Although the p -value was between 0.05 and 0.1, which is marginally significant, this observation suggests that the M protein mutant rVSVs have a slower replication rate in vivo, leading to enhanced reactogenicity compared to rVSV-JN.1.
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Development of COVID-19 Vaccine Candidates Using Attenuated Recombinant Vesicular Stomatitis Virus Vectors with M Protein Mutations.
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