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探索 HVJ-E 在癌症免疫治疗中的潜力

英文原题:Exploring the potential of HVJ-E for cancer immunotherapy.

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Exploring the potential of HVJ-E for cancer immunotherapy.

PubMed 2026/07/09(内容时间) Immunotherapy Q3 · IF 2.3(JCR 2025)

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研究概要

HVJ-Envelope(HVJ-E)是一种源自日本血凝病毒的灭活颗粒,代表了一种独特的基于病毒的癌症免疫治疗方法。

中文摘要

HVJ-Envelope(HVJ-E)是一种源自日本血凝病毒(Hemagglutinating virus of Japan)的灭活颗粒,代表了一种独特的基于病毒的癌症免疫治疗策略。与具有复制能力的溶瘤病毒通过病毒增殖和肿瘤细胞裂解发挥抗肿瘤作用不同,HVJ-E因其病毒基因组被片段化而缺乏复制能力和致病性。相反,尽管大多数非复制型病毒载体主要被设计为递送载体,HVJ-E本身具有内在的抗肿瘤活性。通过保留亲本病毒的天然病毒结构和膜融合能力,HVJ-E能够使片段化的病毒基因组进入靶细胞,从而诱导抗肿瘤免疫激活和肿瘤细胞死亡。机制研究表明,HVJ-E促进树突状细胞成熟,激活NK 细胞,并刺激细胞毒性T淋巴细胞,从而产生系统性抗肿瘤免疫。临床试验已证明其具有良好的安全性特征和令人鼓舞的疗效迹象。此外,反向转化研究已确定了与T细胞共刺激信号通路的联合策略,以及载脂蛋白系统作为增强免疫攻击敏感性的下游介质。本综述总结了HVJ-E作为一种新型癌症免疫治疗平台的历史发展、机制见解和新兴治疗理念。使用PubMed对2002年至2025年间发表的与HVJ-E和癌症相关的文章进行了全面文献检索。当病毒进入人体时,它们进入细胞并增殖。这可能损害我们的细胞并引起感染等疾病。尽管病毒通常是有害的,但它们进入细胞的能力也可能是有用的。研究人员正在利用这一特性,将病毒改造成“载体”,把癌症治疗药物递送到体内。为了确保患者安全,科学家对这些病毒进行改造,使其仍能进入细胞,但不再能够增殖。这些病毒在癌症治疗中被称为“非复制型病毒载体”。HVJ-Envelope(HVJ-E)就是其中一种安全载体,由日本血凝病毒(HVJ)制成。然而,HVJ-E不仅仅是一种载体。它还能直接杀死癌细胞,并刺激机体的防御系统识别并摧毁癌细胞。这意味着HVJ-E是一种高度独特的活性治疗剂。近年来,临床试验已在皮肤癌和其他癌症患者中测试了HVJ-E。这些研究表明,HVJ-E能够安全地缩小肿瘤,且不会引起严重副作用。在这篇综述中,我们阐述了HVJ-E最初如何作为载体被开发出来,其作为抗肿瘤武器的独特特性是如何被发现的,以及研究人员如何对其进行改进以用于癌症治疗,包括在临床试验中的测试。最后,我们讨论了基于HVJ-E的癌症疗法的未来,重点介绍了关于开发新疗法的最新研究,这些疗法能够强烈触发机体的抗肿瘤防御系统,从而有效清除癌细胞。

展开英文摘要原文

HVJ-Envelope (HVJ-E), an inactivated particle derived from the Hemagglutinating virus of Japan, represents a unique virus-based approach for cancer immunotherapy. Unlike replication-competent oncolytic viruses, which exert antitumor effects through viral propagation and tumor cell lysis, HVJ-E lacks replicative capacity and pathogenicity because its viral genome is fragmented. Conversely, although most non-replicative viral vectors are designed primarily as delivery vehicles, HVJ-E itself possesses intrinsic antitumor activity. By preserving the native viral structure and membrane-fusion capacity of the parental virus, HVJ-E enables fragmented viral genomes to enter target cells, thereby inducing antitumor immune activation and tumor cell death. Mechanistic studies have shown that HVJ-E promotes dendritic cell maturation, activates natural killer cells, and stimulates cytotoxic T lymphocytes, leading to systemic antitumor immunity. Clinical trials have demonstrated favorable safety profiles and encouraging signs of efficacy. Furthermore, reverse translational research has identified combination strategies with T cell co-stimulatory signaling and the apolipoprotein system as a downstream mediator that enhances sensitivity to immune attack. This review summarizes the historical development, mechanistic insights, and emerging therapeutic concepts of HVJ-E as a novel cancer immunotherapy platform. A comprehensive literature search was conducted using PubMed for articles related to HVJ-E and cancer published between 2002 and 2025. When viruses enter the human body, they move into cells and multiply. This can damage our cells and cause diseases like infections. Although viruses are usually harmful, their ability to enter cells can also be useful. Researchers are using this property to turn viruses into “carriers” that deliver cancer treatments into the body. To keep patients safe, scientists modify these viruses so they can still enter cells but can no longer multiply. These are used in cancer treatment as “non-replicative viral vectors.” HVJ-Envelope (HVJ-E) is one of these safe carriers, made from the Hemagglutinating Virus of Japan (HVJ). However, HVJ-E is not just a carrier. It can also kill cancer cells directly and stimulate the body’s defense system to recognize and destroy them. This means HVJ-E acts as a highly unique active therapeutic agent. Recently, clinical trials have tested HVJ-E in patients with skin cancer and other cancers. These studies show that HVJ-E can shrink tumors safely without causing major side effects.In this review, we explain how HVJ-E was first developed as a carrier, how its unique features as an anti-tumor weapon were discovered, and how researchers have improved it for cancer treatment, including its testing in clinical trials. Finally, we discuss the future of HVJ-E-based cancer therapies, highlighting the latest research on developing new treatments that strongly trigger the body‘s anti-tumor defense system to eliminate cancer cells effectively.

论文信息

作者
Harada A、Nimura K
单位
Division of Gene Therapy Science, Gunma University Initiative for Advanced Research, Gunma University, Maebashi City, Japan.Japan
文献类型
综述
期刊
Immunotherapy2026 Jun-Jun
原文标识
PubMed 42423067 · DOI 10.1080/1750743X.2026.2697678