Generation and characterization of neutralizing antibodies against M1R and B6R proteins of monkeypox virus

文献类型： 外文期刊

第一作者： Qu, Yuanyuan

作者： Qu, Yuanyuan;Tai, Wanbo;Xiao, Wangcheng;Tian, Chongyu;Liu, Yang;Liu, Jianying;Ma, Enhao;Cheng, Gong;Ma, Enhao;Cheng, Gong;Ma, Enhao;Cheng, Gong;Jiang, Qiwei;Fan, Miao;Ge, Jiwan;Wang, Xinquan

作者机构：

期刊名称：NATURE COMMUNICATIONS （ 影响因子：15.7； 五年影响因子：17.2 ）

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年卷期： 2025 年 16 卷 1 期

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收录情况： SCI

摘要： The global outbreak of monkeypox virus (MPXV), combined with the termination of smallpox vaccination and the lack of specific antiviral treatments, raises increasing concerns. The surface proteins M1R and B6R of MPXV are crucial for virus transmission and serve as key targets for vaccine development. In this study, a panel of human antibodies targeting M1R and B6R is isolated from a human antibody library using phage display technology. Among these antibodies, A138 against M1R and B026 against B6R show the most potent broad-spectrum neutralizing activities against MPXV and Vaccinia virus (VACV). When used in combination, A138 and B026 exhibit complementary neutralizing activity against both viruses in vitro. X-ray crystallography reveales that A138 binds to the loop regions of M1R, similar to the vulnerable epitope of 7D11 on VACV L1R. By contrast, A129 targets a more cryptic epitope, primarily comprising the beta-strands of M1R. Moreover, prophylactic and therapeutic administration of A138 or B026 alone provides partial protection, while combining these two antibodies results in enhanced protection against VACV in male C57BL/6 mice. This study demonstrates of a dual-targeting strategy using two different components of the virion for the prevention and treatment of MPXV infection.

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