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人类内源性逆转录病毒作为神经退行性疾病的新型治疗靶点

Human Endogenous Retroviruses as Novel Therapeutic Targets in Neurodegenerative Disorders.

作者信息

Simula Elena Rita, Jasemi Seyedesomaye, Cossu Davide, Fais Milena, Cossu Ilaria, Chessa Vanna, Canu Mattia, Sechi Leonardo Antonio

机构信息

Department of Biomedical Sciences, Division of Microbiology and Virology, University of Sassari, 07100 Sassari, Italy.

ASL Sassari, SC Anestesia Territoriale Cure Palliatiave, 07100 Sassari, Italy.

出版信息

Vaccines (Basel). 2025 Apr 15;13(4):415. doi: 10.3390/vaccines13040415.

Abstract

Human Endogenous Retroviruses comprise approximately 8% of the human genome, serving as fragments of ancient retroviral infections. Although they are generally maintained in a silenced state by robust epigenetic mechanisms, specific HERV groups, particularly HERV-W and HERV-K, can become derepressed under specific pathological conditions, thereby contributing to the initiation and progression of neuroinflammatory and neurodegenerative processes. Preclinical studies and clinical trials, such as those investigating monoclonal antibodies, indicate that directly targeting these elements may offer a novel therapeutic strategy. In this review, we provide an overview of HERVs' biology, examine their role in neurodegenerative diseases such as amyotrophic lateral sclerosis, multiple sclerosis, Alzheimer's disease, and Parkinson's disease, and explore their therapeutic prospects, highlighting both the challenges and the potential future research directions needed to translate these approaches into clinical interventions.

摘要

人类内源性逆转录病毒约占人类基因组的8%,是古代逆转录病毒感染的片段。尽管它们通常通过强大的表观遗传机制保持沉默状态,但特定的人类内源性逆转录病毒组,特别是人类内源性逆转录病毒-W和人类内源性逆转录病毒-K,在特定病理条件下可能会去抑制,从而促进神经炎症和神经退行性过程的启动和进展。临床前研究和临床试验,如那些研究单克隆抗体的试验,表明直接靶向这些元件可能提供一种新的治疗策略。在这篇综述中,我们概述了人类内源性逆转录病毒的生物学特性,研究它们在肌萎缩侧索硬化、多发性硬化症、阿尔茨海默病和帕金森病等神经退行性疾病中的作用,并探索它们的治疗前景,强调将这些方法转化为临床干预所需面对的挑战和未来潜在的研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2d2/12031449/e78f5d4f9e2c/vaccines-13-00415-g002.jpg

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