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本文引用的文献

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The rabbit papillomavirus model: a valuable tool to study viral-host interactions.兔乳头瘤病毒模型:研究病毒-宿主相互作用的有价值工具。
Philos Trans R Soc Lond B Biol Sci. 2019 May 27;374(1773):20180294. doi: 10.1098/rstb.2018.0294.
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Microvesicles and chemokines in tumor microenvironment: mediators of intercellular communications in tumor progression.微囊泡与肿瘤微环境中的趋化因子:肿瘤进展中细胞间通讯的介质。
Mol Cancer. 2019 Mar 30;18(1):50. doi: 10.1186/s12943-019-0973-7.
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Genomic Characterization of Strain D1701-V () and Development of Novel Sites for Multiple Transgene Expression.D1701-V()株的基因组特征与多个转基因表达新位点的开发
Viruses. 2019 Jan 30;11(2):127. doi: 10.3390/v11020127.
4
Cottontail Rabbit Papillomavirus E1 and E2 Proteins Mutually Influence Their Subcellular Localizations.棉尾兔乳头瘤病毒 E1 和 E2 蛋白相互影响其亚细胞定位。
J Virol. 2018 Oct 12;92(21). doi: 10.1128/JVI.00704-18. Print 2018 Nov 1.
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Therapeutic vaccines for high-risk HPV-associated diseases.用于高危型人乳头瘤病毒相关疾病的治疗性疫苗。
Papillomavirus Res. 2018 Jun;5:46-58. doi: 10.1016/j.pvr.2017.12.006. Epub 2017 Dec 19.
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Therapeutic HPV vaccines.治疗性 HPV 疫苗。
Best Pract Res Clin Obstet Gynaecol. 2018 Feb;47:59-72. doi: 10.1016/j.bpobgyn.2017.09.008. Epub 2017 Sep 28.
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Oncogenic human papillomaviruses.致癌性人乳头瘤病毒
Philos Trans R Soc Lond B Biol Sci. 2017 Oct 19;372(1732). doi: 10.1098/rstb.2016.0273.
8
Keratinocyte Differentiation-Dependent Human Papillomavirus Gene Regulation.角质形成细胞分化依赖性人乳头瘤病毒基因调控
Viruses. 2017 Aug 30;9(9):245. doi: 10.3390/v9090245.
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Genetic susceptibility in cervical cancer: From bench to bedside.宫颈癌的遗传易感性:从实验室到临床
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Human papillomavirus molecular biology.人乳头瘤病毒分子生物学。
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基于口疮病毒的治疗性疫苗治疗乳头瘤病毒诱导的肿瘤。

Orf Virus-Based Therapeutic Vaccine for Treatment of Papillomavirus-Induced Tumors.

机构信息

University Hospital Tuebingen, Institute for Medical Virology and Epidemiology of Viral Diseases, Tuebingen, Germany.

University of Tuebingen, Interfaculty Institute for Cell Biology, Department of Immunology, Tuebingen, Germany.

出版信息

J Virol. 2020 Jul 16;94(15). doi: 10.1128/JVI.00398-20.

DOI:10.1128/JVI.00398-20
PMID:32404527
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7375371/
Abstract

Orf virus (ORFV) represents a suitable vector for the generation of efficient, prophylactic antiviral vaccines against different pathogens. The present study investigated for the first time the therapeutic application of ORFV vector-based vaccines against tumors induced by cottontail rabbit papillomavirus (CRPV). ORFV-CRPV recombinants were constructed expressing the early CRPV gene E1, E2, E7, or LE6. In two independent experiments we used in total 23 rabbits which were immunized with a mixture of the four ORFV-CRPV recombinants or empty ORFV vector as a control 5 weeks after the appearance of skin tumors. For the determination of the therapeutic efficacy, the subsequent growth of the tumors was recorded. In the first experiment, we could demonstrate that three immunizations of rabbits with high tumor burden with the combined four ORFV-CRPV recombinants resulted in significant growth retardation of the tumors compared to the control. A second experiment was performed to test the therapeutic effect of 5 doses of the combined vaccine in rabbits with a lower tumor burden than in nonimmunized rabbits. Tumor growth was significantly reduced after immunization, and one vaccinated rabbit even displayed complete tumor regression until the end of the observation period at 26 weeks. Results of delayed-type hypersensitivity (DTH) skin tests suggest the induction of a cellular immune response mediated by the ORFV-CRPV vaccine. The data presented show for the first time a therapeutic potential of the ORFV vector platform and encourage further studies for the development of a therapeutic vaccine against virus-induced tumors. Viral vectors are widely used for the development of therapeutic vaccines for the treatment of tumors. In our study we have used Orf virus (ORFV) strain D1701-V for the generation of recombinant vaccines expressing cottontail rabbit papillomavirus (CRPV) early proteins E1, E2, LE6, and E7. The therapeutic efficacy of the ORFV-CRPV vaccines was evaluated in two independent experiments using the outbred CRPV rabbit model. In both experiments the immunization achieved significant suppression of tumor growth. In total, 84.6% of all outbred animals benefited from the ORFV-CRPV vaccination, showing reduction in tumor size and significant tumor growth inhibition, including one animal with complete tumor regression without recurrence.

摘要

口疮病毒(ORFV)是一种能够高效生成预防性抗病毒疫苗的合适载体,可用于预防多种病原体感染。本研究首次探索了口疮病毒载体疫苗在对抗兔乳头瘤病毒(CRPV)诱导肿瘤方面的治疗应用。本研究构建了表达 CRPV 早期基因 E1、E2、E7 和 LE6 的 ORFV-CRPV 重组病毒。在两项独立的实验中,我们共使用了 23 只兔子,在皮肤肿瘤出现后 5 周,使用包含这四种 ORFV-CRPV 重组病毒的混合物或空 ORFV 载体进行免疫。为了确定治疗效果,我们记录了随后肿瘤的生长情况。在第一项实验中,我们发现对高肿瘤负担的兔子进行三次联合免疫可显著减缓肿瘤生长,与对照组相比效果明显。第二项实验用于检测低肿瘤负担的兔子接受五次联合疫苗免疫的治疗效果。免疫后肿瘤生长明显减缓,一只接种的兔子甚至出现完全的肿瘤消退,直至 26 周的观察结束。迟发型超敏反应(DTH)皮肤试验的结果表明,ORFV-CRPV 疫苗诱导了细胞免疫反应。本研究首次证明了口疮病毒载体平台具有治疗潜力,鼓励进一步研究开发针对病毒诱导肿瘤的治疗性疫苗。病毒载体被广泛用于开发治疗肿瘤的治疗性疫苗。在本研究中,我们使用 ORFV 株 D1701-V 生成表达兔乳头瘤病毒(CRPV)早期蛋白 E1、E2、LE6 和 E7 的重组疫苗。我们在两个独立的实验中使用 CRPV 兔模型评估了 ORFV-CRPV 疫苗的治疗效果。在这两项实验中,免疫接种都显著抑制了肿瘤生长。总共 84.6%的异系动物受益于 ORFV-CRPV 疫苗接种,表现为肿瘤缩小和显著的肿瘤生长抑制,其中一只动物完全消退且未复发。