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靶向CD47的溶瘤病毒:通往成功的新途径?

Oncolytic viruses targeting CD47: a new road to success?

作者信息

Takimoto Chris H, Wick Michael J

机构信息

START, San Antonio, Texas, USA

XenoSTART, San Antonio, Texas, USA.

出版信息

J Immunother Cancer. 2025 May 7;13(5):e011550. doi: 10.1136/jitc-2025-011550.

Abstract

Clinical success in the therapeutic targeting of the CD47 signaling pathway has thus far remained elusive despite a promising scientific rationale. Use of oncolytic viruses to deliver CD47 targeting agents represents a novel approach to modulate the immunological landscape of the tumor microenvironment and to generate a systemic antitumor immune response. In recent preclinical studies, an oncolytic herpes simplex virus-1 engineered to express an inhibitory CD47-binding nanobody demonstrated promising antitumor activity. Several other oncolytic viruses engineered to express CD47 inhibitory molecules are also in preclinical development. Oncolytic viruses have the potential to mitigate drug delivery issues and may avoid systemic toxicities that have limited conventional CD47 targeting therapeutics. These novel therapeutics warrant further evaluation in clinical trials. The potential advantages, limitations, and remaining critical questions regarding this strategic approach are discussed here.

摘要

尽管有前景良好的科学理论依据,但迄今为止,针对CD47信号通路的治疗靶点在临床上尚未取得成功。使用溶瘤病毒递送靶向CD47的药物代表了一种调节肿瘤微环境免疫格局并产生全身性抗肿瘤免疫反应的新方法。在最近的临床前研究中,一种经过基因工程改造以表达抑制性CD47结合纳米抗体的溶瘤单纯疱疹病毒-1显示出有前景的抗肿瘤活性。其他几种经过基因工程改造以表达CD47抑制分子的溶瘤病毒也正在进行临床前开发。溶瘤病毒有可能缓解药物递送问题,并可能避免限制传统CD47靶向治疗药物的全身毒性。这些新型疗法值得在临床试验中进一步评估。本文讨论了这种战略方法的潜在优势、局限性以及仍然存在的关键问题。

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