Self-replicating RNA vaccines delivered by viral replicon particles (VRPs) induce strong immunity, but repeated dosing on short intervals may be limited by vector responses. In patient samples and mice, VRP-srRNA vaccination generated VRP-neutralizing antibodies and T-cell responses to replicase. In mice, a third dose at two-week intervals minimally boosted transgene immunity, and prior VRP exposure reduced responses to a different-transgene VRP. Optimized schedules or heterologous prime–boost may sustain immunogenicity.
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Ma et al. (Mon,) studied this question.
www.synapsesocial.com/papers/69ba424e4e9516ffd37a266e — DOI: https://doi.org/10.1038/s41541-026-01423-x
Xingru Ma
Robert D. Marek
Susannah Gammell
npj Vaccines
Duke University
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