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本文引用的文献

1
PD-L1 in tumor microenvironment mediates resistance to oncolytic immunotherapy.肿瘤微环境中的 PD-L1 介导了对溶瘤免疫治疗的耐药性。
J Clin Invest. 2018 Apr 2;128(4):1413-1428. doi: 10.1172/JCI98047. Epub 2018 Mar 5.
2
Randomized, Open-Label Phase II Study Evaluating the Efficacy and Safety of Talimogene Laherparepvec in Combination With Ipilimumab Versus Ipilimumab Alone in Patients With Advanced, Unresectable Melanoma.随机、开放标签的 II 期研究评估了替莫唑胺联合伊匹单抗与伊匹单抗单药治疗晚期不可切除黑色素瘤患者的疗效和安全性。
J Clin Oncol. 2018 Jun 10;36(17):1658-1667. doi: 10.1200/JCO.2017.73.7379. Epub 2017 Oct 5.
3
Oncolytic Virotherapy Promotes Intratumoral T Cell Infiltration and Improves Anti-PD-1 Immunotherapy.溶瘤病毒疗法可促进肿瘤内T细胞浸润并改善抗PD-1免疫疗法。
Cell. 2017 Sep 7;170(6):1109-1119.e10. doi: 10.1016/j.cell.2017.08.027.
4
Oncolytic viruses: a new class of immunotherapy drugs.溶瘤病毒:一类新型免疫治疗药物。
Nat Rev Drug Discov. 2015 Sep;14(9):642-62. doi: 10.1038/nrd4663.
5
Local and distant immunity induced by intralesional vaccination with an oncolytic herpes virus encoding GM-CSF in patients with stage IIIc and IV melanoma.瘤内注射 GM-CSF 编码溶瘤单纯疱疹病毒在 IIIc 期和 IV 期黑色素瘤患者中诱导的局部和远处免疫。
Ann Surg Oncol. 2010 Mar;17(3):718-30. doi: 10.1245/s10434-009-0809-6.

释放溶瘤病毒的治疗潜力。

Unleashing the therapeutic potential of oncolytic viruses.

机构信息

Rutgers University, New Brunswick, New Jersey, USA.

Replimune Inc., Woburn, Massachusetts, USA.

出版信息

J Clin Invest. 2018 Apr 2;128(4):1258-1260. doi: 10.1172/JCI120303. Epub 2018 Mar 5.

DOI:10.1172/JCI120303
PMID:29504947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5873873/
Abstract

Oncolytic viruses (OVs) are a versatile new class of therapeutic agents based on native or genetically modified viruses that selectively replicate in tumor cells and can express therapeutic transgenes designed to target cells within the tumor microenvironment and/or host immunity. To date, however, confirmation of the underlying mechanism of action and an understanding of innate and acquired drug resistance for most OVs have been limited. In this issue of the JCI, Zamarin et al. report a comprehensive analysis of an oncolytic Newcastle disease virus (NDV) using both murine melanoma tumor models and human tumor explants to explore how the virus promotes tumor eradication and details of the mechanisms involved. These findings have implications for the optimization of oncolytic immunotherapy, at least that based on NDV, and further confirm that specific combinatorial approaches are promising for clinical development.

摘要

溶瘤病毒 (OVs) 是一类基于天然或经过基因改造的病毒的新型多功能治疗药物,它们能够选择性地在肿瘤细胞中复制,并能够表达设计用于靶向肿瘤微环境内的细胞和/或宿主免疫的治疗性转基因。然而,迄今为止,大多数 OVs 的作用机制的确认以及对先天和获得性耐药性的理解都受到了限制。在本期 JCI 中,Zamarin 等人报告了使用鼠黑色素瘤肿瘤模型和人肿瘤外植体对溶瘤新城疫病毒 (NDV) 进行的全面分析,以探讨病毒如何促进肿瘤清除以及所涉及的机制细节。这些发现对于溶瘤免疫疗法的优化具有重要意义,至少对于基于 NDV 的溶瘤免疫疗法具有重要意义,并进一步证实,特定的组合方法在临床开发中具有广阔前景。