Artificially engineered vesicular vehicles for targeted therapy

Vesicular vehicles have been one of the most potential platforms for therapeutic delivery. Here, we commentate on recent advances in the development of therapeutic vesicular delivery platforms, emphasizing two intriguing works, namely, the chimeric nanobody-decorated immunoliposomes (Wan et al.) and...

Full description

Saved in:
Bibliographic Details
Main Authors: Zhigang Wang, Yufei Yan, Rui Li, Ying Zhu, Gen Yang
Format: Article
Language:English
Published: Elsevier 2024-12-01
Series:Extracellular Vesicle
Online Access:http://www.sciencedirect.com/science/article/pii/S2773041724000143
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1846115548459433984
author Zhigang Wang
Yufei Yan
Rui Li
Ying Zhu
Gen Yang
author_facet Zhigang Wang
Yufei Yan
Rui Li
Ying Zhu
Gen Yang
author_sort Zhigang Wang
collection DOAJ
description Vesicular vehicles have been one of the most potential platforms for therapeutic delivery. Here, we commentate on recent advances in the development of therapeutic vesicular delivery platforms, emphasizing two intriguing works, namely, the chimeric nanobody-decorated immunoliposomes (Wan et al.) and the retrovirus-like capsids incorporated extracellular vesicles (Jiang et al.). In the work of Wan et al., the researchers proposed a novel strategy for antitumor immunoliposome construction by the one-step self-assembly of lipids with rationally designed chimeric nanobody that comprises a nanobody against human epidermal growth factor receptor 2, a flexible peptide linker, and a human single transmembrane domain. By leveraging the natural cell systems (e.g., E coli.) to synthesize the chimeric nanobody, this technique provides a facile and robust strategy for producing immunoliposome platforms, ensuring suitability for industrial manufacturing and distribution, regulatory compliance, and clinical use. In the work of Jiang et al., taking advantage of the natural extracellular vesicle biogenesis system, the researchers introduced the activity-regulated cytoskeleton-associated protein inside the vesicle lumen and thus constructed endogenous retrovirus-like vesicles for mRNA drug delivery to neurons. This technique offers a significative strategy for developing sophisticated delivery platforms, manifesting broad application potential for different disease therapeutics. Overall, these two works have represented two typical paradigms for the artificial construction of vesicular vesicles. Considering their complementary merits, in the future, the integration of artificial engineering technologies and natural biosynthesis systems is anticipated to be a promising strategy to expedite the development of potent delivery systems.
format Article
id doaj-art-a7230d2fd5da4d169badf86aa96e2258
institution Kabale University
issn 2773-0417
language English
publishDate 2024-12-01
publisher Elsevier
record_format Article
series Extracellular Vesicle
spelling doaj-art-a7230d2fd5da4d169badf86aa96e22582024-12-19T11:03:19ZengElsevierExtracellular Vesicle2773-04172024-12-014100047Artificially engineered vesicular vehicles for targeted therapyZhigang Wang0Yufei Yan1Rui Li2Ying Zhu3Gen Yang4Corresponding author. Center of Biomedical Physics, Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, 325001, PR China.; Center of Biomedical Physics, Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, 325001, PR China; School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, 325035, PR ChinaCenter of Biomedical Physics, Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, 325001, PR ChinaCenter of Biomedical Physics, Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, 325001, PR China; Postgraduate Training Base Alliance of Wenzhou Medical University, Wenzhou, 325035, PR ChinaCenter of Biomedical Physics, Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, 325001, PR China; Postgraduate Training Base Alliance of Wenzhou Medical University, Wenzhou, 325035, PR ChinaCorresponding author. Center of Biomedical Physics, Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, 325001, PR China.; Center of Biomedical Physics, Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, 325001, PR China; State Key Laboratory of Nuclear Physics and Technology, School of Physics, Peking University, Beijing, 100871, PR China; School of Public Health and Management, Wenzhou Medical University, Wenzhou, 325035, PR ChinaVesicular vehicles have been one of the most potential platforms for therapeutic delivery. Here, we commentate on recent advances in the development of therapeutic vesicular delivery platforms, emphasizing two intriguing works, namely, the chimeric nanobody-decorated immunoliposomes (Wan et al.) and the retrovirus-like capsids incorporated extracellular vesicles (Jiang et al.). In the work of Wan et al., the researchers proposed a novel strategy for antitumor immunoliposome construction by the one-step self-assembly of lipids with rationally designed chimeric nanobody that comprises a nanobody against human epidermal growth factor receptor 2, a flexible peptide linker, and a human single transmembrane domain. By leveraging the natural cell systems (e.g., E coli.) to synthesize the chimeric nanobody, this technique provides a facile and robust strategy for producing immunoliposome platforms, ensuring suitability for industrial manufacturing and distribution, regulatory compliance, and clinical use. In the work of Jiang et al., taking advantage of the natural extracellular vesicle biogenesis system, the researchers introduced the activity-regulated cytoskeleton-associated protein inside the vesicle lumen and thus constructed endogenous retrovirus-like vesicles for mRNA drug delivery to neurons. This technique offers a significative strategy for developing sophisticated delivery platforms, manifesting broad application potential for different disease therapeutics. Overall, these two works have represented two typical paradigms for the artificial construction of vesicular vesicles. Considering their complementary merits, in the future, the integration of artificial engineering technologies and natural biosynthesis systems is anticipated to be a promising strategy to expedite the development of potent delivery systems.http://www.sciencedirect.com/science/article/pii/S2773041724000143
spellingShingle Zhigang Wang
Yufei Yan
Rui Li
Ying Zhu
Gen Yang
Artificially engineered vesicular vehicles for targeted therapy
Extracellular Vesicle
title Artificially engineered vesicular vehicles for targeted therapy
title_full Artificially engineered vesicular vehicles for targeted therapy
title_fullStr Artificially engineered vesicular vehicles for targeted therapy
title_full_unstemmed Artificially engineered vesicular vehicles for targeted therapy
title_short Artificially engineered vesicular vehicles for targeted therapy
title_sort artificially engineered vesicular vehicles for targeted therapy
url http://www.sciencedirect.com/science/article/pii/S2773041724000143
work_keys_str_mv AT zhigangwang artificiallyengineeredvesicularvehiclesfortargetedtherapy
AT yufeiyan artificiallyengineeredvesicularvehiclesfortargetedtherapy
AT ruili artificiallyengineeredvesicularvehiclesfortargetedtherapy
AT yingzhu artificiallyengineeredvesicularvehiclesfortargetedtherapy
AT genyang artificiallyengineeredvesicularvehiclesfortargetedtherapy