摘要
背景:肿瘤病毒(oncolytic virus,OVS)优先感染癌细胞,诱导宿主抗肿瘤免疫应答,已成为一种有效的黑色素瘤治疗方法。塔那波病毒(TANV)基因组庞大,导致人类轻度自我限制性疾病,是一种潜在的理想的OV候选基因。白细胞介素-2(IL-2)是一种T细胞生长因子,在激活T细胞中起着关键作用,自然杀伤(NK)细胞和巨噬细胞在先天和适应性免疫系统。目的:研制一种重组表达小鼠白细胞介素2(tnvΔ66r/mil-2)的重组病毒。胸腺嘧啶激酶(TK)基因(66r)与小鼠(M)mil-2转基因产生TANVΔ66r/mil-2。 方法:通过皮下注射SKMEL-3细胞,在雌性无胸腺裸鼠中诱导人黑色素瘤肿瘤。 用瘤内注射病毒治疗小鼠肿瘤体积R平均45±4.5mm3。 结果:在细胞培养中,IL-2的表达不仅抑制了TANVΔ66r/mil-2的复制,而且抑制了TANVGFP的复制。结果表明,IL-2可抑制病毒通过细胞内复制。不激活干扰素信号通路的成分。在TANV中引入mil-2可显著提高其抗肿瘤活性,使其明显退行性变。野生型(Wt)TANV和TANVΔ66r.病理组织学研究表明,肿瘤中广泛的细胞变性和肿瘤周围单个核细胞的聚集显著增加。TH TANVΔ66r/mil-2与WtTANV或TANVΔ66r比较。 结论:TANVΔ66r/mil-2在缺乏T细胞的情况下对人黑色素瘤有潜在的治疗作用,而IL-2的表达则导致整体疗效的提高。
关键词: 肿瘤病毒治疗,免疫治疗,黑色素瘤,丹那波病毒,白细胞介素2,天然免疫,病毒复制。
图形摘要
Current Cancer Drug Targets
Title:Oncolytic Tanapoxvirus Expressing Interleukin-2 is Capable of Inducing the Regression of Human Melanoma Tumors in the Absence of T Cells
Volume: 18 Issue: 6
关键词: 肿瘤病毒治疗,免疫治疗,黑色素瘤,丹那波病毒,白细胞介素2,天然免疫,病毒复制。
摘要: Background: Oncolytic viruses (OVs), which preferentially infect cancer cells and induce host anti-tumor immune responses, have emerged as an effective melanoma therapy. Tanapoxvirus (TANV), which possesses a large genome and causes mild self-limiting disease in humans, is potentially an ideal OV candidate. Interleukin-2 (IL-2), a T-cell growth factor, plays a critical role in activating T cells, natural killer (NK) cells and macrophages in both the innate and adaptive immune system.
Objective: We aimed to develop a recombinant TANV expressing mouse IL-2 (TANVΔ66R/mIL- 2), replacing the viral thymidine kinase (TK) gene (66R) with the mouse (m) mIL-2 transgene resulting in TANVΔ66R/mIL-2.
Methods: Human melanoma tumors were induced in female athymic nude mice by injecting SKMEL- 3 cells subcutaneously. Mice were treated with an intratumoral injection of viruses when the tumor volumes reached 45 ± 4.5 mm3.
Results: In cell culture, expression of IL-2 attenuated virus replication of not only TANVΔ66R/ mIL-2, but also TANVGFP. It was demonstrated that IL-2 inhibited virus replication through intracellular components and without activating the interferon-signaling pathway. Introduction of mIL-2 into TANV remarkably increased its anti-tumor activity, resulting in a more significant regression than with wild-type (wt) TANV and TANVΔ66R. Histopathological studies showed that extensive cell degeneration with a significantly increased peri-tumor accumulation of mononuclear cells in the tumors treated with TANVΔ66R/mIL-2, compared to wtTANV or TANVΔ66R.
Conclusion: We conclude that TANVΔ66R/mIL-2 is potentially therapeutic for human melanomas in the absence of T cells, and IL-2 expression resulted in an overall increase of therapeutic efficacy.
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Cite this article as:
Oncolytic Tanapoxvirus Expressing Interleukin-2 is Capable of Inducing the Regression of Human Melanoma Tumors in the Absence of T Cells, Current Cancer Drug Targets 2018; 18 (6) . https://dx.doi.org/10.2174/1568009617666170630143931
DOI https://dx.doi.org/10.2174/1568009617666170630143931 |
Print ISSN 1568-0096 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5576 |
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