A new meta-analysis of 16 studies reveals that, for pre-exposure prophylactic vaccination (PrEP, which is used for disease prevention), the vaccine effectiveness (VE) of one Jynneos dose ranged from 35% to 86%, and VE for post-exposure prophylactic vaccination ranged from 78% and 89% for one dose.
The findings are published on the preprint server medRxiv and represent the most current evidence of vaccine protection offered by Jynneos, Bavarian Nordic's two-dose vaccine used for the past 2 years to fight a global mpox outbreak. The study has not yet been peer-reviewed.
As of February 2024, more than 94,000 confirmed mpox cases have been documented in 117 countries in an outbreak that mostly affected men who have sex with men. Jynneos, also called MVA-BN, can be administered prophylactically either before or after exposure to confirmed mpox cases in two doses, administered 28 days apart.
The analysis included data from six countries: the United States, Canada, Spain, the United Kingdom, Israel, and the Netherlands.
Different administration routes protective
In eight studies, the VE of one dose of MVA-BN administered as PrEP was 35% to 86%, while five studies reported two-dose adjusted VE estimates ranging from 66% to 90%.
Two studies also provided VE estimates for administering Jynneos with intradermal injection or subcutaneously, and found similar ranges of protection regardless of administration route: 80% (95% confidence interval [CI], 23% to 95%) for intradermal administration, 89% (95% CI, 56% to 97%) for subcutaneous administration, and 87% (95% CI, 69% to 95%) when administered via a combination.
The authors conclude that the findings "demonstrated the effectiveness of one or two doses of MVA-BN against symptomatic mpox infection in outbreak settings."