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Antiviral Drugs Against Severe Fever With Thrombocytopenia Syndrome Virus Infection

机译:抗病毒药物免受血小板减少症综合征病毒感染的严重发烧

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摘要

Severe fever with thrombocytopenia syndrome (SFTS) is an emerging tick-borne infectious disease caused by SFTS virus (SFTSV), which is a novel bunyavirus. SFTSV was first isolated from patients who presented with fever, thrombocytopenia, leukocytopenia, and multiorgan dysfunction in China. Subsequently, it was found to be widely distributed in Southeast Asia (Korea, Japan, and Vietnam). SFTSV can be transmitted not only from ticks but also from domestic animals, companion animals, and humans. Because the case fatality rate of SFTS is high (6–30%), development of specific and effective treatment for SFTS is required. Studies of potential antiviral drugs for SFTS-specific therapy have been conducted on existing or newly discovered agents in vitro and in vivo, with ribavirin and favipiravir being the most promising candidates. While animal experiments and retrospective studies have demonstrated the limited efficacy of ribavirin, it was also speculated that ribavirin would be effective in patients with a viral load <1 × 106 copies/mL. Favipiravir showed higher efficacy than ribavirin against SFTSV in in vitro assays and greater efficacy in animal models, even administrated 3 days after the virus inoculation. Although clinical trials evaluating the efficacy of favipiravir in SFTS patients in Japan are underway, this has yet to be confirmed. Other drugs, including hexachlorophene, calcium channel blockers, 2′-fluoro-2′-deoxycytidine, caffeic acid, amodiaquine, and interferons, have also been evaluated for their inhibitory efficacy against SFTSV. Among them, calcium channel blockers are promising because in addition to their efficacy in vitro and in vivo, retrospective clinical data have indicated that nifedipine, one of the calcium channel blockers, reduced the case fatality rate by >5-fold. Although further research is necessary to develop SFTS-specific therapy, considerable progress has been achieved in this area. Here we summarize and discuss recent advances in antiviral drugs against SFTSV.
机译:严重发烧血小板减少症综合征(SFT)是由SFTS病毒(SFTSV)引起的新出现的蜱传染病,这是一种新的Bunyavirus。 SFTSV首先从出现发烧,血小板减少症,白细胞减少症和中国多核功能障碍的患者中孤立。随后,发现它被广泛分布在东南亚(韩国,日本和越南)。 SFTSV不仅可以从蜱虫传播,也可以从家畜,伴侣动物和人类传播。由于SFT的情况高(6-30%),因此需要对SFT进行特异性和有效处理的开发。对SFTS特异性治疗的潜在抗病毒药物的研究已经在体外和体内的现有或新发现的药剂上进行,利用林和FaviPiravir是最有前途的候选者。虽然动物实验和回顾性研究表明了利巴韦林的有限效果,但也推测了利巴韦林在病毒载荷<1×106拷贝/ ml的患者中是有效的。 FaviPiravir在体外测定中对Ribavirin的效率较高,并且在动物模型中的效果较高,甚至在病毒接种后3天给药。虽然评估了日本SFTS患者的FaviPiravir的临床试验正在进行中,但尚未得到证实。还评估了其他药物,包括六氯烯,钙通道阻断剂,2'-氟-2'-脱氧胞苷,咖啡酸,氨基喹和干扰素,对其抑制效果免受SFTSV的抑制作用。其中,钙通道阻滞剂是有前途的,因为除了在体外和体内的功效外,回顾性临床数据表明,尼弗哌单,钙通道阻滞剂之一,通过> 5倍降低了壳体死亡率。虽然进一步研究是制定特定SFTS特定治疗的进一步研究,但该领域取得了相当大的进展。在这里,我们总结并讨论了抗病毒药物对SFTSV的最新进展。

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