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Emerging delivery strategy for oncolytic virotherapy.

作者信息

Zhu Jiao, Ma Jinhu, Huang Meijuan, Deng Hongxin, Shi Gang

机构信息

Department of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, China.

Division of Thoracic Tumor Multimodality Treatment and Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu 610041, China.

出版信息

Mol Ther Oncol. 2024 Apr 29;32(2):200809. doi: 10.1016/j.omton.2024.200809. eCollection 2024 Jun 20.


DOI:10.1016/j.omton.2024.200809
PMID:38845744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11153257/
Abstract

Oncolytic virotherapy represents a promising approach in cancer immunotherapy. The primary delivery method for oncolytic viruses (OVs) is intratumoral injection, which apparently limits their clinical application. For patients with advanced cancer with disseminated metastasis, systemic administration is considered the optimal approach. However, the direct delivery of naked viruses through intravenous injection presents challenges, including rapid clearance by the immune system, inadequate accumulation in tumors, and significant side effects. Consequently, the development of drug delivery strategies has led to the emergence of various bio-materials serving as viral vectors, thereby improving the anti-tumor efficacy of oncolytic virotherapy. This review provides an overview of innovative strategies for delivering OVs, with a focus on nanoparticle-based or cell-based delivery systems. Recent pre-clinical and clinical studies are examined to highlight the enhanced efficacy of systemic delivery using these novel platforms. In addition, prevalent challenges in current research are briefly discussed, and potential solutions are proposed.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a816/11153257/422e196c738d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a816/11153257/63f40c011f5c/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a816/11153257/2578e0e70fb1/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a816/11153257/422e196c738d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a816/11153257/63f40c011f5c/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a816/11153257/2578e0e70fb1/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a816/11153257/422e196c738d/gr2.jpg

相似文献

[1]
Emerging delivery strategy for oncolytic virotherapy.

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[2]
Emerging systemic delivery strategies of oncolytic viruses: A key step toward cancer immunotherapy.

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[3]
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Adv Sci (Weinh). 2024-2

[4]
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Front Immunol. 2022

[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]
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引用本文的文献

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Resistance to oncolytic virotherapy: Multidimensional mechanisms and therapeutic breakthroughs (Review).

Int J Mol Med. 2025-11

[2]
hCCL19-expressing recombinant Newcastle disease virus boosts CAR T cell infiltration and efficacy in solid tumor.

J Immunother Cancer. 2025-7-25

[3]
The role of exosomes in bladder cancer immunotherapy.

J Natl Cancer Cent. 2025-5-2

[4]
Gene therapy strategies for aging intervention.

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[5]
Investigating the potential of oncolytic viruses in the treatment of melanoma: where do we go from here?

Skin Health Dis. 2025-4-22

[6]
Precision oncolytic viral therapy in colorectal cancer: Genetic targeting and immune modulation for personalized treatment (Review).

Int J Mol Med. 2025-7

[7]
Oncolytic Virus Therapy in a New Era of Immunotherapy, Enhanced by Combination with Existing Anticancer Therapies: Turn up the Heat!

J Cancer. 2025-2-18

[8]
Immunotherapeutic Potential of the Yellow Fever Virus Vaccine Strain 17D for Intratumoral Therapy in a Murine Model of Pancreatic Cancer.

Vaccines (Basel). 2025-1-6

[9]
Improving systemic delivery of oncolytic virus by cellular carriers.

Cancer Biol Med. 2025-1-17

[10]
A Novel Oncolytic Virus Formulation Based on Mesenchymal Stem Cell-Derived Vesicles for Tumor Therapy.

J Cancer. 2025-1-1

本文引用的文献

[1]
Tumor-targeted delivery of copper-manganese biomineralized oncolytic adenovirus for colorectal cancer immunotherapy.

Acta Biomater. 2024-4-15

[2]
An oncolytic virus-T cell chimera for cancer immunotherapy.

Nat Biotechnol. 2024-12

[3]
Synergistic Viro-chemoimmunotherapy in Breast Cancer Enabled by Bioengineered Immunostimulatory Exosomes and Dual-Targeted Coxsackievirus B3.

ACS Nano. 2024-2-6

[4]
Development of an optimized, non-stem cell line for intranasal delivery of therapeutic cargo to the central nervous system.

Mol Oncol. 2024-3

[5]
Progress and challenges in the translation of cancer nanomedicines.

Curr Opin Biotechnol. 2024-2

[6]
Clinical application of cytokine-induced killer (CIK) cell therapy in colorectal cancer: Current strategies and future challenges.

Cancer Treat Rev. 2024-1

[7]
Tumor-killing viruses score rare success in late-stage trial.

Science. 2023-12-8

[8]
Cell Membrane-Coated Oncolytic Adenovirus for Targeted Treatment of Glioblastoma.

Nano Lett. 2023-12-13

[9]
Erythrocyte-Leveraged Oncolytic Virotherapy (ELeOVt): Oncolytic Virus Assembly on Erythrocyte Surface to Combat Pulmonary Metastasis and Alleviate Side Effects.

Adv Sci (Weinh). 2024-2

[10]
Systemic delivery of glycosylated-PEG-masked oncolytic virus enhances targeting of antitumor immuno-virotherapy and modulates T and NK cell infiltration.

Theranostics. 2023

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