SARS-CoV-2 vaccine-induced antibodies protect against Omicron breakthrough infection

Eva A M Baerends, Astrid K Hvidt*, Joanne Reekie, Ole S Søgaard, Nina B Stærke, Dorthe Raben, Henrik Nielsen, Kristine T Petersen, Maria R Juhl, Isik S Johansen, Susan O Lindvig, Lone W Madsen, Lothar Wiese, Lene S Knudsen, Mette B Iversen, Thomas Benfield, Kasper Iversen, Sidsel D Andersen, Anna K Juhl, Lisa L DietzSigne R Andreasen, Thea K Fischer, Christian Erikstrup, Palle Valentiner-Branth, Jens Lundgren, Lars Østergaard, Martin Tolstrup, ENFORCE Study Group

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

3 Citations (Scopus)
33 Downloads (Pure)

Abstract

SARS-CoV-2 Omicron quickly spread globally, also in regions with high vaccination coverage, emphasizing the importance of exploring the immunological requirements for protection against Omicron breakthrough infection. The test-negative matched case-control study (N = 964) characterized Omicron breakthrough infections in triple-vaccinated individuals from the ENFORCE cohort. Within 60 days before a PCR test spike-specific IgG levels were significantly lower in cases compared to controls (GMR [95% CI] for BA.2: 0.83 [0.73-0.95], p = 0.006). Multivariable logistic regression showed significant associations between high antibody levels and lower odds of infection (aOR [95% CI] for BA.2 spike-specific IgG: 0.65 [0.48-0.88], p = 0.006 and BA.2 ACE2-blocking antibodies: 0.46 [0.30-0.69], p = 0.0002). A sex-stratified analysis showed more pronounced associations for females than males. High levels of vaccine-induced antibodies provide partial protection against Omicron breakthrough infections. This is important knowledge to further characterize a threshold for protection against new variants and to estimate the necessity and timing of booster vaccination.

Original languageEnglish
Article number107621
JournaliScience
Volume26
Issue number9
Number of pages14
ISSN2589-0042
DOIs
Publication statusPublished - 15 Sept 2023

Bibliographical note

© 2023 The Author(s).

Keywords

  • Immune response
  • Immunology
  • Molecular medicine

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