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严重发热伴血小板减少综合征病毒治疗的最新进展

Recent Advances in Therapeutics for Severe Fever with Thrombocytopenia Syndrome Virus.

作者信息

Dang Huimin, Wang Yuanyuan, Zhang Lihong, Xu Shan, Liu Lei, Tong Yigang

机构信息

School of Basic Medicine, Jiamusi University, Jiamusi 154007, China.

Beijing Advanced Innovation Center for Soft Matter Science and Engineering, College of Life Science and Technology, Beijing University of Chemical Technology, Beijing 100029, China.

出版信息

Viruses. 2025 Aug 28;17(9):1174. doi: 10.3390/v17091174.

Abstract

Severe fever with thrombocytopenia syndrome virus (SFTSV) is a tick-borne bunyavirus with a mortality rate of up to 30%. There is no specific treatment for SFTSV. This article systematically reviews the progress of major anti-SFTSV drugs. The nucleotide analogues (favipiravir, 4'-fluorouridine diphosphate prodrug VV261) have shown clinical potential. Calcium channel blockers (nifedipine, etc.) block virus invasion by inhibiting calcium influx. Monoclonal antibody (S2A5/SNB02) has achieved targeted therapy, and SNB02 nanoantibody has entered clinical trials. However, many candidate agents predominantly focus on a single target, such as viral RdRp or host calcium channels, which makes it difficult to block the entire viral replication cycle and may accelerate the accumulation of resistant mutations. In addition, the low bioavailability of small-molecule drugs, the obstacles to industrial-scale production of antibody-based therapies, and the lack of Phase III clinical evidence severely restrict their clinical translation. Future research should focus on exploring viral replication mechanisms, developing drugs against key viral proteins, and designing multi-target combination therapies and novel drug delivery systems.

摘要

严重发热伴血小板减少综合征病毒(SFTSV)是一种蜱传布尼亚病毒,死亡率高达30%。目前尚无针对SFTSV的特效治疗方法。本文系统回顾了主要抗SFTSV药物的研究进展。核苷酸类似物(法匹拉韦、4'-氟尿苷二磷酸前药VV261)已显示出临床应用潜力。钙通道阻滞剂(硝苯地平等)通过抑制钙内流来阻断病毒入侵。单克隆抗体(S2A5/SNB02)已实现靶向治疗,且SNB02纳米抗体已进入临床试验阶段。然而,许多候选药物主要聚焦于单一靶点,如病毒RNA依赖的RNA聚合酶(RdRp)或宿主钙通道,这使得难以阻断整个病毒复制周期,且可能加速耐药突变的积累。此外,小分子药物的低生物利用度、基于抗体疗法的工业化规模生产障碍以及缺乏III期临床证据,都严重限制了它们的临床转化。未来的研究应集中在探索病毒复制机制、开发针对关键病毒蛋白的药物、设计多靶点联合疗法以及新型药物递送系统。

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