溶瘤病毒在癌症免疫治疗中的治疗实施:挑战和当前临床试验的回顾。

Journal of biomedical science and research Pub Date : 2022-01-01 Epub Date: 2022-10-20 DOI:10.36266/JBSR/164
X Wang, H M Maeng, J Lee, C Xie
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引用次数: 1

摘要

癌症治疗的发展已经从放疗和化疗的一般靶点发展到具有更特定作用机制的治疗,如小分子激酶抑制剂、针对肿瘤抗原的单克隆抗体或检查点抑制剂。最近,溶瘤病毒(OVs)已成为癌症免疫治疗的可行选择,特别是对于“冷”肿瘤,这是一种已知的免疫抑制肿瘤微环境。病毒所需的特征是通过遗传衰减来选择不受控制的毒力,一些基因被肿瘤细胞内增强条件病毒复制的基因所取代。OVs治疗必须克服各种障碍,如宿主免疫系统对病毒的过早抑制和致密的基质屏障。目前,临床研究调查了OVs与各种抗癌疗法(包括放疗、化疗、免疫检查点抑制剂和单克隆抗体)联合使用的疗效。因此,未来的研究应该探索癌症治疗如何与某些OVs协同作用,以创造更有效的联合治疗并改善患者预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Therapeutic Implementation of Oncolytic Viruses for Cancer Immunotherapy: Review of Challenges and Current Clinical Trials.

Therapeutic Implementation of Oncolytic Viruses for Cancer Immunotherapy: Review of Challenges and Current Clinical Trials.

Therapeutic Implementation of Oncolytic Viruses for Cancer Immunotherapy: Review of Challenges and Current Clinical Trials.

The development of cancer therapeutics has evolved from general targets with radiation and chemotherapy and shifted toward treatments with a more specific mechanism of action such as small molecule kinase inhibitors, monoclonal antibodies against tumor antigens, or checkpoint inhibitors. Recently, oncolytic viruses (OVs) have come to the forefront as a viable option for cancer immunotherapy, especially for "cold" tumors, which are known to inhabit an immunologically suppressive tumor microenvironment. Desired characteristics of viruses are selected through genetic attenuation of uncontrolled virulence, and some genes are replaced with ones that enhance conditional viral replication within tumor cells. Treatment with OVs must overcome various hurdles such as premature viral suppression by the host's immune system and the dense stromal barrier. Currently, clinical studies investigate the efficacy of OVs in conjunction with various anti-cancer therapeutics, including radiotherapy, chemotherapy, immune checkpoint inhibitors, and monoclonal antibodies. Thus, future research should explore how cancer therapeutics work synergistically with certain OVs in order to create more effective combination therapies and improve patient outcomes.

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