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解读人类肿瘤生态系统对溶瘤病毒的易感性。

Deciphering permissivity of human tumor ecosystems to oncolytic viruses.

作者信息

Schoeps Benjamin, Lauer Ulrich M, Elbers Knut

机构信息

ViraTherapeutics GmbH, Rum, Austria.

Department of Medical Oncology and Pneumology, Virotherapy Center Tübingen (VCT), Medical University Hospital, Tübingen, Germany.

出版信息

Oncogene. 2025 May;44(16):1069-1077. doi: 10.1038/s41388-025-03357-5. Epub 2025 Mar 27.

DOI:10.1038/s41388-025-03357-5
PMID:40148688
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11996678/
Abstract

Effective cancer therapy involves initiation of a tumor-specific immune response. Consequently, the interest in oncolytic viruses (OV) capable of triggering immunogenic cell death has sparked in recent years. However, the common use of pre-clinical models that fail to mirror patient tumor ecosystems (TES) hinders clinical translation. Here, we provide a condensed view on the intricate interplay between several aspects of TES and OV action and discuss these considerations in the view of recently developed pre-clinical human model systems. Given the urgent demand for innovative cancer treatments, the purpose of this review is to highlight the so-far overlooked complex impact of the tumor microenvironment (TME) on OV permissivity, with the intent to provide a foundation for future, more effective pre-clinical studies.

摘要

有效的癌症治疗涉及启动肿瘤特异性免疫反应。因此,近年来人们对能够引发免疫原性细胞死亡的溶瘤病毒(OV)产生了兴趣。然而,未能反映患者肿瘤生态系统(TES)的临床前模型的普遍使用阻碍了临床转化。在这里,我们简要概述了TES的几个方面与OV作用之间的复杂相互作用,并结合最近开发的临床前人类模型系统讨论了这些考虑因素。鉴于对创新癌症治疗的迫切需求,本综述的目的是强调肿瘤微环境(TME)对OV易感性迄今为止被忽视的复杂影响,旨在为未来更有效的临床前研究提供基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8560/11996678/2325cec2335c/41388_2025_3357_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8560/11996678/c0b877996d0a/41388_2025_3357_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8560/11996678/f3d49f1c2d42/41388_2025_3357_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8560/11996678/ccf60252f885/41388_2025_3357_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8560/11996678/9f91cb37df31/41388_2025_3357_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8560/11996678/2325cec2335c/41388_2025_3357_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8560/11996678/c0b877996d0a/41388_2025_3357_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8560/11996678/f3d49f1c2d42/41388_2025_3357_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8560/11996678/ccf60252f885/41388_2025_3357_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8560/11996678/9f91cb37df31/41388_2025_3357_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8560/11996678/2325cec2335c/41388_2025_3357_Fig5_HTML.jpg

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Further knowledge and developments in resistance mechanisms to immune checkpoint inhibitors.
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Science. 2023 Dec 8;382(6675):1101-1102. doi: 10.1126/science.adn3528. Epub 2023 Dec 7.
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Integrating innate and adaptive immunity in oncolytic virus therapy.将先天免疫和适应性免疫整合到溶瘤病毒治疗中。
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