Discovery of potent cross-neutralizing antibodies against Marburg and Ravn viruses with therapeutic potential
Marburg virus (MARV) and Ravn virus (RAVV) are highly pathogenic filoviruses that cause Marburg virus disease (MVD), for which no approved treatment currently exists. In this study, we describe a panel of 10 novel mouse-derived monoclonal antibodies (mAbs), all exhibiting neutralizing activity against MARV. Notably, five of these mAbs also cross-neutralize RAVV. Based on amino acid sequences, neutralization profiles, and escape mutations in the MARV glycoprotein (GP), the mAbs were classified into three groups. mAbs targeting the receptor-binding domain (RBD) and mucin-like domain exhibited MARV-specific neutralization, whereas those targeting epitopes spanning the RBD and internal fusion loop exhibited cross-neutralization. Post-exposure administration of cross-neutralizing mAbs (AGP-R7, AGP-R12) provided significant protection in MARV and RAVV infection mouse models. These findings identify a conserved neutralizing epitope with therapeutic potential and highlight AGP-R7 and AGP-R12 as promising candidates for MVD treatment. This study offers new insights into cross-reactive antibody strategies against multiple filoviruses.
Authors
- Asuka Nanbo
- Mori-Kajihara Akina
- Gavriella Siman-Tov
- Takeshi Saito (ORCID: https://orcid.org/0000-0002-6908-0702)
- Kirsten Littlefield (ORCID: https://orcid.org/0000-0002-6019-0673)
- Risa Hayashi
- Wakako Furuyama (ORCID: https://orcid.org/0000-0001-7163-6960)
- H. Miyamoto
- Ruchi Paroha
- Manabu Igarashi
- Christine Click
- Slobodan Paessler
- Ayato Takada
- Junki Maruyama
Institutions
- Hokkaido University (JP)
- Sapporo International University (JP)
- University of Zambia (ZM)
- Nagasaki University (JP)
- The University of Texas Medical Branch at Galveston (US)
- Hokkai Gakuen University (JP)
Publication Details
- Journal
- npj Viruses
- Published
- 2025-12-27
- DOI
- https://doi.org/10.1038/s44298-025-00168-z
- Primary Topic
- Viral Infections and Outbreaks Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- John S. Dunn Foundation
- Japan Agency for Medical Research and Development
- Japan Society for the Promotion of Science