Key result
ARCT-154 spike protein clears rapidly from muscle but persists in lymph nodes for ~28 days.
Why the study?
The scientific evidence explaining why the self-amplifying mRNA vaccine ARCT-154 induces higher and more sustained neutralizing antibodies than the conventional mRNA vaccine BNT162b2 remained elusive.
Prolonged lymph node retention may drive superior antibody durability; extends sa-mRNA biodistribution data in preclinical models.
ARCT-154, a recently approved self-amplifying mRNA (saRNA) vaccine, has been shown in clinical trials to induce higher levels of neutralizing antibodies and sustain them for a longer time than the conventional mRNA vaccine BNT162b2. However, the scientific evidence explaining this superiority remain elusive. Hence, we explored the temporal changes in spike protein and replicase components following a single dose of ARCT-154 vaccination in mice. The encoded spike protein reached its highest level approximately 3 days after vaccination and quickly disappeared from the rectus femoris muscle, the injection site. Although the spike protein levels also peaked at an early time point in the lymph nodes, it remained detectable 28 days after the vaccination and then disappeared by 44 days after the vaccination. Expression of nsP1, nsP2 and nsP4 was observed in the injected muscle and/or the lymph nodes for up to 15 days post-vaccination. These data suggest that prolonged expression of spike proteins in lymph nodes may, if not entirely, be responsible for the induction of higher and prolonged levels of neutralizing antibodies by the saRNA vaccine.
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Kanechi et al. (2024) studied Healthy (vaccine biodistribution) (n=45). ARCT-154 vs. Non-immunized baseline was evaluated on Temporal changes and clearance rate of SARS-CoV-2 spike protein and replicase components in tissues. Following a single dose of the ARCT-154 self-amplifying mRNA vaccine in mice, the encoded spike protein was rapidly cleared from the injection site muscle but remained detectable in lymph nodes for up to 28 days.
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