Determining the optimal SARS-CoV-2 mRNA vaccine dosing interval for maximum immunogenicity

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dc.contributor.author
Asamoah-Boaheng, Michael
Goldfarb, David M.
Prusinkiewicz, Martin A.
Golding, Liam
Karim, Ehsanul
Barakauskas, Vilte
Wall, Nechelle
Jassem, Agatha N.
Marquez, Ana Citlali
MacDonald, Chris
O’Brien, Sheila F.
Lavoie, Pascal
Grunau, Brian
dc.date.accessioned
2025-02-05T21:32:36Z
dc.date.available
2025-02-05T21:32:36Z
dc.date.issued
2022-03-04
dc.description.abstract - en
<p>Objective Emerging evidence indicates that longer SARS-CoV-2 vaccine dosing intervals results in an enhanced immune response. However, the optimal vaccine dosing interval for achieving maximum immunogenicity is unclear.</p> <p>Methods This study included samples from adult paramedics in Canada who received two doses of either BNT162b2 or mRNA-1273 vaccines and provided blood samples 6 months (170 to 190 days) after the first vaccine dose. The main exposure variable was vaccine dosing interval (days), categorized as “short” (first quartile), “moderate” (second quartile), “long” (third quartile), and “longest” interval (fourth quartile). The primary outcome was total spike antibody concentrations, measured using the Elecsys SARS-CoV-2 total antibody assay. Secondary outcomes included: spike and RBD IgG antibody concentrations, and inhibition of angiotensin-converting enzyme 2 (ACE-2) binding to wild-type spike protein and several different Delta variant spike proteins. We fit a multiple log-linear regression model to investigate the association between vaccine dosing intervals and the antibody concentrations.</p> <p>Results A total of 564 adult paramedics (mean age 40 years, SD=10) were included. Compared to “short interval” (≤30 days), higher dosing interval quartiles (moderate: 31-38 days; long: 39-73 days and longest: ≥74 days) were all associated with increased Elescys spike total antibody concentration. Compared to the short interval, “long” and “longest” interval quartiles were associated with higher spike and RBD IgG antibody concentrations. Similarly, increasing dosing intervals increased inhibition of ACE-2 binding to viral spike protein, regardless of the vaccine type.</p> <p>Conclusion Increased mRNA vaccine dosing intervals longer than 30 days result in higher levels of circulating antibodies and viral neutralization when assessed at 6 months.</p>
dc.description.sponsorship
This study was supported by funding from Government of Canada, through the COVID-19 Immunity Task Force. M.E.K. is supported in part by a Scholar Award from the Michael Smith Foundation for Health Research, partnered with Centre for Health Evaluation and Outcome Sciences. B.G. is supported by the Michael Smith Foundation for Health Research.
dc.identifier.doi
https://doi.org/10.1101/2022.03.01.482592
dc.identifier.uri
https://open-science.canada.ca/handle/123456789/3397
dc.language.iso
en
dc.publisher - en
bioRxiv
dc.relation.isreplacedby
http://dx.doi.org/10.7759/cureus.34465
dc.rights - en
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
dc.rights - fr
Creative Commons Attribution - Pas d'utilisation commerciale - Pas de modification 4.0 International (CC BY-NC-ND 4.0)
dc.rights.uri - en
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.uri - fr
https://creativecommons.org/licenses/by-nc-nd/4.0/deed.fr
dc.subject - en
Health
Coronavirus diseases
Immunization
dc.subject - fr
Santé
Maladie à coronavirus
Immunisation
dc.subject.en - en
Health
Coronavirus diseases
Immunization
dc.subject.fr - fr
Santé
Maladie à coronavirus
Immunisation
dc.title - en
Determining the optimal SARS-CoV-2 mRNA vaccine dosing interval for maximum immunogenicity
dc.type - en
Submitted manuscript
dc.type - fr
Manuscrit soumis
local.peerreview - en
No
local.peerreview - fr
Non
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