Introduction: Marburg virus disease (MVD) is a highly lethal filovirus infection with case fatality rates of up to 88%. Although no virus-specific interventions have yet been approved, recent laboratory breakthroughs have markedly accelerated translational progress in vaccine and therapeutic development. Areas covered: A hybrid methodological design was employed, combining macro-level bibliometric analysis with a targeted qualitative narrative review. As per the findings, the human monoclonal antibody MR191N provides complete post-exposure protection in non-human primates. Advanced RNA-targeted siRNAs, antisense oligonucleotides, and small-molecule nucleoside analogues (e.g. galidesivir) demonstrate robust preclinical efficacy in suppressing viral replication. Prophylactic platforms–including adenovirus-vectored (ChAd3-MARV), rVSV-MARV, and mRNA-based vaccines–are progressing through early-phase clinical and preclinical evaluation. Bibliometric analysis, however, reveals pronounced geographic disparities: high-income nations dominate scientific output (United States: 31.7%), while endemic African countries remain severely underrepresented in global collaboration networks. Expert opinion: Addressing MVD requires a coordinated transition from experimental research to licensed, field-ready interventions. This necessitates adaptive trial designs, expanded diagnostic models, and synergistic combination therapies. Ultimately, correcting global research inequities and embedding robust, cross-border One Health surveillance infrastructure are essential to transforming scientific advances into equitable, rapid-response solutions for endemic regions.
Advances in therapeutics and vaccines for Marburg virus disease: challenges and future directions
Branda, Francesco;
2026-01-01
Abstract
Introduction: Marburg virus disease (MVD) is a highly lethal filovirus infection with case fatality rates of up to 88%. Although no virus-specific interventions have yet been approved, recent laboratory breakthroughs have markedly accelerated translational progress in vaccine and therapeutic development. Areas covered: A hybrid methodological design was employed, combining macro-level bibliometric analysis with a targeted qualitative narrative review. As per the findings, the human monoclonal antibody MR191N provides complete post-exposure protection in non-human primates. Advanced RNA-targeted siRNAs, antisense oligonucleotides, and small-molecule nucleoside analogues (e.g. galidesivir) demonstrate robust preclinical efficacy in suppressing viral replication. Prophylactic platforms–including adenovirus-vectored (ChAd3-MARV), rVSV-MARV, and mRNA-based vaccines–are progressing through early-phase clinical and preclinical evaluation. Bibliometric analysis, however, reveals pronounced geographic disparities: high-income nations dominate scientific output (United States: 31.7%), while endemic African countries remain severely underrepresented in global collaboration networks. Expert opinion: Addressing MVD requires a coordinated transition from experimental research to licensed, field-ready interventions. This necessitates adaptive trial designs, expanded diagnostic models, and synergistic combination therapies. Ultimately, correcting global research inequities and embedding robust, cross-border One Health surveillance infrastructure are essential to transforming scientific advances into equitable, rapid-response solutions for endemic regions.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
