Pair combinations of human monoclonal antibodies fully protected mice against bunyavirus SFTSV lethal challenge.

IF 4.9 1区 医学 Q1 MICROBIOLOGY PLoS Pathogens Pub Date : 2025-01-31 eCollection Date: 2025-01-01 DOI:10.1371/journal.ppat.1012889
Bang Li, Xiang-Rong Qin, Jia-Chen Qu, Guan-du Wu, Wen-Kang Zhang, Ze-Zheng Jiang, Pan-Pan Liu, Ze-Min Li, Tian-Mei Yu, Chuan-Min Zhou, Yong-Jun Jiao, Xue-Jie Yu
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Abstract

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.

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人单克隆抗体对组合完全保护小鼠免受布尼亚病毒SFTSV致死性攻击。
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,没有针对SFTS的疫苗或有效治疗方法。中和性单克隆抗体治疗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。本研究以人单链可变片段抗体文库为基础,对4种从SFTS恢复期患者淋巴细胞中提取的人单克隆抗体(hmab)在细胞内的中和活性以及在动物体内单独和配对组合的治疗效果进行了检测。中和试验表明,4种hmab在体外对SFTSV感染均表现出较强的中和活性。hmab 4-6、1F6、1B2和4-5对IFNAR1-/- A129小鼠SFTSV致死性攻毒的保护率分别为50%、16.7%、83.3%和66.7%。值得注意的是,识别不同表位的抗体对组合(1B2和4-5,1B2和1F6)保护100%的小鼠免受SFTSV致命攻击。综上所述,我们的研究结果表明,hmab 1B2与4-5或hmab 1B2与1F6的配对组合可能是治疗SFTSV感染的有希望的治疗药物。
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来源期刊
PLoS Pathogens
PLoS Pathogens MICROBIOLOGY-PARASITOLOGY
自引率
3.00%
发文量
598
期刊介绍: Bacteria, fungi, parasites, prions and viruses cause a plethora of diseases that have important medical, agricultural, and economic consequences. Moreover, the study of microbes continues to provide novel insights into such fundamental processes as the molecular basis of cellular and organismal function.
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