4.8 Article

mRNA-based COVID-19 vaccine boosters induce neutralizing immunity against SARS-CoV-2 Omicron variant

Journal

CELL
Volume 185, Issue 3, Pages 457-+

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2021.12.033

Keywords

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Funding

  1. DZIF (German Center for Infection Research) [TTU 01.709, 8009701709]
  2. National Institute of General Medical Sciences [T32GM007753]
  3. National Institute of Allergy and Infectious Diseases [F30 AI160908]
  4. VIC Innovation Fund
  5. NIH [R01 AI146779]
  6. Massachusetts Consortium on Pathogenesis Readiness (MassCPR) grant
  7. Peter and Ann Lambertus Family Foundation
  8. Medscape Young Investigators Lung Cancer Award
  9. National Institute on Drug Abuse (NIDA) Avenir New Innovator Award [DP2DA040254]
  10. MGH Transformative Scholars Program
  11. [T32AI007245]

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Recent surveillance has identified the emergence of the SARS-CoV-2 Omicron variant, which carries up to 36 mutations in the spike protein and has the potential to evade vaccine-induced immunity. This study found that individuals vaccinated with mRNA vaccines exhibited strong neutralization of the Omicron variant, while most vaccinees had weak neutralization. The study also revealed that the Omicron variant infects more efficiently than other tested variants.
Recent surveillance has revealed the emergence of the SARS-CoV-2 Omicron variant (BA.1/B.1.1.529) harboring up to 36 mutations in spike protein, the target of neutralizing antibodies. Given its potential to escape vaccine-induced humoral immunity, we measured the neutralization potency of sera from 88 mRNA-1273, 111 BNT162b, and 40 Ad26.COV2.S vaccine recipients against wild-type, Delta, and Omicron SARS-CoV-2 pseudoviruses. We included individuals that received their primary series recently (<3 months), distantly (6-12 months), or an additional boosterdose, while accounting for prior SARS-CoV-2 infection. Remarkably, neutralization of Omicron was undetectable in most vaccinees. However, individuals boosted with mRNA vaccines exhibited potent neutralization of Omicron, only 4-6-fold lower than wild type, suggesting enhanced cross-reactivity of neutralizing antibody responses. In addition, we find that Omicron pseudo virus infects more efficiently than other variants tested. Overall, this study highlights the importance of additional mRNA doses to broaden neutralizing antibody responses against highly divergent SARS-CoV-2 variants.

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