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针对严重发热伴血小板减少综合征病毒糖蛋白 Gc 的抗体的特征分析。

Characterization of antibodies targeting severe fever with thrombocytopenia syndrome virus glycoprotein Gc.

机构信息

Department of Pathology, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku, Shinjuku, Tokyo, 162-8640, Japan.

Research Center for Influenza and Respiratory Viruses, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.

出版信息

Arch Virol. 2024 Feb 3;169(3):40. doi: 10.1007/s00705-024-05968-x.

Abstract

Severe fever with thrombocytopenia syndrome (SFTS) is a hemorrhagic fever caused by SFTS virus (SFTSV), which is primarily found in East Asian countries. Despite its high mortality rate and increasing incidence, no vaccines or therapeutics have yet been approved for use against SFTS. Antibody drugs have shown promise in treating lethal infectious diseases that currently have no established treatments. In the case of SFTS, however, only a limited amount of research has been done on SFTSV-neutralizing antibodies targeting the transmembrane proteins Gn and Gc, which play critical roles in viral infection. This study focuses on the production and characterization of antibodies targeting the SFTSV Gc protein. Monoclonal antibodies against Gc were generated through immunization of mice, and their antiviral activity was evaluated. Three out of four anti-Gc antibody clones from this study demonstrated dose-dependent SFTSV neutralization activity, two of which exhibited a synergistic effect on the neutralization activity of the anti-Gn antibody clone Mab4-5. Further studies are necessary to identify key sites on the SFTSV glycoprotein and to develop novel agents as well as antibodies with diverse mechanisms of action against SFTSV.

摘要

严重发热伴血小板减少综合征(SFTS)是由SFTS 病毒(SFTSV)引起的一种出血热,主要发生在东亚国家。尽管其死亡率和发病率不断上升,但目前还没有批准用于治疗 SFTS 的疫苗或疗法。抗体药物在治疗目前尚无既定治疗方法的致命传染病方面显示出了前景。然而,对于 SFTS,针对在病毒感染中起关键作用的跨膜蛋白 Gn 和 Gc 的 SFTSV 中和抗体的研究非常有限。本研究专注于针对 SFTSV Gc 蛋白的抗体的生产和特性研究。通过免疫小鼠产生了针对 Gc 的单克隆抗体,并评估了它们的抗病毒活性。本研究的四个抗-Gc 抗体克隆中有三个显示出剂量依赖性 SFTSV 中和活性,其中两个在中和抗 Gn 抗体克隆 Mab4-5 的活性方面表现出协同作用。有必要进一步研究以确定 SFTSV 糖蛋白上的关键位点,并开发新型药物以及具有针对 SFTSV 的不同作用机制的抗体。

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