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外泌体作为脑胶质瘤免疫治疗的药物传递系统。

Exosomes as drug delivery systems in glioma immunotherapy.

机构信息

Stem Cell Clinical Research Center, The First Affiliated Hospital of Dalian Medical University, No. 193 Lianhe Road, Dalian, Liaoning, 116011, China.

Dalian Innovation Institute of Stem Cell and Precision Medicine, No. 57 Xinda Road, Dalian, Liaoning, 116085, China.

出版信息

J Nanobiotechnology. 2024 Jun 18;22(1):340. doi: 10.1186/s12951-024-02611-4.


DOI:10.1186/s12951-024-02611-4
PMID:38890722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11184820/
Abstract

Recently, the significant benefits of cancer immunotherapy for most cancers have been demonstrated in clinical and preclinical studies. However, the efficacy of these immunotherapies for gliomas is limited, owing to restricted drug delivery and insufficient immune activation. As drug carriers, exosomes offer the advantages of low toxicity, good biocompatibility, and intrinsic cell targeting, which could enhance glioma immunotherapy efficacy. However, a review of exosome-based drug delivery systems for glioma immunotherapy has not been presented. This review introduces the current problems in glioma immunotherapy and the role of exosomes in addressing these issues. Meanwhile, preparation and application strategies of exosome-based drug delivery systems for glioma immunotherapy are discussed, especially for enhancing immunogenicity and reversing the immunosuppressive tumor microenvironment. Finally, we briefly describe the challenges of exosome-based drug delivery systems in clinical translation. We anticipate that this review will guide the use of exosomes as drug carriers for glioma immunotherapy.

摘要

近年来,临床和临床前研究已经证明了癌症免疫疗法对大多数癌症的显著益处。然而,由于药物递送受限和免疫激活不足,这些免疫疗法对神经胶质瘤的疗效有限。作为药物载体,外泌体具有低毒性、良好的生物相容性和内在的细胞靶向性等优点,可增强神经胶质瘤的免疫治疗效果。然而,目前尚未有关于基于外泌体的药物递送系统用于神经胶质瘤免疫治疗的综述。本综述介绍了神经胶质瘤免疫治疗中存在的问题以及外泌体在解决这些问题中的作用。同时,讨论了基于外泌体的药物递送系统用于神经胶质瘤免疫治疗的制备和应用策略,特别是用于增强免疫原性和逆转免疫抑制性肿瘤微环境。最后,我们简要描述了外泌体药物递送系统在临床转化中面临的挑战。我们期望本综述将指导外泌体作为药物载体用于神经胶质瘤的免疫治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7487/11184820/148b094c8371/12951_2024_2611_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7487/11184820/ab4dffd4e47e/12951_2024_2611_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7487/11184820/eab09cfffe88/12951_2024_2611_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7487/11184820/e3e499e17bb8/12951_2024_2611_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7487/11184820/148b094c8371/12951_2024_2611_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7487/11184820/ab4dffd4e47e/12951_2024_2611_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7487/11184820/eab09cfffe88/12951_2024_2611_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7487/11184820/e3e499e17bb8/12951_2024_2611_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7487/11184820/148b094c8371/12951_2024_2611_Fig4_HTML.jpg

相似文献

[1]
Exosomes as drug delivery systems in glioma immunotherapy.

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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
A simple self-assembly nanomicelle based on brain tumor-targeting peptide-mediated siRNA delivery for glioma immunotherapy via intranasal administration.

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Combined Hyaluronic Acid Nanobioconjugates Impair CD44-Signaling for Effective Treatment Against Obesity: A Review of Comparison with Other Actors.

Int J Nanomedicine. 2025-8-21

[2]
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Biology (Basel). 2025-6-30

[3]
Evolution of glioma exosome research: emerging trends and global collaborations (2005-2025).

Discov Oncol. 2025-7-16

[4]
Bone marrow-targeted thrombopoietin delivery via engineered platelet-derived vesicle-loaded dissolving microneedles for treating ionizing radiation-induced injury.

Mater Today Bio. 2025-6-12

[5]
From basic to clinical translation: advances and perspectives of photodynamic nanodrugs.

Front Pharmacol. 2025-5-20

[6]
Exosomes in Systemic Autoimmune Diseases: Recent Advances in Diagnostic Biomarkers and Therapeutic Applications.

Int J Nanomedicine. 2025-4-21

[7]
Exploring the roles and clinical potential of exosome-derived non-coding RNAs in glioma.

IBRO Neurosci Rep. 2025-2-5

[8]
Extracellular vesicles as drug and gene delivery vehicles in central nervous system diseases.

Biomater Sci. 2025-2-25

本文引用的文献

[1]
Regulation of cargo selection in exosome biogenesis and its biomedical applications in cancer.

Exp Mol Med. 2024-4

[2]
Circulating extracellular vesicles as biomarker for diagnosis, prognosis, and monitoring in glioblastoma patients.

Neuro Oncol. 2024-7-5

[3]
Exosomes in Glioma: Unraveling Their Roles in Progression, Diagnosis, and Therapy.

Cancers (Basel). 2024-2-18

[4]
Challenges and Promise for Glioblastoma Treatment through Extracellular Vesicle Inquiry.

Cells. 2024-2-13

[5]
Glioma stem cell-derived exosomes induce the transformation of astrocytes via the miR-3065-5p/DLG2 signaling axis.

Glia. 2024-5

[6]
Immunotherapy: a promising approach for glioma treatment.

Front Immunol. 2023

[7]
Anti-glioma effect of ginseng-derived exosomes-like nanoparticles by active blood-brain-barrier penetration and tumor microenvironment modulation.

J Nanobiotechnology. 2023-8-4

[8]
Mesenchymal stem cells, as glioma exosomal immunosuppressive signal multipliers, enhance MDSCs immunosuppressive activity through the miR-21/SP1/DNMT1 positive feedback loop.

J Nanobiotechnology. 2023-7-22

[9]
Hypoxic niches attract and sequester tumor-associated macrophages and cytotoxic T cells and reprogram them for immunosuppression.

Immunity. 2023-8-8

[10]
Biogenesis, Composition and Potential Therapeutic Applications of Mesenchymal Stem Cells Derived Exosomes in Various Diseases.

Int J Nanomedicine. 2023

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