Song Liyuan, Fu Guangcheng, Li Jie, Chen Zhengshan, Fu Ling, Yu Changming, Qiang Li, Li Jiangfan, Fang Ting, Yuan Hongyu, Li Jianmin
Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing 100071, China.
Laboratory of Advanced Biotechnology, ZJU-Hangzhou Global Scientific and Technological Innovation Center, Hangzhou 311215, China.
Int J Mol Sci. 2025 Apr 23;26(9):3982. doi: 10.3390/ijms26093982.
The Chikungunya virus (CHIKV) is a priority endemic pathogen identified by the World Health Organization and its infection induces an acute febrile illness in humans that is often associated with arthritis and musculoskeletal pain. Therefore, specific vaccines and treatments are urgently needed to prevent or treat Chikungunya disease. Here, we identify a series of CHIKV-specific neutralizing nanobodies (Nbs) from an alpaca which exhibit distinct binding modes compared to those previously reported. Two representative anti-CHIKV Nbs, N033-Fc and N053-Fc, demonstrated significant antiviral activity in mice against lethal challenge. Further studies elucidated the functional mechanisms of N033-Fc and N053-Fc in blocking CHIKV infection at multiple stages of the viral life cycle. This study identifies multiple candidate Nbs that may be suitable for next-generation antibody therapies to combat CHIKV infection.
基孔肯雅病毒(CHIKV)是世界卫生组织确定的重点地方性病原体,其感染会引发人类急性发热疾病,常伴有关节炎和肌肉骨骼疼痛。因此,迫切需要特定的疫苗和治疗方法来预防或治疗基孔肯雅病。在此,我们从羊驼中鉴定出一系列CHIKV特异性中和纳米抗体(Nbs),与先前报道的相比,它们表现出不同的结合模式。两种代表性的抗CHIKV Nbs,N033-Fc和N053-Fc,在小鼠中对致死性攻击显示出显著的抗病毒活性。进一步的研究阐明了N033-Fc和N053-Fc在病毒生命周期多个阶段阻断CHIKV感染的功能机制。本研究鉴定出多个可能适用于对抗CHIKV感染的下一代抗体疗法的候选Nbs。