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肿瘤相关抗原完全重定向的溶瘤单纯疱疹病毒载体。

Oncolytic Herpes Simplex Virus Vectors Fully Retargeted to Tumor- Associated Antigens.

机构信息

Division of Bioengineering, Advanced Clinical Research Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.

Department of Life Sciences, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan.

出版信息

Curr Cancer Drug Targets. 2018;18(2):162-170. doi: 10.2174/1568009617666170206105855.

Abstract

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.

摘要

溶瘤病毒治疗是一种治疗恶性疾病的新方法,它利用病毒在癌细胞中的选择性复制。单纯疱疹病毒(HSV)是溶瘤病毒治疗的一种有前途的药物,因为它具有广泛的细胞嗜性,并且已经鉴定出了有利于其在肿瘤细胞中复制而不是在正常细胞中复制的突变。然而,这些减毒突变也往往限制了已进入临床研究的溶瘤性 HSV 载体的效力。作为替代方案,将载体重新靶向到新的进入受体具有在病毒进入阶段实现肿瘤特异性的潜力,从而无需复制减毒突变。在这里,我们总结了 HSV 进入的分子机制以及重新靶向用于溶瘤病毒治疗的完全重新靶向 HSV 载体的最新进展。重新靶向的 HSV 载体为创建新一代具有改善疗效和特异性的溶瘤性 HSV 提供了一个有吸引力的平台。

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