An Update on Mpox: Focussing on Current and Emerging Antiviral Strategies

The 2022 global mpox outbreak and subsequent viral evolution have exposed critical limitations in current therapeutic strategies, which predominantly rely on repurposed smallpox drugs targeting a narrow range of viral proteins. This review provides a timely and comprehensive evaluation of the mpox antiviral landscape, spanning from established clinical agents to cutting-edge preclinical candidates. We critically analyse the 'clinical translation gap' observed in recent clinical trials (e.g., STOMP and PALM007), attributing the limited efficacy in mild cases to host immunopathological responses versus primary viral replication. Highlighting a strategic paradigm shift, we also discuss the 2025 breakthrough in covalent inhibitors targeting the conserved CorePro. Furthermore, we explore the integration of AI-assisted drug design and host-targeted therapies (HTTs) to elevate resistance barriers. By synthesising these emerging targets and multidimensional strategies, this review serves as a strategic roadmap for developing next-generation anti-mpox therapeutics with optimised efficacy and broader resistance profiles.

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Publication Details

Journal
Reviews in Medical Virology
Published
2026-02-16
DOI
https://doi.org/10.1002/rmv.70116
Primary Topic
Poxvirus research and outbreaks
Type
article
Field-Weighted Citation Impact
0.00
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article

An Update on Mpox: Focussing on Current and Emerging Antiviral Strategies

YiZhuo Hou, Jin Ding, Jixi Li, Yu Su
Reviews in Medical Virology
Poxvirus research and outbreaks
article

An Update on Mpox: Focussing on Current and Emerging Antiviral Strategies

YiZhuo Hou, Jin Ding, Jixi Li, Yu Su
article en

Abstract

The 2022 global mpox outbreak and subsequent viral evolution have exposed critical limitations in current therapeutic strategies, which predominantly rely on repurposed smallpox drugs targeting a narrow range of viral proteins. This review provides a timely and comprehensive evaluation of the mpox antiviral landscape, spanning from established clinical agents to cutting-edge preclinical candidates. We critically analyse the 'clinical translation gap' observed in recent clinical trials (e.g., STOMP and PALM007), attributing the limited efficacy in mild cases to host immunopathological responses versus primary viral replication. Highlighting a strategic paradigm shift, we also discuss the 2025 breakthrough in covalent inhibitors targeting the conserved CorePro. Furthermore, we explore the integration of AI-assisted drug design and host-targeted therapies (HTTs) to elevate resistance barriers. By synthesising these emerging targets and multidimensional strategies, this review serves as a strategic roadmap for developing next-generation anti-mpox therapeutics with optimised efficacy and broader resistance profiles.

Reviews in Medical VirologyVol. 36(2)
University of Shanghai for Science and Technology (CN), Fudan University (CN)
Openalex Percentile: Top 55%
Poxvirus research and outbreaks
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