Human antibody combinations determined by epitope mapping of orthopoxvirus A33/A35 confer therapeutic protection in mice

Human infections with mpox virus (MPXV) since 2022 have resulted in more than 188,000 cases reported globally as of June 2026, highlighting the urgent need for effective therapeutics. Here, we recruited smallpox vaccinees and donors with incidental vaccinia virus (VACV) exposure and isolated a panel of human anti-A33/A35 monoclonal antibodies (mAbs) from the latter using recombinant MPXV A35 as a cross-reactive bait. These mAbs recognized four distinct nonoverlapping epitopes (epitopes 1 to 4) and one composite epitope (epitope 3 + 4) on MPXV A35 and exhibited cross-reactivity against multiple orthopoxviruses (OPXVs). Cryo–electron microscopy structural analysis revealed that the high-affinity epitope 3 + 4 mAb HD15 engages an epitope at the A35 dimer interface that is conserved across OPXVs. Combinations of mAbs targeting nonoverlapping epitopes mediated synergistic, Fc-dependent neutralization in vitro; conferred therapeutic protection against lethal VACV challenge; and reduced viral burden and disease severity after MPXV challenge in mice. Together, these findings establish a single-antigen, multiepitope strategy for the development of broadly protective therapeutics against OPXVs.

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Publication Details

Journal
Science Translational Medicine
Published
2026-11-11
DOI
https://doi.org/10.1126/scitranslmed.aeb2836
Primary Topic
Poxvirus research and outbreaks
Type
article
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article

Human antibody combinations determined by epitope mapping of orthopoxvirus A33/A35 confer therapeutic protection in mice

Jieliang Chen, Yi-ou Sha, Cong Zeng, Anqi Xia et al.
Science Translational Medicine
Poxvirus research and outbreaks
article

Human antibody combinations determined by epitope mapping of orthopoxvirus A33/A35 confer therapeutic protection in mice

Jieliang Chen, Yi-ou Sha, Cong Zeng, Anqi Xia, Qiwei Jiang, Yuru Han, Zhenghong Yuan, Weiyu Jiang, Qianqian Zhang, Lu Lu, Xiao Li, Qiao Wang, Rong Zhang, Jie Liu, Rong Xia, Yixiao Zhang, Song Xue, Yidan Gao, Liyuan Hu, Wei Wu, Haiyu Wang, Yingying Song, Xiaojie Wang, Jiannan Chen, Siyuan Sun, Yaming Li, Yiming Long, Haozhe Zhao
article en

Abstract

Human infections with mpox virus (MPXV) since 2022 have resulted in more than 188,000 cases reported globally as of June 2026, highlighting the urgent need for effective therapeutics. Here, we recruited smallpox vaccinees and donors with incidental vaccinia virus (VACV) exposure and isolated a panel of human anti-A33/A35 monoclonal antibodies (mAbs) from the latter using recombinant MPXV A35 as a cross-reactive bait. These mAbs recognized four distinct nonoverlapping epitopes (epitopes 1 to 4) and one composite epitope (epitope 3 + 4) on MPXV A35 and exhibited cross-reactivity against multiple orthopoxviruses (OPXVs). Cryo–electron microscopy structural analysis revealed that the high-affinity epitope 3 + 4 mAb HD15 engages an epitope at the A35 dimer interface that is conserved across OPXVs. Combinations of mAbs targeting nonoverlapping epitopes mediated synergistic, Fc-dependent neutralization in vitro; conferred therapeutic protection against lethal VACV challenge; and reduced viral burden and disease severity after MPXV challenge in mice. Together, these findings establish a single-antigen, multiepitope strategy for the development of broadly protective therapeutics against OPXVs.

Science Translational MedicineVol. 18(875)
Shanghai Medical College of Fudan University (CN), Chinese Academy of Sciences (CN), Fudan University (CN), Academy of Military Medical Sciences (CN), Shandong Tumor Hospital (CN), Shanghai Institute of Organic Chemistry (CN), Wuxi People's Hospital (CN), Huashan Hospital (CN), Shandong First Medical University (CN), Nanjing Medical University (CN)
Poxvirus research and outbreaks
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