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Modeling suggests that multiple immunizations or infections will reveal the benefits of updating SARS-CoV-2 vaccines
Rajat Desikan; Susanne L Linderman; Carl W. Davis; Veronika I Zarnitsyna; Hasan R Ahmed; Rustom Antia.
Affiliation
  • Rajat Desikan; GSK
  • Susanne L Linderman; Emory University
  • Carl W. Davis; Emory University School of Medicine
  • Veronika I Zarnitsyna; Emory University School of Medicine
  • Hasan R Ahmed; Emory University
  • Rustom Antia; Emory University
Preprint in English | bioRxiv | ID: ppbiorxiv-492928
ABSTRACT
When should vaccines to evolving pathogens such as SARS-CoV-2 be updated? Our computational models address this focusing on updating SARS-CoV-2 vaccines to the currently circulating Omicron variant. Current studies typically compare the antibody titers to the new variant following a single dose of the original-vaccine versus the updated-vaccine in previously immunized individuals. These studies find that the updated-vaccine does not induce higher titers to the vaccine-variant compared with the original-vaccine, suggesting that updating may not be needed. Our models recapitulate this observation but suggest that vaccination with the updated-vaccine generates qualitatively different humoral immunity, a small fraction of which is specific for unique epitopes to the new variant. Our simulations suggest that these new variant-specific responses could dominate following subsequent vaccination or infection with either the currently circulating or future variants. We suggest a two-dose strategy for determining if the vaccine needs updating and for vaccinating high-risk individuals.
License
cc_by_nc_nd
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Observational study / Prognostic study / Qualitative research Language: English Year: 2022 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Type of study: Observational study / Prognostic study / Qualitative research Language: English Year: 2022 Document type: Preprint
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