. Among various drugs loaded in EVs for targeted drug delivery, immune checkpoint inhibitors (ICIs), including antibodies against programmed cell death-1 (PD-1), programmed death-ligand 1 (PD-L1), and cytotoxic-T-lymphocyte-associated protein 4 (CTLA-4), have attracted an increasing attention for cancer researchers and clinicians. Animal and clinical studies have shown combination of EVs and immunotherapy antibodies to improve the efficacy and reduce possible side effects in systemic administration of ICIs. In this review, we discuss the EVs and their significance in drug delivery with a focus on cancer immunotherapy agents. GRAPHICAL ABSTRACT: [Image: see text] Springer US 2023-06-01 /pmc/articles/PMC10234250/ /pubmed/37261603 http://dx.doi.org/10.1007/s13346-023-01370-3 Text en © Controlled Release Society 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Review Article Najafi, Sajad Majidpoor, Jamal Mortezaee, Keywan Extracellular vesicle–based drug delivery in cancer immunotherapy |
title | Extracellular vesicle–based drug delivery in cancer immunotherapy |
title_full | Extracellular vesicle–based drug delivery in cancer immunotherapy |
title_fullStr | Extracellular vesicle–based drug delivery in cancer immunotherapy |
title_full_unstemmed | Extracellular vesicle–based drug delivery in cancer immunotherapy |
title_short | Extracellular vesicle–based drug delivery in cancer immunotherapy |
title_sort | extracellular vesicle–based drug delivery in cancer immunotherapy |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234250/ https://www.ncbi.nlm.nih.gov/pubmed/37261603 http://dx.doi.org/10.1007/s13346-023-01370-3 |
work_keys_str_mv | AT najafisajad extracellularvesiclebaseddrugdeliveryincancerimmunotherapy AT majidpoorjamal extracellularvesiclebaseddrugdeliveryincancerimmunotherapy AT mortezaeekeywan extracellularvesiclebaseddrugdeliveryincancerimmunotherapy |