Li Bang, Qin Xiang-Rong, Qu Jia-Chen, Wu Guan-du, Zhang Wen-Kang, Jiang Ze-Zheng, Liu Pan-Pan, Li Ze-Min, Yu Tian-Mei, Zhou Chuan-Min, Jiao Yong-Jun, Yu Xue-Jie
State Key Laboratory of Virology, School of Public Health, Wuhan University, Wuhan, China.
Department of Clinical Laboratory, The Second Hospital of Shandong University, Jinan, China.
PLoS Pathog. 2025 Jan 31;21(1):e1012889. doi: 10.1371/journal.ppat.1012889. eCollection 2025 Jan.
Severe fever with thrombocytopenia syndrome (SFTS) is a viral hemorrhagic fever caused by a tick-borne virus SFTSV with a mortality rate of up to 30%. Currently, there is no vaccine or effective therapy for SFTS. Neutralizing monoclonal antibody therapy, which provides immediate passive immunity and may limit disease progression, has emerged as a reliable approach for developing therapeutic drugs for SFTS. In this study, 4 human monoclonal antibodies (hmAbs) derived from convalescent SFTS patients' lymphocytes based on human single-chain variable fragment antibody libraries were tested for their neutralizing activities in cells and their treatment effect in animals individually and in pair combinations. The neutralization test showed that all 4 hmAbs exhibited strong neutralizing activity against SFTSV infection in vitro. The protection rate of hmAbs 4-6, 1F6, 1B2, and 4-5 against SFTSV lethal challenge in IFNAR1-/- A129 mice are 50%, 16.7%, 83.3%, and 66.7%, respectively. Notably, the pair combination of antibodies (1B2 and 4-5, 1B2 and 1F6) that recognized distinct epitopes protected 100% of mice against SFTSV lethal challenge. In conclusion, our findings indicate that the pair combinations of hmAbs 1B2 and 4-5 or hmAbs 1B2 and 1F6 may serve as promising therapeutic drugs for treating SFTSV infection.
严重发热伴血小板减少综合征(SFTS)是一种由蜱传病毒SFTSV引起的病毒性出血热,死亡率高达30%。目前,尚无针对SFTS的疫苗或有效治疗方法。中和单克隆抗体疗法可提供即时被动免疫并可能限制疾病进展,已成为开发SFTS治疗药物的可靠方法。在本研究中,对4种基于人单链可变片段抗体库从SFTS康复患者淋巴细胞中获得的人单克隆抗体(hmAbs)分别及成对组合检测其在细胞中的中和活性及在动物中的治疗效果。中和试验表明,所有4种hmAbs在体外均对SFTSV感染表现出强大的中和活性。hmAbs 4-6、1F6、1B2和4-5对IFNAR1-/- A129小鼠中SFTSV致死性攻击的保护率分别为50%、16.7%、83.3%和66.7%。值得注意的是,识别不同表位的抗体成对组合(1B2和4-5、1B2和1F6)使100%的小鼠免受SFTSV致死性攻击。总之,我们的研究结果表明,hmAbs 1B2和4-5或hmAbs 1B2和1F6的成对组合可能是治疗SFTSV感染的有前景的治疗药物。