Grandi Nicole, Tramontano Enzo
Laboratory of Molecular Virology, Department of Life and Environmental Sciences, University of Cagliari, Cagliari, Italy.
Istituto di Ricerca Genetica e Biomedica, Consiglio Nazionale delle Ricerche, Cagliari, Italy.
Front Microbiol. 2018 Mar 14;9:462. doi: 10.3389/fmicb.2018.00462. eCollection 2018.
Human endogenous retroviruses (HERVs) are relics of ancient infections accounting for about the 8% of our genome. Despite their persistence in human DNA led to the accumulation of mutations, HERVs are still contributing to the human transcriptome, and a growing number of findings suggests that their expression products may have a role in various diseases. Among HERV products, the envelope proteins (Env) are currently highly investigated for their pathogenic properties, which could likely be participating to several disorders with complex etiology, particularly in the contexts of autoimmunity and cancer. In fact, HERV Env proteins have been shown, on the one side, to trigger both innate and adaptive immunity, prompting inflammatory, cytotoxic and apoptotic reactions; and, on the other side, to prevent the immune response activation, presenting immunosuppressive properties and acting as immune downregulators. In addition, HERV Env proteins have been shown to induce abnormal cell-cell fusion, possibly contributing to tumor development and metastasizing processes. Remarkably, even highly defective HERV genes and alternative splicing variants can provide further mechanisms of pathogenesis. A well-known example is the HERV-K(HML2) gene that, depending on the presence or the absence of a 292-bp deletion, can originate two proteins of different length (Np9 and Rec) proposed to have oncogenic properties. The understanding of their involvement in complex pathological disorders made HERV Env proteins potential targets for therapeutic interventions. Of note, a monoclonal antibody directed against a HERV-W Env is currently under clinical trial as therapeutic approach for multiple sclerosis, representing the first HERV-based treatment. The present review will focus on the current knowledge of the HERV Env expression, summarizing its role in human physiology and its possible pathogenic effects in various cancer and autoimmune disorders. It moreover analyzes HERV Env possible exploitation for the development of innovative therapeutic strategies.
人类内源性逆转录病毒(HERVs)是古代感染的遗迹,约占人类基因组的8%。尽管它们在人类DNA中的持续存在导致了突变的积累,但HERVs仍在对人类转录组产生影响,越来越多的研究结果表明,它们的表达产物可能在各种疾病中发挥作用。在HERV产物中,包膜蛋白(Env)目前因其致病特性而受到高度研究,这些特性可能参与了多种病因复杂的疾病,特别是在自身免疫和癌症的背景下。事实上,一方面,HERV Env蛋白已被证明可触发先天性和适应性免疫,引发炎症、细胞毒性和凋亡反应;另一方面,它又能阻止免疫反应的激活,具有免疫抑制特性并充当免疫下调因子。此外,HERV Env蛋白已被证明可诱导异常的细胞间融合,可能有助于肿瘤的发展和转移过程。值得注意的是,即使是高度缺陷的HERV基因和可变剪接变体也能提供进一步的致病机制。一个著名的例子是HERV-K(HML2)基因,根据是否存在292 bp的缺失,它可以产生两种不同长度的蛋白质(Np9和Rec),这两种蛋白质被认为具有致癌特性。对它们参与复杂病理疾病的了解使HERV Env蛋白成为治疗干预的潜在靶点。值得注意的是,一种针对HERV-W Env的单克隆抗体目前正在作为治疗多发性硬化症的方法进行临床试验,这是第一种基于HERV的治疗方法。本综述将聚焦于HERV Env表达的现有知识,总结其在人类生理学中的作用以及在各种癌症和自身免疫性疾病中可能的致病作用。此外,还分析了HERV Env在开发创新治疗策略方面的可能应用。