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A recombinant live attenuated mumps vaccine based on the Jeryl Lynn strain but engineered to express the fusion (F) and hemagglutinin-neuraminidase (HN) proteins from circulating F or G genotypes of the mumps virus. This design aims to improve immunogenicity and efficacy against currently circulating strains that differ antigenically from older vaccine strains. The construct includes a mutation in the viral protein V gene to reduce virulence while maintaining attenuation, minimizing risks such as aseptic meningitis seen with some previous vaccines. The platform allows for rapid adaptation to new genotypes by facilitating exchange of key antigenic genes. Preclinical studies show robust immune responses and broad protection against divergent strains[1][3][4][5]. The primary indication is prevention of mumps infection.
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