摘要
溶瘤病毒治疗是利用癌细胞中选择性病毒复制的恶性疾病的新型治疗方式。 单纯疱疹病毒(HSV)由于其广泛的细胞取向性以及有利于其在肿瘤中在正常细胞中复制的突变的鉴定,因此是溶瘤病毒治疗的有前途的药剂。 然而,这些减毒突变也倾向于限制已经进入临床研究的当前溶瘤HSV载体的效力。 作为替代方案,向新的进入受体重新导向的载体具有在病毒进入阶段实现肿瘤特异性的潜力,消除了对复制减毒突变的需要。 在这里,我们总结了单纯疱疹病毒进入的分子机制以及最近在完全重靶向单纯疱疹病毒载体的溶瘤病毒治疗方面的进展。 重新靶向的HSV载体提供了一个有吸引力的平台,用于创建具有改进的功效和特异性的新一代溶瘤HSV。
关键词: 癌症,基因治疗,单纯疱疹病毒,溶瘤病毒,靶向,载体,病毒治疗,病毒进入。
图形摘要
Current Cancer Drug Targets
Title:Oncolytic Herpes Simplex Virus Vectors Fully Retargeted to Tumor- Associated Antigens
Volume: 18 Issue: 2
关键词: 癌症,基因治疗,单纯疱疹病毒,溶瘤病毒,靶向,载体,病毒治疗,病毒进入。
摘要: Oncolytic virotherapy is a novel therapeutic modality for malignant diseases that exploits selective viral replication in cancer cells. Herpes simplex virus (HSV) is a promising agent for oncolytic virotherapy due to its broad cell tropism and the identification of mutations that favor its replication in tumor over normal cells. However, these attenuating mutations also tend to limit the potency of current oncolytic HSV vectors that have entered clinical studies. As an alternative, vector retargeting to novel entry receptors has the potential to achieve tumor specificity at the stage of virus entry, eliminating the need for replication-attenuating mutations. Here, we summarize the molecular mechanism of HSV entry and recent advances in the development of fully retargeted HSV vectors for oncolytic virotherapy. Retargeted HSV vectors offer an attractive platform for the creation of a new generation of oncolytic HSV with improved efficacy and specificity.
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Cite this article as:
Oncolytic Herpes Simplex Virus Vectors Fully Retargeted to Tumor- Associated Antigens, Current Cancer Drug Targets 2018; 18 (2) . https://dx.doi.org/10.2174/1568009617666170206105855
DOI https://dx.doi.org/10.2174/1568009617666170206105855 |
Print ISSN 1568-0096 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5576 |
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