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溶瘤病毒的发现和开发:它们是癌症免疫疗法的未来吗?

The discovery and development of oncolytic viruses: are they the future of cancer immunotherapy?

机构信息

Molecular Neurosurgery Laboratory and the Brain Tumor Research Center, Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA.

Harvard Medical School, Boston, MA, USA.

出版信息

Expert Opin Drug Discov. 2021 Apr;16(4):391-410. doi: 10.1080/17460441.2021.1850689. Epub 2020 Dec 14.

Abstract

: Despite diverse treatment modalities and novel therapies, many cancers and patients are not effectively treated. Cancer immunotherapy has recently achieved breakthrough status yet is not effective in all cancer types or patients and can generate serious adverse effects. Oncolytic viruses (OVs) are a promising new therapeutic modality that harnesses virus biology and host interactions to treat cancer. OVs, genetically engineered or natural, preferentially replicate in and kill cancer cells, sparing normal cells/tissues, and mediating anti-tumor immunity.: This review focuses on OVs as cancer therapeutic agents from a historical perspective, especially strategies to boost their immunotherapeutic activities. OVs offer a multifaceted platform, whose activities are modulated based on the parental virus and genetic alterations. In addition to direct viral effects, many OVs can be armed with therapeutic transgenes to also act as gene therapy vectors, and/or combined with other drugs or therapies.: OVs are an amazingly versatile and malleable class of cancer therapies. They tend to target cellular and host physiology as opposed to specific genetic alterations, which potentially enables broad responsiveness. The biological complexity of OVs have hindered their translation; however, the recent approval of talimogene laherparepvec (T-Vec) has invigorated the field.

摘要

尽管有多种治疗方式和新疗法,但许多癌症和患者仍未得到有效治疗。癌症免疫疗法最近取得了突破性进展,但并非对所有癌症类型或患者都有效,并且可能会产生严重的不良反应。溶瘤病毒(OVs)是一种很有前途的新型治疗方式,它利用病毒生物学和宿主相互作用来治疗癌症。OVs 可以是经过基因工程改造的或天然的,它们优先在癌细胞中复制并杀死癌细胞,而不会伤害正常细胞/组织,并介导抗肿瘤免疫。

本综述从历史角度重点介绍了作为癌症治疗剂的 OVs,特别是增强其免疫治疗活性的策略。OVs 提供了一个多方面的平台,其活性可以根据亲本病毒和遗传改变进行调节。除了直接的病毒作用外,许多 OVs 还可以配备治疗性转基因,也可以作为基因治疗载体,和/或与其他药物或疗法联合使用。

OVs 是一类非常灵活多变的癌症治疗方法。它们倾向于针对细胞和宿主生理学,而不是特定的遗传改变,这可能使它们具有广泛的反应能力。OVs 的生物学复杂性阻碍了它们的转化;然而,最近 talimogene laherparepvec(T-Vec)的批准激发了该领域的活力。

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