A cautionary note on the selectivity of oncolytic poxviruses.

IF 6.7
Oncolytic Virotherapy Pub Date : 2019-02-11 eCollection Date: 2019-01-01 DOI:10.2147/OV.S189832
Bingtao Tang, Zong Sheng Guo, David L Bartlett, Jia Liu, Grant McFadden, Joanna L Shisler, Edward J Roy
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引用次数: 12

Abstract

Background: Oncolytic viruses selectively infect cancer cells while avoiding infection of normal cells. Usually, selectivity is demonstrated by injecting a virus into tumor-bearing mice and observing infection and lysis of tumor cells without infection of other tissues. The general view is that this selectivity is due to tropisms of the virus. However, apparent selectivity could be due to accessibility. For example, intravenously injected virus may not gain access to cells within the central nervous system (CNS) because of the blood-brain barrier.

Purpose: We tested the CNS safety of two oncolytic poxviruses that have been demonstrated to be safe for treatment of peripheral tumors (vaccinia virus vvDD-IL15-Rα and myxoma virus vMyx-IL15Rα-tdTr).

Methods: Two poxviruses were tested for selectivity in vitro and in vivo.

Results: Both viruses infected glioma cells in vitro. In vivo, both viruses infected glioma cells and did not infect neurons when injected into a tumor or into the normal striatum. However, viral gene expression was observed in ependymal cells lining the ventricles, implying that these poxviruses were not as selective as originally predicted. For vvDD-IL15-Rα, some tumor-bearing mice died soon after virus treatment. If the same titer of vvDD-IL15-Rα was injected directly into the lateral cerebral ventricle of nontumor-bearing mice, it was uniformly fatal. Infection of ependymal cells, subventricular cells, and meninges was widespread. On the other hand, vMyx-IL15Rα-tdTr only transiently infected ependymal cells and was safe even when injected directly into the lateral cerebral ventricles. The two poxviruses also differed in their infection of dendritic cells; vvDD-IL15-Rα infected dendritic cells and lysed them but vMyx-IL15Rα-tdTr did not.

Conclusion: Vaccinia virus vvDD-IL15-Rα is very promising for treating cancer types outside of the brain. However, for cancers located within the brain, myxoma virus vMyx-IL15Rα-tdTr offers a safer alternative.

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关于溶瘤性痘病毒选择性的警告。
背景:溶瘤病毒选择性地感染癌细胞,同时避免感染正常细胞。通常,通过将病毒注射到荷瘤小鼠体内,观察肿瘤细胞的感染和溶解而不感染其他组织来证明选择性。一般认为,这种选择性是由于病毒的趋向性。然而,明显的选择性可能是由于可及性。例如,由于血脑屏障,静脉注射的病毒可能无法进入中枢神经系统(CNS)内的细胞。目的:我们测试了两种溶瘤痘病毒(牛痘病毒vvDD-IL15-Rα和黏液瘤病毒vMyx-IL15Rα-tdTr)的中枢神经系统安全性,这两种病毒已被证明可以安全治疗周围肿瘤。方法:对两种痘病毒进行体外和体内选择性检测。结果:两种病毒均能在体外感染胶质瘤细胞。在体内,两种病毒都能感染胶质瘤细胞,而注射到肿瘤或正常纹状体时,都不会感染神经元。然而,在室管膜细胞中观察到病毒基因表达,这意味着这些痘病毒不像最初预测的那样具有选择性。对于vvDD-IL15-Rα,一些荷瘤小鼠在病毒治疗后很快死亡。如果将相同滴度的vvDD-IL15-Rα直接注射到非荷瘤小鼠的侧脑室,则均匀致死。室管膜细胞、脑室下细胞和脑膜广泛感染。另一方面,vMyx-IL15Rα-tdTr仅短暂感染室管膜细胞,即使直接注射到侧脑室也是安全的。这两种痘病毒对树突状细胞的感染也不同;vvDD-IL15-Rα感染树突状细胞并使其溶解,而vMyx-IL15Rα-tdTr没有。结论:牛痘病毒vvDD-IL15-Rα在治疗脑外肿瘤方面具有广阔的应用前景。然而,对于位于脑内的癌症,黏液瘤病毒vMyx-IL15Rα-tdTr提供了一个更安全的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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